Scrub typhus is a common and underdiagnosed cause of febrile illness in Southeast Asia, caused by infection with Orientia tsutsugamushi. Inoculation of the organism at a cutaneous mite bite site commonly results in formation of a localized pathological skin reaction termed an eschar. The site of development of the obligate intracellular bacteria within the eschar and the mechanisms of dissemination to cause systemic infection are unclear. Previous postmortem and in vitro reports demonstrated infection of endothelial cells, but recent pathophysiological investigations of typhus patients using surrogate markers of endothelial cell and leucocyte activation indicated a more prevalent host leucocyte than endothelial cell response in vivo. We therefore examined eschar skin biopsies from patients with scrub typhus to determine and characterize the phenotypes of host cells in vivo with intracellular infection by O. tsutsugamushi, using histology, immunohistochemistry, double immunofluorescence confocal laser scanning microscopy and electron microscopy. Immunophenotyping of host leucocytes infected with O. tsutsugamushi showed a tropism for host monocytes and dendritic cells, which were spatially related to different histological zones of the eschar. Infected leucocyte subsets were characterized by expression of HLADR+, with an “inflammatory” monocyte phenotype of CD14/LSP-1/CD68 positive or dendritic cell phenotype of CD1a/DCSIGN/S100/FXIIIa and CD163 positive staining, or occasional CD3 positive T-cells. Endothelial cell infection was rare, and histology did not indicate a widespread inflammatory vasculitis as the cause of the eschar. Infection of dendritic cells and activated inflammatory monocytes offers a potential route for dissemination of O. tsutsugamushi from the initial eschar site. This newly described cellular tropism for O. tsutsugamushi may influence its interaction with local host immune responses.
Scrub typhus is an infectious disease common in Southeast Asia, caused by the intracellular bacteria Orientia tsutsugamushi. These microorgansims infect humans through chigger mite bites, after which O. tsutsugamushi invades cells in the dermis, causing an inflammatory lesion called an eschar. Other rickettsia causing different forms of typhus preferentially invade and grow within endothelial cells lining blood vessels, before spreading systemically. In scrub typhus, unambigous endothelial infection with the bacterium O. tsutsugamushi has been described in autopsy samples. In this study, we examined ex vivo skin biopsies from eschars of scrub typhus patients admitting to hospital and defined the phenotypes of host cells that O. tsutsugamushi invades using specialized immunofluorescence microscopy. In this early phase of disease, we found that endothelial cell infection was rare, but infection of host monocytes and specialist antigen presenting cells, such as dendritic cells, was common. This represents a novel cellular tropism for O. tsutsugamushi, which provides a potential route for bacterial spread to the rest of the body and may affect its interaction with the host immune response.
Citation: Paris DH, Phetsouvanh R, Tanganuchitcharnchai A, Jones M, Jenjaroen K, Vongsouvath M, et al. (2012) Orientia tsutsugamushi in Human Scrub Typhus Eschars Shows Tropism for Dendritic Cells and Monocytes Rather than Endothelium. PLoS Negl Trop Dis 6(1): e1466. doi:10.1371/journal.pntd.0001466
Editor: David H. Walker, University of Texas Medical Branch, United States of America
Received: February 19, 2011; Accepted: November 23, 2011; Published: January 10, 2012
Copyright: © 2012 Paris et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was funded by the Wellcome Trust of Great Britain as part of the Wellcome Trust – Mahidol University – Oxford Tropical Medicine Research Programme and by the NIHR Biomedical Research Centre Programme, Oxford, UK. DHP holds a Wellcome Trust Clinical Research Training Fellowship (Grant Nr. 078990/Z/06/Z). This work was also supported by the Oxford Partnership Comprehensive Biomedical Research Centre with funding from the Department of Health's NIHR Biomedical Research Centres funding scheme. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Scrub typhus is a common and neglected disease caused by Orientia tsutsugamushi in Southeast Asia, accounting for up to 28% of non-malarial fevers in a prospective fever study in Lao PDR , and causing an estimated 1 million clinical cases worldwide every year . Recognition of the disease is difficult, due to its overlapping clinical spectrum with other common causes of fever in this population  and due to limitations of current diagnostic methods . As the early diagnosis of typhus disease is key to directing appropriate therapy, understanding how the organism develops, disseminates within the host, and interacts with the cells of the host immune response is important.
The proportion of acute primary infections with development of an eschar at the site of the chigger bite can vary widely with geographical areas, exposure of the population and level of endemicity of scrub typhus. In eastern Taiwan the percentage of eschars observed has been reported at 23% , in Japan a study observed 97% , and in Thai children from a highly endemic area this was 7% . Accompanying lymphadenopathy is very common in patients with scrub typhus , , which was also observed in volunteers infected with laboratory-reared chiggers . Fever, rash and non-specific symptoms are common, but the clinical course can be complicated by meningo-encephalitis, a disseminated intravascular coagulation (DIC)-like syndrome or severe pneumonitis, which may culminate in acute respiratory distress syndrome (ARDS) and death –.
