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Volume 26, Number 9—September 2020
Research

Molecular Description of a Novel Orientia Species Causing Scrub Typhus in Chile

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Materials and Methods
Results
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Author affiliations: Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile (K. Abarca, C. Martínez-Valdebenito, J. Angulo); Naval Medical Research Center, Silver Spring, Maryland, USA (J. Jiang, C.M. Farris); Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA (A.L. Richards); Facultad de Ciencias Veterinarias, Universidad Austral de Chile, Valdivia, Chile (G. Acosta-Jamett); Clínica Alemana de Santiago, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Santiago (T. Weitzel)

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Abstract

Scrub typhus is a potentially fatal rickettsiosis caused by Orientia species intracellular bacteria of the genus Orientia. Although considered to be restricted to the Asia Pacific region, scrub typhus has recently been discovered in southern Chile. We analyzed Orientia gene sequences of 16S rRNA (rrs) and 47-kDa (htrA) from 18 scrub typhus patients from Chile. Sequences were ≥99.7% identical among the samples for both amplified genes. Their diversity was 3.1%–3.5% for rrs and 11.2%–11.8% for htrA compared with O. tsusugamushi and 3.0% for rrs and 14.8% for htrA compared with Candidatus Orientia chuto. Phylogenetic analyses of both genes grouped the specimens from Chile in a different clade from other Orientia species. Our results indicate that Orientia isolates from Chile constitute a novel species, which, until they are cultivated and fully characterized, we propose to designate as Candidatus Orientia chiloensis, after the Chiloé Archipelago where the pathogen was identified.

Scrub typhus is a potentially fatal rickettsial infection transmitted by larval stage trombiculid mites called chiggers. Scrub typhus is caused by Orientia tsutsugamushi, a strictly intracellular bacterium with a remarkable genetic and antigenic diversity (1,2). Although this disease has been known since at least 313 ce and currently threatens over 1 billion people in Asia and Australasia, it is widely underdiagnosed and underreported (3,4). Disinterest has been influenced by the perception that scrub typhus is a geographically limited disease, threatening rural populations within a certain region, known as the “tsutsugamushi triangle,” and rarely affecting travelers (5,6).

This paradigm, however, has recently been brought into question with evidence of scrub typhus being found in the Middle East, Africa, and South America (7–12). Genomic information on Orientia strains from Chile has been insufficient and scrub typhus in the Middle East region is caused by a new Orientia species, Candidatus Orientia chuto (6), highlighting that our current knowledge on the spectrum of Orientia species is incomplete (13). Here, we discuss the molecular description and phylogenetic analysis of a potential third pathogenic Orientia species detected in 18 patients with scrub typhus in southern Chile.

Materials and Methods

Patients and Samples

The clinical samples described in this study were derived from 18 patients with confirmed scrub typhus diagnosed during February 2016–February 2019. All cases were acquired in southern Chile and diagnosed as part of an ongoing surveillance project of the Chilean Rickettsia and Zoonosis Research Group. The project was approved by the
Comité Ético Científico, Pontificia Universidad Católica de Chile (Santiago, Chile; #12–170 and #160816007) and the Naval Medical Research Center (Silver Spring, MD, USA; PJT-16-24) (9,14,15).

We collected, stored, and extracted DNA from buffy coat preparations and eschar specimens as described elsewhere (9,15). Eschar samples consisted of swab specimens taken from the base or crust material of eschar, which we mechanically desegregated using sterile glass beads. DNA was automatically extracted from eschar and blood samples using MagNA Pure System (Roche Molecular Systems, https://diagnostics.roche.com), according to the manufacturer’s instructions. All included DNA specimens derived from eschar samples, except the BM2016-I sample, which was only from the buffy coat specimen.

PCR Assays and Sequencing

We initially assessed all extracted DNA samples by a newly designed genus-specific quantitative PCR (Orien16S qPCR assay), as described elsewhere (15,16). For further analysis, we performed seminested PCRs targeting the 16S rRNA gene (rrs), 47-kDa high-temperature requirement A gene (htrA), and 56-kDa type-specific antigen gene (tsa) to the qPCR Orien16S–positive samples (Appendix Table 1). We sequenced PCR amplicons for both DNA strands using Sanger sequencing method (Psomagen Inc., https://psomagen.com). Two independent investigators analyzed the chromatogram of each sequence and aligned them using BioEdit version 7.0.5.3 (17) Sequences from these scrub typhus patients in Chile were submitted to GenBank under accession no. MK329247 (rrs), MN231837 (rrs), MT435057 (rrs), MK343091 (htrA), and MT431624 (htrA).

