Loading…
Low genetic polymorphism of merozoite surface proteins 7 and 10 in Colombian Plasmodium vivax isolates
▶Pvmsp-7A, Pvmsp-7K and Pvmsp-10 genes display a low polymorphism among isolates. ▶ A single haplotype for Pvmsp-7A and Pvmsp-10 genes was found in Colombian parasites. ▶ The Pvmsp-7K gene displays 9 haplotypes in the Colombian parasite population. ▶P. vivax msp-7 family members show different genet...
Saved in:
Published in: | Infection, genetics and evolution genetics and evolution, 2011-03, Vol.11 (2), p.528-531 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | ▶Pvmsp-7A, Pvmsp-7K and Pvmsp-10 genes display a low polymorphism among isolates. ▶ A single haplotype for Pvmsp-7A and Pvmsp-10 genes was found in Colombian parasites. ▶ The Pvmsp-7K gene displays 9 haplotypes in the Colombian parasite population. ▶P. vivax msp-7 family members show different genetic variability patterns. ▶ Low variability of Pvmsp-7A and Pvmsp-7K might avoid inducing allele-specific immunity.
The merozoite surface protein (MSP) family is involved in the initial interaction between merozoites and erythrocytes in Plasmodium species, its members are therefore becoming major targets for vaccine development. Considering that antigens included in a subunit malaria vaccine should be both accessible to the immune system and lack genetic diversity or have very limited polymorphism, we have analyzed the genetic diversity of three msp genes (msp-7A, msp-7K and msp-10) in different geographical regions of Colombia. The results showed that these genes follow the neutral model of evolution and also display low genetic diversity. The strong conservation found for msp-7 haplotypes in isolates from geographically different regions further suggests that these proteins could be good components of a vaccine against Plasmodium vivax malaria, thereby avoiding strain-specific immune responses. |
---|---|
ISSN: | 1567-1348 1567-7257 |
DOI: | 10.1016/j.meegid.2010.12.002 |