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Heterogeneity of Orientia tsutsugamushi genotypes in field-collected trombiculid mites from wild-caught small mammals in Thailand

  • Ratree Takhampunya ,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Project administration, Supervision, Visualization, Writing – original draft, Writing – review & editing

    Affiliation Department of Entomology, Armed Forces Research Institute of Medical Sciences-United States Army Medical Directorate, Bangkok, Thailand

  • Achareeya Korkusol,

    Roles Conceptualization, Data curation, Formal analysis, Methodology

    Affiliation Department of Entomology, Armed Forces Research Institute of Medical Sciences-United States Army Medical Directorate, Bangkok, Thailand

  • Sommai Promsathaporn,

    Roles Methodology

    Affiliation Department of Entomology, Armed Forces Research Institute of Medical Sciences-United States Army Medical Directorate, Bangkok, Thailand

  • Bousaraporn Tippayachai,

    Roles Methodology

    Affiliation Department of Entomology, Armed Forces Research Institute of Medical Sciences-United States Army Medical Directorate, Bangkok, Thailand

  • Surachai Leepitakrat,

    Roles Resources

    Affiliation Department of Entomology, Armed Forces Research Institute of Medical Sciences-United States Army Medical Directorate, Bangkok, Thailand

  • Allen L. Richards,

    Roles Writing – original draft, Writing – review & editing

    Affiliation Viral and Rickettsial Diseases Department, Naval Medical Research Center, Silver Spring, Maryland, United States of America

  • Silas A. Davidson

    Roles Funding acquisition, Writing – original draft, Writing – review & editing

    Affiliation Department of Entomology, Armed Forces Research Institute of Medical Sciences-United States Army Medical Directorate, Bangkok, Thailand

Heterogeneity of Orientia tsutsugamushi genotypes in field-collected trombiculid mites from wild-caught small mammals in Thailand

  • Ratree Takhampunya, 
  • Achareeya Korkusol, 
  • Sommai Promsathaporn, 
  • Bousaraporn Tippayachai, 
  • Surachai Leepitakrat, 
  • Allen L. Richards, 
  • Silas A. Davidson


Trombiculid mites are the vectors of scrub typhus, with infected larval mites (chiggers) transmitting the causative agent, Orientia tsutsugamushi, during feeding. Co-existence of multiple O. tsutsugamushi strains within infected mites has previously been reported in naturally infected, laboratory-reared mite lines using molecular methods to characterize the 56-kDa type-specific antigen (TSA) gene. In the current study, more advanced next-generation sequencing technology was used to reveal the heterogeneity of O. tsutsugamushi genotypes in field-collected trombiculid mites from rodents and small mammals in scrub typhus-endemic areas of Thailand. Twenty-eight trombiculid mites collected from 10 small mammals were positive for O. tsutsugamushi, corresponding to a prevalence rate of 0.7% within the mite population. Twenty-four of the infected mites were Leptotrombidium spp., indicating that this genus is the main vector for O. tsutsugamushi transmission in Thailand. In addition, O. tsutsugamushi was detected in the mite genera Ascoschoengastia, Blankaartia, Gahrliepia, and Lorillatum. Of the 10 infested small animal hosts, six had 2–10 infected mites feeding at the time of collection. Deep sequencing was used to characterize mixed infections (two to three O. tsutsugamushi genotypes within an individual mite), and 5 of the 28 infected mites (17.9%) contained mixed infections. Additionally, 56-kDa TSA gene sequence analysis revealed identical bacterial genotypes among co-feeding mites with single or mixed infections. These results suggest that co-feeding transmission may occur during the feeding process, and could explain the occurrence of mixed infections in individual mites, as well as the recovery of multiple infected mites from the same host. This study also revealed highly diverse within-host O. tsutsugamushi genotypes. The occurrence of multiple O. tsutsugamushi genotypes within individual mites has important implications, and could provide a mechanism for pathogen evolution/diversification in the mite vector.

Author summary

Scrub typhus is a leading cause of undifferentiated febrile illness, putting 1 billion people at risk of infection. Trombiculid mites are the major vectors of the causative agent of scrub typhus, Orientia tsutsugamushi (OT), which is transferred through the bite of an infected mite. Previously, we reported the co-existence of multiple OT strains within laboratory-reared mites. Here, we extended our investigation into wild trombiculid mite populations collected from areas of Thailand where scrub typhus is endemic. More advanced next-generation sequencing (NGS) technology was used to examine the presence and abundance of mixed infection in individual mites based on sequence analysis of the 56-kDa type-specific antigen gene. NGS data revealed heterogeneity of OT genotypes in field-collected mites, and mixed infection with two to three OT genotypes was consistently observed (prevalence rate = 17.9%). Moreover, the identical OT genotype detected among co-feeding mites with single or mixed infections suggesting that co-feeding transmission may occur during the feeding process. This result could explain the occurrence of mixed infections in individual mites, as well as the recovery of multiple infected mites from the same host.


Scrub typhus is caused by intracellular Gram-negative bacteria belonging to the genus Orientia, although O. tsutsugamushi was thought to be the only causative agent until recently. Orientia species have been separated from the genus Rickettsia on the basis of differences in genome arrangement and cell wall structure, as well as the substantial genetic distance between the two genera [1, 2]. Recently, the incidence of scrub typhus has drastically increased in several tropical and sub-tropical countries, including Bhutan, Nepal, and Thailand [3, 4]. Environmental changes such as deforestation, urbanization, and even natural disasters have been suggested to play crucial roles in this reemergence [57]. In addition, new species of Orientia and the presence of the pathogen in locations outside of the previously described endemic region of the Tsutsugamushi triangle have been documented [8]. Recent evidence suggests the emergence of new Orientia species in both the Middle East and South America, with infected patients presenting with symptoms similar to those of scrub typhus [9, 10]. Serology testing of patient-paired serum (acute and convalescent) revealed four-fold increases in antibody titers against O. tsutsugamushi antigens in these patients. Comparison of the 16S rRNA, 47-kDa HtrA, and 56-kDa type-specific antigen (TSA) gene sequences against the GenBank database showed that the causative agents were most closely related to, but clearly separated from, O. tsutsugamushi. Based on these findings, one of the isolates was proposed as a new species of Orientia, and named Candidatis Orientia chuto [10].

Currently, there is no vaccine available for scrub typhus infection. The prophylactic treatment with antibiotic as a prevention method is recommended by World Health Organization (WHO) under special circumstances in endemic areas. Other general protective measures include avoiding exposure conditions, wearing appropriate clothing, and using insect and spatial repellents to prevent the chigger bites [11, 12]. Patients initially present with non-specific flu-like symptoms such as fever, rash, headache, myalgia, cough, generalized lymphadenopathy, nausea, vomiting, and abdominal pain approximately 5–14 days after being bitten by an infected mite [13, 14]. The fatality rate can be as high as 50% among these patients if left untreated. An eschar at the bite site is a feature of scrub typhus disease; however, the prevalence of eschar formation varies from 1–97% depending on the geographical area [1517]. Trombiculid mites are the primarily vectors of O. tsutsugamushi, especially species belonging to the genus Leptotrombidium, including L. arenicola, L. deliense, L. pallidum, L. fletcheri, L. scutellare, L. chiangraiensis, L. imphalum, and L. akamushi [1820]. In South Korea and Japan, L. pallidum and L. scutellare are the predominant vector species, and are distributed throughout the islands [2123], while in Taiwan and Thailand, L. deliense is the main vector [24, 25]. Other mite genera are also recognized as potential vectors of scrub typhus, including Blankaartia and Ascoschoengastia; however, O. tsutsugamushi carriage has not been as deeply investigated in these genera [26, 27]. In general, mite species known to be important or potential vectors of O. tsutsugamushi are widely distributed throughout Asia, northern Australia, and the western Pacific Islands, placing an estimated one billion people at risk of scrub typhus [28].

To assess the diversity of O. tsutsugamushi isolates serotyping was developed utilizing serum raised in laboratory animals to individual orientia isolates. The produced antiserum or antisera reactive to new orientia isolates by IFA indicated how closely related the new isolate was to known isolates used to produce the antisera and consequently the lack of reactivity indicated the new isolate was antigenically distinct from the isolate(s) that produced the sera. Early on three prototypes (antigenically distinct isolates) strains were identified, Karp, Kato and Gilliam. Subsequently other antigenically distinct isolates were identified. Utilizing the serotyping technique it was found that Karp was the most prevalent O. tsutsugamushi serotype of isolates found in rodents and vectors in Thailand, with other serotypes appearing to be less common [29].

