Genotypic and phenotypic diversity of Lactobacillus rhamnosus clinical isolates, their comparison with strain GG and their recognition by complement system

Lactobacillus rhamnosus strains are ubiquitous in fermented foods, and in the human body where they are commensals naturally present in the normal microbiota composition of gut, vagina and skin. However, in some cases, Lactobacillus spp. have been implicated in bacteremia. The aim of the study was to examine the genomic and immunological properties of 16 clinical blood isolates of L. rhamnosus and to compare them to the well-studied L. rhamnosus probiotic strain GG. Blood cultures from bacteremic patients were collected at the Helsinki University Hospital laboratory in 2005–2011 and L. rhamnosus strains were isolated and characterized by genomic sequencing. The capacity of the L. rhamnosus strains to activate serum complement was studied using immunological assays for complement factor C3a and the terminal pathway complement complex (TCC). Binding of complement regulators factor H and C4bp was also determined using radioligand assays. Furthermore, the isolated strains were evaluated for their ability to aggregate platelets and to form biofilms in vitro. Genomic comparison between the clinical L. rhamnosus strains showed them to be clearly different from L. rhamnosus GG and to cluster in two distinct lineages. All L. rhamnosus strains activated complement in serum and none of them bound complement regulators. Four out of 16 clinical blood isolates induced platelet aggregation and/or formed more biofilms than L. rhamnosus GG, which did not display platelet aggregation activity nor showed strong biofilm formation. These findings suggest that clinical L. rhamnosus isolates show considerable heterogeneity but are clearly different from L. rhamnosus GG at the genomic level. All L. rhamnosus strains are still normally recognized by the human complement system.

Introduction differences were seen in the organization and the presence of genes encoding surface polysaccharides, including EPS/capsular polysaccharide (CPS), between the clinical strains belonging to the so-called cluster A and cluster B.

Ethics statement
All persons who donated blood for this study provided a written informed consent. The study protocol has been approved by the Academy of Finland (Projects 28 137389, 141140 and 1272870).

Bacterial isolates and growth conditions
Lactobacillus strains used in the study are listed in Table 1 and includes 4 newly sequenced strains and 12 strains previously published [22,23]. Clinical blood isolates of L. rhamnosus strains were obtained from HUSLAB and collected from bacteremic patients between years 2005 and 2011. L. rhamnosus GG (ATCC 53103) was obtained from the Valio culture collection (Valio Ltd., Helsinki, Finland). L. salivarius CCUG 47825 was a kind gift from Prof. Paul W. O'Toole (University College Cork, Cork, Ireland) [19]. Pathogenic control Streptococcus pyogenes strain st369 was obtained from the collection of the National Institute for Health and Welfare (Prof. Jaana Vuopio) and emm8 from ATCC (ATCC catalogue number 12349). S. pyogenes strains were used as controls for complement activity and FH and C4bp binding assays [24]. Lactobacilli were cultured at 37˚C in de Man-Rogosa-Sharpe (MRS) medium (Difco BD, NJ, USA). S. pyogenes strains were grown at 37˚C with 5% CO 2 on blood-agar plates supplemented with colistin and oxolinic acid or in Todd-Hewitt broth (Difco BD, NJ, USA). For in vitro assays Lactobacillus strains were cultured at 37˚C in MRS medium overnight. The overnight bacterial cultures were diluted 1:100 and cultured until the OD 600 reached Table 1 0.5-0.7 for log phase and overnight for stationary phase. The cells were collected by centrifugation and glycerol was added until 20% to freeze the cultures. The strains were stored at -70˚C.

Genome sequencing
DNA was extracted from the bacterial cultures as described previously [23]. Libraries from genomic DNA from L. rhamnosus strains were done for both 454 sequencing and MiSeq sequencing following recommendation from respective manufacturer. The 454 libraries were sequenced using a Genome Sequencer FLX (Roche) and titanium chemistry with read lengths of ca 400 bp. The Illumina libraries were paired-end sequenced (250 bp + 250 bp) using a MISeq (Illumina). All library preparations and sequencing were done at the DNA sequencing and genomics laboratory, Institute Biotechnology, University of Helsinki, Finland. A combined 454 and MiSeq read assembly were performed using the Celera Assembler v6.1 (http:// sourceforge.net/apps/mediawiki/wgs-assembler/index.php?title=Main_Page). Genomes were annotated using the RAST server [25]. The new genome sequences were deposited to public depository databases but most of them were published earlier by Ceapa et al. [23] or by others (see for details Table 1).

