RICKETTSIA SPECIES AMONG TICKS IN AN AREA OF JAPAN ENDEMIC FOR JAPANESE SPOTTED FEVER

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RICKETTSIA SPECIES AMONG TICKS IN AN AREA OF JAPAN ENDEMIC FOR JAPANESE SPOTTED FEVER Makoto Kondo 1, Katsuhiko Ando 2, Keiichi Yamanaka 1 and Hitoshi Mizutani 1 1 Department of Dermatology, 2 Department of Medical Zoology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan Abstract. Rickettsia diseases, such as Japanese spotted fever, are serious infectious diseases. It is important to periodically survey tick species known for carrying pathogens for the presence of Rickettsia in endemic areas. We collected ticks from the field at 4 locations in the Ise-Shima areas of Mie Prefecture, Japan using a standard flagging method. The DNA samples were obtained from each tick using conventional polymerase chain reaction using primers for both the DNA sequences of the ticks and rickettsia. A total of 347 ticks were collected from the 4 study locations. The predominant species of tick found at 3 of 4 study sites was Haemaphysalis longicornis and at the first study site. There was a heterogeneous mix of tick species without a predominant type. Various Rickettsia species were found in 80% of the H. longicornis ticks but Rickettisia japonica, the etiology of Japanese spotted fever, was not detected in any of the studied ticks. Our findings suggest the presence of R.japonica is low in the studied areas among the studied ticks. Keyword: Japanese spotted fever, Rickettsia japonica, Rickettsia tamurae, endemic area, Haemophysalis longicornis INTRODUCTION The Japanese spotted fever (JSF) is a serious infectious disease caused by infection with Rickettsia japonica (Kondo et al, 2010). More than 30 cases of JSF were reported per year in the Ise-Shima areas of Mie Prefecture, Japan during an eight consecutive year period (https://www. pref.mie.lg/jp/hokan/hp/). JSF develops after the bite of a tick carrying R. japonica. The ticks: Haemaphysalis longicornis (H.l) (Uchida et al, 1995, Ishikura et al, 2003, Tabara et al, 2011). Dermacentor taiwanesis Correspondence: Dr Keiichi Yamanaka, Department of Dermatology, Mie University, Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie 514-8507, Japan. Tel: +81 59 2315025; Fax: +81 59 2315206 E-mail: yamake@clin.medic.mie-u.ac.jp (Fournier et al, 2002) and Haemaphysalis flava (H.fl) (Fournier et al, 2002) have been reported to carry R. japonica. Ticks have different species-specific behaviors and life cycles (https://www.cdc.gov/ticks/ life_cycle_and_hosts.html). A step in the prevention of JSF is identification of the ticks that carry R.japonica. We surveyed ticks known to carry R.japonica in an area endemic for JSF in Mie Prefecture, Japan to determine the species of tick associated with JSF and the prevalence of R.japonica in the surveyed ticks. MATERIALS AND METHODS Field surveillance The field surveillance for the studied ticks were conducted in 4 areas of Ise- Shima from November 2014 to February Vol 48 No. 3 May 2017 585

Southeast Asian J Trop Med Public Health Fig 1 Study areas. 2015 (Fig 1). Area A was a grass field covered with the fallen leaves along the road; Area B was a field of short grass in an orange orchard; Area C was an observation deck for the Fall with many visitors; Area D was a field along an animal trail in a forest. Deer spoor was found in Area D; many cases of JSF had been reported among the residents of nearby villages. The ticks were captured using a standard flagging method. Sampling flag consisted of a 1 m 2 piece of white cotton flannel attached to a 1.5 m wooden dowel (Rulison et al, 2013). The collected ticks were placed in 10% ethanol and stored at -80 until examined. Detection of Rickettsia in surveyed ticks DNA was extracted from each tick collected using a QIAamp DNA mini kit (QIAGEN, Germantown, MD) according to manufacturer s instructions. The tick specific DNA sequence was amplified by a conventional polymerase chain reaction (PCR) using tick species-specific identification primers (Ushijima et al, 2003). The outer membrane of any possible rickettsia protein A (OmpA) was amplified using a specific primer set (Forward: 5 -CAACAAGGTCTTAAAGCCGC-3 and Reverse: 5 -AGCATTCACTCCCCCTA- AAG-3 ) we designed. The PCR product sequences were analyzed at Eurofins Genomics (Tokyo, Japan) to detect tick and rickettsia DNA. RESULTS A total of 347 ticks were collected (146 larvae, 193 nymphs and 8 adults). A total of 7 species were identified. The distribution and types of ticks found are shown in Table 1. Haemaphysalis longicornis was the most common species of tick 586 Vol 48 No. 3 May 2017