With advances in genetic characterization of bacteria the relationship between serotyping and genotyping of orientia isolates was assessed. Early studies showed that serotyped O. tsutsugamushi isolates using hyperimmune serum raised against prototype strains of the genotypes (genetically distinct) Karp, Gilliam, Kato, and TA716, resulted in cross-reactivity against genetically diverse isolates suggesting that many serotypes existed [30, 31]. Interestingly, the Gilliam and Japanese Gilliam serotypes suggested that these orientia isolates were closely related antigenically, however with genotyping based on the 56-kDa TSA gene they were shown to be genetically disparate (25). Thus, the genotyping method based on the 56-kDa TSA gene sequence and subsequent phylogenetic analysis, revealed substantial genotypic diversity among O. tsutsugamushi isolates from patients and rodent hosts in many parts of Thailand contrary to the serotyping study just mentioned above and that many of these new isolates were found to have much less similarity to the prototype strains than previously thought using serotyping techniques [25, 32, 33].

O. tsutsugamushi is maintained through both transovarial and transstadial transmission processes in the mite population, with these mechanisms thought to be the main ways in which the bacterium is maintained in the wild [20, 3436]. Nevertheless, a small number of studies have reported the acquisition of O. tsutsugamushi from an infected host to naïve mites, although the bacteria failed to transmit transovarially [3739]. Moreover, co-feeding transmission of O. tsutsugamushi from infected mite(s) to co-feeding naïve mites of the same or different species has been demonstrated in a laboratory setting; however, the study did not confirm whether this type of infection resulted in subsequent transstadial and transovarial transmission [40]. In ticks, co-feeding transmission of pathogens such as viruses occurs when infected individuals co-fed with uninfected individuals [4144]. This direct tick-to-tick mode of transmission is thought to be an important process in maintaining viruses in nature. In addition, the bacterial pathogens responsible for Lyme disease, Borrelia burgdorferi and Borrelia afzelii, can be transmitted from infected nymphal Ixodes ricinus L. ticks to co-fed uninfected larval ticks [45, 46]. Although co-feeding transmission of these bacterial spirochetes is thought to occur in nature, albeit to a lesser extent than was observed in the laboratory, the perpetuation of the bacteria in nature largely depends on acquisition from systemically-infected hosts. Co-feeding transmission of Rickettsia has been observed among ticks, with uninfected Rhipicephalus sanguineus ticks being much more likely to acquire a R. conorii infection when feeding in close proximity to infected ticks, compared to feeding on an infected animal host [47]. A recent study has also demonstrated the co-feeding transmission of Rickettsia felis from infected cat fleas (Ctenocephalides felis) to naïve cat fleas or rat fleas (Xenopsylla cheopis) on a vertebrate host, and this mode of transmission could be crucial for the maintenance of R. felis within the vector population [48]. Although the occurrence of horizontal transmission and co-feeding transmission of O. tsutsugamishi has not been well documented, this mode of transmission might play an important role in maintaining O. tsutsugamushi in nature.

Our previous study showed the co-existence of two O. tsutsugamushi genotypes in single laboratory-reared mite lines [35]. Twelve colonies from three species of Leptotrombidium mites (L. chiangraiensis (Lc), L. imphalum (Li), and L. deliense (Ld)) were studied. An O. tsutsugamushi Karp-like genotype was found as a single genotype in the L. chiangraiensis line, but as part of a co-infection with an UT302-like genotype in L. imphalum lines or with a Gilliam-like genotype in the L. deliense line. Moreover, the co-existing genotypes were well maintained through transovarial and transstadial transmission in L. imphalum mites [36]. Co-infection with multiple O. tsutsugamushi sequence types was observed in 25% of patients in a study conducted by Sonthayanon et al. [49]. The study, along with several others, also identified a high degree of genetic diversity within the O. tsutsugamushi isolates recovered from patients [4951]. Indeed, the genome of O. tsutsugamushi shows a high level of plasticity, with 50% of the genome containing repetitive sequences derived from integrative and conjugative elements. Amongst these, several hundred transposases, phage integrases, and transposable elements have been identified, as well as a massive duplication of components of the conjugative type IV secretion system (359 tra genes), which is distributed throughout the genome [52, 53]. These findings indicate that genetic recombination, duplication, and rearrangement are major mechanisms driving O. tsutsugamushi genomic diversity and complexity. As O. tsutsugamushi is an obligate intracellular parasite, recombination would occur during coinfection of different bacterial strains within the same mammalian host or vector, resulting in the exchange of genetic material between the bacterial strains. The co-existence of O. tsutsugamushi strains of different genotypes in a single trombiculid mite is confirmation that these mechanisms are likely to contribute to the genomic diversity/complexity of the bacterial pathogen.

In this study, we aimed to examine the prevalence of mixed infection of O. tsutsugamushi genotypes in individual field-collected mites in high and low scrub typhus-endemic areas of Thailand. Next generation sequencing (deep sequencing) of the 56-kDa TSA gene was used to accurately determine the presence and abundance of each O. tsutsugamushi genotype in individual infected mites. Additionally, the evidence for horizontal transmission of O. tsutsugamushi between co-feeding mites was discussed based on the study data. The results presented in this study represent an epidemiological assessment of O. tsutsugamushi carriage in a wild vector population in an area with active scrub typhus transmission.


Study sites and trombiculid mite collection

Rodents and mites were collected during the wet season (Jun–Aug) in the northeastern (Sisaket and Loei provinces), western (Tak Province), and southern (Pang Nga and Chumphon provinces) regions of Thailand in 2015 (Table 1). All study sites were on private land, and permission was obtained from each of the owners to conduct research on their land. None of the field studies involved endangered or protected species. Rodents were captured using live traps baited with bananas, palm fruit, or dried fish, and were collected from orchards, palm and rubber plantations, cultivated rice-fields, grassland areas, edges of dense forest, stream margins, and around dwellings. Traps were set for 3–5 nights and were checked early in the morning. Captured rodents were removed from the traps, euthanized using carbon dioxide, and processed immediately at the site of collection. Blood, serum, and tissue samples (liver, spleen, kidney, and lung) were collected and stored on dry ice. Ears were removed and stored in 70% ethanol for mite collection. All tissues were then transported to the AFRIMS laboratory for further processing. All rodents were later identified to the species level as described previously [54]. A recent genetic analysis of rodents in Southeast Asia showed that the black rat, Rattus rattus sensu stricto, is not found in Thailand. However, three morphologically similar species are present; Rattus tanezumi, Rattus sakeratensis, and an additional mitochondrial lineage of unclear taxonomic status referred to as ‘Rattus R3’ [55]. These three species were not separated in this study using molecular methods and are referred to collectively as Rattus rattus complex. Meanwhile, all other members of the genus Rattus are identified to species.

Table 1. Prevalence of Orientia tsutsugamushi in rodents, small mammals, and associated trombiculid mites captured from June–August 2015 from five provinces in three regions of Thailand.

Genomic DNA extraction from rodent tissue

Genomic DNA was extracted from rodent spleen samples using a Wizard Genomic DNA Purification Kit (Promega, Madison, WI) according to the manufacturer’s instructions, with some modifications as per a previously published protocol [56]. Briefly, spleen tissue was cut into pieces (~3 mm in diameter) and added to 600 μl of Nuclei Lysis Solution (Promega, Madison, WI). The mixture was homogenized with beads using a TissueLyser II apparatus (Qiagen, Hilden, Germany) at 25 Hz for two rounds of 5 min each. The homogenized solution was then incubated with 20 μl of Proteinase K solution (20 mg/ml) at 55°C for 1 h, and then with 3 μl of RNase A (10 mg/ml) at 37°C for 15 min. A 200-μl volume of protein precipitation solution was then added, and the sample was mixed vigorously by vortex then incubated on ice for 5 min. Insoluble materials were removed by centrifugation at 20,000 x g for 4 min, and the supernatant was transferred to a new tube. DNA was precipitated by adding 600 μl of isopropanol, followed by centrifugation at 20,000 x g for 1 min. The resulting DNA pellet was washed with 70% ethanol and then air dried. Dried DNA was resuspended in 200 μl of EB buffer (10 mM Tris Cl, pH 8.5) and stored at −20°C until further analysis.

