Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 25, Number 6—June 2019

Scrub Typhus in Continental Chile, 2016–20181

Article Metrics
citations of this article
EID Journal Metrics on Scopus
Thomas WeitzelComments to Author , Katia AbarcaComments to Author , Constanza Martínez-Valdebenito, Gerardo Acosta-Jamett, Ju Jiang, and Allen L. Richards
Author affiliations: Clinica Alemana, Universidad del Desarrollo, Santiago, Chile (T. Weitzel); Pontificia Universidad Católica de Chile, Santiago (C. Martínez-Valdebenito, K. Abarca); Universidad Austral de Chile, Valdivia, Chile (G. Acosta-Jamett); Naval Medical Research Center, Silver Spring, Maryland, USA (J. Jiang, A.L. Richards)

Cite This Article


Endemic scrub typhus was recently detected on Chiloé Island in southern Chile. We report a series of cases, acquired over a wide geographical range in continental Chile during 2016–2018, demonstrating that this emerging rickettsial infection is also found on the mainland of South America.

Scrub typhus is a vectorborne zoonosis caused by Orientia spp. bacteria; infection carries a potentially severe outcome (1). Although widely underrecognized, scrub typhus is considered one of the most important rickettsial infections worldwide in terms of prevalence and severity (2). Until recently, scrub typhus was associated with only a single species, O. tsutsugamushi, which is transmitted by larvae of trombiculid mites (chiggers) and threatens >1 billion human inhabitants within the so-called tsutsugamushi triangle in the Asia–Pacific region (1). Since 2006, the discoveries of scrub typhus in 4 patients on Chiloé Island in Chile (3,4) and in 1 patient from Dubai, United Arab Emirates (5), have suggested the emergence of the disease farther afield (6). This change of paradigm has been reinforced by recent studies mainly from Africa (7). The emergence of endemic scrub typhus on Chiloé Island has been confirmed by ongoing studies of our working group in Chile (8,9). Whether this disease is only endemic to Chiloé Island or has a wider distribution is unknown. We report 9 patients who had scrub typhus diagnosed after visiting different regions of continental Chile during 2016–2018.

The Study

After the confirmation of autochthonous scrub typhus cases in Chiloé in 2016 (4), the Chilean Ministry of Health issued a clinical alert advising healthcare providers in Chile to confirm possible cases in cooperation with our research group. Most of the patients described in this report were identified as a result of the clinical alert and are included in an ongoing clinical–epidemiologic scrub typhus project.

We tested serum samples obtained during acute and convalescent phases of infection for Orientia-specific antibodies by using a commercial IgG indirect immunofluorescence assay (Fuller Laboratories,, based on whole-cell O. tsutsugamushi Gilliam, Karp, Kato, and Boryong strains, and by using Scrub Typhus Detect IgG and IgM ELISA (InBios International Inc., with recombinant 56-kD type–specific antigens of O. tsutsugamushi Karp, Kato, Gilliam, and TA716 strains. We examined DNA extracted from eschar material by using 16S rRNA (rrs) and 47 kDa gene (htrA) seminested PCR and sequencing, as previously described (10), except that we changed the forward primer of the PCR step of rrs from 16SU17 to 16SOR155f. We also tested all samples by using a recently developed Orientia genus–specific quantitative real-time PCR assay targeting rrs (11).

Among the 37 patients with suspected scrub typhus who were tested during 2016–2018, 13 were from mainland Chile. Of those, 9 had scrub typhus diagnosed both serologically and molecularly. None of these 9 patients lived in or traveled to Chiloé Island or other regions with endemic scrub typhus, but all were exposed to natural habitats on mainland Chile (Table 1). Seven patients were male and 2 female; median age was 28 years.


Thumbnail of Locations of probable exposures (red circles) of 9 scrub typhus patients in continental Chile, 2016–2018. Inset map shows the study area (red box) and the location of Chile (grey shading) within South America.

Figure. Locations of probable exposures (red circles) of 9 scrub typhus patients in continental Chile, 2016–2018. Inset map shows the study area (red box) and the location of Chile (grey shading) within...

All cases occurred after outdoor activities during the summer months of February and March. We defined probable exposure sites as those locations where patients reported outdoor activities with close contact to natural environments within the 7–20 days before symptom onset. Most infections were acquired in the Los Lagos Region, which includes Chiloé Island. However, 2 cases were acquired farther south, in the Aysén Region, and another case farther north, in the Bio Bío Region (Figure). The sites of exposure ranged over a total distance of >1,120 km (, from 38°03′S to 47°47′S. Details of the activities leading to the exposure have been described elsewhere (12).

