Severe fever with thrombocytopenia syndrome virus, South Korea, 2013.
Ixodid tick species are implicated as vectors of SFTSV (1,5,6). One study described a SFTSV prevalence in Haemaphysalis longicornis ticks, a major vector of SFTSV, of 0.46% minimum infection rate in South Korea (7); in another study, SFTSV was detected in ticks that had bitten humans (6). From these studies, we realized that SFTSV was common throughout the country. We aimed to evaluate the prevalence of SFTS in South Korea and isolate the SFTSV to analyze its phylogenetic properties.
In March 2013, we established molecular diagnostic methods to detect SFTSV. During April-December 2013, from 125 hospitals throughout the country, we collected 301 serum samples from hospitalized persons who had SFTS signs and symptoms, such as high fever (temperatures [greater than or equal to]38[degrees]C), vomiting, diarrhea, and/or fatigue and showed laboratory parameters consistent with thrombocytopenia and/or leukocytopenia. We conducted reverse transcription PCR (RT-PCR) to detect the SFTSV medium (M) segment gene from acute-phase serum specimens with a previously described method (6). We also detected the SFTSV small (S) segment gene by RT-PCR with specific primers (SF3, 5'-GGGTCCCTGAAGGAGTTGTAAA-3'; SRI, 5'-TGGTGAGCAGCAGCTCAATT-3'). The RT-PCR conditions were as follows: an initial step of 30 min at 50[degrees]C for reverse transcription and 15 min at 95[degrees]C for denaturation, followed by 35 cycles of 20 s at 95[degrees]C, 40 s at 58[degrees]C (for M segment) or 55[degrees]C (for S segment), and 30 s at 72[degrees]C and a final extension step of 5 min at 72[degrees]C.
From the 301 samples, we detected M and S segment genes from 34 and 29 samples, respectively. The nucleotide sequences were assembled by the SeqMan program implemented inDNASTAR software (version 5.06; Madison, WI, USA) to determine the consensus sequences. The nucleotide sequences of the Korea isolates showed 93%-98% homology to the China and Japan isolates.
To isolate SFTSV, we inoculated subconfluent mono layers of Vero E6 cells with the RT-PCR-positive semm. After the monolayers underwent 3 blind passages in new monolayers of Vero E6 cells (8), we examined the Vero E6 cells for SFTSV by RT-PCR. We considered the vims to be isolated when the specific genes were amplified by RTPCR. The viruses did not cause cytopathic effects in Vero E6 cells during isolation. Isolation of SFTSV also was confirmed by indirect immunofluorescent assay (IFA) (Figure 1, panels A,B) and electron microscopy (Figure 1, panel C). For IF A, Vero E6 cells infected with SFTSV were incubated at 37[degrees]C in a C02 incubator. Cells were harvested, inoculated, and fixed with acetone on Teflon-coated well slides. IFA was conducted by using a monoclonal SFTSV nucleocapsid protein (N) antibody (manufactured in our laboratory) as the primary antibody. N proteins of SFTSV were distributed throughout the cytoplasm (Figure 1, panels A,B). By electron microscopy, Vero E6 cells infected with the SFTSV Korea isolate KAJJH showed bunyavirus-like particles, 80-100 nm in diameter, located in cytoplas mic vacuoles, presumably in the Golgi apparatus (Figure 1, panel C).
The amplified DNA products from the isolates were sequenced and compared with the sequences of other Gen Bank-registered SFTSV isolates. The sequences of partial M and S segments of the 26 Korea isolates (GenBank accession nos. KF282701, KF282702, and KJ739543KJ739592) were closely related to those of the SFTSV isolates from China and Japan with 92%-100% identity. A phylogenetic tree was constructed by the neighbor-joining method on the basis of the partial M (Figure 2, panel A, http://wwwnccdc.gOv/EID/article/20/l 1/14-0888-F2 .htm) and S segment (Figure 2, panel B) sequences of the Korea SFTSVs in the study and 15 SFTSVs from China and Japan registered in GenBank. SFTSV isolates formed 2 major clusters in M and S segment sequences, and 1 other small group comprising only Korea isolates, KAGNH2 and KAUSH, was formed in M-segment sequences. Many Korea isolates formed the first cluster with the Japan isolates. Some Korea isolates clustered with the major group of China isolates, forming the second group.