Mite morphological identification and DNA extraction

Mites in their larval stage (chigger) were collected from rodent ears by paintbrush under the stereomicroscope and stored separately. Each mite was individually identified to the genus level under a high resolution microscope (400×, Nikon ECLIPSE Ni-U microscope, Tokyo, Japan) using a taxonomic key [57]. Mites were not identified to the species level because this would have required the mites to be cleared and slide-mounted, which would prevent molecular testing. The genus of each mite was recorded, along with its host species and other field site information. Mites collected from wild-caught rodents were individually subjected to genomic DNA extraction using a modified tissue protocol from the QIAamp DNA Mini Kit (Qiagen) with a previously published protocol [35]. Mites were punctured with a fine needle under stereomicroscope to release the tissue from the hard chitin exoskeleton prior to DNA extraction. Eluted DNA solution was stored at −20°C until further use in O. tsutsugamushi quantitative polymerase chain reaction (qPCR) screening assays. Chigger cytochrome oxidase subunit 1 (host COI gene) was examined by conventional PCR on all mite samples before being subjected to Otsu47 qPCR assay as describe previously [58].

Screening of O. tsutsugamushi from field-collected trombiculid mites and animal tissue

Field-collected mites and animal tissue (spleen) samples were screened for the presence of O. tsutsugamushi by qPCR analysis. The primers and probe were designed to detect a portion of the 47-kDa HtrA gene [59]. The reaction mixtures (25 μl) contained 12.5 μl of 2× Platinum Quantitative PCR SuperMix-UDG (Invitrogen, Foster City, CA), 0.2 mM probe, and 0.2 mM each primer. The qPCR assay, referred to as Otsu47, was performed by incubating samples at 95°C for 2 min, followed by 45 cycles of 95°C for 15 s and 60°C for 1 min. Reactions were carried out using the ABI 7500 Fast Real-time PCR System (Life Technologies, Carlsbad, CA).

Amplification of the 56-kDa TSA gene for next-generation sequencing

Trombiculid mites or animal tissue found to be positive for the presence of O. tsutsugamushi was then used as the basis for amplification and next-generation sequencing (NGS) of the 56-kDa TSA gene from O. tsutsugamushi. A fragment of the 56-kDa TSA gene (variable domains I–III, 600–700 bp) was amplified in a first-round PCR using primers RTS-8 and RTS-9 [60]. The reaction was performed in a 20-μl volume containing 5 μl of DNA template, 300 nM each primer, 200 μM dNTPs, 1.5 mM MgCl2, 1× PCR buffer, and 0.4 U of iProof High-Fidelity DNA Polymerase (Bio-Rad, Hercules, CA). Amplification was performed using a DNA thermal cycler under the following conditions: initial denaturation at 98°C for 2 min; 30 cycles of 98°C for 10 s, 45°C for 20 s, and 72°C for 45s; and a final extension at 72°C for 10 min. The second amplification was performed using fusion primers for NGS. The fusion primers comprised three parts: (i) 21-bp A and B sequencing adapters plus 4 bp of key sequence (bold letters) (5′-CGTATCGCCTCCCTCGCGCCATCAG-3′ and 5′-CTATGCGCCTTGCCAGCCCGCTCAG-3′, respectively), (ii) 10-bp multiplex identifier (MID) sequences (with a unique MID for each sample), and (iii) 56-kDa TSA gene-specific sequences RTS-6 and RTS-7 [60]. PCR assays were carried out in 50-μl reaction volumes containing 1.5 mM MgCl2, 200 μM dNTPs, 0.3 μM each primer, and 0.5 U of iProof High-Fidelity DNA Polymerase. Five microliter of diluted product from the first amplification (1:50) was used as template. The thermal cycler parameters consisted of 98°C for 2 min, followed by 30 cycles of 98°C for 10 s, 55°C for 30 s, and 72°C for 30 s. The resulting amplicons were purified using AMPure beads (Agencourt Bioscience Corporation, Beverly, MA), and amplicon concentrations were measured using the Quant-iT PicoGreen dsDNA Assay (Invitrogen) according to the manufacturer’s protocol. Each PCR amplicon was then diluted to 109 copies/μl and pooled (10–15 amplicons per pool). Sample pools were amplified by emulsion PCR using a GS Junior+ emPCR Kit (Lib-A) with a ratio of 0.5 copies per bead. Amplicons were then sequenced in both forward and reverse directions at 5000× coverage per sample on a 454 GS Junior Genome Sequencer Instrument using the GS Junior+ Sequencing Kit XL+ chemistry (Roche 454 Life Sciences, Branford, CT). The average read length obtained from the NGS runs was 633 nucleotides, with a median number of reads per sample of 10,198, (range 3,749–28,943).

Data analysis

Raw reads were quality filtered and de-multiplexed with standard quality filtering parameters using CLC Genomics Workbench v 9.0 software (Qiagen). After quality trimming, reads < 500 bp and > 800 bp in length were discarded. All trimmed reads were then de-multiplexed using the MID barcodes. All reads from each sample were mapped to a full reference set (S1 Table) using the Map Reads to Reference function in the CLC Genomics Workbench software. Each read was mapped to the reference sequences for which it showed the best match using the parameters length fraction = 0.5 and similarity fraction = 0.8 (at least 50% of the total alignment and 80% identity), then the reads were counted and extracted from each reference. In order to be assigned to a O. tsutsugamushi genotype, the number of reads aligned to each reference had to be at least 5% of the total reads. The extracted reads per reference were assembled using de novo assembly, and the consensus sequence was extracted. The GenBank accession numbers for consensus sequences reported in this study were provided at the end of this article. The consensus sequences were aligned with reference sequences retrieved from the GenBank database using the MUSCLE codon alignment algorithm [61]. A maximum likelihood phylogenetic tree was then constructed based on the 56-kDa TSA gene variable domain I–III sequences using the GTR+G model of nucleotide substitution with bootstrapping (1000 replicates) in MEGA 6 [62] (S1 Fig).

Characterization of O. tsutsugamushi genotypes by cloning

The 56-kDa TSA gene was amplified by nested polymerase chain reaction using our previously designed primer [35] for the first-round PCR, and then nested PCR was carried out as previously described [63]. The resulting 615-678-bp amplicon was purified using a Qiagen DNA Purification Kit to remove salts and primer dimers. The purified fragment was then cloned into pCR2.1-TOPO and transformed into Escherichia coli DH5a-T1R as per the manufacturer’s instructions (Invitrogen). Transformants were randomly selected and screened by nested PCR. Between 6 and 28 clones from individual chiggers appeared to contain the correct 56-kDa TSA gene insert fragment. Plasmids containing the correct 56-kDa TSA gene insert were then purified from the E. coli host using a QIAprep Spin Miniprep Kit (Qiagen), and sent for DNA sequencing (Sanger method) by AITBiotech (Singapore).

Statistical analysis and data visualization

All statistical analyses (Chi-square tests) and graphical illustrations presented in this study were performed in the R environment for statistical computing [6466]. A nucleotide distance matrix was generated using “DNADist DNA Distance Matrix” in BioEdit [67]. A heatmap dendrogram was generated in R using the heatmap.2 function from the package Gplots and applying complete linkage clustering and Euclidean distances computed among 36 genotypes from 28 infected mites [68].

Ethics statement

Rodents were trapped according to the institutional animal collection protocol titled “Field Sampling of Small Mammal (Orders: Erinaceomorpha, Soricomorpha, Scandentia, Macroscelidea, and Rodentia) Populations to Support Zoonotic Diseases Surveillance and Ectoparasite Collection” (PN# 12–06), reviewed and approved by the USAMC-AFRIMS Institutional Animal Care and Use Committee (IACUC). All sampling procedures and experimental manipulations were reviewed and approved as part of obtaining the animal collection protocol (PN# 12–06). Research was conducted in compliance with the Animal Welfare Act and other federal statutes and regulations relating to animals and experiments involving animals, and adhered to principles outlined in the Guide for the Care and Use of Laboratory Animals, NRC Publication, 2011 edition.

