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Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model

  • Jully Gogoi-Tiwari,

    Affiliations School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia, College of Veterinary Sciences and Animal Husbandry, Central Agricultural University, Selesih, Aizawl, Mizoram, India

  • Vincent Williams,

    Affiliation School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia

  • Charlene Babra Waryah,

    Affiliations School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia, Department of Medicine and Cell Biology, Albert Einstein College of Medicine, Bronx, New York, United States of America

  • Paul Costantino,

    Affiliation School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia

  • Hani Al-Salami,

    Affiliation School of Pharmacy, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia

  • Sangeetha Mathavan,

    Affiliation School of Pharmacy, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia

  • Kelsi Wells,

    Affiliation School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia

  • Harish Kumar Tiwari,

    Affiliation School of Veterinary and Life Sciences, Murdoch University, Perth, Western Australia, Australia

  • Nagendra Hegde,

    Affiliation Ella Foundation, Genome Valley, Hyderabad, India

  • Shrikrishna Isloor,

    Affiliation Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Bangalore, India

  • Hesham Al-Sallami,

    Affiliation School of Pharmacy, University of Otago, Dunedin, New Zealand

  • Trilochan Mukkur

    tk_mukkur@hotmail.com

    Affiliation School of Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, Western Australia, Australia

Mammary Gland Pathology Subsequent to Acute Infection with Strong versus Weak Biofilm Forming Staphylococcus aureus Bovine Mastitis Isolates: A Pilot Study Using Non-Invasive Mouse Mastitis Model

  • Jully Gogoi-Tiwari, 
  • Vincent Williams, 
  • Charlene Babra Waryah, 
  • Paul Costantino, 
  • Hani Al-Salami, 
  • Sangeetha Mathavan, 
  • Kelsi Wells, 
  • Harish Kumar Tiwari, 
  • Nagendra Hegde, 
  • Shrikrishna Isloor
PLOS
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Abstract

Background

Biofilm formation by Staphylococcus aureus is an important virulence attribute because of its potential to induce persistent antibiotic resistance, retard phagocytosis and either attenuate or promote inflammation, depending upon the disease syndrome, in vivo. This study was undertaken to evaluate the potential significance of strength of biofilm formation by clinical bovine mastitis-associated S. aureus in mammary tissue damage by using a mouse mastitis model.

Methods

Two S. aureus strains of the same capsular phenotype with different biofilm forming strengths were used to non-invasively infect mammary glands of lactating mice. Biofilm forming potential of these strains were determined by tissue culture plate method, ica typing and virulence gene profile per detection by PCR. Delivery of the infectious dose of S. aureus was directly through the teat lactiferous duct without invasive scraping of the teat surface. Both bacteriological and histological methods were used for analysis of mammary gland pathology of mice post-infection.

Results

Histopathological analysis of the infected mammary glands revealed that mice inoculated with the strong biofilm forming S. aureus strain produced marked acute mastitic lesions, showing profuse infiltration predominantly with neutrophils, with evidence of necrosis in the affected mammary glands. In contrast, the damage was significantly less severe in mammary glands of mice infected with the weak biofilm-forming S. aureus strain. Although both IL-1β and TNF-α inflammatory biomarkers were produced in infected mice, level of TNF-α produced was significantly higher (p<0.05) in mice inoculated with strong biofilm forming S. aureus than the weak biofilm forming strain.

Conclusion

This finding suggests an important role of TNF-α in mammary gland pathology post-infection with strong biofilm-forming S. aureus in the acute mouse mastitis model, and offers an opportunity for the development of novel strategies for reduction of mammary tissue damage, with or without use of antimicrobials and/or anti-inflammatory compounds for the treatment of bovine mastitis.

Introduction

Despite advances in diagnosis and management practices aimed at reducing the incidence of ruminant mastitis associated with the contagious pathogens, Staphylococcus aureus (S. aureus) is one of the major contagious causative agents of clinical and subclinical bovine mastitis worldwide causing significant economic loss to the dairy industry [13]. Reduced milk production due to mastitis is associated with irreversible mammary tissue damage in majority of the cases [4]. A wide array of virulence factors including surface-associated polysaccharide antigens including capsular polysaccharides (CP), teichoic acid (TA) and Poly-β-1, 6-N-acetylglucosamine (PNAG), MSCRAMM (microbial surface components recognizing adhesive matrix molecules), cytotoxins and enterotoxins are produced by S. aureus, which compromise host’s innate and adaptive immune systems [5, 6], resulting in the establishment of infection. Staphylococcus aureus enters the mammary gland, most likely via the orifice of chapped or injured teats [7]. Once the organism enters into the mammary gland, it adheres to epithelial cell receptors for bacterial adhesins [8] resulting in the production of virulence factors mentioned above and intracellular uptake of the small colony variants of S. aureus. Once the intra-mammary infection is established, damage to the mammary gland epithelial lining is initiated by ulceration and occlusion of lactiferous ducts, alveoli and infiltration of inflammatory cells in the parenchyma [4]. Mammary tissue damage is further compounded by various toxins and extracellular enzymes produced by S. aureus, including α, β, γ, and δ toxins, toxic shock syndrome toxin (TSST-1), enterotoxins, nuclease, coagulase, catalase, hyaluronidase, phosphatase, lipase, staphylokinase and proteases [9]. Some toxins act as super-antigens promoting the release of inflammatory cytokines, while others are leukocidins and cytolysins including haemolysins [10, 11]. Inflow of somatic cells, predominantly of polymorphonuclear (PMN) leukocytes into mammary gland is possibly due to breach of blood-milk barrier, worsens the damage to mammary epithelial cells owing to release of proteolytic enzymes and superoxide resulting in mammary tissue damage [12].

Staphylococcus aureus is capable of forming biofilms on both natural body surfaces and medical devices including indwelling catheters and prostheses resulting in acute or chronic infections [13]. Biofilm is a cluster of bacterial cells, extracellular matrix and water which is more tolerant to host defense mechanism and antibiotics [14] facilitating chronic infections [1518]. The ability to produce biofilm by S. aureus in the mammary gland has been demonstrated both in vitro [19] and in vivo [20]. Development of biofilm by S. aureus has been proposed to occur in two steps. Regardless of the clinical manifestation of mastitis, acute/clinical or chronic/subacute/subclinical [21], the 1st step is the adherence of S. aureus cells to mammary epithelial cells via microbial surface component recognizing adhesive matrix molecules (MSCRAMMs), including fibrinogen binding proteins (ClfA, ClfB), collagen binding protein (Cna), fibronectin binding proteins (FnBpA, FnBPB) and bone sialoprotein binding protein (BBP) [2225]. Biofilm forming S. aureus can attach to mammary epithelium more efficiently than non-biofilm forming S. aureus [26, 27]. The 2nd step involves multiplication, interaction and accumulation of adherent S. aureus cells embedded by bacterial extracellular matrix. The main constituent of extracellular matrix accredited for its role in the formation of biofilms by S. aureus is the polysaccharide intercellular adhesion (PIA) comprised of poly-β-1, 6-linked N-acetylglucosamine (PNAG) synthesized by icaADBC [28]. PNAG, a surface-associated polysaccharide is the most studied virulence factor associated with biofilm formation by S. aureus. However, ica-independent biofilm formation by S. aureus has also been reported, albeit in a small percentage of clinical isolates [29] suggesting potential importance of MSCRAMM and secretory proteins in replacing the function of PIA [30, 31]. Cytolytic toxins produced by S. aureus such as alpha (hla) and beta (hlb) have also been reported to be important in biofilm formation [32]. Alpha-toxin is required for cell-cell interactions during biofilm formation [10], whereas beta-toxin forms covalent cross-links to self to form insoluble nucleoprotein matrix in the presence of DNA in the staphylococcal biofilm [32]. Both alpha (α) and beta (β) toxins can directly damage milk-producing tissue by destruction of the mammary epithelial cells lining the teats and gland cisterns within the quarter. This eventually leads to establishment of deep-seated pockets of infection in the milk secreting cells (alveoli) and formation of scar tissue in acute mastitis, comparable to the formation of chronic wounds due to biofilm-mediated infection of the skin with this pathogen [33]. Other S. aureus proteins that potentially may be associated with biofilm formation include the immune evasion molecule, protein A [34], and biofilm-associated protein, Bap [35].

