Literature DB >> 18503166

PCR-based identification of Culex pipiens complex collected in Japan.

Shinji Kasai1, Osamu Komagata, Takashi Tomita, Kyoko Sawabe, Yoshio Tsuda, Hiromu Kurahashi, Takeshi Ishikawa, Mitsugu Motoki, Tomoya Takahashi, Tsutomu Tanikawa, Masahiro Yoshida, Goro Shinjo, Tomoyuki Hashimoto, Yukiko Higa, Mutsuo Kobayashi.   

Abstract

The Culex pipiens complex consists of vector mosquitoes that transmit important human pathogens. In this study we established a simplified method to distinguish three members of the Cx. pipiens complex, Cx. p. pallens Coquillet, Cx. p. form molestus Forskal, and Cx. quinquefasciatus Say, collected in Japan. Sequence analysis of the Drosophila Ace-orthologous acetylcholinesterase (Ace) gene (668 to 680 bp) revealed that a single polymorphic region characterizes each species. Based on this region, specific primers that distinguish Cx. p. form molestus (ACEpip2) and Cx. p. pallens (ACEpall2) were newly designed. Polymerase chain reactions were performed with the genomic DNA of Culex mosquitoes as the template, and these primers clearly distinguished two Culex spp. The accuracy of the designed primers was evaluated with 38 colonies of mosquito samples collected from 9 prefectures of Japan. The testing revealed that the distribution of anautogenous Cx. p. pipiens has not been confirmed in Japan. It also revealed that the male of Cx. p. pallens possesses an Ace gene haplotype that is highly similar to the sequence of Cx. quinquefasciatus. This improved method allows the evaluation of vector competence of Cx. p.molestus, which is the suspected vector of West Nile virus.

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Year:  2008        PMID: 18503166

Source DB:  PubMed          Journal:  Jpn J Infect Dis        ISSN: 1344-6304            Impact factor:   1.362


  13 in total

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