Accession numbers

The GenBank ( accession numbers for the 56-kDa TSA gene described in this paper are: MH290189 (Lep.DS092.9c), MH290190 (Lep.DS092.8c), MH290191 (Lep.DS021.b), MH290192 (Lep.DS016.b), MH290193 (Lep.DS092.6b), MH290194 (Lep.DS020.2a), MH290195 (Lep.DS092.8a), MH290196 (Lep.DS021.1h), MH290197 (Lep.DS016.e), MH290198 (Lep.DS092.8e), MH290199 (Lep.DS092.9e), MH290200 (Lep.DS092.10e), MH290201 (Lep.DS123.1e), MH290202 (Lep.DS078.d), MH290203 (Lep.DS021.3f), MH290204 (Lep.DS092.7g), MH290205 (Lep.DS092.5g), MH290206 (Lep.DS092.4g), MH290207 (Lep.DS092.2g), MH290208 (Lep.DS092.1g), MH290209 (Lep.DS020.1g), MH290210 (Lep.DS021.4g), MH290211 (Lep.DS123.2g), MH290212 (Lep.DS027.g), MH290213 (Lep.DS030.g), MH290214 (Asc.MS651.g), MH290215 (Lep.DS024.b), MH290216 (Bla.DS123.a), MH290217 (Lep.DS092.3e), MH290218 (Bla.DS123.e), MH290219 (Lep.DS024.d), MH290220 (Lep.DS024.g), MH290221 (Bla.DS123.g), MH290222 (Gah.DS024.g), MH290223 (Lep.DS021.2g), and MH290224 (Lor.MS651.g).


Abundance of small mammals and rodents in the study areas

Collection sites were selected based on our annual surveillance data (2012–2016) on scrub typhus prevalence in small mammals and trombiculid mites in Thailand (S2 Fig). The data revealed a high prevalence of O. tsutsugamushi in Chumphon and Pang Nga provinces (southern Thailand), while low prevalence rates were observed in Sisaket and Loei (northeastern Thailand) and Tak (western Thailand) provinces. Therefore, we decided to survey both high and low prevalence areas for comparison. Small mammals and rodents were collected during the rainy season (Jun–Aug) of 2015. In total, 275 small mammals and rodents were collected from five provinces in three regions of Thailand (Table 1). The collected animals belonged to eight genera and 15 species (Table 2). The greatest rodent species diversity was observed in Pang Nga Province, followed by Tak Province. R. rattus complex (n = 113), Bandicota indica (greater bandicoot rat, n = 54), and Mus caroli (ryukyu mouse, n = 42) were the most abundant species sampled in this study, accounting for 41.1%, 19.6%, and 15.3% of total rodents collected, respectively. R. rattus complex were the most abundant species in all provinces (34.5–65.3%) except Tak Province, in which M. caroli (46.2%) was the most abundant species collected.

Table 2. Chigger infestation rates and population diversity of mites recovered from small mammals, Thailand.

Infestation rates and abundance and diversity of mites among small mammal and rodent populations, and geographical variation of mite genera among the study areas

A total of 4,281 trombiculid mites were collected from 176 of the 275 (64.0%) small mammals and rodents examined in this study (Table 2). The infestation rate by host species was determined for the most abundant species, with the highest infestation rates observed in R. rattus complex (101/113, 89.4%), B. indica (45/54, 83.3%), and Tupaia glis (common tree shrew; 9/13, 69.2%). Overall, mite infestation rates among animals collected from each of the provinces ranged from 33–86.7%. Of the infested animals, those from Sisaket, Chumphon, and Pang Nga provinces were heavily infested, with a chigger index (average number of chiggers per animal) ranging from 19.1–21.4 (Table 2). However, when present, the number of mites on individual hosts was highly variable (1–181). The most abundant mite genus collected from animals in this study was Leptotrombidium (49.1%), followed by Gahrliepia (24.4%) and Ascoschoengastia (20.4%). Overall, a significantly greater proportion of Leptotrombidium mites were collected relative to other mite genera (P < 0.001, Chi-square test), with the abundance of Leptotrombidium spp. clearly observed in Pang Nga and Chumphon provinces (southern Thailand) (Table 2). The greatest numbers of mites were collected from R. rattus complex (2,831, 66.1%), B. indica (987, 23.1%), and T. glis (223, 5.2%), with mean chigger index scores of 25.1 (2,831/113), 18.3 (987/54), and 12.2 (223/13), respectively (Fig 1A). However, when considering the proportion of Leptotrombidium spp. amongst all mite genera collected from these hosts, T. glis individuals showed the highest proportion of Leptotrombidium spp. mites (Chi-square test, P < 0.001). The majority of animals were infested with mites belonging to one (n = 74, 42%) or two (n = 73, 41.5%) different genera, while only 27 (15.3%) and two (1.1%) animals were infested with three or four different mite genera, respectively, with R. rattus complex accounting for the majority of these animals (19/29, 65.5%) (Fig 1B).

Fig 1. Abundance and diversity of field-collected trombiculid mites on wild-caught rodents and small mammals.

(A) Abundance of chigger(s) from three dominant small mammal species. (B) Diversity of chigger(s) collected from animal(s).

Prevalence of O. tsutsugamushi in rodent and small mammal populations

The overall prevalence of O. tsutsugamushi in the animal populations was very low (1.1%, 3/275). The three infected rodents were identified as R. rattus complex (n = 2) and B. indica (n = 1), and were collected from Pang Nga Province (southern Thailand) (Table 1). However, trombiculid mites collected from the infected animals were all negative for O. tsutsugamushi. Genotyping of O. tsutsugamushi from these three rodents revealed single infections with Karp A-genotype strains (26–30 clones, S2 Table).

Prevalence of O. tsutsugamushi in mite populations and genotyping by deep sequencing of the 56-kDa TSA gene (variable domains I–III)

Screening of the 4,281 individual mites for the presence of O. tsutsugamushi using the Otsu47 qPCR assay revealed positive results for 28 mites (prevalence = 0.7%). Twenty-four of the 28 infected mites were Leptotrombidium spp. (85.7%), while the remaining four mites were Ascoschoengastia spp., Lorillatum spp., Gahrliepia spp., and Blankaartia spp. (Table 3). The 28 trombiculid mites were collected from 10 animals: two mites were from one R. rattus complex individual collected in Srisaket Province, while the remaining 26 infected mites were from nine animals collected in Pang Nga Province (four R. rattus complex, three B. indica, and two T. glis). However, tissue samples from all 10 animals were negative for O. tsutsugamushi infection using the same assay. The overall infection rate among mites collected from these 10 animals was 8.4% (28/333), whereas the O. tsutsugamushi prevalence among mites per host varied from 2.2–21.3%. Prevalence rates for infection among the same mite species per host ranged from 0–21.3% (Table 3). The number of infected mites per host varied from 1–10, with four hosts having one infected mite and six hosts with more than two infected mites (2–10 infected mites).

Table 3. Orientia tsutsugamushi-positive rate in mite populations collected from 10 animals, Thailand.

Genotyping of O. tsutsugamushi was conducted for the 28 positive mites by NGS. Of these, the 56-kDa TSA gene was successfully amplified and sequenced from 21 mites using the NGS method. The target gene from the remaining seven mites was genotyped by cloning, as shown in Table 4. The genotypic characterization was based on 56-kDa TSA gene sequence identity to reference sequences in the database, as well as phylogenetic analysis (S1 Table and S1 Fig). Overall, eight O. tsutsugamushi genotypes were detected in the mite population. The majority of infected mites showed single infection (23/28, 82.1%), with only five mites (5/28, 17.9%) showing mixed infection with 2–3 different O. tsutsugamushi genotypes. The most prevalent O. tsutsugamushi genotype found in the mites was TA763 B (44.4%), followed by Kato B (19.4%) (Table 4). The majority of single infections (n = 23) were identified as genotype TA763 B strains (14/23, 60.9%), followed by Kato B (3/23, 13.0%) and Karp A (2/23, 8.7%). The remaining four single infections were identified as genotypes TA763 A, Kato A, and Gilliam JG-C, as well as an unknown genotype. Twenty of the 23 infected mites (86.9%) with single infection were Leptotrombidium spp., while the remaining mites were Gahrliepia spp., Ascoschoengastia spp., and Lorillatum spp.