Staphylococcus aureus in biofilm is different from its planktonic state in various aspects including phenotypes [36], antibiotic resistance patterns [15] and innate immune responses [37]. More recently, it was demonstrated that S. aureus in biofilm induced stronger and differential immune responses against experimentally induced acute mastitis in mice than planktonic cultures [29]. Although many chronic infections are associated with bacteria in biofilm state as there is aggregation of colonies producing exopolysaccharide matrix offering resistance against phagocytosis and antibiotics [15], acute infection can also lead to the establishment of chronic carrier state. Baselga and co-workers (1993) compared slime producing (SP) versus non-slime producing (NSP) S. aureus in-vitro and in-vivo, and reported the NSP S. aureus strains to be more virulent than SP strains whereas the latter strains were more important in colonisation of mammary tissue [26]. Due to the ability of S. aureus in biofilm to induce inflammatory responses distinct from those induced by planktonic cultures [37, 38], it is important to know the extent of mammary tissue damage associated with infection of the mammary gland with strong biofilm forming versus weak or non-biofilm forming S. aureus. A pilot study by Breyne and co-workers [39] aimed at determining the differences between bovine associated coagulase-negative staphylococci (CNS) versus the laboratory S. aureus Newbould 305 strain. Bacterial inoculum containing low colony forming units (CFU) representing chronic or subclinical bovine mastitis in the non-invasive mouse model [40] resulted significantly lower bacterial growth of CNS versus the laboratory S. aureus strain. While S. aureus was reported to induce IL-6 and IL- 1β locally but not TNF-α, the CNS-infected mammary glands lacked strong cytokine host response [39]. This was in contrast to expression and induction/production of high levels of IL- 1β and TNF-α, with a low level of IL-6 in the plasma [41] in which the mouse mammary glands were infected with low CFUs of a clinical S. aureus isolate. However, no studies on the impact of biofilm formation on production of cytokines and mammary tissue damage were conducted. Our pilot study, presented in this communication, provides this information adding new knowledge in the area of bovine mastitis. Bovine mastitis in dairy cattle can manifest as clinical or acute, or subclinical/subacute, latter frequently leading to development of chronic mastitis [21]. Due to paucity of knowledge of the mammary gland pathology and cytokine profiles post-infection with strong biofilm-forming versus weak biofilm-forming S. aureus, this pilot study was carried out. Because of limited knowledge on the relative contribution of individual surface-associated antigens, such as polysaccharides (CP, TA, PNAG), MSCRAMM proteins and/or toxins to biofilm formation,in vitro or in vivo, it was decided to use S. aureus clinical isolates with the desired biofilm forming properties in this pilot study. The inflammatory cytokine response of lactating mice infected with large doses of strong versus weak biofilm-forming S. aureus to induce acute mastitis, suggested potential association of mammary tissue damage with high levels of TNF-α. Although IL-1β production was significantly greater in infected versus placebo mice also, there was no significant difference between the levels produced post-infection of the mammary glands with strong versus weak biofilm-forming S. aureus. The overall similarity of the cytokine profile induced by infection of the mammary gland with low [41] or high CFUs of S. aureus (this study) offers opportunities for development of treatment strategies aimed at eliminating or reducing mammary tissue damage in acute clinical bovine mastitis with or without the use of antibiotics and/or anti-inflammatory molecules.

Materials and Methods

Bovine S. aureus phenotypes

Two capsular polysaccharide-8 (CP8) positive S. aureus strains, isolated from mastitic milk of cows, with strong or weak biofilm forming potential, were used in this study (Table 1). These strains were selected from a collection of 154 strains, obtained through the courtesy of Professor Margaret Deighton, (RMIT University), Dr. Sharon de Wet (Queensland Biosecurity laboratory) and Dr. Justine Gibson (University of Queensland). These strains were collected from cows in dairy farms in Victoria and Queensland, Australia suffering from both clinical and subclinical mastitis. Selection of these strains was solely on the basis of in vitro biofilm forming ability [42] and presence or absence of biofilm-associated intercellular adhesin genes, icaA and icaD [6].

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Table 1. Phenotypic and genotypic characteristics of S. aureus strains used in this study.

https://doi.org/10.1371/journal.pone.0170668.t001

Capsular typing of S. aureus isolates

Capsular typing of the two S. aureus strains used in this investigation was carried out using molecular as well as serological methods as described elsewhere [43]. Briefly, genomic DNA was extracted from 2 strains of S. aureus using extraction kit (MO BIO laboratories, Inc, Carlsbad, CA). Conventional Polymerase Chain Reaction (PCR) was carried out using the cycling parameters for cap1, cap5 and cap8 described previously [43]. The primers used for typing cap1 are 5’-AGG TCT GCT AAT TAG TGC AA-3’ (forward) and 5’-GAA CCC AGT ACA GGT ATC ACC A-3’ (reverse) with an expected band size of 550bp. The primers used for typing cap5 and cap8 were 5′-GTC AAA GAT TAT GTG ATG CTA CTG AG-3′ (forward) and 5′-ACT TCG AAT ATA AAC TTG AAT CAA TGT TAT ACA G-3′ (reverse) for cap5 [42, 44] and 5′-GCC TTA TGT TAG GTG ATA AAC C-3′ (forward) and 5′-GGA AAA ACA CTA TCA TAG CAG G-3′ (reverse) for cap8 [43, 45], respectively. The expected band size for cap5 and cap8 were 881 bp and 1148 bp, respectively. Strain M, strain Newman and USA 400 and were used as positive control for cap1, cap5 and cap8 respectively, and LAC (USA 300) was used as negative control. For serological typing of S. aureus isolates, CP-specific antisera (CP 1, 2, 5 and 8) were produced using Quackenbush Swiss line 5 mice after gaining approval from the Animal Ethics Committee of Curtin University (Approval number: AEC_2011_65). The preparation of the vaccines for infection of mice and production of CP-specific sera were carried out according to the methods described elsewhere [46]. Strain M, strain Smith diffuse, strain Newman and USA 400 were used for production of CP1, 2, 5 and 8—specific sera, respectively. A slide agglutination test to determine the serotype of the four strains was carried out as described previously [46].

Determination of biofilm forming potential of S. aureus isolates

Biofilm assay.

Biofilm forming characteristics of the strains were determined using the Tissue Culture Plate method as described previously [42, 47].

Tissue culture plate method.

S. aureus strains were inoculated in 200 μL of nutrient broth supplemented with 1% glucose in a 96-well sterile microtiter plate [48]. The plates were left overnight in a 37°C incubator to ensure adequate biofilm production. This was followed by assessment of their biofilm-forming property using the following method:

Crystal violet staining.

This method, which measures the amount of biofilm attached to the polystyrene plate, was an adaptation of the procedures described elsewhere [47, 49]. S. aureus strains were grown to produce biofilm in a 96-well micro titre plate. The plates were washed with phosphate buffer saline (PBS) [pH 7.2] to remove planktonic or free-floating bacteria [49]. The biofilm was fixed at 55°C for 10 mins and stained with 2% crystal violet. Biofilms were de-stained with alcohol and read using a microplate reader at 570 nm. The assay was repeated three times and the data averaged. The arbitrary cut-off points for non-biofilm former, weak-biofilm former, intermediate and strong biofilm formers were 0.120 A570nm, 0.130–4.00 x 0.120 A570nm, 4.10–5.90 x 0.120 A570nm and greater than 6 x 0.120 A570nm, respectively [50].

ica typing of S. aureus isolates

The ica typing of the isolates was performed as per the method described elsewhere [51]. Briefly, The primers used for typing icaA [52] were 5’-CCTAACTAACGAAAGGTAG-3’ (forward) and 5’-AAGATATAGCGATAAGTG C-3’ (reverse) and 5’-AAACGTAAGAGAGGTGG-3’ (forward) and 5’-GGCAATATGATCAAGATAC-3’ (reverse) for icaD [52] typing. The expected band size for icaA and icaD were 1315bp and 381bp, respectively. The PCR cycles were run at 95°C for 5mins, 95°C for 30secs, Tm 48°C (icaA) and 47°C (icaD) for 30secs, 72°C for 45secs with 30 cycles and final extension at 72°C for 10 mins. Gel electrophoresis was carried out using 1.5% agarose gel in 1x TAE buffer and visualizing under UV trans-illuminator. The positive control used for this study was USA 400 strain which was positive for both icaA and icaD.

