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Molecular taxonomy of phlebotomine sand flies (Diptera, Psychodidae) with emphasis on DNA barcoding: A review

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ACTA TROPICA
卷 238, 期 -, 页码 -

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DOI: 10.1016/j.actatropica.2022.106778

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Phlebotomine; Sand flies; Integrative taxonomy; Molecular marker; Molecular systematics

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The taxonomy and systematics of sand flies are crucial for identifying vector populations and the diseases they transmit. Traditional methods of classification relying on morphological traits have been complemented with DNA sequencing, particularly using the coi gene as a DNA barcoding marker. However, only a limited number of sand fly species have been sequenced, and there is a lack of sequences for certain genera, limiting our understanding of these groups. More efforts should be made to sequence sand fly species using multiple markers to improve phylogenetic analyses.
The taxonomy and systematics of sand flies (Diptera, Psychodidae, Phlebotominae) are one of the pillars of research aimed to identifying vector populations and the agents transmitted by these insects. Traditionally, the use of morphological traits has been the main line of evidence for the definition of species, but the use of DNA sequences is useful as an integrative approach for their delimitation. Here, we discuss the current status of the molecular taxonomy of sand flies, including their most sequenced molecular markers and the main results. Only about 37% of all sand fly species have been processed for any molecular marker and are publicly available in the NCBI GenBank or BOLD Systems databases. The genera Phlebotomus, Nyssomyia, Psathyromyia and Psychodopygus are well-sampled, accounting for more than 56% of their sequenced species. However, less than 34% of the species of Sergentomyia, Lutzomyia, Trichopygomyia and Trichophoromyia have been sampled, representing a major gap in the knowledge of these groups. The most sequenced molecular markers are those within mtDNA, especially the DNA barcoding fragment of the cytochrome c oxidase subunit I (coi) gene, which has shown promising results in detecting cryptic diversity within species. Few sequences of conserved genes have been generated, which hampers higher-level phylogenetic inferences. We argue that sand fly species should be sequenced for at least the coi DNA barcoding marker, but multiple markers with different mutation rates should be assessed, whenever possible, to generate multilocus analysis.

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