Table 4. Genotyping of Orientia tsutsugamushi from individual mites by next-generation sequencing.

All mixed O. tsutsugamushi genotype infections (n = 5) were identified in animals from Pang Nga Province. Four infected mites were Leptotrombidium spp., and one was Blankaartia spp. Two Leptotrombidium mites had a mixed infection with two O. tsutsugamushi genotypes, whereas the rest of the mites (two Leptotrombidium spp. and one Blankaartia spp.) showed mixed infection with three genotypes. The genotype composition and the relative abundance of each of the genotypes were determined by the number of NGS reads, or by the number of clones for those sequences amplified using the cloning technique (Table 4).

O. tsutsugamushi genotypes in co-feeding mites

Of the 10 small mammal and rodent hosts infested with Orientia-infected mites, six were found to have 2–10 infected mites feeding on them at the time of collection (Table 3). Three of these animals had two Orientia-infected mites, while the remaining three hosts had 3, 5, and 10 Orientia-infected mites, respectively. The relationship between the O. tsutsugamushi genotypes and the mite genera collected from each host was then examined. The majority of infected mites were Leptotrombidium spp., and were collected from hosts where this genus was predominant (86.2–100%). However, when a host was infested with several mite genera, the number of infected mites proportionately reflected the relative abundance of each of the mite genera. For example, 90 mites were collected from R. rattus complex individual MS0651, and belonged to three different genera: 71 Ascoschoengastia spp., 16 Lorillatum spp., and 3 Gahrliepia spp. Of these 90 mites, only three were infected with O. tsutsugamushi, two of which were Ascoschoengastia spp. and one was Lorillatum spp. No infection was detected in Gahrliepia spp. mites, which were present on the host in the lowest numbers. The same situation occurred with mites collected from R. rattus complex individual DS024 (n = 19), which showed an almost equal prevalence of Leptotrombidium spp. (n = 10) and Gahrliepia spp. (n = 9). In this case, one infected mite was identified from each genus. Also, among mites collected from B. indica individual DS123 (n = 36), two of the infected mites were Leptotrombidium spp. (n = 26), while the remaining infected mite was Blankaartia spp. (n = 10).

A network graph was generated to determine the relationships between O. tsutsugamushi genotypes detected in mites collected from the same animal host (Fig 2A). From hosts infested with 2–10 infected mites, identical O. tsutsugamushi genotypes were detected among infected mites collected from the same host (Table 3). For example, two R. rattus complex individuals (MS0651, black line; DS024, purple line in Fig 2A) each had two infected mites (MS0651: Ascoschoengastia and Lorillatum mites; DS024: Gahrliepia and Leptotrombidium mites), each of which carried the TA763 B genotype. An interesting case was observed in a B. indica rat (DS123, red line in Fig 2A) infested with three infected mites. Two of the mites (Leptotrombidium spp.) had the Kato B and TA763 B genotypes, respectively, while the third infected mite (Blankaartia spp., white circle) contained both genotypes. A similar situation was observed in another B. indica rat (DS092, green line) infested with 10 infected Leptotrombidium mites. Eight mites had a single infection, while two had mixed infection. Among the mites with a single infection, five shared the same TA763 B genotype and two had the Kato B genotype. The latter genotype was also detected in two infected mites with mixed infection, and both of these mites also shared the Karp C genotype. In contrast, in a common tree shrew (DS021, T. glis, blue line in Fig 2A), only two out of five infected mites (Leptotrombidium spp.) shared the same genotype (TA763 B). Likewise, two infected Leptotrombidum spp. infested on another common tree shrew (DS020, T. glis, pink line in Fig 2A) carried different O. tsutsugamushi genotypes (TA763 B and Gilliam). The heatmap shown in Fig 2B outlines the nucleotide sequence distance matrix of the 36 O. tsutsugamushi 56-kDa TSA gene genotypes detected in 28 infected mites. Alignment and identity analysis of the 56-kDa TSA gene sequences belonging to the same genotypes revealed a high level of similarity for each of the genotypes, with percent identities ranging from 98–100%, except for the Kato A genotype, where only 89% identity was observed.

Fig 2. Relationship between co-feeding mites and diversity of Orientia tsutsugamushi 56-kDa TSA gene sequence-based genotypes detected in mite populations.

(A) Network graph demonstrates the potential co-feeding transmission of O. tsutsugamushi genotypes (yellow circle) among infected mites on the same host (indicated by colored lines). Only hosts with multiple infected mites were included in the analysis. Hosts infested with single O. tsutsugamushi-infected mite were indicated with grey line. The graph was created in the igraph R package. (B) Heatmap demonstrating a pair-wise distance matrix of the 56-kDa TSA gene sequences among 36 O. tsutsugamushi genotypes identified in 28 infected mites. The heatmap was generated using the Heatmap.2 function of the gplots R package.


This study is the first to provide evidence of the co-existence of multiple O. tsutsugamushi genotypes in field-collected trombiculid mites using NGS based on the 56-kDa TSA gene (variable domains I–III). These findings build on our previous research showing that different O. tsutsugamushi strains can co-exist in laboratory-reared Leptotrombidium mites maintained in an ABSL-3 facility [35, 36]. Co-existing genotypes, representative of mixed infections, occurred in five out of 28 infected mites (17.9%) examined in the current study. In addition, identical O. tsutsugamushi genotypes were detected among co-feeding trombiculid mites, which may indicate co-feeding transmission. Co-feeding transmission of O. tsutsugamushi occurs among laboratory-reared infected and uninfected mites (Leptotrombidium spp. and Blankaartia spp.) that had co-fed on ICR mice [40]. The current study suggests that co-feeding transmission may also occur naturally among field-collected trombiculid mites feeding on the same animal host, leading to mixed infections or multiple infected mites carrying identical O. tsutsugamushi genotypes. This conclusion is supported by two main observations. First, a single O. tsutsugamushi genotype was detected in multiple mites belonging to different genera. Second, one O. tsutsugamushi genotype was detected in a mite with mixed infection, with the same genotype also found in a co-feeding mite with single infection (Table 4; Fig 2A). For example, B. indica hosts DS092 and DS123 were infested with 10 and 3 infected mites, respectively, all of which shared similar/identical O. tsutsugamushi genotypes in both single and mixed infections. In addition, the majority of mites with mixed infection (three Leptotrombidium spp., one Blankaartia spp.) were found on hosts infested with more than two infected mites. Thus, a higher number of infected mites per host increases the likelihood of an uninfected mite acquiring O. tsutsugamushi during co-feeding [40].

Among the rodents collected in the current study, mites were mostly collected from the inner earlobe, and some hosts were heavily infested (as many as 181 mites/host). Only a small number of mites were found on the soft tissues of the ventral and genital areas. From previous field experience, clusters of mites are rarely found on the ventral surfaces of rodents, possibly because rodents are able to groom these areas; whereas, they cannot groom inside their ears and clusters of mites are able to form. In contrast, mites on the common tree shrew (T. glis) were predominantly found on the ventral and genital areas, with few mites in the inner earlobe. This is probably because the skin in the inner ear of shrews is very thick compared to rodents, and is not conducive to chigger feeing. The observation that mites were more widely dispersed on shrews and did not feed in tight clusters within the inner earlobe could be one possible hypothesis to explain why infected mites on shrews did not have identical O. tsutsugamushi genotypes, and showed no evidence of co-feeding transmission.

Larval mites usually feed once on a rodent host for a period of 2–5 days [40, 69]. Mites on rodents were most often observed feeding in tight clusters in the inner earlobe, supporting the likelihood that if there was an infected mite, the close proximity and duration of feeding would provide the opportunity for co-feeding transmission of O. tsutsugamushi from infected to naïve mites. Similar observations have been made for Rhipicephalus sanguines ticks, where co-feeding transmission efficiency of R. conorii is greatly increased by close proximity of infected and naïve ticks [47]. Therefore, we speculate that co-feeding transmission could be another mode of O. tsutsugamushi transmission, in addition to transstadial and transovarial transmission processes, and play a significant role in maintaining O. tsutsugamushi in mite populations in nature.