Detection of different virulence genes of S. aureus using PCR

Conventional PCR was carried out to detect MSCRAMM associated and toxin genes of the two S. aureus strains isolated from both clinical and subclinical bovine mastitis cases in Australia. The primers, Tm, for all the MSCRAMM-encoding including icaA icaD (intercellular adhesion molecule, PNAG), cna (collagen-binding adhesion protein), clfA (clumping factor A), clfB (clumping factor B), spa (protein A), fnbpA (fibronectin-binding protein A), fnbpB (fibronectin-binding protein B), bbp (bone sialoprotein binding protein), isdA (iron regulated protein A), isdB (iron regulated protein B), sdrD (serine-aspartate repeat proteins D), sdrE (serine-aspartate repeat proteins E) and bap (biofilm-associated surface protein) and cytolytic toxin genes (hla (haemolysin A), hlb (haemolysin B), pvl (panton-valentine leukocidin) of the two S. aureus strains used in this study have been described elsewhere [6, 51].

Infection of mammary gland

Preparation of bacterial inocula.

The S. aureus strains were grown on Mueller Hinton (MH) agar plates at 37°C for 18h. The organisms were washed from the plates using 20 ml of isotonic saline and suspended in isotonic saline to give a final viable bacterial count of 4 x 1011 ml-1 [53].

Animals.

All animal work described in this investigation was approved by the Animal Ethics Committee of Curtin University (Approval number: AEC_2012_14) prior to commencement of the experiment. The mice were used for the study ensuring compliance with the Western Australian Animal Welfare Act 2002. A total of 12 Balb/c first-pregnancy mice, in three groups of 4 mice each were used for the experiment. Pups were removed from the lactating mice when they were between 5–15 days old, approximately 1h prior to infection of the mammary glands of mice. The pups were euthanized and not allowed to suckle after inoculation of the mammary gland with the S. aureus strains or normal saline in case of the control group of mice.

Method of infection of the mammary gland.

Inoculation of the different S. aureus phenotypes into mammary glands was carried out using a modification to the procedure described previously [54]. The modification involved inoculation of S. aureus strains directly into the mammary duct without making any incision or scraping of the superficial layer of the mammary gland with a scissors or scalpel. Briefly, mice were anaesthetised using 100 mg kg-1 ketamine and 10 mg kg-1 xylazine administered by the intraperitoneal route and laid in the supine position. The area surrounding the 5th pair of mammary glands (L5 and R5) was disinfected with 70% ethanol. A binocular dissecting microscope was used to locate the duct orifice of the teat. While controlling the teats with sterile forceps, 0.05 ml of bacterial suspension equivalent to 2x 1010 CFU S. aureus was injected using a blunt smooth 31-gauge hypodermic needle to a depth of not more than 4mm. The infection was allowed to progress for 48 h and the mice were observed at six-hour intervals to assess development of macroscopic clinical signs of infection. All animals were administered one dose of Buprenorphine hydrochloride (0.05–0.1 mg kg-1) subcutaneously pre-operation so that anticipated pain relief was available for up to 12 h post bacterial inoculation. A control group of mice was injected with normal saline using the same procedure.

Post-inoculation examination

Macroscopic examination.

The mammary glands of mice were examined for the development of mastitis. The clinical signs of mastitis observed were redness, swelling and discoloration of mammary gland, and extrusion of exudate with or without squeezing of the mammary gland. Monitoring of mice for morbidity and mortality was carried out at 6 hourly intervals up to 48h. The level of clinical signs was graded as 0 (no macroscopic changes), + (low) grade, ++ (medium grade) and +++ (severe grade) based on the observed clinical features.

Mice were euthanized 48h after infection, and investigated for the extent of infection by determining the bacterial load [53] as described below, and the mammary gland tissue collected for estimating the level of inflammation and histological changes [53].

Bacteriological procedures for mammary glands and blood.

At post-mortem examination, the L5 mammary glands from control and test mice were collected and individually ground in sterile Griffith’s tubes containing 2 ml of sterile normal saline. The homogenates from the mammary glands were subjected to serial tenfold dilutions and inoculated on Baird Parker (BP) agar plates by the spread plate method and incubated at 37°C for 48h, followed by determination of colony counts of S. aureus per mammary gland.

Blood samples obtained by cardiac puncture were inoculated on BP agar plates by streaking to obtain isolated colonies and incubated at 37°C for 48 h.

Histological procedures

Mammary gland and blood.

After aseptically shaving the hair around the gland the R5 mammary glands were collected for histological examination. The R5 glands were fixed in 10% neutral buffered formalin for 24 h, processed on an automatic tissue processor and embedded in paraffin wax. Sections were cut at 4 μm thickness at three levels and stained by the Haematoxylin and Eosin stain [55]. An additional section was stained for bacteria using Gram Twort Method [56].

Blood smears were prepared following standard procedure and stained by the Diff-Quik method [57].

Grading of histological changes observed in mammary glands.

The histopathological changes observed in mammary glands of mice, infected with different strains of S. aureus, were graded as Level 0 [no inflammatory reaction post-inoculation with PBS (Fig 1a)], Level 1 [minimal inflammatory response in mammary tissue post-inoculation with S. aureus (Fig 1b)], Level 2 [Moderate inflammation in peri-mammary and intramammary tissue post-inoculation with S. aureus, with intra luminal organisms observed (Fig 1b and 1c), and Level 3 [Marked inflammatory cell infiltration into mammary tissue post-inoculation with S. aureus with evidence of tissue degeneration including necrosis (Fig 1d to 1f)].

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Fig 1. Histopathological changes observed in mouse mammary tissue.

Control mouse showing absence of inflammatory response (Level 0) in mammary tissue (A) to inoculation of sterile normal saline, H&E x100, bar, 200 μm (Fig 1a); Level 1 inflammatory response induced in the mouse teat by inoculation of S. aureus via the mammary duct (A), characterized by acute neutrophil rich response in the intraductal exudate, H&E x400, bar, 50 μm (Fig 1b); Level 2 inflammation of the mammary glands (A) Infiltrate of acute inflammatory cells, predominantly neutrophils, in supporting connective tissue, with intraluminal organisms, H&E x200, bar, 100 μm (Fig 1b); Level 2 inflammation of the mammary tissue post-inoculation of mammary gland with S aureus, characterized by infiltration of acute inflammatory cells, predominantly neutrophils (A), in supporting connective tissue and intraluminal space, H&E x200, bar, 100 μm (Fig 1c); Level 3 inflammation of mammary tissue post-inoculation of mammary gland with S. aureus, characterized by marked acute neutrophil rich infiltrate (A) with tissue necrosis (B), H&E x200, bar, 100 μm (Fig 1c); Level 3 inflammation of the mammary tissue post-inoculation of mammary gland with S. aureus, characterized by marked acute neutrophil-rich infiltrate (A) with tissue necrosis (B), H&E x200, bar, 100 μm (Fig 1d); Level 3 inflammation of the mammary tissue post-inoculation of mammary gland with S. aureus, characterized by neutrophil-rich inflammatory exudate, H&E x1000, bar, 20 μm (Fig 1e); Level 3 inflammation of the mammary tissue post-inoculation of mammary gland with S. aureus, characterized by presence of Gram-positive bacteria and neutrophil-rich inflammatory exudate, Gram Twort x400, bar, 50 μm (Fig 1f).

https://doi.org/10.1371/journal.pone.0170668.g001

Quantification of inflammatory cytokines

Quantification of inflammatory cytokines, IL-1β and TNF-α in serum samples of mice was performed by using BD Cytometric Bead Array (CBA) Mouse/Rat soluble protein Master Buffer Kit (BD Biosciences), USA. Preparation of Mouse/Rat soluble protein flex set standards, capture beads and detection reagents were performed as per the standard protocol provided with the reagent kit. Briefly, 50μL of Mouse/Rat soluble protein flex set standard dilutions ranging from 1:2 to 1:256 and one negative control containing only assay diluent was prepared. To 10μL of each unknown serum sample, 10μL of each capture bead and mixed PE detection reagent was added. Tubes were incubated at 4°C for one hour each after addition of capture beads and PE detection reagent protected from light. Following incubation, 200μL of wash buffer was added to each tube and centrifuged at 200g for 5min. The supernatant was aspirated carefully and discarded. The remaining pellet was reconstituted using 200μL of wash buffer and analysed using Attune Acoustic Focussing Flow Cytometer using the FlowJo software.

Statistical analysis

To compare the IL-1β and TNF-α levels, bacterial loads between groups of mice infected with strong biofilm and weak biofilm forming S. aureus phenotypes, student’s t-test was performed using Microsoft Excel. Statistical significance was set at p < 0.05.