Phylogenetic Analysis

We compared Orientia DNA sequences from the 2016–2019 scrub typhus patients with DNA from the first Orientia scrub typhus patient in Chile from 2006 and that of distinct Orientia species, including O. tsutsugamushi and Candidatus O. chuto, different Rickettsia species, and other microorganisms retrieved from GenBank and aligned using ClustalW (http://www.clustal.org). We used MEGAX software (https://www.megasoftware.net) to infer phylogenetic analyses by the maximum-likelihood method (18) and to perform the search for the most appropriate model of nucleotide substitution for phylogenetic analysis according to the Bayesian information criterion. For the maximum-likelihood method, we obtained initial trees for the heuristic search automatically by applying neighbor-joining and Bio neighbor-joining algorithms to a matrix of pairwise distances estimated using the maximum composite likelihood approach and then selecting the topology with superior log likelihood value. We based the support of the topology on a bootstrapping of 1,000 replicates; the positions equivalent to gaps or missing data were deleted.

Comparison of Nucleotide Diversity

We created consensus sequences of the generated amplicons after alignment in BioEdit version 7.0.5.3, which we compared with respective sequences of O. tsutsugamushi and Candidatus O. chuto strains as well as the first Orientia case from Chile, obtained from GenBank. A sequence identity matrix was constructed in BioEdit version 7.0.5.3. The selected databases and algorithms used for alignment and comparison of sequences were in accordance with current recommendations for the taxonomical characterization of prokaryote strains (19).

Results

Cases

The 18 investigated scrub typhus cases were acquired in 3 regions currently known to be endemic for scrub typhus (15), Biobío, Los Lagos, and Aysen, which span >1,120 km (latitude 38°03¢S to 47°47¢S) in Chile; 5 of the 18 cases were from Chiloé Island (Los Lagos), where the initial case was reported (Table 1). At the time they sought treatment, all but 1 patient exhibited the 3 clinical signs characteristic of scrub typhus: fever, maculopapular rash, and inoculation eschar. The presence of Orientia genomic DNA was confirmed in all cases by qPCR Orien16S from buffy coat or eschar material (Table 1). All of the patients recovered from scrub typhus without sequelae, 16 after treatment with doxycycline, 1 after treatment with azithromycin, and 1 without specific antimicrobial therapy. Further epidemiologic and clinical details of some of the patients have been published elsewhere (9,15,20).

DNA Sequences and Phylogenetic Analyses

Figure 1

Thumbnail of Phylogenetic analyses of sequences of the 16S rRNA gene (rrs) from scrub typhus cases in Chile compared with those from different Orientia and Rickettsia species and other microorganisms. We inferred the evolutionary history by using the maximum-likelihood method based on the Kimura 2-parameter model (21), according to the Bayesian information criterion for these sequences. The analysis involved 39 nt sequences and a total of 875 positions in the final dataset. The trees is drawn to

Figure 1. Phylogenetic analyses of sequences of the 16S rRNA gene (rrs) from scrub typhus cases in Chile compared with those from different Orientia and Rickettsia species and other microorganisms. We inferred the...

Figure 2

Thumbnail of Phylogenetic analyses of sequences of the 47-kDa gene (htrA) from scrub typhus cases from Chile in comparison to different Orientia species. For the phylogenetic tree, the maximum-likelihood method based on the Hasegawa-Kishino-Yano model was applied (22). A discrete gamma distribution was used to model evolutionary rates differences among sites. The analysis involved 37 nucleotide sequences and a total of 736 positions in the final dataset. The tree is drawn to scale, with branch l

Figure 2. Phylogenetic analyses of sequences of the 47-kDa gene (htrA) from scrub typhus cases from Chile in comparison to different Orientia species. For the phylogenetic tree, the maximum-likelihood method based on the...

