Ookinete-Specific Genes and 18S SSU rRNA Evidenced in Selection and Adaptation by Sympatric Vectors.

Journal: Frontiers in genetics
Published Date:

Abstract

In the southern Pacific coast of Chiapas, Mexico (SM), the two most abundant vector species, and , were susceptible to different Pvs25/28 haplotypes. To broaden our understanding of the existing in the area, genes encoding proteins relevant for ookinete development and the 18S rRNA were studied. infectivity (percentage of infected mosquitoes and oocyst numbers) was evaluated by simultaneously feeding infected blood samples from patients to and female mosquitoes. Three infectivity patterns were identified: one group of parasites were more infective to than to , another group was more infective to , while a third group infected both vectors similarly. In 29 parasite isolates, the molecular variations of ookinete-specific genes and the 18S rRNA-type S were analyzed. Using concatenated sequences, phylogenetic trees, and Structure analysis, parasite clustering within SM isolates and between these and those from other geographical origins were investigated. A ML phylogenetic tree resolved two parasite lineages: PvSM-A and PvSM-B. They were associated to a different 18S rRNA variant. PvSM-A parasites had 18S rRNA variant rV2 and correspond to parasites causing high oocyst infection in . A new ML tree and Structure analysis, both comprising global sequences, showed PvSM-A clustered with Latin American parasites. Meanwhile, all isolates of PvSM-B had 18S rRNA variant rV1 and remained as unique genetic cluster comprising two subgroups: PvSM-Ba, producing high infection in , and PvSM-Bb, causing similar oocyst infection in both vector species. PvSM-A parasites were genetically similar to parasites from South America. Meanwhile, PvSM-B were exclusive to southern Mexico and share ancestry with Asian parasites. The results suggest that these lineages evolved separately, likely by geographic and vector restriction.

Authors

  • Lilia González-Cerón
    Regional Center of Research in Public Health, National Institute of Public Health, Ministry of Health, Tapachula, Mexico.
  • Mario H Rodríguez
    Vector Borne Diseases, Center for Research on Infectious Diseases, National Institute of Public Health, Ministry of Health, Cuernavaca, Mexico.
  • Marbella T Ovilla-Muñoz
    Chronic Infections and Cancer, Center for Research on Infectious Diseases, National Institute of Public Health, Ministry of Health, Cuernavaca, Mexico.
  • Frida Santillán-Valenzuela
    Regional Center of Research in Public Health, National Institute of Public Health, Ministry of Health, Tapachula, Mexico.
  • Juan E Hernández-Ávila
    Center of Information for Public Health Decisions, National Institute of Public Health, Ministry of Health, Mexico City, Mexico.
  • María Carmen Rodríguez
    Vector Borne Diseases, Center for Research on Infectious Diseases, National Institute of Public Health, Ministry of Health, Cuernavaca, Mexico.
  • Jesús Martínez-Barnetche
    Chronic Infections and Cancer, Center for Research on Infectious Diseases, National Institute of Public Health, Ministry of Health, Cuernavaca, Mexico.
  • Cuauhtémoc Villarreal-Treviño
    Regional Center of Research in Public Health, National Institute of Public Health, Ministry of Health, Tapachula, Mexico.

Keywords

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