Bioinformatics analysis
The orthology prediction was performed using sequence clustering and search program Usearch v8.0.1623 [26]. To define orthologous groups, all the predicted ORF amino acid sequences of all the strains were first ordered by length using the sortbylength command, and then clustered with the cluster_smallmem command using identity threshold of 0.9. Thus, the members of each ORF sequence cluster shared at least 90% amino acid identity over their whole sequence lengths. The longest sequence in each cluster was chosen as the representative sequence of that orthologous group. The pangenome was defined as the set of representative sequences of the orthologous groups. The ortholog data was managed using R v. 3.2.2 (R) with Biostrings library v. 2.40.2 [27] and in-house scripts. The ortholog copy number data was used for hierarchical clustering of the strains by first removing orthologs that had variance <0.06 over the strains, and then calculating Euclidean distances between the strains and applying Ward's minimum variance method to the distances using R functions dist and hclust, respectively. Clustering dendrograms were drawn with R library dendextend v. 1.3.0 [28], and the function heatmap.2 from R library gplots v. 3.0.1. [29] was used for producing a row-wise centered and scaled heatmap of the filtered ortholog number matrix. Strains were compared at nucleotide level to the L. rhamnosus GG genome using blastn program v. 2.2.31+ with parameters -task magablast, -evalue 0.001 and -perc_identity 95. Mean similarity of aligned fragments over 10 kb was calculated for each strain.

Complement activity determination using C3a and TCC ELISA
The frozen batches of log phase bacteria were used to activate complement in the serum pool of healthy volunteers. Bacterial cells were washed with PBS and adjusted to have 10 7 bacterial cells in 100 μl of PBS. The bacteria were mixed with the same volume of serum and incubated for 30 minutes at 37˚C in agitation at 500 rpm. The reactions were stopped by adding EDTA to a final concentration of 15 mM and by transferring the samples on ice. Cells were separated from serum samples by centrifugation at 5,900g for 3 minutes and stored at -70˚C for C3a and SC5b-9 (TCC) analysis. Complement C3a and SC5b-9 were analyzed from the samples using the commercial MicroVue C3a EIA (Quidel, Tecomedical) and ELISA for TCC determination as described earlier [30]. For C3a measurements serum samples were diluted 1 to 10,000 and for TCC assay 1 to 2,000.

Direct 125 I-factor H and C4bp binding assays
The binding of FH and C4bp were performed as described earlier [31]. Shortly, FH and C4bp were labelled with iodine ( 125 I; Perkin Elmer) using the Iodogen method [32]. The specific activities of the labelled proteins were 1-2 x 10 7 cpm/μg. Each bacterial strain (3 × 10 7 log phase bacteria/reaction) was incubated with 25,000 cpm of radiolabeled FH or C4bp in 100 μl of gelatin-Veronal buffered saline for 30 minutes at 37˚C. The reaction mixtures were centrifuged (at 10,000g for 3 minutes) through 20% sucrose, and the radioactivity of each pellet and supernatant was measured with gamma counter. S. pyogenes strains were used as a negative (emm8) and positive (st369) controls for FH binding and positive control for C4bp binding [33]. The ratios of bound (pellet) to total activity (pellet + supernatant) were calculated as percentage.

Platelet preparation and aggregometry
Blood samples were collected from healthy donors as previously described [34]. Nine ml of blood was collected into 3.2% Na-citrate tubes (Vacuette, ref. 455322, Greiner-bio-one) via venipuncture from a cubital vein from a healthy donor using 20G needle. Whole blood was centrifuged at 180g for 12 minutes at 22˚C without using brake. Platelet rich plasma (PRP) was collected slowly above the buffy coat with a plastic Pasteur pipette into separate plastic tube.
The remaining blood was mixed and centrifuged again at 2,000g for 10 minutes at 22˚C to obtain platelet poor plasma (PPP). The platelet count was measured with Sysmex XK-21 cell counter and adjusted with PPP to the desired concentration.
Platelet aggregation was carried out in a profiler aggregometer (PAP-4, Bio/Data corp.), with light transmission through PPP presenting 100% aggregation and that through PRP representing 0% aggregation. PRP was used in a test well and the change in transmission over time was a signal of the platelet aggregation. The frozen batches of bacterial cells were washed with PBS three times. The final volume was adjusted to get 2 x 10 9 cfu/ml in PBS for platelet aggregation experiments. Lactobacillus strains were determined for their ability to induce platelet aggregation by the addition of 25 μl of a bacterial suspension to 475 μl of PRP. One minute after agonist ADP or bacteria was added into the well the platelet response was monitored for a maximum 30 minutes. Platelet viability was confirmed by addition to PRP of agonist adenosine diphosphate (ADP) to a final concentration of 5 μM.