Results

Determination of biofilm forming potential of S. aureus isolates

Tissue culture plate (TCP) method.

Between the two S. aureus strains selected for this study, S. aureus strain 51 was strong biofilm former in vitro whereas S. aureus strain 104 was a weak biofilm former in vitro (Table 1).

ica typing of S. aureus isolates.

Staphylococcus aureus strains 51 harboured the icaA and icaD genes encoding production of PNAG whereas these genes were not detectable in S. aureus strain 104.

Detection of different MSCRAMM-encoding genes of S. aureus using conventional PCR.

The virulence-associated genes detected in the two bovine S. aureus strains are shown in Table 1. Both S. aureus strains harboured genes encoding alpha and beta toxin. S. aureus 51 carried icaA icaD, cna, clfA, clfB, spa, isdA, isdB, sdrD and sdrE MSCRAMM genes and also genes encoding alpha and beta haemolysins. S. aureus 104 was found to carry cna, clfB, isdA, isdB, sdrD and sdrE genes, the gene encoding spa and clfA being undetectable (Table 1).

Macroscopic examination of mammary glands.

The control group showed no gross/macroscopic pathological change in the inoculated glands. On the other hand, all the test mice showed varying degrees of change in the gross appearance of mammary glands (Table 2).

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Table 2. Clinical signs observed in mice infected with strong versus weak-biofilm forming S. aureus strains by intra-mammary route (observations up to 48 hours post inoculum).

https://doi.org/10.1371/journal.pone.0170668.t002

Clinical features used to make a judgement on the macroscopic pathology of the mammary glands inoculated with S. aureus strains include redness, swelling, and discolouration of mammary gland, exudate, morbidity and mortality. Macroscopic pathological changes were assigned scores as no change (0) low grade (+), medium grade (++) and severe grade (+++). The criteria used for grading of clinical signs are shown Supporting Information (S1 Table).

Bacterial load and histopathological changes of mammary gland.

The bacterial loads in the mammary glands as a measure of proliferation of S. aureus at the infection site and the associated histopathological grade observed in the mammary tissue are shown in Table 3 and Fig 1. The bacteriological load study demonstrated that mice (M) infected with encapsulated S. aureus strains with in vitro strong biofilm forming ability (S. aureus 51) had higher bacterial count than the encapsulated in vitro weak biofilm producing strain (S. aureus 104). Statistical analysis of the bacterial burden of the mammary glands of mice infected with strong biofilm-forming versus weak biofilm-forming S. aureus strains revealed significant differences in the bacterial load between the different groups (P < 0.001).

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Table 3. Total viable counts of S. aureus recovered from mammary glands 48 h post-harvest and the grade of histopathological changes.

https://doi.org/10.1371/journal.pone.0170668.t003

Histopathological studies showed that mice infected with encapsulated S. aureus with strong biofilm forming characteristics (S. aureus 51) produced severe mastitis lesions characterised as level 3 lesions, showing a profuse inflammatory infiltrate with severe tissue damage including necrosis in mammary tissue. On the other hand, S. aureus strain 104 with weak biofilm forming ability demonstrated only level 2 histopathological changes (Table 3).

Bacteriology of blood and and histopathology of liver, lung and spleen.

The culture of blood and organs (liver, lung and spleen) in BP agar plates was negative for S. aureus consistent with no evidence of systemic infection. No overt microscopic evidence of inflammation was observed in tissue sections of lung, liver and spleen from any of the mice as judged by normal histological appearance (data not shown).

Histopathology of mammary glands pre- or post-infection with biofilm forming S. aureus.

No evidence of inflammatory response was recorded in mammary tissue of control mice which were inoculated with sterile normal saline. The mammary tissue of mice infected with S.aureus 51 demonstrated level 3 inflammation with marked neutrophil rich infiltration and tissue necrosis. The mammary tissue of all the mice infected with S. aureus 104 showed level 2 inflammation characterised by acute inflammatory cells, predominantly neutrophils, in supporting connective tissue and intraluminal spaces (Fig 1).

Quantification of inflammatory cytokines.

Quantification data of inflammatory cytokines, IL-1β and TNF-α is presented in Table 4. The result showed that there was no significant difference in the level of IL-1β produced by strong biofilm forming versus the weak biofilm forming S. aureus strain. However, the levels of TNF-α were significantly higher (p<0.05) in the sera of mice inoculated with strong biofilm forming S. aureus strain 51 versus infection with the weak biofilm forming S. aureus strain 104.

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Table 4. Detection of IL-1β and TNF-α levels in serum samples of mice 48 h post-infection.

https://doi.org/10.1371/journal.pone.0170668.t004

Discussion

Biofilm formation by S. aureus has been studied extensively with respect to methods of detection, potential role in chronicity of infection and resistance to antibiotics and innate immune defences for both human and animal infectious diseases [1315, 38, 41, 58]. Demonstrated ability of S. aureus biofilm to resist innate immune defences against intra-mammary infections (IMI) in the last few years [31, 37, 59, 60] and the difficulty encountered in treating such infections with antibiotics [9] has highlighted the urgency of developing effective vaccines against bovine mastitis. This also highlights the urgency of discovering ways to disperse the biofilms for improvement in the efficacy of the available antibiotics in the treatment of intra-mammary infections. Potential reasons underpinning mammary tissue damage due to S. aureus infection have been reported previously [4, 61]. However, limited studies have been reported on the potential impact of biofilm formation by S. aureus on the integrity of the mammary tissue post-infection with the pathogen [26, 62]. Most studies have been confined to characterization of the inflammatory immune responses to porcine dermal explants [63], murine tibial implants [64], nasal explant model [65] and prosthetic implant infections [64, 66]. Baselga and co-workers (1993) reported slime producing (SP) S. aureus isolates from ruminant mastitis cases to exhibit higher colonisation capacity than the non-slime producing (NSP) variant of the same strain obtained by repeated subculturing on Congo red agar at a medium frequency [26]. The NSP variants were shown to have higher virulence than the SP S. aureus revertants as measured by moderate to severe clinical signs and inflammatory lesions in mammary glands of lactating ewes at 48 h post-infection. It was hypothesized that the SP isolates of S. aureus were responsible for attachment to mammary epithelia and colony formation, whereas the NSP S. aureus variant led to the development of severe mastitis. Since some NSP strains can produce slime in vivo as demonstrated by immunoperoxidase staining of mammary tissue [26], it is important to obtain information on the strength of the biofilm formation of SP versus NSP strains cultured in vitro as well as for isolates cultured from infected mammary tissues for confirmation of the stated hypotheses.

In our study, the main aim was to compare the pathology subsequent to infection of the mammary glands with a high dose of mammary infection (2x 1010 CFU/0.05 ml) [53] of strong biofilm versus weak-biofilm producing clinical S. aureus strains. Development of acute mastitis was measured by the level of mammary tissue damage based upon clinical manifestations, histopathology, and the production of inflammatory cytokines. The only differences between the 2 isolates used in this investigation are the detection of icaA and icaD genes encoding production of PNAG, previously reported to be associated with biofilm formation [67, 68] and the spa and clfA genes encoding the production of protein A and clfA clumping factor A respectively in the strong biofilm forming strain 51, which were undetectable in the weak biofilm forming S. aureus isolate/strain 104 (Table 1). The strong biofilm forming property of S. aureus strain 51 may also be attributable, in part, to the presence spa and clfA genes encoding protein A and clumping factor A respectively. The relative contribution of protein A and ClfA to colonisation of mammary glands warrants further investigations. Other genes that have all been reported previously to contribute to biofilm formation and were detectable in both the isolates included cna, clfB, isdA, isdB, sdrD, sdrE, hla and hlb [22, 23, 32, 6971]. Had information about the relative contribution of each of the genes detected in this investigation been available, it may have been possible to confirm the biofilm forming property of the strains used in this investigation by constructing isogenic mutants. However, given the recent report of major potential contribution of PNAG to biofilm formation [72], the weak biofilm forming S. aureus strain 104 with no detectable icaA and icaD genes, appears to be a reasonable choice for this investigation. It is also to be noted that all the S. aureus strains used in this study were negative for the gene encoding bap, which has been reported to facilitate formation of biofilm in chronic bovine mastitis [15].