We successfully amplified fragments of rrs from 18 cases and htrA from17 cases; the primers for tsa failed to produce amplicons. For all assays, we successfully amplified a well-defined Orientia strain (Kawasaki clade) from South Korea as a positive control (6). The lengths of clean reads were 886 nt for rrs and 950 nt for htrA. Sequences of the isolates showed a high nucleotide identity (99.7%–100%) for both genes (Appendix Table 1), with a maximum divergence of 2 nucleotides. We were able to distinguish 3 distinct rrs genotypes (1, 2, and 3) and 2 genotypic variants of htrA (a and b) (Appendix Table 2). HtrA variants, although determined by only 1 nucleotide, led to distinct DNA codons with leucine versus phenylalanine. The genotype 1a samples (n = 10) derived from Los Lagos (continental and Chiloé Island), Biobío, and Aysén regions, whereas genotypes 2b (n = 3) occurred in the continental Los Lagos region, 3a (n = 1) in Chiloé Island, and genotype 3b (n = 3) in the Los Lagos region, both continental and Chiloé Island. For 1 genotype 2 strain, we could not amplify htrA (Appendix Table 2). Phylogenetic analyses of both genes from the DNA specimens from Chile formed a unique cluster separate from the 14 O. tsutsugamushi strains included in the analysis as well as from Candidatus O. chuto (Figures 1, 2). However, the rrs sequence from the 2016–2019 samples grouped together with that from the first scrub typhus case in Chile (Figure 1) (8).

Details of discrepancies in the nucleotide sequences were evaluated by identity matrices. For rrs from the isolates from Chile, identity of the consensus sequence ranged from 96.5% to 97.0% compared with O. tsutsugamushi and Candidatus O. chuto (Table 2). A higher diversity was observed for htrA, with sequence identity of 88.2%–88.8% compared with O. tsutsugamushi and 85.2% with Candidatus O. chuto (Table 3). We observed a GTA insertion (valine) in position 28 of htrA in all 18 samples, similar to Candidatus O. chuto, but this substitution was not observed in O. tsutsugamushi strains.

Species Designation

The rrs sequences we analyzed showed a divergence of ≥3% from known Orientia species, indicating that the isolates from Chile constitute a novel species within the genus Orientia (family Rickettsiaceae, order Rickettsiales, class Alphaproteobacteria). Our designation of the bacteria as a new species was corroborated by the divergence of htrA and our inability to generate amplicons with primers of O. tsutsugamushi type-specific antigen gene tsa. Until a type strain is cultivated and characterized, we propose the designation Candidatus Orientia chiloensis for the novel species, after the Chiloé Archipelago (Los Lagos Region, Chile) where the pathogen was first identified (8,9).

Discussion

Because of new diagnostic tools and increasing clinical awareness, our knowledge of rickettsial infections has increased over recent decades (23,24). For scrub typhus, which has been considered the most important rickettsiosis in Asia and Australasia, the discovery of new endemic regions outside of the traditional tsutsugamushi triangle raises questions about established paradigms (25). Since 2006, multiple patients with scrub typhus have been reported in southern Chile, >12,000 km away from known endemic regions (8,9,15). In addition, a case of scrub typhus caused by a novel species, Candidatus O. chuto, was diagnosed on the Arabian Peninsula (7). These findings, together with serologic and molecular data from sub-Saharan Africa and Europe, suggest that scrub typhus caused by various Orientia species might have a much wider than previously known, possibly global, distribution (4,26,27).

Most clinicoepidemiologic and ecologic aspects of scrub typhus in South America are currently unknown. A recent study on Chiloé Island suggested that trombiculid mites of the genus Herpetacarus, which were found to be infected with Orientia-species bacteria, might serve as vectors (28); preliminary phylogenetic analyses showed that the mite-associated strains were 99%–100% identical to those from patients (29). Clinically, the >40 patients with scrub typhus diagnosed in southern Chile during 2015–2019 sought treatment for conditions similar to those for scrub typhus from the Asia Pacific region—fever, generalized rash, and inoculation eschar—and, similarly, had a rapid response to treatment with tetracycline or azithromycin (30). Early molecular and serologic data suggest that the Orientia species in Chile diverge from those in the Asia-Pacific region (8,9,15), but whether they represent distinct O. tsutsugamushi strains or a new species remained inconclusive. Our phylogenetic analyses of larger DNA segments from 2 conserved genes support the conclusion that the isolates from patients in Chile cluster outside known Orientia species and represent a distinct species.

Culture-independent sequencing techniques play an important role in prokaryotic taxonomy, especially for strictly intracellular bacteria (31,32). For the description of new species, sequence analyses of the 16S rRNA gene (rrs) are paramount. A ≥3% divergence of rrs sequences from those in known species is the accepted threshold suggesting a novel species (19), although corrected levels of ≥1.30%–1.35% have been suggested (33,34). Isolates with rrs sequence differences of >5%–6% might belong to a distinct genus, if they display unique phenotypic differences (35). Distinct, lower thresholds have been developed for Rickettsia spp. (31), but this approach remains controversial among rickettsiologists (36). As should be the case for all molecularly defined novel species and genera, we have classified this proposed species as Candidatus, until type strains can be cultivated and fully described (37).

