Molecular studies of Anopheles culicifacies (Diptera : Culicidae) in Sri Lanka: Sibling species B and E show sequence identity at multiple loci

Sinnathamby Noble Surendran, Nicola J. Hawkes, Andrew Steven, Janet Hemingway, Ranjan Ramasamy

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13 Citations (Scopus)

Abstract

The anomaly that Anopheles culicifacies (Diptera: Culicidae) Species B is a major vector of malaria in Sri Lanka, but a non-vector in India, has been noted for several years. In 1999, a Y chromosome dimorphism associated with Plasmodium vivax infectivity within the Indian A. culicifacies species B suggested that this was itself a complex of two sibling species, B and E. A recent cytogenetic analysis shows the sympatric presence of these sibling species in Sri Lanka, a situation similar to that reported from nearby Rameshwaram Island, India. Species E, with a submetacentric Y chromosome, is a more effective vector of P. vivax than species B with an acrocentric Y chromosome. Larval karyotyping, however, is time-consuming and labour-intensive. Recently, the development of a PCR-RFLP assay distinguishing species B and E of A. culicifacies from India, based oil differences in one region of the cytochrome oxidase subunit II (COII) gene, was reported. Here we show that whilst this diagnostic approach reveals polymorphism in Sri Lankan A. culicifacies, this variation is not correlated with Y chromosome karyotype. Hence this assay will not be useful for distinguishing Species B and E in Sri Lanka. Further, we found no difference between the sequences of Sri Lankan specimens in any of three other regions (ITS2, D3 region of 28S rDNA, and guanylate cyclase intron) often Used for species discrimination.

Original languageEnglish
Pages (from-to)233-237
Number of pages5
JournalEuropean Journal of Entomology
Volume103
Issue number1
DOIs
Publication statusPublished - 30 Jan 2006

Keywords

  • 28S rDNA
  • Anopheles culicifacies
  • Cytochrome oxidase II
  • Guanylate cyclase
  • ITS2
  • Species B
  • Species E
  • Y-chromosome dimorphism

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