Biofilm assay
The microtiter plate biofilm assay is a static assay that has been used for examining biofilm formation [35]. The wells of 24-well cell culture plate (Greiner Bio-One, Germany) were filled in with serial dilution (1 to 10) of an overnight bacterial culture. After an incubation for 18 hour at 37˚C, the wells were washed with aqua and stained with crystal violet. The crystal violet stained plates were dried and scanned with Odyssey IR scanner (Licor) at 700 nm channel and integrated intensities analyzed using Odyssey (v 2.1) analysis software. The bound dye was also solubilized in 250 μl of 70% ethanol, transferred into 96-well plate and the optical density of the ethanol-dye solution was determined at 600 nm using a microplate reader (Fluostar Optima, BMG Labtech, Germany). The correlation between the methods was high (97.3%) indicating that the crystal violet was a strong fluorophore at 700 nm and Odyssey scanner is a useful tool for determining biofilms.

Western blot analysis of cell wall proteins
Cell wall proteins were extracted and the presence of SpaCBA and SpaFED pili were determined using Western Blot analysis as earlier described [22].

Statistical analysis
All values are presented as a mean ± SD. Where applicable, a 2-tailed Student's t-test was used to analyse the differences between groups (Excel software; Microsoft, Redmond, WA, USA).

Results
Genomic features and organization of L. rhamnosus clinical blood isolates vs. L. rhamnosus GG All L. rhamnosus strains described in the present study were isolated from clinical blood cultures collected during 2005-2011 from the Helsinki University Hospital laboratory. The genomes of four strains are reported here while that of the other 12 have been described earlier [23]. Their general genomic information was compared to that of L. rhamnosus GG (Table 1 and Table 2). Genome size, G+C content and open reading frame (ORF) count of annotated protein coding sequences varied greatly between the strains and differed from L. rhamnosus GG. The genome sizes ranged from 2.86 to 3.17 Mb. The average genome size was 3.0 Mb ± 0.16 Mb which is in the same range as other members of the L. rhamnosus species [23]. The G+C content varied among the genomes from 46.6 to 46.8% being closely similar to L. rhamnosus GG (46.7%) while the number of ORF predictions varied between 2648 and 3010, exceeding that of L. rhamnosus GG (2926).
To analyze the similarity of the strains against L. rhamnosus GG at sequence level, a dendrogram based on cluster analysis of the presence of orthologs at 90% sequence identity was created (Fig 1). This showed that the strains could be grouped into two main clusters and one separate strain (Lrh20). It shows that the L. rhamnosus isolates are different from each other at the sequence level and more remarkably, all are very different at the genomic level from L. rhamnosus GG. The strains in cluster A have sequence similarity at nucleic acid level to L. rhamnosus GG between 99.942 and 99.984% whereas the strains in cluster B differ remarkably more having the similarity between 97.0 and 98.5% (Fig 1). Interestingly, all the genomes of five isolated L. rhamnosus strains (Lrh13, Lrh22, Lrh28, Lrh30 and Lrh47) that contain plasmids belong to the cluster B ( Table 2, Fig 1). The presence of unique orthologs between clusters were compared (S1 Table). Most of the differing orthologs that could be annotated, and are not phage sequences, are exopolysaccharide-related. Cluster A consists of 66 orthologs that were not found from cluster B and 35 orthologs that were missing from cluster A but present in cluster B. Interestingly, there were 8 EPS related ORFs present and 10 absent in cluster A.