Definitive evidience of endothelial tropism of O. tsutsugamushi requires immunophenotyping and ultrastructural co-localisation, which is available in one report of human post-mortem autopsies . Further data in the literature refers to histopathological reports from patient eschar biopsies and animal studies. Histopathological studies of eschars in humans – and cynomolgus monkeys  have described perivascular collections of mononuclear cells, including lymphocytes, plasma cells and macrophages. In recent studies, immunophenotyping revealed a dominance of CD3+ T-cells and CD68+ monocyte/macrophages within infiltrates  and an association of O. tsutsugamushi with the epithelial lining covering the surface of the sweat ducts and glands . Eschars can have high bacterial loads and have been shown to be useful specimens for both PCR-based and immunohistochemical diagnosis , .
Parallel studies of human ex vivo eschar biopsies in the spotted fever group (SFG) rickettsioses show evidence for infection of endothelium and surrounding leucocytes, with a predominance of neutrophils in the infiltrates in cases of R. africae , R. rickettsii  and R. conorii  although lacking ultrastructural demonstration. In summary, the literature provides limited evidence for the in vivo cellular tropism of O. tsutsugamushi in humans, due to a lack of co-localization studies allowing phenotypic characterization of the infected leucocyte subsets.
The eschar offers an accessible model for studying O. tsutsugamushi interactions during early infection of the human host, including colocalization studies for phenotyping of infected cells to elucidate the immune mechanisms involved in control or dissemination of O. tsutsugamushi from the local inoculation site. The study was designed to examine the cellular tropism of O. tsutsugamushi in eschars of patients with scrub typhus, characterize host leucocyte responses and determine the role of endothelial infection by O.tsutsugamushi in early disease.
Materials and Methods
The study was approved by the National Ethics Committee For Health Research, Ministry of Public Health, Lao PDR, and the Oxford Tropical Research Ethics Committee, UK. Patients were enrolled at Mahosot hospital, Vientiane, Lao PDR after the written consent (translated into Lao) of each patient was obtained by local clinicians. An additional separate written consent (translated into Lao) of each patient was obtained before performing the skin biopsy.
The clinical diagnosis of scrub typhus was confirmed with a positive scrub typhus immunochromatographic rapid diagnostic test (RDT; Panbio, Australia) and 4.5 mL of whole blood was taken into EDTA and serum separately for rickettsial culture, PCR and serology testing.
Only patients who had a visible eschar were asked to participate. During the course of the study, 1467 patients with a clinical diagnosis of scrub typhus were tested using serology, culture and/or PCR diagnosis. Of these, 188/1467 (12.8%) were confirmed to have scrub typhus by RDT and of these patients 57/188 (30.3%) had visible eschars. Only 14/57 patients (24.5%) had eschars on a part of the body appropriate for a biopsy (ie not the genitals or exposed areas) and gave consent for biopsy. No patients declined consent. 131/188 (69.7%) of confirmed scrub typhus patients lacked an eschar and were therefore not approached for inclusion in this study.
Skin biopsies were performed with disposable 3 mm circular punch biopsies (Stiefel Laboratories Inc., Offenbach, Germany) to sample a part of the central necrosis with perifocal inflamed skin, after local anesthesia with 1% lidocaine. Each patient had one biopsy, which was fixed using one of three different methods. The biopsies were either i) fixed in 10% Formalin and processed later into paraffin blocks (n = 7), ii) or stored in 2.5% glutaraldehyde for electron microscopy (n = 4), iii) or frozen in OCT for immunohistochemistry (n = 3, total cases = 14). The cases used in this study were the formalin fixed and EM cases (n = 11), shown in Table 1.
Gold standard serological diagnosis for scrub typhus was performed using paired serum samples with the indirect microscopic immunofluorescence assay for detection of IgM, with a cut-off titer of 1∶400 and a four-fold increase on paired serum samples, using pre-coated microscopic slides with antigen derived from validated O. tsutsugamushi type-strains (Karp, Kato and Gilliam), prepared and provided by the Australian Rickettsial Reference Laboratory . Region-specific and previously determined positivity criteria of 1∶400 IgM or a fourfold (or greater) rising titer was taken as indicative of an active infection , .
Quantitational PCR assay
Samples were examined by a previously described method using quantitative realtime PCR assay based on the groEL gene to confirm infection during diagnosis, and to quantitate rickettsial DNA copy numbers in samples from peripheral blood buffy coat preparations and skin biopsy sections . Diagnostic positivity was confirmed using a nested PCR technique for the 56 KDa surface protein as previously described .
Sample preparation for Electron Microscopy
Cell culture pellets or skin biopsies for EM examination were fixed in 4% glutaraldehyde in 0.1 M phosphate buffer and stored at 4°C before use. The samples were post-fixed in 2% osmium tetroxide in phosphate buffer and dehydration in ethanol followed by treatment with propylene oxide, prior to embedding in Spurr's epoxy resin. 1 µm ultrathin sections were cut with a diamond knife ultratome, stained with Azure A and examined by light microscopy to identify areas of interest. Thin sections of suitable areas were examined using a Jeol 1200EX electron microscope.
In vitro human cell line cultures
U937 immortilised human cell lines were used as a model of cells with the characteristics of monocyte/macrophages . Cells were grown in suspension in antibiotic free RPMI+10% FCS+1 mM Glutamine. Infection with O.tsutsugamushi strain UT-76 was achieved by a multiplicity of infection (MOI) of 10∶1. The infected VERO cells were incubated at 37°C for 45 minutes to then be harvested for PCR, electron microscopy and immunohistochemistry.