All patients had fever, generalized maculopapular rash, eschar, and headache; other frequent symptoms were myalgia (8 patients) and regional lymphadenopathy (5 patients). Laboratory abnormalities included elevated C-reactive protein (8 patients) and transaminases (6 patients), thrombocytopenia (4 patients), and leukopenia (4 patients). Eight patients required hospitalization. We noted a serologic response to O. tsutsugamushi antigens in all 9 patients. Eight patients were positive for IgG by indirect immunofluorescence assay, mostly with low titers, and 3 of the 6 patients for whom convalescent-phase samples were available showed seroconversion or a >4-fold rise in titer. IgG and IgM results by ELISA were positive in 6 of 9 patients on the basis of local cutoff values (Table 2). All cases were confirmed by detection of Orientia-specific DNA from eschar material using 3 different PCR assays (Table 2). After treatment with doxycycline (7 patients) or azithromycin (1 patient), patients recovered rapidly; 1 patient recuperated after 6 days of fever without receiving any scrub typhus–specific treatment.


Our understanding of the global epidemiology of Orientia spp. as human pathogens has undergone important changes. Most importantly, the paradigm of the geographic limitation of scrub typhus to the Asia–Pacific region, which had been unchallenged since the first scientific description of this disease at the beginning of the last century, has been superseded in light of the recent identification of scrub typhus cases on the Arabian Peninsula (Dubai) and South America (Chiloé Island in Chile) (4,5). The Dubai patient was infected by a distinct Orientia species, Candidatus O. chuto; the complete description of the isolates from Chile is pending.

Further studies in rodents and vectors have demonstrated molecular evidence of Orientia spp. or Orientia-like organisms in South Africa, Kenya, Senegal, and France (6,13,14). In addition, serologic reports point to possible human exposure to Orientia microorganisms in Djibouti, Kenya, Republic of the Congo, Cameroon, and Peru (6,7,15). Current data suggest that Candidatus O. chuto might be the Orientia species from Africa and the Arabian Peninsula (5,14). Clinical data from these regions are scarce, but 1 molecularly proven case and 2 cases diagnosed on the basis of serologic results occurred in patients with typical symptoms of scrub typhus (5,6).

The case series we report provides important epidemiologic information for South America, highlighting that scrub typhus is not limited to Chiloé Island but also occurs over a wide range of continental Chile. The actual incidence of the infection remains unknown; the observed increase from 1 case in 2016 to 6 cases in 2018 most probably reflects the growing awareness of scrub typhus among infectious diseases physicians in Chile. Because all of the case-patients we describe were included through a surveillance based on passive case detection, we believe that they only represent the tip of the iceberg for scrub typhus in Chile and South America.

The clinical data of this series showed the classical scrub typhus manifestation: fever, generalized maculopapular rash, and eschar at the inoculation site. However, this finding has to be interpreted cautiously because our epidemiologic alert describes these manifestations as typical, which biases the physicians’ attention toward these presentations. Less typical clinical signs and symptoms (e.g., without rash or with predominant respiratory symptoms), which are present in Asia in a relevant percentage of cases (1), might go undiagnosed in Chile.

All patients were serologically positive according to >1 of the applied commercial assays, which were based on O. tsutsugamushi antigens. The low seroreactivity against these antigens, however, suggests a distinct strain or species, which is supported by our preliminary molecular analyses (data not shown). Eschar material, which can be stored and transported under simple conditions (i.e., in a dry plastic tube at 4°C), proved to be the best and most practical specimen, permitting a rapid and reliable confirmation by molecular methods. Studies are ongoing to culture the Orientia species in Chile and to understand its life cycle, including vectors and possible zoonotic reservoirs.

Dr. Weitzel is a clinical microbiologist and infectious diseases physician specializing in tropical and travel medicine at Clínica Alemana and a professor at the Clínica Alemana Medical School of the Universidad del Desarrollo in Santiago, Chile. His main research interests include vectorborne zoonoses and imported tropical infections.



We thank the following physicians, who clinically suspected scrub typhus and permitted the confirmation of the patients of this case series, for their important contribution: Teresa Bidart, Johanna Cabrera, Mario Calvo, María Pilar Gambra, Iván Jara, Miguel Lagos, Alejandra Marcotti, José Manuel Munita, and Luis Thompson.

This work was supported by the Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT grant no. 1170810) and the Global Emerging Infectious Diseases Section (work unit no. A1402).

The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Department of the Navy, Department of Defense nor the U.S. Government. A.L.R. is an employee of the US Government. This work was prepared as a part of his official duties. Title 17 U.S.C. §105 provides that “copyright protection under this title is not available for any work of the United States Government.” Title 17 U.S.C. §101 defines a US Government work as a work prepared by a military service member or employee of the US Government as part of that person’s official duties. J.J. and A.L.R. provided training and consultation, but did not have contact with patients or participate in the data collection at Naval Medical Research Center, USA.