Complement activation and binding of complement regulators
The recovery of L. rhamnosus isolates from the blood of bacteremic patients raised questions about their survival within the human bloodstream and also their (possible) recognition or killing by the host immunological system. Initial experiments indicated L. rhamnosus GG and clinical isolates showed only little survival in blood (less than 31% survival after 3 hours at 37˚C) in contrast to strain st369, a known pathogen belonging to the Group A Streptococci, which multiplies rapidly in blood (at least 5 cell divisions after 3 hours at 37˚C; see S2 Table).
To further explore these, we studied in vitro if the isolated strains can activate the complement system and thus, be recognized by the human innate immune system, and if they are able to bind complement regulators to evade complement in the manner of pathogenic bacteria. Clinical blood isolate of L. rhamnosus Strains were incubated with human serum to trigger the complement activation response. All the isolates as well as L. rhamnosus GG induced the formation of C3a and soluble terminal component TCC in serum (Fig 2 and S3 Table). All tested L. rhamnosus strains induced significantly higher C3a concentrations in serum than the negative control (S. pyogenes st369). Similar observations were made for the levels of TCC, although more variations were seen among isolates (notably between Lrh14 (the lowest) and Lrh7, Lrh13, Lrh18, Lrh20 and Lrh30 (the highest values)). Taken together, the amounts of both complement activity markers (C3a and TCC), indicated that the complement system was activated in the presence of the isolated L. rhamnosus strains in vitro, as opposed to the S. pyogenes st369, which did not activate the complement system similarly as earlier described [24]. To further explore additional factors mediating activation of the complement and to assess the ability of these strains to potentially inhibit complement activation, we examined the direct binding of complement regulators FH and C4bp to all L. rhamnosus strains (Fig 2, S3 Table). No binding of FH or C4bp to any of the L. rhamnosus strains was observed. The FH binding ranged between 0.3-0.55% and the C4bp binding between 1.6-5.8%, which corresponds to background levels (0.40 ± 0.15% and 3.1 ± 0.6%, respectively). In contrast, the control strain S. pyogenes st369 showed strong FH binding (46.7 ± 14.1%) and both S. pyogenes emm8 (35.7 ± 0.2%) and st369 (31.9 ± 14.7%) exhibited strong C4bp binding as previously reported [33].
These results indicate that the L. rhamnosus blood isolates and the probiotic strain GG do not bind these complement regulators and therefore do not escape complement using studied mechanisms as known in pathogens [38,39]. Human platelet aggregation by the L. rhamnosus strains Next we studied the capacity of the L. rhamnosus strains to promote platelet aggregation. Platelets are cell fragments that plug the leakage in a damaged blood vessel but they are also key components in the innate immune system [40]. Many Gram-positive bacteria causing sepsis have been shown to induce platelet aggregation [41]. The L. rhamnosus strains were tested for platelet aggregation using isolated platelets from different human donors (Fig 2, S3 Table). Four out of 16 L. rhamnosus isolates (Lrh11, Lrh18, Lrh22, Lrh28) induced platelet aggregation. It is noteworthy that platelet aggregation was donor-dependent. Hence the same strain did not always induce platelet aggregation for every donor tested and this was also noted for the positive control L. salivarius CCUG 47825 (S3 Table). Two of the aggregating strains, Lrh22 and Lrh28, induced platelet aggregation with platelets from every donor tested. Similar to previous studies [17] L. rhamnosus GG and the rest of the twelve isolates did not induce platelet aggregation for any tested donors. The experimental data shown here suggest that the L. rhamnosus blood isolates differ in their ability to cause platelet aggregation and that platelet aggregation was not a common phenotypic trait associated with L. rhamnosus blood isolates although 2 clinical strains were highly proficient platelet aggregators.

Biofilm formation by the L. rhamnosus strains
Biofilm formation is a feature found in both pathogenic and commensal bacteria, as it promotes colonization and persistence in an ecological habitat. Hence, we assessed the formation of biofilms for L. rhamnosus strains in 24-well plates (Fig 2 and S3 Table). Some differences in biofilm formation could be seen between the isolated strains. Four of the strains (from cluster B) tested (Lrh13 (8.9 ± 3.1%), Lrh28 (13.1 ± 4.7%), Lrh30 (7.1 ± 2.3%), Lrh32 (5.4 ± 1.3%)) showed a stronger ability for biofilm formation than GG (3.8 ± 0.8%). L. salivarius CCUG 47825 was used as a positive control and produced a strong biofilm (relative biofilm formation 100 ± 25.7%). Summarizing, biofilm formation varied between L. rhamnosus isolates with some strains displaying higher biofilm formation than L. rhamnosus GG. All those strains that showed clear biofilm formation phenotype belong to cluster B.