Skin biopsies were immediately fixed in 10% PBS buffered formalin, stored at 4°C and subsequently processed into paraffin wax blocks. These were prepared using standard histological techniques, and 3 µm sections cut with a rotatory microtome either onto standard glass slides (for histology) or Vectabond coated slides (Vector Laboratories, Inc., Burlingame, CA, USA) for immunohistochemistry or immunofluorescence.
Sections were de-waxed with Citroclear (TCS Biosciences, Buckingham, UK): 2 baths of each 5 min, and ethanol: 2 baths of each 2 min in 100% EtOH then one bath for 2 min in 50% EtOH. The sections underwent antigen retrieval by pressure cooking in Tris-EDTA buffer (pH 9), at 120°C for 2 min before double-immunological labelling.
The DAKO EnVision™+ System, HRP kit was used. Briefly, endogenous peroxidase activity was blocked by incubating the specimen for 5 minutes with DAKO Peroxidase Block (included in the kit). Slides were incubated at room temperature in a dark, humidified chamber with primary mouse or rabbit antibody for 30 minutes or, as a negative control, incubated with PBS with omission of the primary antibody, followed by three washes with PBS and then incubation with the labeled polymer for 30-minutes. Staining was completed by a further three washes with PBS andd then a 5–10 minute incubation with 3,3′-diaminobenzidine (DAB)+ substrate-chromogen, which resulted in a brown-coloured precipitate at the antibody binding site. Double immunolabelling with immunoperoxidase staining utilized secondary labeled antibodies against different isotype specific primary monoclonals, one for which labeled with Diaminobenzidine (DAB) in brown and the other with alkaline phosphatase (AAP) in red to allow co-localisation. This was followed by counterstaining with hematoxylin for 30 seconds, washing with PBS, application of mounting media (VectaMount medium, Vector Labs, Burlingame, USA) and coverslipping the slides.
Immunofluorescence and confocal microscopy
The 3 µm thin sections underwent pressure cooking for antigen retrieval, were incubated with the proprietory protein blocking solution (DAKO) for 10 minutes, washed three times with 10% PBS, then incubated in a humidified darkened slide chamber at room temperature with primary monoclonal antibodies (mAbs) for 30–45 min, washed and incubated with the secondary isotype specific mAbs conjugated with a fluorochrome for 30 mins. The fluorochromes used for detection of O. tsutsugamushi was FITC- (absorbtion 488 nm/emission 520 nm, bright apple green colour) and for cellular phenotyping Texas Red (absorbtion 596 nm/emission 615 nm, deep red colour). These were then washed in a PBS bath for 2 minutes, the slides mounted and coverslipped in VectaMount (Vector Laboratories, Burlingame, CA, USA) into which was added the nuclear intercalating counterstain DAPI (4′,6-diaminidimo-2-phenylindole), and examined using standard fluorescence microscopy and a confocal laser scanning microscope (Zeiss LSM 700). Both microscopes used the AxioVision 40 v126.96.36.199 software from Carl Zeiss Imaging Solutions Gmbh, Germany. Images were merged and optimised with Photoshop CS3 extended, version 10.0.
Generation of anti-O.tsutsugamushi monoclonal antibodies
The in-house monoclonal antibody used for staining O. tsutsugamushi in this study was generated in our laboratory by immunization of mice using whole protein extracts of O. tsutsugamushi (Karp UT76, Kato, Gilliam and 716-like strains), which were cultured in L929 cells, or intra-peritoneal mouse infection with live O. tsutsugamushi (MSc thesis of Ampai Tanganuchitcharnchai, Faculty of Tropical Medicine, Mahidol University, Thailand). Prospective hybridomas were further chartacterised by indirect ELISA and immuno-fluorescence assays (IFA) using a panel of crude surface membrane lysates including O. tsutsugamushi (Karp, Kato, Gilliam and TA716-like strains), R. typhi, R. prowazekii, R. honei, R. conorii, and a wide range of negative control bacteria including Aeromonas hydrophilia (American Tissue Culture Collection reference 4965), Escherichia coli (ATCC 25922), Shigella flexneri (ATCC 12022), Plesimonias shigelloides (ATCC 14029), Salmolella choleraesuis (ATCC14028), Vibrio spp. (ATCC33812), Salmonella spp, Yersinia enterocolitica, Pseudamonas aeruginosa and Leptospira spp. Selected clones showing positive reaction specifically to O.tsutsugamushi were tested using Western blotting on SDS-PAGE gels of crude protein extracts of VERO infected cells. Eight mAbs were assessed for their suitability for immunostaining of cell culture preparations by IFA staining of infected and uninfected Vero cell culture pellets as positive and negative controls performed in triplicate and immuno-enzymatic staining on cell cultures (HRP-based enzyme-conjugated polymer kit, Envision, DAKO). The antibody clone 1C4B11 was a highly O. tsutsugamushi-specific monoclonal antibody (isotype IgG2bκ) recognizing the 56 kDa surface antigen on Western blotting, which stained O. tsutsugamushi strongly and specifically as ringforms with a central lucency, reflecting recognition of antigen on the outer membrane, with no staining of uninfected VERO or L929 cell lines as negative controls. It also produced regular and highly specific staining of O. tsutsugamushi in formalin fixed sections using AAP, HRP enzymatic and fluorescence labeling.
