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Background <p><i>Anopheles squamosus</i> is a widespread mosquito species in sub-Saharan Africa. It is a potential vector for human malaria parasites and has been found naturally infected with <i>Plasmodium falciparum</i> and <i>Plasmodium vivax</i>. Morphological identification is challenging even with pristine specimens and current molecular methods such as the use of the internal transcribed spacer 2 (ITS2) polymerase chain reaction (PCR) cannot distinguish <i>An. squamosus</i> from morphologically similar <i>Anopheles</i> species<i>.</i> Described in the following methods is the development and validation of a new PCR assay that will reliably identify <i>An. squamosus</i><i>.</i></p> Methods <p>Multiple alignments of previously published ITS2 contig sequences in NCBI from <i>An. squamosus</i> and <i>An.</i> species 11 and 15, were used to identify candidate ITS2 regions for primer design. Six sets of primers were evaluated overall for specificity of species identification. The one set with <i>An. squamosus</i> species-specific amplification was tested using 78 specimens morphologically identified from Zambia and South Africa.</p> Results <p>A new assay consisting of a forward (ITS2-ASQ-R10, 5’-CCC TCG AAG GGT GCT GTG-3’) and reverse (ITS2-ASQ-R10 5’-AAT CCA CGG TGT GAT GGC-3’) primer reliably (&gt; 94.9%) amplified an ITS2 fragment of 301&#xa0;bp length for <i>An. squamosus</i>. The <i>An. squamosus-</i>specific primer set can be multiplexed with existing ITS2 assays frequently used for anopheline species identification.</p> Conclusions <p>The development of this robust PCR assay for <i>An. squamosus</i> is vital to accurate identification of this species in malaria vector surveillance efforts. Improved understanding of the anopheline community composition will lead to better targeted methods of vector eradication and malaria prevention. To further the validation of this ITS2 PCR assay, more species of <i>Anopheles</i> should be compared in addition to <i>An. squamosus</i> collected in different regions. To refine and optimize the PCR process with these primers, touchdown PCR can be used to increase specificity. Applying genomic tools to correctly identify <i>An. squamosus</i> will allow for a better understanding of their role in malaria transmission and may lead to genomic insights into what influences their behaviour, thus leading to new innovations in malaria elimination.</p>

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A new assay for molecular identification of Anopheles squamosus (Diptera: Culicidae) using internal transcribed spacer 2

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年10月16日

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  • Valerie T. Nguyen,
  • Renee L. M. N. Ali,
  • Bianca C. Burini,
  • Dalia S. Dryden,
  • Megan A. Riddin,
  • Kochelani Saili,
  • Edgar Simulundu,
  • Lawrence E. Reeves,
  • Douglas E. Norris,
  • Yoosook Lee

摘要

Background

Anopheles squamosus is a widespread mosquito species in sub-Saharan Africa. It is a potential vector for human malaria parasites and has been found naturally infected with Plasmodium falciparum and Plasmodium vivax. Morphological identification is challenging even with pristine specimens and current molecular methods such as the use of the internal transcribed spacer 2 (ITS2) polymerase chain reaction (PCR) cannot distinguish An. squamosus from morphologically similar Anopheles species. Described in the following methods is the development and validation of a new PCR assay that will reliably identify An. squamosus.

Methods

Multiple alignments of previously published ITS2 contig sequences in NCBI from An. squamosus and An. species 11 and 15, were used to identify candidate ITS2 regions for primer design. Six sets of primers were evaluated overall for specificity of species identification. The one set with An. squamosus species-specific amplification was tested using 78 specimens morphologically identified from Zambia and South Africa.

Results

A new assay consisting of a forward (ITS2-ASQ-R10, 5’-CCC TCG AAG GGT GCT GTG-3’) and reverse (ITS2-ASQ-R10 5’-AAT CCA CGG TGT GAT GGC-3’) primer reliably (> 94.9%) amplified an ITS2 fragment of 301 bp length for An. squamosus. The An. squamosus-specific primer set can be multiplexed with existing ITS2 assays frequently used for anopheline species identification.

Conclusions

The development of this robust PCR assay for An. squamosus is vital to accurate identification of this species in malaria vector surveillance efforts. Improved understanding of the anopheline community composition will lead to better targeted methods of vector eradication and malaria prevention. To further the validation of this ITS2 PCR assay, more species of Anopheles should be compared in addition to An. squamosus collected in different regions. To refine and optimize the PCR process with these primers, touchdown PCR can be used to increase specificity. Applying genomic tools to correctly identify An. squamosus will allow for a better understanding of their role in malaria transmission and may lead to genomic insights into what influences their behaviour, thus leading to new innovations in malaria elimination.