Abstract

Simple SummaryThe most dangerous vectors of malaria in the northern regions of the world belong to the Maculipennis group. Among the 22 species in this group, six are considered dominant vectors of malaria. Of these six, Anopheles messeae represents the most widely spread and genetically diverse species in Eurasia and Anopheles daciae, a cryptic species whose taxonomic status is still under debate, has been differentiated from An. messeae based on differences in their ribosomal DNA. However, genetic studies of these species are scarce. The availability of well-developed polytene chromosomes in malaria mosquitoes provides an opportunity to construct high-resolution cytogenetic photomaps that can be used to investigate the genetic divergence between these species. In this study, we created a standard universal cytogenetic map for the salivary gland polytene chromosomes of An. messeae and An. daciae and developed a simple and robust molecular approach for species diagnostics. The quality of the cytogenetic map was validated by studying inversion polymorphisms in populations of An. messeae and An. daciae from a location in the Asian part of Russia. The map will facilitate further investigation of the genetic diversity of these cryptic species.The Eurasian malaria vector Anopheles messeae is a widely spread and genetically diverse species. Five widespread polymorphic chromosomal inversions were found in natural populations of this mosquito. A cryptic species, Anopheles daciae, was differentiated from An. messeae by the presence of several nucleotide substitutions in the Internal Transcribed Spacer 2 (ITS2) region of ribosomal DNA. However, because of the absence of a high-quality reference cytogenetic map, the inversion polymorphisms in An. daciae and An. messeae remain poorly understood. Moreover, a recently determined heterogeneity in ITS2 in An. daciae questioned the accuracy of the previously used Restriction Fragment Length Polymorphism (RFLP) assay for species diagnostics. In this study, a standard-universal cytogenetic map was constructed based on orcein stained images of chromosomes from salivary glands for population studies of the chromosomal inversions that can be used for both An. messeae and An. daciae. In addition, a new ITS2-RFLP approach for species diagnostics was developed. Both methods were applied to characterize inversion polymorphism in populations of An. messeae and An. daciae from a single location in Western Siberia in Russia. The analysis demonstrates that cryptic species are remarkably different in their frequencies of chromosomal inversion variants. Our study supports previous observations that An. messeae has higher inversion polymorphism in all autosomes than the cryptic species An. daciae.

Highlights

  • Anopheles messeae is one out of six of the dominant malaria vectors in the EurasianMaculipennis group

  • We developed a standard-universal cytogenetic photomap based on digital images of orcein-stained salivary gland polytene chromosomes that enables fast and accurate identification of the chromosomal inversion variants in natural populations of the cryptic species An. daciae and An. messeae

  • A diploid chromosome complement in the malaria mosquitoes An. messeae and An. daciae consists of six chromosomes, which appear as five chromosome arms in salivary glands because of homologous chromosome pairing [39]

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Summary

Introduction

Anopheles messeae is one out of six of the dominant malaria vectors in the EurasianMaculipennis group. As a result of such a distribution, An. messeae is characterized by a high level of genetic diversity [4], including five chromosomal inversions in different chromosome arms [5,6] These inversions are associated with geographic, ecological, and behavioral adaptations of the species [7,8,9,10,11]. A deeper investigation of the inversion frequencies indicated that these inversions were associated unevenly in natural populations and led to the formation of two chromosomal complexes [12]. These chromosomal complexes were referred to as cryptic species An. messeae A and B [13]. A later study indicated that the species An. messeae A is synonymous to the cryptic species Anopheles daciae [14,15,16], which was discriminated from An. messeae based on five nucleotide substitutions in the Internal Transcribed Spacer

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