In the high-prevalence area (Pang Nga Province), Leptotrombidium species were the most abundant mites, and were mainly associated with R. rattus complex and B. indica rats. Moreover, Leptotrombidium was the most commonly infected mite genus in this area, which is consistent with previous studies showing that Leptotrombidium spp. are still the main vectors for scrub typhus transmission [23, 7073]. Interestingly, our findings confirm a previous study that used direct immunofluorescence assays (DFA) to show that O. tsutsugamushi was present in Blankaartia acuscutellaris mites collected from rodents in central Thailand [27]. However, further investigation by the same group failed to isolate O. tsutsugamushi in laboratory mice from field-collected B. acuscutellaris [26]. The authors suggested that the detection of O. tsutsugamushi by DFA in B. acuscutellaris, which has been reported previously by Tanskul et al. [27], might be a result of co-feeding transmission or acquisition of the bacterium from a systemically infected host, as these modes of transmission have been shown to occur in an experimental mice and laboratory-reared mites [40]. However, our current study used molecular detection methods to identify O. tsutsugamushi infection not only in Bankaartia spp., but also in Ascoschoengastia spp., Gahrliepia spp., and Lorillatum spp. Additionally, some of these genera were found feeding in the earlobe in close proximity to Leptotrombidium spp. Acquisition from a systemically infected host could be excluded, as all hosts infested with O. tsutsugamushi-positive mites were negative for O. tsutsugamushi infection by molecular assay. Therefore, the presence of O. tsutsugamushi in these mites could be a result of co-feeding transmission from infected Leptotrombidium mite(s) feeding in the close proximity on the same host. This could explain the finding of an identical O. tsutsugamushi genotype in Gahrliepia spp. and Leptotrombidium spp. mites on R. rattus complex individual DS024, and in a Blankaartia spp. mite on B. indica individual DS123. However, the Blankaartia mite collected from DS123 also carried the Gilliam genotype, which was not detected in its co-feeding Leptotrombidium mites. So, the question remains of how the Blankaartia mite acquired the Gilliam genotype. A similar observation was made among Ascoschoengastia and Lorillatum mites co-feeding on R. rattus complex MS651, where both mites carried TA763 B genotype bacteria. However, because all of these conclusions are based solely on data from field-collected mites, where transmission could not be monitored, other unknown factors could have influenced the results. For example, Gilliam genotype detected in Blankaartia mite infested on host DS123 may have been present in the mite prior to attachment to this host (i.e. it has been maintained in the mite via transovarial transmission). Further study is therefore needed to investigate whether other genera are capable of transmitting O. tsutsugamushi in nature, and to confirm whether co-feeding transmission results in mixed infection of O. tsutsugamushi genotypes. Such co-feeding transmission studies can be conducted using laboratory-reared infected mites and animal models, allowing for more controlled experimentation.

It is worth noting that an abundance of Leptotrombidium mites or a higher chigger index does not necessarily directly correspond to an increased prevalence of O. tsutsugamushi in mite populations. This was the case in Chumphon Province, which had the second highest abundance of mites, and where the majority of mites were Leptotrombidium spp. However, no infected mites were detected in this area. In addition, two infected mites (Ascoschoengastia spp. and Lorillatum spp.) were collected from a R. rattus complex in Sisaket Province; however, no Leptotrombidium spp. mites were collected from animals captured in this area. Based on our study data, Pang Nga Province could be considered a hotspot for scrub typhus transmission within mite populations, as multiple infected mites were usually found on each animal host. Interestingly, during the study period, 211 human cases of scrub typhus were reported in Pang Nga Province by the Thai Ministry of Public Health. The current study also revealed highly diverse within-host O. tsutsugamushi genotypes, with as many as three different O. tsutsugamushi genotypes found in individual mites. The ecological dynamics of multiple O. tsutsugamushi genotypes in one host could drive pathogen evolution/diversification in the vector. This may be consistent with the hypothesis that genetic recombination among different O. tsutsugamushi genotypes can occur in the mite vector [74].

Supporting information

S1 Fig. Phylogenetic analysis of Orientia tsutsugamushi 56-kDa type-specific antigen gene sequences for each of the genotypes (consensus sequences from next-generation sequencing reads or cloning) detected in field-collected trombiculid mites and reference sequences retrieved from the GenBank database.

A maximum likelihood tree was constructed using the GTR+G model of nucleotide substitution in the MEGA 6 program with bootstrapping (1000 replicates). Percent abundance of each genotype detected in individual mites is indicated in parenthesis after each sequence.


S2 Fig. Orientia tsutsugamushi prevalence in small mammals and trombiculid mites collected from several provinces in Thailand (2012–2016).


S1 Table. List of Orientia tsutsugamushi 56-kDa type-specific antigen gene reference sequences used as local references in Map Reads to Reference analysis.

Analysis was performed using CLC Genomics Workbench.


S2 Table. Characterization of O. tsutsugamushi genotypes (based on 56-kDa TSA gene, variable domains I-III) from three rodents collected from Phang Nga province by cloning.

A nucleotide distance matrix was generated using “DNADist DNA Distance Matrix” in BioEdit.



We thank Tamsin Sheen, PhD, from Edanz Group ( for critically reviewing and editing a draft of this manuscript.


Material has been reviewed by the Walter Reed Army Institute of Research. There is no objection to its presentation and/or publication. The opinions or assertions contained herein are the private views of the authors, and are not to be construed as official, or as reflecting true views of the Department of the Army or the Department of Defense. Research was conducted under an approved animal use protocol in an AAALACi accredited facility in compliance with the Animal Welfare Act and other federal statutes and regulations relating to animals and experiments involving animals, and adheres to principles stated in the Guide for the Care and Use of Laboratory Animals, NRC Publication, 2011 edition.


