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Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase
For 20 years, Plasmodium vivax has been the only prevalent malaria species in Mexico, and cases have declined significantly and continuously. Spatiotemporal genetic studies can be helpful for understanding parasite dynamics and developing strategies to weaken malaria transmission, thus facilitating...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779127/ https://www.ncbi.nlm.nih.gov/pubmed/35056635 http://dx.doi.org/10.3390/microorganisms10010186 |
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author | Flores-Alanis, Alejandro González-Cerón, Lilia Santillán-Valenzuela, Frida Ximenez, Cecilia Sandoval-Bautista, Marco A. Cerritos, Rene |
author_facet | Flores-Alanis, Alejandro González-Cerón, Lilia Santillán-Valenzuela, Frida Ximenez, Cecilia Sandoval-Bautista, Marco A. Cerritos, Rene |
author_sort | Flores-Alanis, Alejandro |
collection | PubMed |
description | For 20 years, Plasmodium vivax has been the only prevalent malaria species in Mexico, and cases have declined significantly and continuously. Spatiotemporal genetic studies can be helpful for understanding parasite dynamics and developing strategies to weaken malaria transmission, thus facilitating the elimination of the parasite. The aim of the current contribution was to analyze P. vivax-infected blood samples from patients in southern Mexico during the control (1993–2007) and pre-elimination phases (2008–2011). Nucleotide and haplotype changes in the pvmsp1(42) fragment were evaluated over time. The majority of multiple genotype infections occurred in the 1990s, when the 198 single nucleotide sequences exhibited 57 segregating sites, 64 mutations, and 17 haplotypes. Nucleotide and genetic diversity parameters showed subtle fluctuations from across time, in contrast to the reduced haplotype diversity and the increase in the R(2) index and Tajima’s D value from 2008 to 2011. The haplotype network consisted of four haplogroups, the geographical distribution of which varied slightly over time. Haplogroup-specific B-cell epitopes were predicted. Since only high-frequency and divergent haplotypes persisted, there was a contraction of the parasite population. Given that 84% of haplotypes were exclusive to Mesoamerica, P. vivax flow is likely circumscribed to this region, representing important information for parasite surveillance. |
format | Online Article Text |
id | pubmed-8779127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87791272022-01-22 Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase Flores-Alanis, Alejandro González-Cerón, Lilia Santillán-Valenzuela, Frida Ximenez, Cecilia Sandoval-Bautista, Marco A. Cerritos, Rene Microorganisms Article For 20 years, Plasmodium vivax has been the only prevalent malaria species in Mexico, and cases have declined significantly and continuously. Spatiotemporal genetic studies can be helpful for understanding parasite dynamics and developing strategies to weaken malaria transmission, thus facilitating the elimination of the parasite. The aim of the current contribution was to analyze P. vivax-infected blood samples from patients in southern Mexico during the control (1993–2007) and pre-elimination phases (2008–2011). Nucleotide and haplotype changes in the pvmsp1(42) fragment were evaluated over time. The majority of multiple genotype infections occurred in the 1990s, when the 198 single nucleotide sequences exhibited 57 segregating sites, 64 mutations, and 17 haplotypes. Nucleotide and genetic diversity parameters showed subtle fluctuations from across time, in contrast to the reduced haplotype diversity and the increase in the R(2) index and Tajima’s D value from 2008 to 2011. The haplotype network consisted of four haplogroups, the geographical distribution of which varied slightly over time. Haplogroup-specific B-cell epitopes were predicted. Since only high-frequency and divergent haplotypes persisted, there was a contraction of the parasite population. Given that 84% of haplotypes were exclusive to Mesoamerica, P. vivax flow is likely circumscribed to this region, representing important information for parasite surveillance. MDPI 2022-01-15 /pmc/articles/PMC8779127/ /pubmed/35056635 http://dx.doi.org/10.3390/microorganisms10010186 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Flores-Alanis, Alejandro González-Cerón, Lilia Santillán-Valenzuela, Frida Ximenez, Cecilia Sandoval-Bautista, Marco A. Cerritos, Rene Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase |
title | Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase |
title_full | Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase |
title_fullStr | Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase |
title_full_unstemmed | Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase |
title_short | Spatiotemporal Changes in Plasmodium vivax msp1(42) Haplotypes in Southern Mexico: From the Control to the Pre-Elimination Phase |
title_sort | spatiotemporal changes in plasmodium vivax msp1(42) haplotypes in southern mexico: from the control to the pre-elimination phase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779127/ https://www.ncbi.nlm.nih.gov/pubmed/35056635 http://dx.doi.org/10.3390/microorganisms10010186 |
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