Population genetics of the yellow fever mosquito in Trinidad: comparisons of amplified fragment length polymorphism (AFLP) and restriction fragment length polymorphism (RFLP) markers

Authors

  • G. Yan,

    1. Department of Animal Health and Biomedical Sciences, University of Wisconsin, Madison, WI 53706, USA,
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    • Correspondence: G. Yan.Present address: Department of Biological Sciences, State University of New York — Buffalo, Buffalo, NY 14260, USA. Fax: + 01 (716) 645 2975; E-mail:gyan@acsu.buffalo.edu

      † † Present address: Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556-5645, USA.

    • Present address: Department of Biological Sciences, State University of New York — Buffalo, Buffalo, NY 14260, USA. Fax: + 01 (716) 645 2975; E-mail:
  • J. Romero-Severson,

    1. PE AgGen, 1361 Squire Dr., Suite H, South Bend, IN 46637, USA,
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  • M. Walton,

    1. PE AgGen, 2411 South 1070 West, Suite B, Salt Lake City, UT 84119, USA,
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  • D. D. Chadee,

    1. Insect Vector Control Division, Ministry of Health, 3 Queen Street, St. Joseph, Trinidad and Tobago, West Indies
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  • D. W. Severson

    1. Department of Animal Health and Biomedical Sciences, University of Wisconsin, Madison, WI 53706, USA,
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      † † Present address: Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556-5645, USA.

Abstract

Recent development of DNA markers provides powerful tools for population genetic analyses. Amplified fragment length polymorphism (AFLP) markers result from a polymerase chain reaction (PCR)-based DNA fingerprinting technique that can detect multiple restriction fragments in a single polyacrylamide gel, and thus are potentially useful for population genetic studies. Because AFLP markers have to be analysed as dominant loci in order to estimate population genetic diversity and genetic structure parameters, one must assume that dominant (amplified) alleles are identical in state, recessive (unamplified) alleles are identical in state, AFLP fragments segregate according to Mendelian expectations and that the genotypes of an AFLP locus are in Hardy–Weinberg equilibrium (HWE). The HWE assumption is untestable for natural populations using dominant markers. Restriction fragment length polymorphism (RFLP) markers segregate as codominant alleles, and can therefore be used to test the HWE assumption that is critical for analysing AFLP data. This study examined whether the dominant AFLP markers could provide accurate estimates of genetic variability for the Aedes aegypti mosquito populations of Trinidad, West Indies, by comparing genetic structure parameters using AFLP and RFLP markers. For AFLP markers, we tested a total of five primer combinations and scored 137 putative loci. For RFLP, we examined a total of eight mapped markers that provide a broad coverage of mosquito genome. The estimated average heterozygosity with AFLP markers was similar among the populations (0.39), and the observed average heterozygosity with RFLP markers varied from 0.44 to 0.58. The average FST (standardized among-population genetic variance) estimates were 0.033 for AFLP and 0.063 for RFLP markers. The genotypes at several RFLP loci were not in HWE, suggesting that the assumption critical for analysing AFLP data was invalid for some loci of the mosquito populations in Trinidad. Therefore, the results suggest that, compared with dominant molecular markers, codominant DNA markers provide better estimates of population genetic variability, and offer more statistical power for detecting population genetic structure.

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