Other antibodies used for immunohistochemistry
The cell-specific monoclonal antibodies used to characterize and immunophenotype different host cells within eschar biopsies are summarized in Table 1. Staining of the cellular components in sections was expressed as a percentage of all inflammatory cells. The extent of immunopositivity in the inflammatory cells for specific cell markers was graded in the following manner: (−) in 0%, (±) in <1%, (+) in 1%–25%, (++) in 26%–50%, (+++) in >50% and (++++) in >75% of infiltrated cells.
Clinical details of scrub typhus patients
Eschar biopsies from patients with a confirmed diagnosis of scrub typhus were examined by histology, immunohistochemistry, immunofluorescence and electron microscopy (Table 2).
All patients presented with fever and suffered from headache or severe retro-orbital pain (10/11), myalgia (10/11) or rigors (10/11). No skin rash was observed in any of the patients. One patient presented with confusion and deafness, which resolved fully following antibiotic therapy. Four patients were referred after β-lactam based antibiotics had been administered with no effect. All patients were subsequently treated with doxycycline, with exception of a pregnant woman, who was treated successfully with azithromycin. No patients suffered severe manifestations of the disease and all made a full recovery during hospitalization [median 8 days (range 4–20)].
Histological features of eschar biopsies
Histological examination of the eschar revealed common features between patients, with sharply demarcated areas of ulceration and necrosis of the overlying epidermis, acute inflammatory slough and artifactual shedding and blistering of the epidermis (Figure 1). The neighbouring intact epidermis showed mild spongiosis with focal inflammation. There was focal parakeratosis, probably reflecting the relatively short time period over which the eschar is established. Basal vacuolar and necrotic changes within keratinocytes were accompanied with focal red cell extravasation, and in patient TM2644 there was established intraepidermal splitting, and in patient TM2646 marked subepidermal blistering. These features appeared secondary to necrosis, and associated with marked neutrophilic acute inflammation, rather than representing a primary bullous disease .
Panels A and B. Intraepidermal splitting and sub-epidermal blistering with basal vacuolar changes, inflammatory exocytosis and focal red blood cell extravasation in the superficial dermis. Patient TM2644 (Panel A) and TM2646 (Panel B), magnification ×400. Panel C. Acute inflammatory sloughing and artefactual separation of the epidermis. A demarcated area of ulceration and necrosis of the overlying epidermis with subepidermal vacuolation, necrosis and mononuclear infiltration, patient TM2663, magnification ×250. Panel D. Perivascular infiltrates and leucocytoclastic vasculitis. On the right hand side the cross-section of an arteriole, on the left, a venous vessel with intravascular obliteration and secondary thrombus. There is prominent perivascular cuffing with mononuclear cells and fibrinoid necrosis of the arteriolar wall. Patient TM2193, magnification ×250. All panels Haematoxylin & Eosin (H&E) staining.
In the underlying dermis the histological pattern was dominated by inflammatory infiltrates at all levels, including perivascular infiltrates in subdermal fat consistent with superficial panniculitis. The dermis showed mild edema and marked mononuclear cell infiltrates, distributed in perivascular, interstitial, perifollicular, periglandular and focally in perineural areas. Patient TM2193 showed a leucocytoclastic vasculitis, with dense infiltrates of mononuclear cells around dermal vasculature, karryorhectic neutrophil debris, fibrinoid necrosis of the vessel wall and associated thrombosis.
Immunophenotyping of leucocyte subsets in eschar infiltrates
The dermal cell infiltrates were phenotyped using multiple markers against different leucocyte subsets as detailed in Table 1. A mixed inflammatory infiltrate with a strong predominance of antigen presenting cells (APCs) was present within all the eschar biopsies studied. The extensive infiltrates, in both superficial and deep dermis, consisted predominantly of mononuclear cells with high expression levels of MHC class II receptors (HLADR). High leucocyte densities were found at the dermo-epidermal junction, around vessels and sebaceous and sweat glands reaching into the subcutaneous fat (Figure 2). More detailed examination of HLADR intense zones in the eschar revealed that more than 80% of these cells consisted of monocytes, macrophages and dendritic cells (Supplemental Figure S1). Lymphocytes were found interspersed and whilst T cells were common, B cells were rare. T lymphocytes presented with a ratio of T helper cells (CD4+) to cytotoxic T cells (CD8+) of approximately 1∶2. The presence of dermal dendritic cells (DDCs) was more intense at the dermal-epidermal junction, with a macrophage to DDC ratio of approximately 1, which increased towards the deeper dermis. DDCs displayed an immunophenotype of CD1a+, CD11c+, DCSIGN+, S100+, and FXIIIa+ (using double immunofluorescence labelling on multiple sequential sections). Neutrophils were relatively uncommon in perivascular infiltrates but formed an intense zone of infiltration around the necrotic centre of the eschar (Supplemental Figure S2).
