期刊论文详细信息
Particle and Fibre Toxicology
Karyotypic assignment of Sri Lankan Anopheles culicifacies species B and E does not correlate with cytochrome oxidase subunit I and microsatellite genotypes
Catherine Walton4  S. H. P. Parakrama Karunaratne5  Lalanthika B. S. Peiris6  Kanapathy Gajapathy1  Ranjan Ramasamy2  Pavilupillai J. Jude1  Devojit K. Sarma3  Nathan Truelove4  Sinnathamby N. Surendran4 
[1] Department of Zoology, Faculty of Science, University of Jaffna, Jaffna 40000, Sri Lanka;Faculty of Science and Technology, Anglia Ruskin University, Cambridge CB1 1PT, UK;Regional Medical Research Centre, NE region (ICMR), Dibrugarh 786001, Assam, India;Faculty of Life Sciences, University of Manchester, Oxford Road, Manchester M13 9PT, UK;Department of Zoology, Faculty of Science, University of Peradeniya, Peradeniya 20400, Sri Lanka;Regional Office, Anti Malaria Campaign, Hambantota 82000, Sri Lanka
关键词: Y-chromosome karyotype;    Sri Lanka;    Species complex;    Mosquito vector;    Microsatellite;    Malaria;    COI;    Anopheles culicifacies;   
Others  :  1224194
DOI  :  10.1186/s13071-015-0944-9
 received in 2015-04-22, accepted in 2015-06-08,  发布年份 2015
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【 摘 要 】

Background

The identification of species B and E in the Anopheles culicifacies complex in the Indian subcontinent has been based on Y-chromosome karyotype. Since no detectable variations were previously found in DNA markers commonly used for sibling species identification, further molecular characterization using cytochrome oxidase subunit I (COI) and microsatellite markers was carried out on Y-chromosome karyotyped Anopheles culicifacies specie B and E from Unnichchai, Kallady and Ranawarunawa in Sri Lanka.

Findings

COI sequence analysis (n = 22) revealed the presence of nine unique haplotypes with six in each species. Three haplotypes were shared by both species. The two sibling species had a pairwise F STvalue of 1.338 (p < 0.05) with the number of migrants (Nm) value <1. The genetic structure analysis resulted in two genetic clusters not 100 % associated with karyotypes. While none of the species B were incorrectly assigned two were inconclusive. Five out of 26 specimens karyotyped as species E were incorrectly assigned, while further 9 were inconclusive.

Conclusions

The new molecular data support the existence of two genetically different populations of the Culicifacies Complex in Sri Lanka that are not associated with the Y-chromosome karyotype. Detailed analysis with more microsatellite markers and assortative mating experiments are needed to establish the presence of the two genetically distinct populations and relate them to Y-chromosome morphology.

