Scrub Typhus Outbreak, Northern Thailand, 2006–2007

During a scrub typhus outbreak investigation in Thailand, 4 isolates of O. tsutsugamushi were obtained and established in culture. Phylogenetic analysis based on the 56-kDa type-specific antigen gene demonstrated that the isolates fell into 4 genetic clusters, 3 of which had been previously reported and 1 that represents a new genotype.

S crub typhus is a febrile disease endemic to the Asia-Australia-Pacific region, where ≈1 million cases occur annually (1). The causative agent of scrub typhus in this region is the gram-negative obligate intracellular bacterium Orientia tsutsugamushi (2). The bacterium maintains itself in trombiculid mites, and small mammals serve as reservoir hosts in the natural life cycle of the mites. Chiggers, the larval stage of mites, act as the transmission vector for O. tsutsugamushi (1). Humans and small animals become infected following the bite of chiggers harboring O. tsutsugamushi. After an incubation period of 7-14 days, high fever, chills, headache, rash, and an eschar usually develop in infected persons (3).
Scrub typhus is endemic to northern Thailand, especially Chiang Mai Province, where >200 cases are reported each year (4). During June 2006-May 2007, a total of 142 febrile children with clinically suspected scrub typhus were admitted to Nakornping Hospital in the city of Chiang Mai. Serologic and molecular laboratory test results showed that 65 of the children were positive for O. tsutsugamushi. Among the 142 hospitalized children, 30 were Hmong hill tribe people living in Ban Pongyeang, a village in the mountain area located north of the Chiang Mai. Laboratory testing also confirmed that 26 of the 30 Hmong children had scrub typhus.
To better characterize the specific strain(s) of O. tsutsugamushi present in the area and to determine how the agent(s) is transmitted to humans, we genetically typed O. tsutsugamushi obtained from these 26 children and small mammals. The Royal Thai Army Medical Department Ethical Committee approved all procedures (protocol S014q/45). Small mammals were handled according to guidelines in the Guide for the Care and Use of Laboratory Animals (National Institutes of Health publication no. 85-23, revised 1985).

The Study
We obtained clinical information and blood samples from 26 scrub typhus-infected children from Ban Pongyeang after their parents gave informed consent. Blood specimens were stored in liquid nitrogen and shipped on dry ice to the Armed Forces Research Institute of Medical Sciences in Bangkok, Thailand, for serologic testing, genetic characterization, and isolation of O. tsutsugamushi.
We assessed serum samples for the presence of antibodies against O. tsutsugamushi by using an indirect fluorescence antibody assay (5) with an in-house antigen preparation from propagated O. tsutsugamushi Karp, Kato, and Gilliam strains. Single specimens with an IgM or IgG titer >400 were considered positive; paired specimens were considered positive if they showed seroconversion or a >4-fold rise in titer (6). To genetically characterize O. tsutsugamushi, we amplified a fragment of the 56-kDa type-specific antigen gene from patients' blood genomic DNA by using a modified nested PCR procedure as described (7). A newly designed forward primer (F584, 5′-CAA TGT CTG CGT TGT CGT TGC-3′) was used with the previously reported reverse primers RTS9 and RTS8 (7). The expected 693-bp products were purified, directly sequenced, and aligned according to ClustalW algorithm (www.clustal.org/). Using PAUP 4.0b10 software and maximum parsimony methods, we generated phylogenetic relationships (8). O. tsutsugamushi was isolated by using animal inoculation and L-929 mouse fibroblast cell culture techniques as described (9).
Patient clinical information and laboratory test results are shown in the online Technical Appendix (wwwnc.cdc.gov/EID/article/19/5/12-1445-Techapp1.pdf). The patients' ages ranged from 11 months to 13 years. Common signs and symptoms of illness were fever (100.0%), chills (73.1%), eschar (73.1%), headache (57.7%), and rash (23.1%) (online Technical Appendix; Figure 1 grassland, woods, and rice fields. Cases also occurred in infants who were carried on their mother's back during work in those areas ( Figure 1E). In addition, the opportunity to become infected was increased by frequent exposure to vector mites living in vegetation-rich areas.
To investigate O. tsutsugamushi transmission, we trapped small mammals from different terrains in Ban Pongyeang, identified them to species level, and collected tissue specimens (whole blood, liver, and spleen). The specimens were kept in liquid nitrogen and delivered to the Armed Forces Research Institute of Medical Sciences for laboratory testing. Chiggers were removed from captured mammals and stored in 70% ethanol. The chiggers were slide-mounted and identified to species by using a microscope.
Thirty-six (65.5%) of 51 animals tested were seroreactive to O. tsutsugamushi (Table 1). Compared with the other animals, a higher percentage (100%) of B. indica rats had O. tsutsugamushi infections, indicating that this species might serve as a reservoir host for the bacterium (Table 1).   (10,11); the sequence of the fourth isolate presented as a divergent distinct genotype ( Figure 2). Most of the children were infected with a strain genetically similar to the LA cluster ( Figure 2). Moreover, this major pathogenic strain was recovered from B. indica bandicoot rats (isolate PYA5), the most commonly found rats in the village and the small mammals with the highest densities of L. deliense chiggers. These findings indicate possible transmission between animals and humans. Many studies have demonstrated that chiggers can acquire O. tsutsugamushi during the feeding process (12)(13)(14)(15). Therefore, rodents could play a critical role as reservoir hosts for O. tsutsugamushi and for feeding vector mites, causing widespread distribution of O. tsutsugamushi in Ban Pongyeang.

Conclusions
Investigation of scrub typhus in Ban Pongyeang, northern Thailand, demonstrated O. tsutsugamushi infection in children and rodent hosts, and it demonstrated the potential for transmission between small mammal reservoirs and humans. Campaigns concerning protection from scrub typhus should be established in areas where O. tsutsugamushi is endemic, and local medical clinics should be made aware of the campaigns. Specific plans for protecting against/preventing O. tsutsugamushi transmission are crucially needed to prevent scrub typhus infection in humans.