  1. 1. Silverman DJ, Wisseman CL Jr. Comparative ultrastructural study on the cell envelopes of Rickettsia prowazekii, Rickettsia rickettsii, and Rickettsia tsutsugamushi. Infection and immunity. 1978;21(3):1020–3. pmid:101465
  2. 2. Tamura A, Ohashi N, Urakami H, Miyamura S. Classification of Rickettsia tsutsugamushi in a new genus, Orientia gen. nov., as Orientia tsutsugamushi comb. nov. International journal of systematic bacteriology. 1995;45(3):589–91. pmid:8590688
  3. 3. Upadhyaya BP, Shakya G, Adhikari S, Rijal N, Acharya J, Maharjan L, et al. Scrub Typhus: An Emerging Neglected Tropical Disease in Nepal. Journal of Nepal Health Research Council. 2016;14(33):122–7. pmid:27885295
  4. 4. Tshokey T, Graves S, Tshering D, Phuntsho K, Tshering K, Stenos J. Scrub Typhus Outbreak in a Remote Primary School, Bhutan, 2014. Emerging infectious diseases. 2017;23(8):1412–4. pmid:28726604
  5. 5. Lindahl JF, Grace D. The consequences of human actions on risks for infectious diseases: a review. Infection ecology & epidemiology. 2015;5:30048.
  6. 6. Neiderud CJ. How urbanization affects the epidemiology of emerging infectious diseases. Infection ecology & epidemiology. 2015;5:27060.
  7. 7. Morse SS. Factors in the emergence of infectious diseases. Emerging infectious diseases. 1995;1(1):7–15. pmid:8903148
  8. 8. Jiang J, Richards AL. Scrub Typhus: No Longer Restricted to the Tsutsugamushi Triangle. Tropical Medicine and Infectious Disease. 2018;3(11):1–7.
  9. 9. Balcells ME, Rabagliati R, Garcia P, Poggi H, Oddo D, Concha M, et al. Endemic scrub typhus-like illness, Chile. Emerging infectious diseases. 2011;17(9):1659–63. pmid:21888791
  10. 10. Izzard L, Fuller A, Blacksell SD, Paris DH, Richards AL, Aukkanit N, et al. Isolation of a novel Orientia species (O. chuto sp. nov.) from a patient infected in Dubai. Journal of clinical microbiology. 2010;48(12):4404–9. pmid:20926708
  11. 11. Xu G, Walker DH, Jupiter D, Melby PC, Arcari CM. A review of the global epidemiology of scrub typhus. PLoS neglected tropical diseases. 2017;11(11):e0006062. pmid:29099844
  12. 12. Bonell A, Lubell Y, Newton PN, Crump JA, Paris DH. Estimating the burden of scrub typhus: A systematic review. PLoS neglected tropical diseases. 2017;11(9):e0005838. pmid:28945755
  13. 13. Mahajan SK. Scrub typhus. The Journal of the Association of Physicians of India. 2005;53:954–8. pmid:16515236
  14. 14. Jeong YJ, Kim S, Wook YD, Lee JW, Kim KI, Lee SH. Scrub typhus: clinical, pathologic, and imaging findings. Radiographics: a review publication of the Radiological Society of North America, Inc. 2007;27(1):161–72.
  15. 15. Tsay RW, Chang FY. Serious complications in scrub typhus. Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi. 1998;31(4):240–4. pmid:10496165
  16. 16. Tang Y-W SM, Liu D, Poxton I, Schwartzman J. Orientia. Molecular medical microbiology. Academic press. 2014;2ed:2057–96.
  17. 17. Kawamura A. Tsutsugamushi disease: an overview. Tokyo: University of Tokyo Press; c1995.
  18. 18. Wright JD, Hastriter MW, Robinson DM. Observations on the ultrastructure and distribution of Rickettsia tsutsugamushi in naturally infected Leptotrombidium (Leptotrombidium) arenicola (Acari: Trombiculidae). Journal of medical entomology. 1984;21(1):17–27. pmid:6420571
  19. 19. Lerdthusnee K, Khuntirat B, Leepitakrat W, Tanskul P, Monkanna T, Khlaimanee N, et al. Scrub typhus: vector competence of Leptotrombidium chiangraiensis chiggers and transmission efficacy and isolation of Orientia tsutsugamushi. Annals of the New York Academy of Sciences. 2003;990:25–35. pmid:12860596
  20. 20. Phasomkusolsil S, Tanskul P, Ratanatham S, Watcharapichat P, Phulsuksombati D, Frances SP, et al. Transstadial and transovarial transmission of Orientia tsutsugamushi in Leptotrombidium imphalum and Leptotrombidium chiangraiensis (Acari: Trombiculidae). Journal of medical entomology. 2009;46(6):1442–5. pmid:19960694
  21. 21. Ree HI, Cho MK, Lee IY, Jeon SH. Comparative epidemiological studies on vector/reservoir animals of tsutsugamushi disease between high and low endemic areas in Korea. The Korean journal of parasitology. 1995;33(1):27–36. pmid:7735783
  22. 22. Ogawa M, Ono T. Epidemiological characteristics of tsutsugamushi disease in Oita Prefecture, Japan: yearly and monthly occurrences of its infections and serotypes of its causative agent, Orientia tsutsugamushi, during 1984–2005. Microbiology and immunology. 2008;52(3):135–43. pmid:18402595
  23. 23. Roh JY, Song BG, Park WI, Shin EH, Park C, Park MY, et al. Coincidence between geographical distribution of Leptotrombidium scutellare and scrub typhus incidence in South Korea. PloS one. 2014;9(12):e113193. pmid:25500568
  24. 24. Kuo CC, Lee PL, Chen CH, Wang HC. Surveillance of potential hosts and vectors of scrub typhus in Taiwan. Parasites & vectors. 2015;8:611.
  25. 25. Kelly DJ, Fuerst PA, Ching WM, Richards AL. Scrub typhus: the geographic distribution of phenotypic and genotypic variants of Orientia tsutsugamushi. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America. 2009;48 Suppl 3:S203–30.
  26. 26. Frances SP, Watcharapichat P, Phulsuksombati D, Tanskul P. Investigation of the role of Blankaartia acuscutellaris (Acari: Trombiculidae) as a vector of scrub typhus in central Thailand. The Southeast Asian journal of tropical medicine and public health. 2001;32(4):863–6. pmid:12041564
  27. 27. Tanskul P, Strickman D, Eamsila C, Kelly DJ. Rickettsia tsutsugamushi in chiggers (Acari: Trombiculidae) associated with rodents in central Thailand. Journal of medical entomology. 1994;31(2):225–30. pmid:8189414
  28. 28. Rosenberg R. Drug-resistant scrub typhus: Paradigm and paradox. Parasitology today. 1997;13(4):131–2. pmid:15275098
  29. 29. Shirai A, Tanskul PL, Andre RG, Dohany AL, Huxsoll DL. Rickettsia tsutsugamushi strains found in chiggers collected in Thailand. The Southeast Asian journal of tropical medicine and public health. 1981;12(1):1–6. pmid:6789455
  30. 30. Shirai A, Wisseman CL Jr. Serologic classification of scrub typhus isolates from Pakistan. The American journal of tropical medicine and hygiene. 1975;24(1):145–53. pmid:46135
  31. 31. Ohashi N, Nashimoto H, Ikeda H, Tamura A. Diversity of immunodominant 56-kDa type-specific antigen (TSA) of Rickettsia tsutsugamushi. Sequence and comparative analyses of the genes encoding TSA homologues from four antigenic variants. The Journal of biological chemistry. 1992;267(18):12728–35. pmid:1618776
  32. 32. Rodkvamtook W, Ruang-Areerate T, Gaywee J, Richards AL, Jeamwattanalert P, Bodhidatta D, et al. Isolation and characterization of Orientia tsutsugamushi from rodents captured following a scrub typhus outbreak at a military training base, Bothong district, Chonburi province, central Thailand. The American journal of tropical medicine and hygiene. 2011;84(4):599–607. pmid:21460017
  33. 33. Ruang-Areerate T, Jeamwattanalert P, Rodkvamtook W, Richards AL, Sunyakumthorn P, Gaywee J. Genotype diversity and distribution of Orientia tsutsugamushi causing scrub typhus in Thailand. Journal of clinical microbiology. 2011;49(7):2584–9. pmid:21593255
  34. 34. Frances SP, Watcharapichat P, Phulsuksombati D. Vertical transmission of Orientia tsutsugamushi in two lines of naturally infected Leptotrombidium deliense (Acari: Trombiculidae). Journal of medical entomology. 2001;38(1):17–21. pmid:11268685
  35. 35. Takhampunya R, Tippayachai B, Promsathaporn S, Leepitakrat S, Monkanna T, Schuster AL, et al. Characterization based on the 56-Kda type-specific antigen gene of Orientia tsutsugamushi genotypes isolated from Leptotrombidium mites and the rodent host post-infection. The American journal of tropical medicine and hygiene. 2014;90(1):139–46. pmid:24297814
  36. 36. Takhampunya R, Tippayachai B, Korkusol A, Promsathaporn S, Leepitakrat S, Sinwat W, et al. Transovarial Transmission of Co-Existing Orientia tsutsugamushi Genotypes in Laboratory-Reared Leptotrombidium imphalum. Vector borne and zoonotic diseases. 2016;16(1):33–41. pmid:26771218
  37. 37. Walker JS, Chan CT, Manikumaran C, Elisberg BL. Attempts to infect and demonstrate transovarial transmission of R. tsutsugamushi in three species of Leptotrombidium mites. Annals of the New York Academy of Sciences. 1975;266:80–90. pmid:829478