Comparison of LPXTG protein encoding genes, SpaCBA pilus proteins and EPS related genes
In an attempt to further characterize the phenotypes of these different isolate, we examined some of the relevant genomic features related to surface exposed structures and molecules of these strains. Typically, the genomes of Gram-positive bacteria harbor genes that code for LPXTG proteins as well as the sortase enzymes. Sortases are involved in the surface display and cell wall anchoring of surface proteins carrying the sortase-specific recognition motif LPXTG in Gram-positive bacteria [42]. Based on the genome sequences of the blood isolates, we investigated the repertoire of all gene sequences that are predicted to code for LPXTG proteins, as they are most likely to interact with the environment and the host, in that particular context with the human vascular system. All strains possessed a distinct and unique set of proteins (S2 Fig). It has been well established that the presence of pili depends on a specific set of LPXTG proteins that include major pilin, minor pilin and, tip pilin subunit proteins and these are widely spread in various Lactobacillus spp. [2]. In L. rhamnosus GG, two pili gene clusters have been identified but only SpaCBA pili have been found to be produced [22,43]. Hence, we used Western blot analysis with SpaA and SpaD antibodies to show that 8 out of 16 L. rhamnosus strains produced SpaCBA pili while none were producing the SpaFED pili (Fig 2) even though the SpaFED locus was found in all strains (S1 Fig). Five of these showed phenotypic characters (platelet aggregation (Lrh18, Lrh11) or biofilm formation (Lrh13, Lrh30) or both (Lrh28; Fig 2)). When the strains were divided into two groups based on the presence of SpaCBA pilus there was a significant association between the biofilm formation and the presence of pilus among the isolated strains (6.5 ± 3.11% (present) vs 3.87 ± 0.72% (absent), p = 0.047, S3 Table).
As the surface polysaccharides are known to participate in important functions during pathogenesis, such as tissue adherence, biofilm formation and evasion of host defence [44,45] and our clusters of L. rhamnosus strains showed differences between the ORFs related to EPS/CPS gene clusters (S1 Table), we wanted to study if the genomic organization of EPS gene clusters in the studied blood isolates of L. rhamnosus are similar to L. rhamnosus GG [46]. This cluster consists of genes coding proteins for the regulation of EPS production and polymerization (wzd, wze, wzr, wzb), polysaccharide transportation and polymerization (wzx, wzy), glycosyltransferases (welJ, welI, welH, welG, welF, welE), biosynthesis of the dTDP-rhamnose precursor (rmlA, rmlC, rmlB) and UDP-galactopyranose mutase for biosynthesis of the sugar nucleotide precursor for galactofuranose (glf) [46]. Interestingly, after annotation analysis our data showed that the strains in cluster A had the EPS cluster consisting 16 putative ORFs/genes with similar identity (> 78%) to those present in L. rhamnosus GG (Fig 3A). However, the strains in cluster B had only some of these genes (wzd, wze, wzr, wzb and rmlB (except Lrh22)) with similar identity (> 78%) to genes in EPS cluster of L. rhamnosus GG (Fig 3B). The other genes found in this cluster were annotated to encode genes for mostly glycosyl transferases with different specificities, hypothetical proteins and several mobile element proteins. However, we were not able to characterize these clusters in details because multiple mobile elements were present and they spliced the sequences into multiple contigs. Interestingly, the strains in cluster B consist also a different type of polysaccharide (EPS/CPS) cluster comprising of 19 genes (Fig 3B) including an additional flippase (6.) gene essential for EPS production. The cluster was similar in most of the strains (Lrh22, Lrh30, Lrh32 and Lrh47) in the cluster B (Fig 3B). The strain Lrh11 had a mobile element in the PS cluster before the gene coding for lysozyme and the strains Lrh13 and Lrh28 had two point mutations within the lysozyme gene (resulting in a split gene). The differences in the organization and existence of the polysaccharide clusters may have an influence on the polysaccharide surface of the strains and could potentially lead differences in the phenotype of these isolates.