Serial sections at the dermal-epidermal border, demonstrate that APCs are the dominant cell type adjacent to the central necrotic zone of the eschar. Immunophenotyping by MHC class II receptor for APCs (Panel A: HLADR), macrophages (B: CD68) and DCs (C: DC-SIGN, D: FXIIIa, G: S100 and H: LSECtin), neutrophils (E: CD15) and lymphocytes (F: CD4). The proportion of dendritic cells was higher in the dermal-epidermal border zone, than in the deeper dermis. Subepidermal vacuolization is prominent. Patient TM2663, magnification ×400, counterstained with haematoxylin, peroxidase immunostaining in brown.
Characterization of O. tsutsugamushi-infected cells in eschars
Intracellular infection of endothelial cells by O. tsutsugamushi in the dermal vascular plexus of these specimens was extremely rare and found in only three sections (patients TM2193 and 2508). While O. tsutsugamushi co-localization with the endothelium was often seen, the high resolution thin sections using confocal laser scanning microscopy (LSM) revealed O. tsutsugamushi to be located within adjacent perivascular mononuclear cells or cells in the process of diapedesis through the endothelial monolayer (Supplemental Figure S3).
Antigen presenting cells (APCs).
APCs, characterized by MHC class II receptor and HLADR positivity, were the main cell type associated with intracellular O. tsutsugamushi infection (Figure 3). HLADR positive cells contained high numbers of O. tsutsugamushi, (6–7 organisms per cell per section), but also small immuno-positive intracellular microparticles, with high refractive indices on confocal LSM. This ‘microparticle’ phenomenon could not be observed in any other of the cell types characterized. HLADR-positive dermal dendritic cells (DDCs) cells were differentiated from monocyte/macrophages by their CD1a, S100, LSECtin and/or DC-SIGN positivity. DDCs were the predominant HLADR+ cell type found in the sub-epidermal zone. A focal subpopulation of CD1a-positive Langerhan's cells infected with O. tsutsugamushi were seen entering the dermis in conjunction with overlying nodule-like epidermal proliferations of Langerhan's cells (Figure 4). This was more pronounced in immediate vicinity of the necrotic zone. Although CD1a is a hallmark antigen for Langerhan's cells, these surface markers can also be found on activated lymphocytes, and DDCs , . DCSIGN+ cells were present in large numbers in the dermis, and two subsets of DDCs were characterized by either weak or strong intensity, in both immunoperoxidase and immunofluorescence staining. LSM images demonstrated intracellular O. tsutsugamushi within DDCs, and a strong DCSIGN+ signal was observed with evidence of O. tsutsugamushi infection in the same cell, as shown by co-localization with O. tsutsugamushi in LSM thin sections (Figure 5). Similar observations were made for subsets of LSECtin+ and S100+ DCs (data not shown).
APCs are characterised by MHC class II receptor (HLADR) positivity and were associated with intracellular O. tsutsugamushi in admission samples of an eschar from a patient with acute scrub typhus. Panel A: HLADR-positive cells in red, O. tsutsugamushi in green. Panels B and C: Laser Scanning Micrographs. Panel B depicts the same infected cell as in Panel A as a 0.3 µm thin section. Panel C shows a 3D stack projection (of 0.3 µm thin sections) of intracytosolic O. tsutsugamushi (in green), with small, high-density granules with high refractive index, staining positively for O. tsutsugamushi antigen. Patient TM2193, magnification ×400, LSM inserts ×1000, double-immunolabeling: HLADR in red, O. tsutsugamushi in green and DAPI nuclear counterstain in blue.
Local proliferation of Langerhans cells in the epidermis, with a distinct CD1a+ nodule formation and O. tsutsugamushi infected cells located in the dermis (white arrows) of an eschar from a patient with acute scrub typhus. Erythrocytes appear yellow due to autofluorescence. Insert: Laser Scanning Micrograph (LSM), 0.3 µm thin section visualizing the intracytosolic location of O. tsutsugamushi, accompanied by small intracellular microparticles with high refractile index. Patient TM2193, magnification ×400, insert ×1000. Labeling: CD1a in red, O. tsutsugamushi in green and DAPI nuclear counterstain in blue.
Panel A: High numbers of DCSIGN+ cells in the dermal-epidermal zone of the eschar. The variance of staining-intensity of individual positive cells ranged from strong (long black arrow) to weak (short black arrow). Patient TM2644, magnification ×400, peroxidase immunostaining in brown. Panels B, C and D: Immuno-double-labelling with HLADR (Panel B), DC-SIGN (Panel C) and LSP-1 (Panel D) stained red. The signal intensity of these markers in infected cells with O. tsutsugamushi (in green) appeared more pronounced (long white arrows) than in uninfected cells (short white arrows). Patient TM2193 (Panel B), patient TM2508 (Panel C and D). Magnification ×400, blue nuclear counterstaining with DAPI.