  1. Kim  IS, Walker  DH. Scrub Typhus. In: Guerrant RL, Walker DH, Weller PF, editors. Tropical infectious diseases: principles, pathogens and practice. 3rd edition. New York: Elsevier Inc.; 2011. p. 334–8.
  2. Paris  DH, Shelite  TR, Day  NP, Walker  DH. Unresolved problems related to scrub typhus: a seriously neglected life-threatening disease. Am J Trop Med Hyg. 2013;89:3017. DOIPubMedGoogle Scholar
  3. Balcells  ME, Rabagliati  R, García  P, Poggi  H, Oddó  D, Concha  M, et al. Endemic scrub typhus-like illness, Chile. Emerg Infect Dis. 2011;17:165963. DOIPubMedGoogle Scholar
  4. Weitzel  T, Dittrich  S, López  J, Phuklia  W, Martinez-Valdebenito  C, Velásquez  K, et al. Endemic scrub typhus in South America. N Engl J Med. 2016;375:95461. DOIPubMedGoogle Scholar
  5. 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. J Clin Microbiol. 2010;48:44049. DOIPubMedGoogle Scholar
  6. Luce-Fedrow  A, Lehman  ML, Kelly  DJ, Mullins  K, Maina  AN, Stewart  RL, et al. A review of scrub typhus (Orientia tsutsugamushi and related organisms): then, now, and tomorrow. Trop Med Infect Dis. 2018;3:8. DOIPubMedGoogle Scholar
  7. Xu  G, Walker  DH, Jupiter  D, Melby  PC, Arcari  CM. A review of the global epidemiology of scrub typhus. PLoS Negl Trop Dis. 2017;11:e0006062. DOIPubMedGoogle Scholar
  8. Weitzel  T, Jiang  J, Acosta-Jamett  G, Martínez-Valdebenito  C, López  J, Richards  AL, et al. Canine seroprevalence to Orientia species in southern Chile: A cross-sectional survey on the Chiloé Island. PLoS One. 2018;13:e0200362. DOIPubMedGoogle Scholar
  9. Abarca  K, Weitzel  T, Martínez-Valdebenito  C, Acosta-Jamett  G. Scrub typhus, an emerging infectious disease in Chile [in Spanish]. Rev Chilena Infectol. 2018;35:6969.
  10. Weitzel  T, Aylwin  M, Martínez-Valdebenito  C, Jiang  J, Munita  JM, Thompson  L, et al. Imported scrub typhus: first case in South America and review of the literature. Trop Dis Travel Med Vaccines. 2018;4:10. DOIPubMedGoogle Scholar
  11. Jiang  J, Martínez-Valdebenito  C, Weitzel  T, Abarca  K, Richards  AL. Development of an Orientia genus-specific quantitative real-time PCR assay and the detection of Orientia species in DNA preparations from O. tsutsugamushi, Candidatus Orientia chuto, and Orientia species from Chile. In: Abstracts of the 29th Meeting of the American Society for Rickettsiology; Milwaukee, USA; 2018 Jun 16–19, Abstract no. 46.
  12. Weitzel  T, Acosta-Jamett  G, Martínez-Valdebenito  C, Richards  AL, Grobusch  MP, Abarca  K. Martínez-Valdebenito, Richards AL, Grobusch MP, Abarca K. Scrub typhus risk in travelers to southern Chile. Travel Med Infect Dis. 2019 Jan 9 [Epub ahead of print]. PMID 30639781
  13. Kolo  AO, Sibeko-Matjila  KP, Maina  AN, Richards  AL, Knobel  DL, Matjila  PT. Molecular detection of zoonotic rickettsiae and Anaplasma spp. in domestic dogs and their ectoparasites in Bushbuckridge, South Africa. Vector Borne Zoonotic Dis. 2016;16:24552. DOIPubMedGoogle Scholar
  14. Masakhwe  C, Linsuwanon  P, Kimita  G, Mutai  B, Leepitakrat  S, Yalwala  S, et al. Identification and characterization of Orientia chuto in trombiculid chigger mites collected from wild rodents in Kenya. J Clin Microbiol. 2018;56:e0112418. DOIPubMedGoogle Scholar
  15. Kocher  C, Jiang  J, Morrison  AC, Castillo  R, Leguia  M, Loyola  S, et al. Serologic evidence of scrub typhus in the Peruvian Amazon. Emerg Infect Dis. 2017;23:138991. DOIPubMedGoogle Scholar




Cite This Article

DOI: 10.3201/eid2506.181860

Original Publication Date: March 05, 2019

1Preliminary results from this study were presented at the 67th Annual Meeting of the American Society of Tropical Medicine and Hygiene, October 28–November 2, 2018, New Orleans, Louisiana, USA.

Table of Contents – Volume 25, Number 6—June 2019

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.



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

Thomas Weitzel, Laboratorio Clínico, Clínica Alemana, Av Vitacura 5951, Santiago, Chile; ; Katia Abarca, Departamento de Enfermedades Infecciosas e Inmunología Pediátricas, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, Santiago, Chile

Send To

10000 character(s) remaining.


Page created: May 20, 2019
Page updated: May 20, 2019
Page reviewed: May 20, 2019
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.