The bacteriological load study demonstrated significantly higher bacterial counts in the mammary glands of mice infected with strong biofilm forming S. aureus strain 51 than those infected with the weak biofilm forming strain 104. Although severity of mastitis has been reported to vary from cow to cow, level of bacterial load may also play a role in the extent of mammary tissue damage. Significantly higher bacterial load in the mammary glands of mice infected with strong biofilm forming S. aureus versus those infected with weak biofilm former may be associated with the ability of the former strains to attach and colonize mammary epithelia more efficiently, a perquisite for manifestation of clinical mastitis. This suggestion is supported by previous studies [73] in which significant correlation between the bacterial load and severity of mastitis within 6 h of intramammary inoculation of Escherichia coli into mammary gland of cows was reported.

Histopathological analysis is an important and widely used tool to assess mammary tissue damage incurred by bacterial invasion of mammary gland [4, 74]. Extensive PMN infiltration, reduced alveolar luminal space, necrosis of mammary tissue and replacement of damaged secreting mammary tissue with non-secretory mammary tissue are the characteristic histopathological findings in bovine mastitis caused by S. aureus [7577]. PMN plays a vital role in host defence mechanism against S. aureus invasion of mammary gland [78]. However, excessive levels of PMN, which may rise as high as 90% in bovine mastitis cases [79], can potentially damage mammary epithelia by respiratory burst and degranulation leading to release of granular enzymes [60]. In the present study, inflammation in peri-mammary and intra-mammary tissue with intra-luminal organisms and marked inflammatory cell infiltration into mammary tissue with evidence of tissue degeneration including necrosis were observed. Given the production of greater mammary tissue damage (grade 3 histopathological changes) by the strong biofilm-producing S. aureus strains versus grade 2 lesions by the PNAG-independent weak biofilm-producing strain in this study, there appeared to be an association between the strength of the biofilms produced by S. aureus and damage to the mouse mammary tissue (Table 3, Fig 1d).

The vital mediators of inflammatory process during IMI are the cytokines [80]. Many investigators have reported higher concentrations of IL-1 [81] and TNF- α [82] in milk and plasma during mastitis potentially mediating local and systemic inflammatory responses. The level of TNF-α in serum has been reported to be highly elevated in cases of acute clinical mastitis [83] resulting in activation and migration of neutrophils [84]. Nevertheless, no studies on the role of these mediators in mammary tissue damage caused by strong versus weak biofilm-forming S. aureus have been performed. TNF-α was reported to induce apoptosis in bovine endothelial cells [85] and human mammary gland epithelial cells [86]. In our study, the level of TNF-α was significantly higher (p<0.05) in mice inoculated with the strong biofilm forming S. aureus than the weak biofilm forming strain even at 48 h post-infection indicating an important role for TNF-α in the observed mammary tissue damage in the mouse mastitis model (Table 4). An earlier investigation [87] reported a potential protective role of TNF-α against S. aureus-associated mastitis provided it was administered by the i/mam route prior to infection (4 to 0 hours) of the mouse mammary gland, accompanied by administration of ciprofloxacin or pirlimycin 1 hour post-infection of the mammary gland. However, no information on the potential association of S. aureus biofilms with inflammatory cytokines and mammary tissue damage post-infection was reported. In contrast, Breyne and co-workers (2015) reported that infection of the mouse mammary gland with S. aureus resulted in local induction of IL-1β and IL-6 but not TNF-α [39]. However, these authors found that mice inoculated with CNS lacked a strong cytokine response although IL-1β was produced locally. Clearly, an analysis of the cytokine profile post-infection with the biofilm forming Newbould strain 305, which is genotypically different from a virulent field isolate, RF122, a strain representative of the major clone involved in severe bovine mastitis worldwide [88], using a dose high enough to produce acute mouse mastitis warrants further investigations. Similarly, further studies on the extent of mammary tissue damage post-infection of the mammary glands with doses low enough to induce subclinical or chronic mouse mastitis by the strong versus weak biofilm forming strains used in this investigation and association/correlation with the levels inflammatory cytokines produced, warrants further investigations.

In summary, the extent of tissue damage in the mammary gland of mice infected with strong biofilm forming S. aureus was found to be significantly greater than that associated with infection with weak biofilm forming S. aureus in this pilot study. It was concluded that the severe tissue damage in mammary glands of mice infected with S. aureus might be due to the strength of biofilm formation by the pathogen and production of the inflammatory cytokine, TNF-α, mediating the influx of phagocytic cells in the mammary gland [89]. However, the limitation of this study is the lack of availability of bovine mastitis-associated clinical S. aureus isolates that are genotypically and phenotypically identical, with the only difference comprising the strength of biofilm formation. Although beyond the scope of this study, it would be interesting to determine the extent of mammary tissue damage caused by a triple deletion mutant of the strong biofilm forming strain 51, in which the genes encoding protein A (spa), clfA (clfA) and PNAG (icaA, icaD) have been deleted, with a view to confirming their potential contribution to the strength of biofilm formation and associated mammary gland pathology. Mouse mastitis model, although requiring larger number of organisms for establishment of acute mammary gland infection, has been considered to be a viable alternative to dairy cattle for cost considerations and similarities between mice and cows because of the locale of mammary glands in the inguinal region [90] despite differences in the predominance of different immunoglobulin isotypes in the serum or milk of mice, depending upon the nature of the pathogen viz., extracellular versus intracellular.

The next phase of this study is to determine the attachment potential, a pre-requisite for biofilm formation [72], of the S. aureus strains used in this study for the mammary gland epithelial cells in vitro using bovine mammary epithelial cells (MAC-T), followed by in vivo studies using the non-invasive mouse mastitis model described in this investigation. Furthermore, because of the unlikelihood of compromising the cutaneous immune system [91], the non-invasive mouse mastitis model should be considered as a preferred alternative to the invasive mouse mastitis model, in which the skin covering the surface of the mammary gland is scraped off using a scalpel or scissors [27, 54], for assessment of the biofilm dispersing potential of biofilm disrupting molecules, including quorum quenching compounds, for discovery of novel anti-biofilm antimicrobials and anti-inflammatory molecules/compounds, notwithstanding its’ cost-effectiveness in the evaluation of novel vaccine candidates against bovine mastitis.

Supporting Information

S1 Table. Criteria used for assignment of grades based on the extent of inflammation in infected versus control mice at 48 hours post-infection.

Assignment of zero (0) denotes no inflammation, + denoted low grade, ++ denoted medium grade and +++ severe inflammation using redness, swelling, discoloration of mammary gland, presence of exudate in the teat, morbidity and mortality.

https://doi.org/10.1371/journal.pone.0170668.s001

(DOCX)

S2 Table. Raw data of total viable counts (CFU/infected mammary gland) of strong versus weak biofilm forming S. aureus recovered from mammary glands at 48 hours post-infection.

A total of 4 mice were infected with each S. aureus strain and euthanized at 48 hours post-infection for collection of mammary glands and total bacterial load/mammary gland obtained in each mouse.

https://doi.org/10.1371/journal.pone.0170668.s002

(DOCX)

S3 Table. Raw data of IL-1β and TNF-α levels (Pg/mL) in serum samples of mice infected with S. aureus at 48 hours post-infection.

Blood samples were collected post-euthanasia at 48 hours post-infection for collection of sera and cytokines estimated for each experimental mouse.

https://doi.org/10.1371/journal.pone.0170668.s003

(DOCX)

Acknowledgments

The authors acknowledge the provision of research facilities and the scientific and technical assistance of the staff of CHIRI Biosciences Research Precinct Core Facility, Curtin University. Our sincere thanks to Karl Fairhurst, senior technician, School of Biomedical Sciences, Curtin University for assisting with histopathology and Tammy De Jong, Life Sciences Research Facility, Office of Research and Development, Building 300, Curtin University, Perth for helping us to look after the experimental animals during the study. Our sincere thanks to Dr. Beng Hooi Chua, Facility Manager, Life Sciences Research Facility, Curtin University and Dr. Tara Pike, Veterinarian, Life Sciences Research Facility, Curtin University for technical support and assistance while carrying out the animal work. The authors acknowledge the provision of research facilities and the scientific and technical assistance of the staff of CHIRI Biosciences Research Precinct core facility, Curtin University. The authors are grateful to Professor Gerard Pier, Brigham and Women’s Hospital, Channing Laboratory, Harvard Medical School for providing S. aureus isolates expressing specific capsular polysaccharides.