Characterisation of monocytes/macrophages included immunophenotyping for CD14, CD68 for moncytes and macrophages and CD163 for subtypes expressing scavenger receptors. Monocytes and macrophages were the predominant cell type characterizing peri-glandular and peri-vascular dermal infiltrates and co-localized regularly with O. tsutsugamushi, however unambiguous intracellular location could not always be proven due to podocyte formation and dendritic cellular morphology (Figure 6). Infected cells contained on average fewer intracellular O. tsutsugamushi than DDCs (2–4 organisms per cell per section, Figure 7). In CD163+ macrophages, the O. tsutsugamushi often appeared fragmented and not as round intact bacteria (Figure 8). No intracellular microparticle formation was observed in macrophages. Bacterial staining in association with B cells (positive for CD20 and nuclear BCL11a) was extremely rare and seen in only 2 individual B-cells (<1%).
Panel A: Perivascular cuff formation and clusters of predominantly CD68+ macrophages, co-localizing closely with O. tsutsugamushi. Patient TM2193, magnification ×400. Magnification ×400, insert ×1000, double-immunolabeling: CD1a in red, O. tsutsugamushi in green and DAPI nuclear counterstain in blue. Panels B and C: Laser Scanning Micrographs with 3D stack projections of multiple 0.3 µm thin sections, depicting intact O. tsutsugamushi associated with CD68+ macrophages (panel B). Unambigous intracellular location of O. tsutsugamushi in a CD68+ cell (panel C). Patient TM2508, magnification ×1000, CD68 labeled in red, O. tsutsugamushi in green.
Characteristics were defined as follows: (a) Number of O. tsutsugamushi per cell per section. (b) Proportion of cells in infiltrate. (c) Morphological aspects of intracellular O. tsutsugamushi. Infiltrates were estimated in a semi-quantitative manner: The extent of immunopositivity in the inflammatory cells for specific cell markers was graded in the following manner: (−) in 0%, (±) in <1%, (+) in 1%–25%, (++) in 26%–50%, (+++) in >50% and (++++) in >75% of infiltrated cells.
Panel A: High density of CD163+ monocye/macrophages at the dermal-epidermal border and after intraepidermal translocation adjacent to the inoculation of O. tsutsugamushi. Patient TM2391 (panel A), magnification ×200, peroxidase immunostaining in brown. Panels B and D: Perivascular CD14+ monocyte/macrophages conglomerates containing O. tsutsugamushi. Cross-section of perivascular cuff formation (panel B) and longitudinal section (panel D). Patient TM2644, magnification ×400, double-immunolabeling: CD14 in red, O. tsutsugamushi in green and DAPI nuclear counterstain in blue. Panel C: Laser Scanning Micrograph, 0.3 µm thin section confirms the intracellular co-localization of O. tsutsugamushi in a CD163+ monocyte/macrophage. A large proportion of O. tsutsugamushi in these cells appeared in a fragmented state. Patient TM2508, magnification ×1000, double-immunolabeling: CD163 in red, O. tsutsugamushi in green and DAPI nuclear counterstain in blue.
Non-antigen presenting cells.
CD3+ T lymphocytes co-localized with O. tsutsugamushi and confocal LSM revealed the external attachment of O. tsutsugamushi to be more common than true intracytoplasmic infection (Figure 9). CD3 stains both CD8+ cytotoxic T-cells (MHC class I) and CD4+ regulatory T-cells (MHC class II), but immuno-fluorescence staining for CD8+ T-cells showed co-localization in only 3 cells (<1%).
Panel A: Perivascular cuff formation of predominantly mononuclear cells containing large numbers of CD3+ cells co-localising with O. tsutsugamushi. Panels B and C: Laser Scanning Micrographs. The association of T cells with O. tsutsugamushi was commonly by external attachment rather than definite intracellular location. Panel B depicts a 3-D stack projection showing external O. tsutsugamushi attachment to the T lymphocyte, in the lateral vertical sections. Panel B is a 0.6 µm thin section. Patient TM2193, magnification in panel A ×400, in panels B and C ×1000. Double-immunolabeling: CD3 in red, O. tsutsugamushi in green and DAPI nuclear counterstain in blue.
LSP1 is expressed in lymphocytes, neutrophils, macrophages, and endothelium and may regulate neutrophil motility, adhesion to fibrinogen matrix proteins, and transendothelial migration. LSP1 can also be expressed by plasma cells, dendritic cells and Langerhans cells . O. tsutsugamushi co-localized intracellularly with LSP1+ cells in the upper dermis and infected cells appeared to stain more intensively for LSP1 (Figure 5).
Neutrophils were most dense at the delineating zone of the central necrosis and CD15/neutrophil elastase-positive cells co-localized regularly with intracytoplasmic O. tsutsugamushi. While many bacteria appeared intact, a proportion appeared to vary in size and morphology, suggestive of intracytoplasmic degradation.
Quantitation of bacterial loads and leucocyte responses.
As summarized in Table 2, semiquantitative estimation of bacterial load within the eschar showed high levels of infected cells in eschars taken earlier in the course of febrile illness (days 5–7) and decreased (or absent) Orientia seen in later eschars from days 7–12. Bacterial load per infected cell ranged from 1–7 recognisable separate bacteria per section. Semiquantitative estimation of specific infected cell phenotypes showed activated inflammatory monocytes and dendritic cells were present in both the upper and lower dermis, although the nodules of CD1a+ Langerhan's cells were limited to the basal epidermis and superficial dermis. Quantitative PCR estimation of bacterial load in peripheral blood leucocytes from Buffy coat samples indicated that early dissemination of Orientia into the blood stream was already established at presentation of the eschar. The decrease in bacterial numbers in the eschar over time (taking the series as a whole) and the early positive PCR results in Buffy coat samples imply that the eschar is not the major site for bacterial replication.