Discussion
Although Lactobacillus spp. are commensals, part of the normal flora of the gastrointestinal tract, oral cavity and female urogenital tract [47], they have been occasionally isolated from immunocompromised and other hospitalized patients [6]. In the present study, we have isolated and sequenced 4 new strains and 12 already described L. rhamnosus strains from blood cultures collected from bacteremic patients between years 2005 and 2011 in HUSLAB. The main purpose of this study was to first identify the isolated strains at the sequence level and compare them to the widely consumed probiotic L. rhamnosus GG and, secondly, to investigate the phenotypic features related to complement evasion, platelet aggregation and biofilm formation in these isolated L. rhamnosus strains and compare these characteristics with L. rhamnosus GG. Our data revealed that L. rhamnosus isolates were clearly different from L. rhamnosus GG and each other at sequence level and they did not possess any distinctive niche specific (blood) genotypic traits as compared to L. rhamnosus GG. The strains were clustered into two main clusters A and B. Cluster A includes L. rhamnosus GG and its related strains. A model summarizing our findings (Fig 4) shows that all the isolated L. rhamnosus strains, including L. rhamnosus GG, were able to activate the complement system when it was measured as C3a and TCC formation in serum. Similarly, the strains did not bind complement inhibitors C4bp or FH. These results indicate that L. rhamnosus strains have not acquired mechanisms or traits to escape the complement system as opposed to the tested pathogens. However, some differences were seen in other phenotypic features, since four of the sixteen strains induced platelet aggregation and four strains formed stronger biofilm compared to L. rhamnosus GG. Most of these strains belong to the cluster B. The L. rhamnosus blood isolates showed a high level of heterogeneity and showed no common phenotypic trait that is involved in the persistence in the host, like biofilm formation, platelet aggregation and specific pilus production. Interestingly, analysis of genes encoding polysaccharide clusters showed differences between the strains in cluster A and B that might be also influencing the differences seen in phenotypes. Our results of the current study extend the results of the earlier survey by Salminen and coworkers [48] and unambiguously demonstrate that the widely consumed L. rhamnosus GG was not associated with the bacteremia cases. The techniques used for the analysis of the strains at sequence level have been highly improved from earlier used PFGE method to full genome Lrh7, Lrh8, Lrh9, Lrh14, Lrh20, Lrh46, Lrh47, Lrh38 and Lrh39 displayed comparable properties as observed in L. rhamnosus GG. All these strains activate the complement in serum. Strains Lrh13, Lrh30 and Lrh32 also induced more biofilm formation more than GG. Strains Lrh11, Lrh18 and Lrh22 were aggregating with platelets. Strain Lrh28 was doing both causing platelet aggregation and biofilm formation. The pathogenic group A Streptococcus strain emm8 induced complement activation, but it could bind complement regulator C4bp to evade complement. The pathogenic strain st369 could bind complement regulators C4bp and factor H and did not induce complement activation. A similar type of GAS strain has been shown to cause platelet aggregation [36] and biofilm formation [37]. The bolded strains have SpaCBA pili similar to GG. https://doi.org/10.1371/journal.pone.0176739.g004 Clinical blood isolate of L. rhamnosus sequence analyses up to 100% coverage of the sequence that allow to distinguish the strains at species level. However, there are reports that some cases of bacteremia have been associated with the consumption of probiotics among certain special conditions including hematopoietic stem cell transplantation [49], HIV-infection [50], severe active ulcerative colitis [13] and in a newborn with intrauterine growth restriction [51]. However, not all studies have determined the strains at species level. Only Sadowska-Krawczenko (2014) analyzed the identity at 100% (16S sequencing and PCR) in the case of intrauterine growth restriction [51]. A case report demonstrates that it is important to use the molecular diagnostic tools that can distinguish the strains at species level when we want study if the blood isolate originates from the probiotic strain consumed [52]. It is known earlier that immuno-compromised patients and patients with underlying diseases such as cancer are the ones who usually suffer from bacteremia caused by lactobacillus [48,53]. Based on our and others' studies we conclude that healthy people can use probiotics safely but among risk patients having disturbed immune function and mucosal disruption as in the case of inflammatory bowel diseases, the consumption of probiotics should be considered with caution before new studies have carefully assessed the risk to these patients.
