Signatures of competition and strain structure within the major blood-stage antigen of Plasmodium falciparum in a local community in Ghana
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| Publication date | 04-2018 |
| Journal | Ecology and Evolution |
| Volume | Issue number | 8 | 7 |
| Pages (from-to) | 3574-3588 |
| Number of pages | 15 |
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| Abstract |
The concept of niche partitioning has received considerable theoretical attention
at the interface of ecology and evolution of infectious diseases. Strain theory postulates
that pathogen populations can be structured into distinct nonoverlapping strains by
frequency‐dependent selection in response to intraspecific competition for host immune
space. The malaria parasite Plasmodium falciparum presents an opportunity to investigate this phenomenon in nature, under conditions
of high recombination rate and extensive antigenic diversity. The parasite's major
blood‐stage antigen, PfEMP1, is encoded by the hyperdiverse var genes. With a dataset that includes thousands of var DBLα sequence types sampled from asymptomatic cases within an area of high endemicity
in Ghana, we address how var diversity is distributed within isolates and compare this to the distribution of
microsatellite allelic diversity within isolates to test whether antigenic and neutral
regions of the genome are structured differently. With respect to var DBLα sequence types, we find that on average isolates exhibit significantly lower overlap
than expected randomly, but that there also exists frequent pairs of isolates that
are highly related. Furthermore, the linkage network of var DBLα sequence types reveals a pattern of nonrandom modularity unique to these antigenic
genes, and we find that modules of highly linked DBLα types are not explainable by neutral forces related to var recombination constraints, microsatellite diversity, sampling location, host age,
or multiplicity of infection. These findings of reduced overlap and modularity among
the var antigenic genes are consistent with a role for immune selection as proposed by strain
theory. Identifying the evolutionary and ecological dynamics that are responsible
for the nonrandom structure in P. falciparum antigenic diversity is important for designing effective intervention in endemic
areas.
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| Document type | Article |
| Note | With supplementary file |
| Language | English |
| Published at | https://doi.org/10.1002/ece3.3803 |
| Other links | https://www.scopus.com/pages/publications/85042561669 |
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