We confirmed the SFTS in several localities around South Korea. We also isolated several SFTSVs from case-patient serum and analyzed the phylogenetic properties of the isolates. A total of 36 SFTS case-patients were reported in South Korea. The first SFTS case was identified in a retrospective study from 2012 (3). Subsequently, SFTS was diagnosed in 35 additional case-patients in South Korea. Another group diagnosed the first of the 35 cases in the country; we diagnosed the other 34 cases, from which we isolated the 26 SFTSVs. The major signs and symptoms of the 35 case-patients, including fever (100%), gastrointestinal symptoms (74%), fatigue (74%), thrombocytopenia (100%), and leukocytopenia (100%), were similar to those of case-patients in China and Japan (9).
The case-fatality rate for SFTS in South Korea was 47.2% (17/36), higher than that of the recent China cases ([approximately equal to]8.7%) (10). The low sensitivity of the detection method, the conventional 1-step RT-PCR, and the absence of a serologic diagnosis may have contributed to the relatively high case-fatality rate. Most cases occurred in older persons; [approximately equal to]80% of patients were >50 years of age. Approximately 70% were farmers, including persons who cultivated vegetable gardens (9). In many case-patients, the disease evolved during a relatively warm time of year, from late spring to early autumn (Figure 3, panel A). The geographic distribution of SFTS case-patients also indicated that environmental temperature affected the SFTS prevalence because many (86%, 30/35) SFTS cases evolved in relatively warm southern provinces and cities south of Chungcheongbuk, Chungcheongnam, and Gangwon Provinces (Figure 3, panel B). We have also observed that the tick density is high during May-August, a generally warm season in South Korea (7). SFTSV was also mainly detected during this season. These results indicate that the virus infection in humans is closely related to a high tick density and SFTSV infection in ticks in a warm climate.
As described in another report, Japan isolates formed an independent cluster from the China isolates (2). In our current study, SFTSV isolates fonned 2 major clusters. Most of the Korea isolates formed a cluster with the Japan isolates, although some Korea and China isolates were in eluded in the other group, perhaps not surprising given the geographic location of South Korea between China and Japan.
We thank all involved in SFTS diagnosis in 2013, especially the staff in 17 regional Institutes of Health and Environment. We also thank Young Eui Jeong and Ki Ju Choi for technical support with molecular evolution and the electron microscope.
This study was financially supported by the Korea National Institute of Health, Korea Centers for Disease Control and Pre vention (program no. 4800-4837-300-210-13 and 4800-4861304-210-13 [grant no. 2014-NG53002-00]).
Dr. Sun-Whan Park is a senior researcher at tire Division of Arboviruses, National Institute of Health, Korea Centers for Dis ease Control and Prevention. His research focuses on bunyavi ruses, including SFTSV and hantavirus.
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Address for correspondence: Jungsang Ryou, Division of Arboviruses, Center for Immunology and Pathology, National Institute of Health, Korea Centers for Disease Control and Prevention, 187 Osongsaengmyeong2-ro, Osong-eup, Cheongwon-gun, Chungbuk, 363-951, South Korea; email: email@example.com
Sun-Whan Park, Myung-Guk Han, Seok-Min Yun, Chan Park, Won-Ja Lee, Jungsang Ryou
Author affiliation: Korea Centers for Disease Control and Prevention, Cheongwon-gun, South Korea
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|Author:||Park, Sun-Whan; Han, Myung-Guk; Yun, Seok-Min; Park, Chan; Lee, Won-Ja; Ryou, Jungsang|
|Publication:||Emerging Infectious Diseases|
|Date:||Nov 1, 2014|
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