All the Lactobacillus strains were recognized by the complement system and had no properties to inhibit the complement system by binding complement regulators (C4bp or FH). Thus, in this respect they can be categorized as commensals in contrast to pathogenic GAS strains emm8 and st369 that we used in this and an earlier study [24]. However, some variation in the level of TCC formation between the strains could be seen. Recently, piliation of L. rhamnosus GG has been shown to bind macrophages through a pattern recognition receptor namely complement receptor type 3 (CR3, iC3b receptor, CD11b/18) that mediates phagocytosis and removal of bacteria [54]. The SpaCBA piliation was also analyzed in the current study (Fig 2). The group having pili showed to have only a borderline increase in the complement TCC level (483.9 ± 76.4 AU/ml and 407.3 ± 68.1 AU/ml, p = 0.053; S2 Table) compared to the group without the SpaCBA pili. However, when the difference in complement activation as TCC between the SpaCBA pilus-deficient mutant strain of L. rhamnosus (PB12) [55] and L. rhamnosus GG was tested no significant difference was seen (441.5 ± 78.4 AU/ml vs 398.4 ± 87.1 AU/ ml, p = 0.07, respectively). Both of these strains induced similarly TCC formation in serum indicating that pilus as a structure is not inducing more complement activation. Thus, our data suggest that the isolated strains are recognized by the complement and they do not differ from each other in the ability to induce complement activation in serum and have not developed properties similar to pathogens.
Moreover, in our study we demonstrated that some of the strains have phenotypic features that are different from L. rhamnosus GG but can be found from pathogenic strains. These phenotypic features were abilities to cause platelet aggregation and biofilm formation. Earlier studies with a handful of strains have also shown that some of the clinical isolates of L. rhamnosus have been able to cause platelet aggregation [16,18]. Those strains were isolated from infectious endocarditis (5/5 tested strains), laboratory strains (8/16 strains) [15] and strains from infection of aortic aneurysm graft and carcinoma with liver metastasis [18]. Similar to our findings, L. rhamnosus GG did not cause aggregation with platelets in previous studies [17,18]. The ability to bind fibrinogen is known to help Gram-positive pathogens escape the immune system, and can be sufficient to induce platelet aggregation which can lead to e.g. endocarditis [41]. Recently a L. salivarius isolate from a case of sepsis, was found to aggregate human platelets via binding human fibrinogen through a novel fibrinogen-binding protein [19]. In our study a gene encoding fibrinogen/fibronectin binding proteins was present but we could not show that it causes the platelet aggregation phenotype (Fig 3).
We found that five of the isolated L. rhamnosus strains (Lrh28, Lrh13, Lrh30, Lrh32) were able to form biofilm more than L. rhamnosus GG (Fig 2). Interestingly, one strain (Lrh28) had the platelet aggregation phenotype, as well. Biofilms of lactobacilli can be located in many natural environments. Pathogenic bacteria can utilize the biofilm formation capacity for better survival in human body [56]. Various genetic pathways including clusters producing surface polysaccharides (EPS) have been shown to influence the biofilm formation capacity of L. rhamnosus GG in an earlier study [46]. Similar to a previous study we found in our experiments that L. rhamnosus GG was able to form small amounts of biofilms in the MRS medium [57]. Interestingly, we found that the strains in cluster A and cluster B possessed different EPS clusters so that the strains in cluster A had the EPS cluster similar to L. rhamnosus GG but the strains in cluster B had different sets of genes encoding proteins needed for EPS/CPS production such as glycosyltransferases and hypothetical proteins than GG. They also had an additional polysaccharide cluster that was found from all those strains in cluster B. However, one of the limitations of our study is that the genomic sequences of the isolated L.rhamnosus strains were not complete and contained some gaps. Moreover, we did not compare the gene expression of the L. rhamnosus strains and hence could not correlate all our functional analyses to the gene level. At least partly some of the phenotypic features could be caused by differences in the organization of EPS/CPS clusters. Recently, it has been shown that alterations in the genes involved in EPS synthesis in Lactobacillus johnsonii changed their surface properties and influenced on biofilm formation, cell adhesion, and autoaggregation [58]. Two clinical L. rhamnosus strains isolated from dental pulp infections have been shown to have modified exopolysaccharide clusters [21]. Such a biofilm producing phenotype can provoke the development of infections e.g. in the case of dental pulps, during catheter usage or endocarditis and be detrimental to a patient during bacteremia. However, biofilm formation is usually a feature associated with niche colonization in a different context than in clinical cases.
To conclude, our data demonstrate that L. rhamnosus strains isolated from blood cultures are distinct from L. rhamnosus GG and well-recognized by the body through the complement system and differ clearly from pathogenic strains. This supports the safe use of L. rhamnosus GG in healthy subjects with a functional immune system. Clinical blood isolates of L. rhamnosus do not possess any distinctive niche-specific genotypic traits for the blood environment similar to pathogens, which may be explained by the fact that they resided for a short period of time in blood and originally derived from other niches such as mouth, vagina, intestine or food products. In that regard, some of the strains that have platelet aggregation and biofilm formation properties might originate from those types of niches, where these properties are central for the stability and vitality of the strain.
Supporting information S1