【 授权许可】

   
2015 Surendran et al.

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【 参考文献 】
  • [1]Surendran SN, Ramasamy R. The Anopheles culicifacies and An. subpictus complexes in Sri Lanka and their implications for malaria control in the country. Trop Med Health. 2010; 38(1):1-10.
  • [2]Sinka ME, Bangs MJ, Manguin S, Chareonviriyaphap T, Patil AP, Temperley WH et al.. The dominant Anopheles vectors of human malaria in the Asia-Pacific region: occurrence data, distribution maps and bionomic précis. Parasit Vectors. 2011; 4:89. BioMed Central Full Text
  • [3]Kar I, Subbarao SK, Eapen A, Ravindran J, Satyanarayana TS, Raghavendra K et al.. Evidence for a new vector species E within the Anopheles culicifacies complex (Diptera: Culicidae). J Med Entomol. 1999; 36:595-600.
  • [4]Abhayawardana TA, Dilrukshi RKC, Wijesuriya SRE. Cytotaxonomic examination for sibling species in the taxon Anopheles culicifacies Giles in Sri Lanka. Indian J Malariol. 1996; 33:74-80.
  • [5]Surendran SN, Abhayawardana TA, de SDilva BGDNK, Ramasamy MS, Ramasamy R. Anopheles culicifacies Y-chromosome dimorphism indicates the presence of sibling species (B and E) with different malaria vector potential in Sri Lanka. Med Vet Entomol. 2000; 14:437-40.
  • [6]Surendran SN, Ramasamy MS, de Silva BGDNK, Ramasamy R. Anopheles culicifacies sibling species B and E in Sri Lanka differ in longevity and in their susceptibility to malaria parasite infection and common insecticide. Med Vet Entomol. 2006; 20(1):153-6.
  • [7]Surendran SN, Hawkes NJ, Steven A, Hemingway J, Ramasamy R. Molecular studies of Anopheles culicifacies (Diptera: Culicidae) in Sri Lanka: sibling species B and E show sequence identity at multiple loci. Eur J Entomol. 2006; 103:233-7.
  • [8]Amerasinghe FP. A guide to the identification of the anopheline mosquitoes (Diptera: Culicidae) of Sri Lanka -I Adult females. Cey J Sci (Biological Science). 1990; 21:1-16.
  • [9]Surendran SN, Sarma DK, Jude PJ, Kemppainen P, Kanthakumaran N, Gajapathy K, Peiris LBS, Ramasamy R, Walton C: Molecular characterization and identification of members of the Anopheles subpictus complex in Sri Lanka. Malar J, 12: 304 doi: 10.1186/1475-2875-12-304.
  • [10]Simon C, Frati F, Beckenbach A, Crepsi B, Liu H, Flook P. Evolution, weighting and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers. Ann Entomol Soc Am. 1994; 87:651-701.
  • [11]Drummond AJ, Ashton B, Buxton S, Cheung M, Cooper A, Heled J, Kearse M, Moir R, Stones-Havas S, Sturrock S, Thierer T, Wilson A: Geneious version 4.8.5.http://www.geneious.com.
  • [12]Librado P, Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009; 25:1451-2.
  • [13]Excoffier L, Smouse PE, Quattro JM. Analysis of molecular variance inferred for metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics. 1992; 131:479-91.
  • [14]Excoffier L, Laval G, Schneider S. Arlequin (ver 3.0): An integrated software package for population genetics data analysis. Evol Bioinform Online. 2005; 1:47-50.
  • [15]Clement MD, Posada D, Crandall KA. TCS: a computer programme to estimate gene genealogies. Mol Ecol. 2000; 9:1657-9.
  • [16]Sunil S, Raghavendra K, Singh OP, Malhotra P, Huang Y, Zheng L et al.. Isolation and characterization of microsatellite markers from malaria vector, Anopheles culicifacies. Mol Ecol Notes. 2004; 4:440-2.
  • [17]Pritchard JK, Stephens M, Donnelly P. Inference of population structure using multilocus genotypes. Genetics. 2000; 155:945-59.
  • [18]Earl DA, von Holdt BM. STRUCTURE HARVESTER: a website and programme for visualizing STRUCTURE output and implementing Evanno method. Conserv Genet Resour. 2012; 4(2):359-61.
  • [19]Rousset F. Genepop’007: a complete reimplementation of the Genepop software for Windows and Linux. Mol Ecol Resour. 2008; 8:103-6.
  • [20]Paetkau D, Calvert W, Stirling I, Strobeck C. Microsatellite analysis of population structure in Canadian polar bears. Mol Ecol. 1995; 4:347-54.
  • [21]Choochote W. Evidence to support karyotypic variation of the mosquito Anopheles peditaeniatus in Thailand. J Insect Sci. 2011; 11:10.
  • [22]Goswami G, Singh OP, Nanda N, Raghavendra K, Gakhar SK, Subbarao SK. Identification of all members of the Anopheles culicifacies complex using allele-specific polymerase chain reaction assays. Am J Trop Med Hyg. 2006; 75(3):454-60.
  • [23]Manonmani AM, Mathivanan AK, Sadanandane C, Jambulingam P. Evaluation of the mtDNA-COII region based species specific assay for identifying members of the Anopheles culicifacies complex. J Arthropod-Borne Dis. 2013; 7(2):154-63.
  • [24]Adak T, Sarbjit K, Wattal S, Nanda N, Sharma VP. Y-chromosome polymorphism in species B and C of the Anopheles culicifacies complex. J Am Mosq Control Assoc. 1997; 13:379-83.
  • [25]Della Torre A, Fanello C, Akogbeto M, Dossou-Yovo J, Favia G, Petrarca V et al.. Molecular evidence of incipient speciation within Anopheles gambiae s.s. in West Africa. Insect Mol Biol. 2001; 10:9-18.
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