Table 1 The numbers and species of ticks captured in the study areas. Area Total number Tick species Tick growth stages Larva Nymph Adult A 100 H.m 4 1 0 H.l 64 31 0 Total 68 32 0 B 67 H.c 0 1 0 H.l 5 59 0 H.fl 0 2 0 Total 5 62 0 C 97 A.t 0 0 1 H.l 48 41 0 H.m 2 3 0 H.c 0 2 0 Total 50 46 1 D 83 H.fo 0 1 0 H.l 0 1 0 H.m 6 34 1 H.fl 15 2 1 A.t 1 13 5 H.j 1 2 0 Total 23 53 7 H.l, Haemaphysalis longicornis; H.m, Haemaphysalis megaspinosa; H.fl, Haemaphysalis flava; H.c, Haemaphysalis cornigera; A.t, Amblyomma testudinarium; H.j, Haemaphysalis japonica; H.fo, Haemaphysalis formosensis. found in areas A, B and C and the most common species of tick found in Area D was Haemaphysalis megaspinosa (H.m). The rickettsia DNA found in the collected ticks is summarized in Table 2. Rickettsia lon (R. lon) was the most frequently isolated species of Rickettsia in our study and most frequently found in H.l in all 4 study areas. Rickettsia tamurae has been reported to be carried primarily by Amblyomma testudinarium (A.t) (Fournier et al, 2006), but it was detected in H.l in our study as well. No R. japonica was detected in any of the collected ticks in our study. DISCUSSION Various pathogenic species of Rickettsia have been reported in Japan including R. japonica (Kondo et al, 2010), R. tamurae (Imaoka et al, 2011) and R. heilongjiangensis (Ando et al, 2010). Delay in diagnosis and treatment of JSF caused by R. japonica can result in life-threating liver disease and disseminated intravascular coagulation (DIC) (Kondo et al, 2010). It is important to know the distribution of rickettsia-carrying ticks in JSF endemic areas. R. japonica, the cause of JSF, was not detected in our study. R.tamurae is a human pathogen causing mild general symptoms (Imaoka et al, 2011). R. tamurae was detected in a small percentage of ticks in our study. H.l. has been reported to be a competent host for R. japonica (Uchida et al, 1995; Vol 48 No. 3 May 2017 587

Southeast Asian J Trop Med Public Health Table 2 Prevalence of Rickettsia species by tick type at study location. Study No. (%) of studied ticks Number Tick Rickettsia Tick types positive Area positive for Rickettsia of ticks speies for Rickettsia species Larva Nymph Adult A 83/95 (87.4) 95 H.l R.L 55 28 0 1/5 (20) 5 H.m R.L 1 0 0 B 59/64 (92) 64 H.l R.L 5 54 0 0/2 (0) 2 H.fl R.sp 0 0 0 0/1 (0) 1 H.c R.sp 0 0 0 C 64/89 (71.9) 89 H.l R.L 27 35 0 R.T 2 0 0 1/5 (20) 5 H.m R.L 0 1 0 0/2 (0) 2 H.c R.sp 0 0 0 0/1 (0) 1 A.t R.sp 0 0 0 D 1/1 (100) 1 H.l R.L 0 1 0 7/40 (17.5) 40 H.m R.L 3 4 0 0/18 (0) 18 H.fl R.sp 0 0 0 6/19 (31.2) 19 A.t R.L 1 3 0 RT 0 0 2 2/3 (66.7) 3 H.j R.L 1 1 0 0/1 (0) 1 H.fo R.sp 0 0 0 H.l, Haemaphysalis longicornis; H.m, Haemaphysalis megaspinosa; H.fl, Haemaphysalis flava; H.c, Haemaphysalis cornigera; A.t, Amblyomma testudinarium; H.j, Haemaphysalis japonica; H.fo, Haemaphysalis formosensis; R.L, Rickettsia lon type; R.T, Ricekttsia tamurae; R.sp, Rickettsia species. Ishikura et al, 2003; Tabara et al, 2011). H.l was the most common tick in study areas A, B and C. Rickettsia DNA was found in 80% of H.l ticks collected in our study, suggesting it as an effective carrier of Rickettsia species, mostly of the R. lon type. A variety of tick species were detected in area D, an area known as endemic for Rickettsia infections. R. japonica was not detected in any area, including area D, which is endemic for JSF, suggesting the sample size may have been too small or the study site inappropriate. Further studies with larger sample sizes in other areas known to be endemic for JSF are needed to determine of the presence of R.japonica carrying ticks and their species. REFERENCES Ando S, Kurosawa M, Sakata A, et al. Human Rickettsia heilongjiangensis infection, Japan. Emerg Infect Dis 2010; 16: 1306-8. Fournier PE, Fujita H, Takada N, Raoult D. Genetic identification of rickettsiae isolated from ticks in Japan. J Clin Microbiol 2002; 40: 2176-81. Fournier PE, Takada N, Fujita H, Raoult D Rickettsia tamurae sp. nov., isolated from Amblyomma testudinarium ticks. Int J Syst Evol Microbiol 2006; 56: 1673-5. Imaoka K, Kaneko S, Tabara K, Kusatake K, Morita E. The first human case of Rickettsia tamurae infection in Japan. Case Rep Dermatol 2011; 3: 68-73. Ishikura M, Ando S, Shinagawa Y, et al. Phy- 588 Vol 48 No. 3 May 2017

logenetic analysis of spotted fever group rickettsiae based on glta, 17-kDa, and rompa genes amplified by nested PCR from ticks in Japan. Microbiol Immunol 2003; 47: 823-32. Kondo M, Nishii M, Gabazza EC, Kurokawa I, Akachi S. Nine cases of Japan spotted fever diagnosed at our hospital in 2008. Int J Dermatol 2010; 49: 430-4. Rulison EL, Kuczaj I, Pang G, et al. Flagging versus dragging as sampling methods for nymphal Ixodes scapularis (Acari: Ixodidae). J Vector Ecol 2013; 38: 163-7. Tabara K, Kawabata H, Arai S, et al. High incidence of rickettsiosis correlated to prevalence of Rickettsia japonica among Haemaphysalis longicornis tick. J Vet Med Sci 2011; 73: 507-10. Uchida T, Yan Y, Kitaoka S. Detection of Rickettsia japonica in Haemaphysalis longicornis ticks by restriction fragment length polymorphism of PCR product. J Clin Microbiol 1995; 33: 824-8. Ushijima Y, Oliver JH, Jr, Keirans JE, et al. Mitochondrial sequence variation in Carlos capensis (Neumann), a parasite of seabirds, collected on Torishima Island in Japan. J Parasitol 2003; 89: 196-8. Vol 48 No. 3 May 2017 589