Author Contributions

  1. Conceptualization: TM.
  2. Data curation: JG-T.
  3. Formal analysis: JG-T VW CBW SM KW HKT PC HaA HeA.
  4. Funding acquisition: TM NH SI.
  5. Investigation: JG-T VW CBW SM KW HKT.
  6. Methodology: JG-T VW CBW SM KW HKT.
  7. Project administration: TM.
  8. Resources: TM PC NH SI.
  9. Software: HaA.
  10. Supervision: TM VM.
  11. Validation: TM JG-T VW.
  12. Visualization: TM JG-T VW.
  13. Writing – original draft: JG-T TM VM.
  14. Writing – review & editing: JG-T VW TM NH SI.

References

  1. 1. Bannerman DD. Pathogen-dependent induction of cytokines and other soluble inflammatory mediators during intramammary infection of dairy cows. J Anim Sci. 2009;87(13 Suppl):10–25. Epub 2008/08/19. pmid:18708595
  2. 2. Pereira UP, Oliveira DG, Mesquita LR, Costa GM, Pereira LJ. Efficacy of Staphylococcus aureus vaccines for bovine mastitis: a systematic review. Vet Microbiol. 2011;148(2–4):117–24. Epub 2010/12/01. pmid:21115309
  3. 3. Tiwari JG, Babra C, Tiwari HK, Williams V, Wet SD, Gibson J, et al. Trends In Therapeutic and Prevention Strategies for Management of Bovine Mastitis: An Overview. J Vaccines Vaccin. 2013;4:1–11.
  4. 4. Zhao X, Lacasse P. Mammary tissue damage during bovine mastitis: causes and control. J Anim Sci. 2008;86(13 Suppl):57–65. Epub 2007/09/06. pmid:17785603
  5. 5. Zecconi A, Scali F. Staphylococcus aureus virulence factors in evasion from innate immune defenses in human and animal diseases. Immunol lett. 2013;150(1–2):12–22. Epub 2013/02/05. pmid:23376548
  6. 6. Gogoi-Tiwari J, Waryah CB, Eto KY, Tau M, Wells K, Costantino P, et al. Relative distribution of virulence-associated factors among Australian bovine Staphylococcus aureus isolates: Potential relevance to development of an effective bovine mastitis vaccine. Virulence. 2015;6(5):419–23. Epub 2015/06/24. pmid:26103596
  7. 7. Prasad LB, Newbould FH. Initial response of the bovine mammary gland to invasion by Staphylococcus aureus. Can Vet J. 1968;9(8):170–7. Epub 1968/08/01. pmid:5671135
  8. 8. Foster TJ, Geoghegan JA, Ganesh VK, Hook M. Adhesion, invasion and evasion: the many functions of the surface proteins of Staphylococcus aureus. Nat Rev Microbiol. 2014;12(1):49–62. Epub 2013/12/18. pmid:24336184
  9. 9. Middleton JR. Staphylococcus aureus mastitis: Have we learned anything in the last 50 years? NMC Regional Meeting Proceedings. 2013:1–8.
  10. 10. Caiazza NC, O'Toole GA. Alpha-toxin is required for biofilm formation by Staphylococcus aureus. J Bact. 2003;185(10):3214–7. Epub 2003/05/06. pmid:12730182
  11. 11. Gordon RJ, Lowy FD. Pathogenesis of methicillin-resistant Staphylococcus aureus infection. Clin Infect Dis. 2008;46 Suppl 5:S350–9. Epub 2008/05/28.
  12. 12. Boulanger V, Zhao X, Lacasse P. Protective effect of melatonin and catalase in bovine neutrophil-induced model of mammary cell damage. J Dairy Sci. 2002;85(3):562–9. pmid:11949860
  13. 13. Fitzpatrick F, Humphreys H, O'Gara JP. The genetics of staphylococcal biofilm formation—will a greater understanding of pathogenesis lead to better management of device-related infection? Clin Microbiol Infect. 2005;11(12):967–73. Epub 2005/11/26. pmid:16307550
  14. 14. Bjarnsholt T. The role of bacterial biofilms in chronic infections. APMIS Supplementum. 2013;(136):1–51. Epub 2013/05/03.
  15. 15. Cucarella C, Tormo MA, Ubeda C, Trotonda MP, Monzon M, Peris C, et al. Role of biofilm-associated protein bap in the pathogenesis of bovine Staphylococcus aureus. Infect Immun. 2004;72(4):2177–85. Epub 2004/03/25. pmid:15039341
  16. 16. Zhao G, Usui ML, Lippman SI, James GA, Stewart PS, Fleckman P, et al. Biofilms and Inflammation in Chronic Wounds. Adv Wound Care. 2013;2(7):389–99. Epub 2014/02/15 2014/10/16.
  17. 17. Archer NK, Mazaitis MJ, Costerton JW, Leid JG, Powers ME, Shirtliff ME. Staphylococcus aureus biofilms: properties, regulation, and roles in human disease. Virulence. 2011;2(5):445–59. Epub 2011/09/17. pmid:21921685
  18. 18. Tankersley A, Frank MB, Bebak M, Brennan R. Early effects of Staphylococcus aureus biofilm secreted products on inflammatory responses of human epithelial keratinocytes. J inflamm. 2014;11:17. Epub 2014/06/18.
  19. 19. Periasamy S, Joo HS, Duong AC, Bach TH, Tan VY, Chatterjee SS, et al. How Staphylococcus aureus biofilms develop their characteristic structure. PNAS USA. 2012;109(4):1281–6. Epub 2012/01/11. pmid:22232686
  20. 20. Prenafeta A, March R, Foix A, Casals I, Costa L. Study of the humoral immunological response after vaccination with a Staphylococcus aureus biofilm-embedded bacterin in dairy cows: possible role of the exopolysaccharide specific antibody production in the protection from Staphylococcus aureus induced mastitis. Vet Immunol Immunopathol. 2010;134(3–4):208–17. Epub 2009/10/20. pmid:19836084
  21. 21. Boonyayatra S R-uS, Punyapornwithaya V. Association of intramammary infection caused by biofilm-producing pathogens with chronic mastitis in dairy cows. Int J Dairy Sci. 2014;9:89–95.
  22. 22. McDevitt D, Francois P, Vaudaux P, Foster TJ. Molecular characterization of the clumping factor (fibrinogen receptor) of Staphylococcus aureus. Mol Microbiol. 1994;11(2):237–48. Epub 1994/01/01. pmid:8170386
  23. 23. Patti JM, Jonsson H, Guss B, Switalski LM, Wiberg K, Lindberg M, et al. Molecular characterization and expression of a gene encoding a Staphylococcus aureus collagen adhesin. JBC. 1992;267(7):4766–72. Epub 1992/03/05.
  24. 24. O'Neill E, Pozzi C, Houston P, Humphreys H, Robinson DA, Loughman A, et al. A novel Staphylococcus aureus biofilm phenotype mediated by the fibronectin-binding proteins, FnBPA and FnBPB. J Bact. 2008;190(11):3835–50. Epub 2008/04/01. pmid:18375547
  25. 25. Tung H, Guss B, Hellman U, Persson L, Rubin K, Ryden C. A bone sialoprotein-binding protein from Staphylococcus aureus: a member of the staphylococcal Sdr family. Biochem J. 2000;345 Pt 3:611–9. Epub 2000/01/22.
  26. 26. Baselga R, Albizu I, De La Cruz M, Del Cacho E, Barberan M, Amorena B. Phase variation of slime production in Staphylococcus aureus: implications in colonization and virulence. Infect Immun. 1993;61(11):4857–62. pmid:8406887
  27. 27. Brouillette E, Malouin F. The pathogenesis and control of Staphylococcus aureus-induced mastitis: study models in the mouse. Microbes and infection / Institut Pasteur. 2005;7(3):560–8. Epub 2005/03/22.
  28. 28. Cramton SE, Gerke C, Schnell NF, Nichols WW, Gotz F. The intercellular adhesion (ica) locus is present in Staphylococcus aureus and is required for biofilm formation. Infect Immun. 1999;67(10):5427–33. Epub 1999/09/25. pmid:10496925
  29. 29. Gogoi-Tiwari J, Williams V, Waryah CB, Eto KY, Tau M, Costantino P, et al. Comparative studies of the immunogenicity and protective potential of biofilm vs planktonic Staphylococcus aureus vaccine against bovine mastitis using non-invasive mouse mastitis as a model system. Biofouling. 2015;31(7):543–54. Epub 2015/08/22. pmid:26293793
