| Literature DB >> 26350381 |
Kai Meng1, Wenjing Sun1, Ziqiang Cheng1, Huijun Guo1, Jianzhu Liu2, Tongjie Chai3.
Abstract
The aim of this study was to detect severe fever with thrombocytopenia syndrome virus (SFTSV) infection using polymerase chain reaction (PCR) amplification in adult Haemaphysalis concinna ticks. A total of 72 adult H. concinna ticks were obtained from 35 goats, three adult H. concinna ticks (4.17 %) collected from two goats were found to be infected with SFTSV via PCR assay. Sequence analysis showed that the partial segment M glycoprotein gene of SFTSV was about 500 bases long by polymerase chain reaction (PCR) amplification and that the PCR products from the samples had an identical sequence (KP714259). With regard to the phylogenetic analysis, the Nei-Gojobri (Kimura 2-parameter) method was used to construct the phylogenetic trees. Phylogenetic analysis indicated that the obtained sequence closely resembled SFTSV strain from Zhejiang Province (KC189856) and belonged to the same clade. The similarity of these strains was up to 96.62 % (only differing by 17 bases). In addition, phylogenetic analysis also indicated that the sequence obtained from adult H. concinna ticks was most closely related to the sequence isolated from Haemaphysalis longicornis (KF781498) with 97.22 % similarity (differing only by 4 bases) and belonged to the same clade.Entities:
Keywords: Fever with thrombocytopenia syndrome virus; Goat; Haemaphysalis concinna tick; PCR; Sequencing analysis
Mesh:
Year: 2015 PMID: 26350381 DOI: 10.1007/s00436-015-4718-2
Source DB: PubMed Journal: Parasitol Res ISSN: 0932-0113 Impact factor: 2.289