Formation of Orientia membrane protrusions.
Ultrastructural examination of in vitro O. tsutsugamushi-infected U937 monocytic cells revealed formation of multiple intracytopalsmic membrane protrusions from bacteria, leading to microparticles budding from the outer leaflet of normal-sized, intracellular bacteria were found in in the cytoplasm of infected U937 cells (Figure 10). This mirrored morphological observations in both HLADR and CD1a positive cells in eschar biopsies in vivo.
Panel A: Bizarre morphology of O. tsutsugamushi (B) in the U937 cell line, with corners and tent-like stretching within the cytoplasm with adjacent mitochondria (Mi). Bar length corresponds to 1 µm. Panel B: A number of O. tsutsugamushi (B) with associated microparticles (arrowheads) within the host cell cytoplasm. Bar represents 500 nm. Panel C: Enlargement of the enclosed bacterium from Panel B showing blebbing of the outer membrane (arrow). ‘mp’ - detached microparticle. Bar length corresponds to 100 nm. Panel D: Detail of two microparticles (mp) formed by the outer, but not inner leaflet of O. tsutsugamushi. These microparticles carry the surface antigens of the ‘mother’ Orientia, and their function remains unclear. Bar length corresponds to 100 nm. Insert - Enlargement of the enclosed area in D showing the structure of the limiting membrane of the microparticle. Bar length corresponds to 10 nm.
Evidence from post mortem studies and extrapolation of findings in other rickettsial diseases have implied that scrub typhus is predominantly an endothelial infection, with pathological features of a disseminated vasculitis. Early histopathological studies from the 1940s suggested different pathogenic mechanisms between Orientia and Rickettsia spp.  and recent clinico-pathophysiological studies in Southeast Asia highlighted marked differences in the expression patterns of endothelial and mononuclear cell activation markers, as well as coagulation parameters and cytokines for the clinically similar diseases murine typhus (caused by Rickettsia typhi) and scrub typhus (O. tsutsugamushi) , . While murine typhus patients had high levels of endothelial-specific soluble E-selectin, implying widespread endothelial cell activation, this was not the case in scrub typhus, where significantly raised sL-selectin levels implied mononuclear cell activation.
This study provides evidence that within the eschar site, at the clinically relevant timepoint of hospital presentation after 5 to 10 days of fever, O. tsutsugamushi co-localized mainly with monocyte/macrophages and dermal dendritic cells, rather than the endothelium (Figure 7). Both of these cell types act as APCs and have the ability to re-circulate systemically via the lymphatic vasculature. The O. tsutsugamushi organisms within these cells did not appear fragmented and formed clusters or groups, often at a perinuclear location, suggestive of intracellular replication. B-cells were very rarely infected and T-cells often showed O. tsutsugamushi adherent to the surface of the cell rather than invading intracellularly.
Endothelial cells on the other hand were not a common site for cellular invasion and replication and seemed to be a less important target than mononuclear cells in this early phase of infection in the eschar. A recent report demonstrated that monocytes are activated in vitro and ex vivo following exposure to O. tsutsugamushi . These pathogenic findings offer an explanation for the rapid clearance of organisms from the eschar and early hematogenous and/or lymphatic dissemination (due to re-circulation of infected cells and/or direct hematogenous dissemination), consistent with the presence of early and co-existent rickettsiaemia by PCR examination of peripheral blood.
The eschar provides a unique opportunity to study cellular interactions in humans in vivo, though the biopsy specimen of each patient represents a single time window, usually early in the disease course. Although data from serial sections at different timepoints from the same eschar are not available, eschars biopsied on days 5 to 7 of clinical illness had higher bacterial counts per section than those biopsied on days 10 to 12, suggestive of a gradual decline of detectable O. tsutsugamushi within an eschar over time. While the number of O. tsutsugamushi in the eschars studied decreased rapidly from day 7, rickettsaemia as measured in the buffy coat preparation of peripheral blood leucocytes from the same patients decreased around day 10 of fever/illness, and did not relate directly to the presence of O. tsutsugamushi in the eschar. This implies that the main site of replication of O. tsutsugamushi prior to dissemination is not the eschar. Regional lymphadenopathy at this timepoint is common, which coupled with the tropism of O. tsutsugamushi to APC in eschars, suggests that one source of replication may be within infected, recirculated APCs in the regional (and other) lymph nodes. Previous investigations of intradermal inoculations with R. mooseri (R. typhi) in guinea pigs demonstrated that the organisms rapidly access draining lymph nodes then sequentially appeared in spleen, kidney, and blood . However if O. tsutsugamushi is disseminated to other organs by this time then further studies are required to determine the sites of replication and cellular tropism within other tissues, in relation to disease progression (days of fever or similar parameters). As no studies addressing these issues in eschars of SFG and TG rickettsial disease are available, direct pathogenic comparisons of infected cell phenotypes to related rickettsioses are unfortunately not possible.