  30. 30. O'Gara JP. ica and beyond: biofilm mechanisms and regulation in Staphylococcus epidermidis and Staphylococcus aureus. FEMS Microbiol lett. 2007;270(2):179–88. Epub 2007/04/11. pmid:17419768
  31. 31. Otto M. Staphylococcal infections: mechanisms of biofilm maturation and detachment as critical determinants of pathogenicity. Ann Rev Med. 2013;64:175–88. Epub 2012/08/22. pmid:22906361
  32. 32. Huseby MJ, Kruse AC, Digre J, Kohler PL, Vocke JA, Mann EE, et al. Beta toxin catalyzes formation of nucleoprotein matrix in staphylococcal biofilms. PNAS USA. 2010;107(32):14407–12. Epub 2010/07/28. pmid:20660751
  33. 33. Petersson-Wolfe C MI, Jones GM. Damage caused by Staphylococcus aureus mastitis. VCES. 2010;404:229.
  34. 34. Merino N, Toledo-Arana A, Vergara-Irigaray M, Valle J, Solano C, Calvo E, et al. Protein A-mediated multicellular behavior in Staphylococcus aureus. J Bact. 2009;191(3):832–43. Epub 2008/12/03. pmid:19047354
  35. 35. Valle J, Latasa C, Gil C, Toledo-Arana A, Solano C, Penades JR, et al. Bap, a biofilm matrix protein of Staphylococcus aureus prevents cellular internalization through binding to GP96 host receptor. PLoS pathogens. 2012;8(8):e1002843. Epub 2012/08/10. pmid:22876182
  36. 36. Shemesh M, Tam A, Steinberg D. Differential gene expression profiling of Streptococcus mutans cultured under biofilm and planktonic conditions. Microbiology;. 2007;153(Pt 5):1307–17. Epub 2007/04/28. pmid:17464045
  37. 37. Thurlow LR, Hanke ML, Fritz T, Angle A, Aldrich A, Williams SH, et al. Staphylococcus aureus biofilms prevent macrophage phagocytosis and attenuate inflammation in vivo. J Immunol. (Baltimore, Md: 1950). 2011;186(11):6585–96. Epub 2011/04/29.
  38. 38. Hanke ML, Kielian T. Deciphering mechanisms of staphylococcal biofilm evasion of host immunity. Front Cell Infect Microbiol. 2012;2:62. Epub 2012/08/25. pmid:22919653
  39. 39. Breyne K, De Vliegher S, De Visscher A, Piepers S, Meyer E. Technical note: a pilot study using a mouse mastitis model to study differences between bovine associated coagulase-negative staphylococci. J dairy Sci. 2015;98(2):1090–100. Epub 2014/12/17. pmid:25497801
  40. 40. Chandler RL. Experimental bacterial mastitis in the mouse. J Med Microbiol. 1970;3(2):273–82. Epub 1970/05/01. pmid:4989101
  41. 41. Nazemi S, Aalbaek B, Kjelgaard-Hansen M, Safayi S, Klaerke DA, Knight CH. Expression of acute phase proteins and inflammatory cytokines in mouse mammary gland following Staphylococcus aureus challenge and in response to milk accumulation. J Dairy Res. 2014;81(4):445–54. Epub 2014/09/18. pmid:25230141
  42. 42. Babra C, Tiwari JG, Pier G, Thein TH, Sunagar R, Sundareshan S, et al. The persistence of biofilm-associated antibiotic resistance of Staphylococcus aureus isolated from clinical bovine mastitis cases in Australia. Folia Microbiol. 2013;58(6):469–74. Epub 2013/03/01.
  43. 43. Gogoi-Tiwari J, Babra Waryah C, Sunagar R, Veeresh HB, Nuthanalakshmi V, Preethirani PL, et al. Typing of Staphylococcus aureus isolated from bovine mastitis cases in Australia and India. Aust Vet J. 2015;93(8):278–82. pmid:26220320
  44. 44. Moore PC, Lindsay JA. Genetic variation among hospital isolates of methicillin-sensitive Staphylococcus aureus: evidence for horizontal transfer of virulence genes. J Clin Microbiol. 2001;39(8):2760–7. Epub 2001/07/28. pmid:11473989
  45. 45. Verdier I, Durand G, Bes M, Taylor KL, Lina G, Vandenesch F, et al. Identification of the capsular polysaccharides in Staphylococcus aureus clinical isolates by PCR and agglutination tests. J Clin Microbiol. 2007;45(3):725–9. Epub 2007/01/05. pmid:17202275
  46. 46. Fournier JM, Vann WF, Karakawa WW. Purification and characterization of Staphylococcus aureus type 8 capsular polysaccharide. Infect Immun. 1984;45(1):87–93. Epub 1984/07/01. pmid:6429051
  47. 47. Christensen GD, Simpson WA, Younger JJ, Baddour LM, Barrett FF, Melton DM, et al. Adherence of coagulase-negative staphylococci to plastic tissue culture plates: a quantitative model for the adherence of staphylococci to medical devices. J Clin Microbiol. 1985;22(6):996–1006. Epub 1985/12/01. pmid:3905855
  48. 48. Kogan G, Sadovskaya I, Chaignon P, Chokr A, Jabbouri S. Biofilms of clinical strains of Staphylococcus that do not contain polysaccharide intercellular adhesin. FEMS Microbiol Lett. 2006;255(1):11–6. Epub 2006/01/27. pmid:16436056
  49. 49. Mathur T, Singhal S, Khan S, Upadhyay DJ, Fatma T, Rattan A. Detection of biofilm formation among the clinical isolates of Staphylococci: an evaluation of three different screening methods. Ind J Med Microbiol. 2006;24(1):25–9. Epub 2006/03/01.
  50. 50. Stepanovic S, Vukovic D, Dakic I, Savic B, Svabic-Vlahovic M. A modified microtiter-plate test for quantification of staphylococcal biofilm formation. J Microbiol Methods 2000;40(2):175–9. Epub 2000/03/04. pmid:10699673
  51. 51. Babra C, Tiwari J, Costantino P, Sunagar R, Isloor S, Hegde N, et al. Human methicillin-sensitive Staphylococcus aureus biofilms: potential associations with antibiotic resistance persistence and surface polysaccharide antigens. J Basic Microbiol. 2014;54(7):721–8. Epub 2013/05/21. pmid:23686411
  52. 52. Vasudevan P, Nair MK, Annamalai T, Venkitanarayanan KS. Phenotypic and genotypic characterization of bovine mastitis isolates of Staphylococcus aureus for biofilm formation. Vet Microbiol. 2003;92(1–2):179–85. Epub 2002/12/19. pmid:12488081
  53. 53. Anderson JC, Chandler RL. Experimental Staphylococcal mastitis in the mouse. Histological, ultrastructural and bacteriological changes caused by a virulent strain of Staphylococcus aureus. J Comp Pathol. 1975;85(4):499–510. Epub 1975/10/01. pmid:1237501
  54. 54. Brouillette E, Grondin G, Lefebvre C, Talbot BG, Malouin F. Mouse mastitis model of infection for antimicrobial compound efficacy studies against intracellular and extracellular forms of Staphylococcus aureus. Vet Microbiol. 2004;101(4):253–62. Epub 2004/07/21. pmid:15261998
  55. 55. Bancroft JD, Gamble M. Theory and practice of histological techniques. 6th ed. Edinburgh: Churchill Livingston; 2008:pp. 121–34.
  56. 56. Ollett WS. A method for staining both gram-positive and gram-negative bacteria in sections. The J Pathol Bacteriol. 1947;59(1–2):357. Epub 1947/01/01. pmid:20266387
  57. 57. Skipper R, Destephano D. Diff quik stain set* 64851. J Histotechnol. 1989;4:303.
  58. 58. Ramakrishnan Y, Shields RC, Elbadawey MR, Wilson JA. Biofilms in chronic rhinosinusitis: what is new and where next? J Laryngol Otol. 2015:1–8. Epub 2015/06/30.
  59. 59. Lee SH, Mangolin BL, Goncalves JL, Neeff DV, Silva MP, Cruz AG, et al. Biofilm-producing ability of Staphylococcus aureus isolates from Brazilian dairy farms. J Dairy Sci. 2014;97(3):1812–6. pmid:24440248
  60. 60. Paape M, Mehrzad J, Zhao X, Detilleux J, Burvenich C. Defense of the bovine mammary gland by polymorphonuclear neutrophil leukocytes. J Mammary Gland Biol Neoplasia. 2002;7(2):109–21. pmid:12463734
