Characterization of P. vivax blood stage transcriptomes from field isolates reveals similarities among infections and complex gene isoforms
Our understanding of the structure and regulation of Plasmodium vivax genes is limited by our inability to grow the parasites in long-term in vitro cultures. Most P. vivax studies must therefore rely on patient samples, which typically display a low proportion of parasites and asynchronous parasites...
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| Published in | Scientific reports Vol. 7; no. 1; pp. 7761 - 12 |
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| Main Authors | , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
10.08.2017
Nature Publishing Group Nature Portfolio |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2045-2322 2045-2322 |
| DOI | 10.1038/s41598-017-07275-9 |
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| Summary: | Our understanding of the structure and regulation of
Plasmodium vivax
genes is limited by our inability to grow the parasites in long-term
in vitro
cultures. Most
P. vivax
studies must therefore rely on patient samples, which typically display a low proportion of parasites and asynchronous parasites. Here, we present stranded RNA-seq data generated directly from a small volume of blood from three Cambodian vivax malaria patients collected before treatment. Our analyses show surprising similarities of the parasite gene expression patterns across infections, despite extensive variations in parasite stage proportion. These similarities contrast with the unique gene expression patterns observed in sporozoites isolated from salivary glands of infected Colombian mosquitoes. Our analyses also indicate that more than 10% of
P. vivax
genes encode multiple, often undescribed, protein-coding sequences, potentially increasing the diversity of proteins synthesized by blood stage parasites. These data also greatly improve the annotations of
P. vivax
gene untranslated regions, providing an important resource for future studies of specific genes. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 PMCID: PMC5552866 |
| ISSN: | 2045-2322 2045-2322 |
| DOI: | 10.1038/s41598-017-07275-9 |