  38. 38. Takahashi M, Murata M, Misumi H, Hori E, Kawamura A Jr., Tanaka H. Failed vertical transmission of Rickettsia tsutsugamushi (Rickettsiales: Rickettsiaceae) acquired from rickettsemic mice by Leptotrombidium pallidum (Acari: trombiculidae). Journal of medical entomology. 1994;31(2):212–6. pmid:8189412
  39. 39. Traub R, Wisseman CL Jr., Jones MR, O'Keefe JJ. The acquisition of Rickettsia tsutsugamushi by chiggers (trombiculid mites) during the feeding process. Annals of the New York Academy of Sciences. 1975;266:91–114. pmid:829479
  40. 40. Frances SP, Watcharapichat P, Phulsuksombati D, Tanskul P. Transmission of Orientia tsutsugamushi, the aetiological agent for scrub typhus, to co-feeding mites. Parasitology. 2000;120 (Pt 6):601–7.
  41. 41. Gordon SW, Linthicum KJ, Moulton JR. Transmission of Crimean-Congo hemorrhagic fever virus in two species of Hyalomma ticks from infected adults to cofeeding immature forms. The American journal of tropical medicine and hygiene. 1993;48(4):576–80. pmid:8480867
  42. 42. Linthicum KJ, Logan TM. Feeding nymphs of Hyalomma truncatum (Acari: Ixodidae) on guinea pigs previously exposed to nymphs. Journal of medical entomology. 1993;30(6):1064–7. pmid:8271249
  43. 43. Jones LD, Davies CR, Green BM, Nuttall PA. Reassortment of Thogoto virus (a tick-borne influenza-like virus) in a vertebrate host. The Journal of general virology. 1987;68 (Pt 5):1299–306.
  44. 44. Randolph SE, Gern L, Nuttall PA. Co-feeding ticks: Epidemiological significance for tick-borne pathogen transmission. Parasitology today. 1996;12(12):472–9. pmid:15275266
  45. 45. Richter D, Allgower R, Matuschka FR. Co-feeding transmission and its contribution to the perpetuation of the lyme disease spirochete Borrelia afzelii. Emerging infectious diseases. 2002;8(12):1421–5. pmid:12498658
  46. 46. Gern L, Rais O. Efficient transmission of Borrelia burgdorferi between cofeeding Ixodes ricinus ticks (Acari: Ixodidae). Journal of medical entomology. 1996;33(1):189–92. pmid:8906929
  47. 47. Zemtsova G, Killmaster LF, Mumcuoglu KY, Levin ML. Co-feeding as a route for transmission of Rickettsia conorii israelensis between Rhipicephalus sanguineus ticks. Experimental & applied acarology. 2010;52(4):383–92.
  48. 48. Brown LD, Christofferson RC, Banajee KH, Del Piero F, Foil LD, Macaluso KR. Cofeeding intra- and interspecific transmission of an emerging insect-borne rickettsial pathogen. Molecular ecology. 2015;24(21):5475–89. pmid:26414611
  49. 49. Sonthayanon P, Peacock SJ, Chierakul W, Wuthiekanun V, Blacksell SD, Holden MT, et al. High rates of homologous recombination in the mite endosymbiont and opportunistic human pathogen Orientia tsutsugamushi. PLoS neglected tropical diseases. 2010;4(7):e752. pmid:20651929
  50. 50. Duong V, Blassdell K, May TT, Sreyrath L, Gavotte L, Morand S, et al. Diversity of Orientia tsutsugamushi clinical isolates in Cambodia reveals active selection and recombination process. Infection, genetics and evolution: journal of molecular epidemiology and evolutionary genetics in infectious diseases. 2013;15:25–34. pmid:20854933
  51. 51. Wongprompitak P, Duong V, Anukool W, Sreyrath L, Mai TT, Gavotte L, et al. Orientia tsutsugamushi, agent of scrub typhus, displays a single metapopulation with maintenance of ancestral haplotypes throughout continental South East Asia. Infection, genetics and evolution: journal of molecular epidemiology and evolutionary genetics in infectious diseases. 2015;31:1–8. pmid:25577986
  52. 52. Cho NH, Kim HR, Lee JH, Kim SY, Kim J, Cha S, et al. The Orientia tsutsugamushi genome reveals massive proliferation of conjugative type IV secretion system and host-cell interaction genes. Proceedings of the National Academy of Sciences of the United States of America. 2007;104(19):7981–6. pmid:17483455
  53. 53. Nakayama K, Yamashita A, Kurokawa K, Morimoto T, Ogawa M, Fukuhara M, et al. The Whole-genome sequencing of the obligate intracellular bacterium Orientia tsutsugamushi revealed massive gene amplification during reductive genome evolution. DNA research: an international journal for rapid publication of reports on genes and genomes. 2008;15(4):185–99.
  54. 54. MacKinnon K. Mammals of Thailand, by Boonsong Lekagul and Jeffrey A. McNeely. Association for the Conservation of Wildlife, 4 Old Custom House Lane, Bangkok 5, US $49. Oryx. 1978;14(03):262–.
  55. 55. Pages M, Bazin E, Galan M, Chaval Y, Claude J, Herbreteau V, et al. Cytonuclear discordance among Southeast Asian black rats (Rattus rattus complex). Molecular ecology. 2013;22(4):1019–34. pmid:23278980
  56. 56. Klangthong K, Promsthaporn S, Leepitakrat S, Schuster AL, McCardle PW, Kosoy M, et al. The Distribution and Diversity of Bartonella Species in Rodents and Their Ectoparasites across Thailand. PloS one. 2015;10(10):e0140856. pmid:26484537
  57. 57. Nadchatram M DA. A Pictorial key to the subfamilies, genera and subgenera of Southeast Asian chiggers (Acari, Prostigmata, Trombiculidae). Kuala Lumpur: Institute for Medical Research; 1974.
  58. 58. Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Molecular marine biology and biotechnology. 1994;3(5):294–9. pmid:7881515
  59. 59. Jiang J, Chan TC, Temenak JJ, Dasch GA, Ching WM, Richards AL. Development of a quantitative real-time polymerase chain reaction assay specific for Orientia tsutsugamushi. The American journal of tropical medicine and hygiene. 2004;70(4):351–6. pmid:15100446
  60. 60. Horinouchi H, Murai K, Okayama A, Nagatomo Y, Tachibana N, Tsubouchi H. Prevalence of genotypes of Orientia tsutsugamushi in patients with scrub typhus in Miyazaki Prefecture. Microbiology and immunology. 1997;41(6):503–7. pmid:9251062
  61. 61. Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic acids research. 2004;32(5):1792–7. pmid:15034147
  62. 62. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Molecular biology and evolution. 2013;30(12):2725–9. pmid:24132122
  63. 63. Horinouchi H, Murai K, Okayama A, Nagatomo Y, Tachibana N, Tsubouchi H. Genotypic identification of Rickettsia tsutsugamushi by restriction fragment length polymorphism analysis of DNA amplified by the polymerase chain reaction. The American journal of tropical medicine and hygiene. 1996;54(6):647–51. pmid:8686786
  64. 64. Wickham H. ggplot2: Elegant Graphics for Data Analysis. New York: Springer-Verlag. 2009.
  65. 65. R Core Team. R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2013. Available from
  66. 66. Csardi G, Nepusz T. The igraph software package for complex network research. InterJournal, Complex Systems. 2006:1695. Available from
  67. 67. Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acids Symp Ser 1999;41:95–8.
  68. 68. Warnes GR, Bolker B, Bonebakker L, Gentleman R, Huber W, Liaw A, et al. gplots: Various R programming tools for plotting data. R package version 3.0.1. 2016. Available from
  69. 69. Lerdthusnee K, Khlaimanee N, Monkanna T, Sangjun N, Mungviriya S, Linthicum KJ, et al. Efficiency of Leptotrombidium chiggers (Acari: Trombiculidae) at transmitting Orientia tsutsugamushi to laboratory mice. Journal of medical entomology. 2002;39(3):521–5. pmid:12061450
  70. 70. Tanskul P, Linthicum KJ, Watcharapichat P, Phulsuksombati D, Mungviriya S, Ratanatham S, et al. A new ecology for scrub typhus associated with a focus of antibiotic resistance in rice farmers in Thailand. Journal of medical entomology. 1998;35(4):551–5. pmid:9701943
  71. 71. Kuo CC, Huang CL, Wang HC. Identification of potential hosts and vectors of scrub typhus and tick-borne spotted fever group rickettsiae in eastern Taiwan. Medical and veterinary entomology. 2011;25(2):169–77. pmid:21223345
  72. 72. Zhang WY, Wang LY, Ding F, Hu WB, Soares Magalhaes RJ, Sun HL, et al. Scrub typhus in mainland China, 2006–2012: the need for targeted public health interventions. PLoS neglected tropical diseases. 2013;7(12):e2493. pmid:24386495
  73. 73. Ebisawa II. Current Epidemiology and Treatment of Tsutsugamushi Disease in Japan. Journal of travel medicine. 1995;2(4):218–20. pmid:9815394
  74. 74. Kim G, Ha NY, Min CK, Kim HI, Yen NT, Lee KH, et al. Diversification of Orientia tsutsugamushi genotypes by intragenic recombination and their potential expansion in endemic areas. PLoS neglected tropical diseases. 2017;11(3):e0005408. pmid:28248956