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Next generation sequencing improves the resolution of detecting mixed host blood meal sources in field collected arboviral mosquito vectors.
Tchouassi, David P; Kisero, Robinson O; Rotich, Gilbert; Dunlap, Christopher; Torto, Baldwyn; Muturi, Ephantus J.
Affiliation
  • Tchouassi DP; International Centre of Insect Physiology and Ecology, Nairobi, Kenya.
  • Kisero RO; International Centre of Insect Physiology and Ecology, Nairobi, Kenya.
  • Rotich G; International Centre of Insect Physiology and Ecology, Nairobi, Kenya.
  • Dunlap C; USDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Crop Bioprotection Research Unit, Peoria, Illinois, USA.
  • Torto B; International Centre of Insect Physiology and Ecology, Nairobi, Kenya.
  • Muturi EJ; USDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Crop Bioprotection Research Unit, Peoria, Illinois, USA.
Med Vet Entomol ; 2024 May 15.
Article in En | MEDLINE | ID: mdl-38747253
ABSTRACT
Accurate knowledge of blood meal hosts of different mosquito species is critical for identifying potential vectors and establishing the risk of pathogen transmission. We compared the performance of Miseq next generation sequencing approach relative to conventional Sanger sequencing approach in identification of mosquito blood meals using genetic markers targeting the 12S rRNA and cytochrome oxidase I (COI) genes. We analysed the blood meals of three mosquito vector species (Aedes aegypti, Aedes simpsoni s.l. and Culex pipiens s.l.) collected outdoors, and compared the frequency of single- versus multiple-blood feeding. Single host blood meals were mostly recovered for Sanger-based sequencing of the mitochondrial 12S rRNA gene, whereas Miseq sequencing employing this marker and the COI marker detected both single and multiple blood meal hosts in individual mosquitoes. Multiple blood meals (two or more hosts) which mostly included humans were detected in 19%-22.7% of Ae. aegypti samples. Most single host blood meals for this mosquito species were from humans (47.7%-57.1%) and dogs (9.1%-19.0%), with livestock, reptile and rodent hosts collectively accounting for 4.7%-28.9% of single host blood meals. The frequency of two or more host blood meals in Ae. simpsoni s.l. was 26.3%-45.5% mostly including humans, while single host blood meals were predominantly from humans (31.8%-47.4%) with representation of rodent, reptile and livestock blood meals (18.2%-68.2%). Single host blood meals from Cx. pipiens s.l. were mostly from humans (27.0%-39.4%) and cows (11.5%-27.36%). Multiple blood meal hosts that mostly included humans occurred in 21.2%-24.4% of Cx. pipiens s.l. samples. Estimated human blood indices ranged from 53%-76% for Ae. aegypti, 32%-82% for Ae. simpsoni s.l. and 26%-61% for Cx. pipiens s.l. and were consistently lower for Sanger-based sequencing approach compared to Miseq-based sequencing approach. These findings demonstrate that Miseq sequencing approach is superior to Sanger sequencing approach as it can reliably identify mixed host blood meals in a single mosquito, improving our ability to understand the transmission dynamics of mosquito-borne pathogens.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Med Vet Entomol Journal subject: BIOLOGIA / MEDICINA VETERINARIA Year: 2024 Document type: Article Affiliation country: Kenia Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Med Vet Entomol Journal subject: BIOLOGIA / MEDICINA VETERINARIA Year: 2024 Document type: Article Affiliation country: Kenia Country of publication: Reino Unido