The novel Orientia species presented here fulfills the rrs gene criteria described in the previous sections. Our designation of a novel species was affirmed by a high divergence of another genomic marker, htrA, which diverged >11% from O. tsutsugamushi and of >14% from Candidatus O. chuto (Table 3). This conserved gene diverges only <3.7% among O. tsutsugamushi isolates (38). The O. tsutsugamushi type-specific antigen gene, tsa, which has a much higher diversity than htrA (1), was not amplifiable from isolates from Chile using primers designed for O. tsutsugamushi. This suggests that the Candidatus O. chiloensis tsa is unique, requiring the assessment of additional primers, possibly based on results from a future WGS. Currently, no Orientia culture isolate from Chile is available.

Surprisingly, the rrs and htrA sequences from the 18 Orientia samples from Chile were almost identical, showing a maximum variability of only 2 nucleotides. This genetic homogeneity over a wide geographic range is in sharp contrast to O. tsutsugamushi (38). As a unique characteristic among obligate intracellular pathogens, this species displays a dramatic genomic and phenotypic heterogeneity (1), which might be related to homologous recombination and lateral gene transfer (39). Among O. tsutsugamushi isolates, for example, the divergence of reported rrs sequences are up to 1.5% and for htrA sequences up to 3.6% (1,38), compared with ≤0.3% observed among isolates from Orientia DNA from Chile.

The most frequently applied phenotypic and molecular marker of O. tsutsugamushi strain heterogeneity is the highly variable 56-kDa TSA. This Orientia-specific surface protein is also known to be an important determinant of strain-specific pathogenicity and immunity (1). As we mentioned, we were not able to generate amplicons of strains from Chile with the applied tsa PCR or with tsa qPCR (41) or other commonly used primers (e.g., r56_2057). In a previous report, short tsa sequences were produced from 2 samples, but only after prolonged amplification cycles (9). These findings strongly suggest that tsa of Candidatus O. chiloensis is highly divergent from those of other Orientia species. Because the TSA surface protein is the main antigenic determinant, such divergence might explain the low serologic cross-reactivity, which was observed in patients with scrub typhus and in seroprevalence studies in Chile using O. tsutsugamushi whole-cell or recombinant antigens (9,41).

In conclusion, our results indicate that scrub typhus in Chile is caused by a novel Orientia species, suggesting an ancient origin of the disease in South America, rather than recent introduction. However, after obtaining cultured isolates of Candidatus O. chiloensis and larger gene sequences including from WGS, deeper comparative studies of the 3 Orientia species and their vectors are necessary to understand the ecology and evolution of these emerging intracellular pathogens, including the mechanisms responsible for the differences in strain variability and surface proteins.

Dr. Abarca is a pediatric infectious diseases specialist and professor at the School of Medicine, Pontificia Universidad Católica de Chile in Santiago, Chile. Her main research interests include vectorborne zoonoses and rickettsial infections as well as vaccine development.

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Acknowledgments

We acknowledge Katia Velasquez and all other physicians who participated in identifying the scrub typhus cases included in this study. We also thank Teresa Azócar and Romina Alarcón for their technical help in processing the clinical samples.

This work was supported by a grant from the Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT N° 1130817 and N° 1170810) and the Armed Forces Health Surveillance Branch and its Global Emerging Infections Surveillance and Response (GEIS) Section (funding year 2018, ProMIS ID P0017_19_NM_02 NMRC work unit number A0047).

The views expressed in this article reflect the results of research conducted by the authors and do not necessarily reflect the official policy or position of the Department of the Navy, Department of Defense, or the United States Government.

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Cite This Article

DOI: 10.3201/eid2609.200918

Original Publication Date: August 05, 2020

1These authors contributed equally to this article.

Table of Contents – Volume 26, Number 9—September 2020

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Please use the form below to submit correspondence to the authors or contact them at the following address:

Thomas Weitzel, Laboratorio Clínico, Clínica Alemana de Santiago, Av. Vitacura 5951, Santiago, Chile; ; and Katia Abarca, Departamento de Enfermedades Infecciosas e Inmunología Pediátricas, Pontificia Universidad Católica de Chile, Santiago, Chile

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Page created: May 26, 2020
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