A novel observation in these studies was of small membranous protrusions forming microparticles in the cytoplasm of infected monocyte/macrophages and dendritic cells, in vivo (CD1a+ and HLADR+) (Figures 3 and 4) and in vitro in the monocyte cell line U937 (Figure 10). These microparticles stained strongly positive with the monoclonal antibody targeting the surface type specific antigen p56. Similar microbial protuberances leading to shedding of microparticles have been described in salivary gland cells of the transmitting vectors (trombiculid mites) in EM studies, with an apparently similar membrane structure . They may represent particles of degenerating O. tsutsugamushi. Other intracellular organisms with similar membrane characteristics, such as Ehrlichia spp. have been reported to produce membranous rounded or filamentous extensions, which can contribute to the pathogenicity of infection , .
Dermal dendritic cells comprise at least two major phenotypic populations, immature DCs expressing CD1, CD11c and CD208; and macrophages expressing DC-SIGN (CD209), CD206, CD163, and CD68 . This study showed evidence of DDC subgroups with differential expression of either HLADR, DCSIGN, LSECtin, S100 and/or LSP1. O. tsutsugamushi-infected DDCs appeared to express higher levels of DC-SIGN, arguing either for the selection of these cells for infection, or upregulation of this marker in response to infection. The immunomodulatory effects of O. tsutsugamushi infection on local APCs in the eschar site could also interfere with downstream host immune responses. Activated DDCs (such as dermal Langerhans cells) can recirculate from skin to lymph nodes and represent a potential route of intracellular spread away from the eschar site, This offers an alternative explanation for rapid systemic dissemination other than interendothelial cell migration, and may not be restricted solely to O. tsutsugamushi, but also other rickettsioses.
These observations of the cellular tropism of O.tsutsugamushi in the eschar raise the question of which cellular phenotypes are infected in the lymph node and distant organs following dissemination, where endothelial cells could be a preferential site of infection. Such data are unlikely to become available from large autopsy based studies and hence the development of good animal models for scrub typhus is important.
Further investigations are warranted into the phenotypes of cells infected in the lymph node and other organs following dissemination to determine where Orientia invade, survive and replicate, as this will contribute to our understanding of immunopathophysiology of scrub typhus.
Immunohistochemical characterization of cellular phenotypes and their distribution within dermal infiltrates. Markers used to define antigen presenting cells (panel A: HLADR), monocytes (B: CD14), macrophages (C: CD68, D: CD163), neutrophils (E: CD15), dendritic cells (F: CD11c, G: DCSIGN, H: S100, and I: FXIIIa), endothelium (J: CD31), B lymphocytes (K: CD20, L: BCL11a), T lymphocytes (M: CD4, N: CD8) and cytokeratin (O: CK). While T lymphocytes were ubiquitously present, the most prominent cellular phenotype found in dermal infiltrates were APCs, consisting predominantly of macrophages and dendritic cells, but not B cells. Patient TM2425, magnification ×400, counterstain haematoxylin, peroxidase immunostaining in brown.
Neutrophil polymorphnuclear cells delineate the central necrotic zone of the eschar. The necrotic centre (labelled ‘N’, in upper left of both panels) is delineated by a granulocyte-dense zone depicted in red, buy immunofluorescent staining for neutrophil elastase NP57 (Panel A), and CD15 (Panel B). Accumulation of CD15+ neutrophils along the vasculature (yellow arrows) can be seen in panel B. Patient TM2193, magnification ×200, erythrocytes in yellow-green, NP57 and CD15 labeled in red, DAPI nuclear counterstain in blue.
Longitudinal section of a superficial dermal blood vessel with perivascular mononuclear cells. A longitudinal cross-section of a blood vessel with endothelium stained by CD31 (in red) and O. tsutsugamushi (in green). A small cluster of O. tsutsugamushi (long white arrow) were examined using a LSM (insert). The insert is a 0.3 LSM micrograph with CD31+ cells (short arrows) with adjacent cells containing O. tsutsugamushi (long white arrow) One cell contains O. tsutsugamushi and three small ‘bleb-like’ inclusions, typically seen in HALDR-positive cells. Patient TM2193, magnification ×400, LSM insert ×1000, double-immunolabeling: CD31 in red, O. tsutsugamushi in green and DAPI nuclear counterstain in blue.
We would like to thank the staff at Mahosot Hospital, Lao PDR, who cared for the patients involved in the study, especially Dr Vilada Chansamouth and Sengkham Symanivong for assistance. We also thank the Minister of Health, His Excellency Dr. Ponmek Dalaloy, and the Director of the Curative Department, Ministry of Health, Professor Sommone Phousavath, Government of Laos, for support for this study.
We gratefully acknowledge the help and advice of members of the NDCLS/OxFABs laboratory for their help with immunohistochemistry and cell culture techniques, in particular Jackie Cordell.
Conceived and designed the experiments: DHP PNN NPJD GDHT. Performed the experiments: DHP AT MJ KJ. Analyzed the data: DHP DPJF SDB GDHT. Contributed reagents/materials/analysis tools: RP MV MJ SDB DPJF PNN. Wrote the paper: DHP GDHT NPJD.
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