  61. 61. Kuroishi T, Komine K, Asai K, Kobayashi J, Watanabe K, Yamaguchi T, et al. Inflammatory responses of bovine polymorphonuclear neutrophils induced by staphylococcal enterotoxin C via stimulation of mononuclear cells. Clin Diagn Lab Immunol. 2003;10(6):1011–8. pmid:14607860
  62. 62. Cucarella C, Tormo MA, Knecht E, Amorena B, Lasa I, Foster TJ, et al. Expression of the biofilm-associated protein interferes with host protein receptors of Staphylococcus aureus and alters the infective process. Infect Immun. 2002;70(6):3180–6. Epub 2002/05/16. pmid:12011013
  63. 63. Lone AG, Atci E, Renslow R, Beyenal H, Noh S, Fransson B, et al. Staphylococcus aureus induces hypoxia and cellular damage in porcine dermal explants. Infect Immun.2015;83(6):2531–41. Epub 2015/04/08. pmid:25847960
  64. 64. Prabhakara R, Harro JM, Leid JG, Harris M, Shirtliff ME. Murine immune response to a chronic Staphylococcus aureus biofilm infection. Infect Immun. 2011;79(4):1789–96. pmid:21282411
  65. 65. Cantero D, Cooksley C, Jardeleza C, Bassiouni A, Jones D, Wormald PJ, et al. A human nasal explant model to study Staphylococcus aureus biofilm in vitro. Int Forum Allergy & Rhinol. 2013;3(7):556–62.
  66. 66. Hanke ML, Heim CE, Angle A, Sanderson SD, Kielian T. Targeting macrophage activation for the prevention and treatment of Staphylococcus aureus biofilm infections. J Immunol. 2013;190(5):2159–68. Epub 2013/02/01. pmid:23365077
  67. 67. Kropec A, Maira-Litran T, Jefferson KK, Grout M, Cramton SE, Gotz F, et al. Poly-N-acetylglucosamine production in Staphylococcus aureus is essential for virulence in murine models of systemic infection. Infect Immun. 2005;73(10):6868–76. Epub 2005/09/24. pmid:16177366
  68. 68. Waryah CB, Gogoi-Tiwari J, Wells K, Costantino P, Al-Salami H, Sunagar R, et al. Serological versus molecular typing of surface-associated immune evading polysaccharide antigens-based phenotypes of Staphylococcus aureus. J Med Microbiol. 2014;63(Pt 11):1427–31. Epub 2014/08/22. pmid:25142964
  69. 69. Lin MH, Shu JC, Huang HY, Cheng YC. Involvement of iron in biofilm formation by Staphylococcus aureus. PloS One. 2012;7(3):e34388. Epub 2012/04/06. pmid:22479621
  70. 70. Liu H, Lv J, Qi X, Ding Y, Li D, Hu L, et al. The carriage of the serine-aspartate repeat protein-encoding sdr genes among Staphylococcus aureus lineages. Braz J Infect Dis. 2015;19(5):498–502. Epub 2015/08/19. pmid:26277345
  71. 71. Otto M. Staphylococcal biofilms. Curr Top Microbiol Immunol. 2008;322:207–28. Epub 2008/05/06. pmid:18453278
  72. 72. Waryah CB, Gogoi-Tiwari J, Wells K, Mukkur T. An immunological assay for identification of potential biofilm-associated antigens of Staphylococcus aureus. Folia Microbiol. 2016;61(6):473–8. Epub 2016/04/24.
  73. 73. Kornalijnslijper JE, Daemen AJ, van Werven T, Niewold TA, Rutten VP, Noordhuizen-Stassen EN. Bacterial growth during the early phase of infection determines the severity of experimental Escherichia coli mastitis in dairy cows. Vet Microbiol. 2004;101(3):177–86. Epub 2004/06/30. pmid:15223122
  74. 74. Frost AJ, Hill AW, Brooker BE. The early pathogenesis of bovine mastitis due to Escherichia coli. Proc Royal Soc London Series B, Biol Sci. 1980;209(1176):431–9. Epub 1980/09/26.
  75. 75. Chandler RL, Reid IM. Ultrastructural and associated observations on clinical cases of mastitis in cattle. J Comp Pathol. 1973;83(2):233–41. Epub 1973/04/01. pmid:4761663
  76. 76. Heald CW. Morphometric study of experimentally induced Staphylococcus bovis mastitis in the cow. Am j Vet Res. 1979;40(9):1294–8. Epub 1979/09/01. pmid:525935
  77. 77. Nickerson SC, Heald CW. Histopathologic response of the bovine mammary gland to experimentally induced Staphylococcus aureus infection. Am J Vet Res. 1981;42(8):1351–5. Epub 1981/08/01. pmid:7294468
  78. 78. Paape MJ, Bannerman DD, Zhao X, Lee JW. The bovine neutrophil: Structure and function in blood and milk. Vet Res. 2003;34(5):597–627. pmid:14556697
  79. 79. Leitner G, Shoshani E, Krifucks O, Chaffer M, Saran A. Milk leucocyte population patterns in bovine udder infection of different aetiology. J Vet Med B Infect Dis Vet public health. 2000;47(8):581–9. pmid:11075546
  80. 80. Persson K, Larsson I, Hallen Sandgren C. Effects of certain inflammatory mediators on bovine neutrophil migration in vivo and in vitro. Veterinary Immunol Immunopathol. 1993;37(2):99–112. Epub 1993/07/01.
  81. 81. Bannerman DD, Paape MJ, Lee JW, Zhao X, Hope JC, Rainard P. Escherichia coli and Staphylococcus aureus elicit differential innate immune responses following intramammary infection. Clin Diagn Lab Immunol. 2004;11(3):463–72. Epub 2004/05/13. pmid:15138171
  82. 82. Kauf AC, Vinyard BT, Bannerman DD. Effect of intramammary infusion of bacterial lipopolysaccharide on experimentally induced Staphylococcus aureus intramammary infection. Res Vet Sci. 2007;82(1):39–46. Epub 2006/08/05. pmid:16887158
  83. 83. Nakajima Y, Mikami O, Yoshioka M, Motoi Y, Ito T, Ishikawa Y, et al. Elevated levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) activities in the sera and milk of cows with naturally occurring coliform mastitis. Res Vet Sci. 1997;62(3):297–8. Epub 1997/05/01. pmid:9300553
  84. 84. Blum JW, Dosogne H, Hoeben D, Vangroenweghe F, Hammon HM, Bruckmaier RM, et al. Tumor necrosis factor-alpha and nitrite/nitrate responses during acute mastitis induced by Escherichia coli infection and endotoxin in dairy cows. Domest Anim Endocrinol. 2000;19(4):223–35. Epub 2000/12/19. pmid:11118787
  85. 85. Messmer UK, Briner VA, Pfeilschifter J. Tumor necrosis factor-alpha and lipopolysaccharide induce apoptotic cell death in bovine glomerular endothelial cells. Kidney Int. 1999;55(6):2322–37. Epub 1999/06/03. pmid:10354280
  86. 86. Burow ME, Tang Y, Collins-Burow BM, Krajewski S, Reed JC, McLachlan JA, et al. Effects of environmental estrogens on tumor necrosis factor alpha-mediated apoptosis in MCF-7 cells. Carcinogenesis. 1999;20(11):2057–61. Epub 1999/11/05. pmid:10545406
  87. 87. Sanchez MS, Ford CW, Yancey RJ Jr. Efficacy of tumor necrosis factor-alpha and antibiotics in therapy of experimental murine staphylococcal mastitis. J Dairy Sci. 1994;77(5):1259–66. Epub 1994/05/01. pmid:8046067
  88. 88. Peton V, Bouchard DS, Almeida S, Rault L, Falentin H, Jardin J, et al. Fine-tuned characterization of Staphylococcus aureus Newbould 305, a strain associated with mild and chronic mastitis in bovines. Vet Res. 2014;45:106. Epub 2014/10/16. pmid:25316113
  89. 89. Vieira SM, Lemos HP, Grespan R, Napimoga MH, Dal-Secco D, Freitas A, et al. A crucial role for TNF-alpha in mediating neutrophil influx induced by endogenously generated or exogenous chemokines, KC/CXCL1 and LIX/CXCL5. Br J Pharmacol2009;158(3):779–89.
  90. 90. Notebaert S, Meyer E. Mouse models to study the pathogenesis and control of bovine mastitis. A review. Veterinary Quart. 2006;28(1):2–13. Epub 2006/04/12.
  91. 91. Di Meglio P, Perera GK, Nestle FO. The multitasking organ: recent insights into skin immune function. Immunity. 2011;35(6):857–69. Epub 2011/12/27. pmid:22195743