| Literature DB >> 26503281 |
Jonathan J Juliano1, Christian M Parobek2, Nicholas F Brazeau2, Billy Ngasala2, Milijaona Randrianarivelojosia2, Chanthap Lon2, Kashamuka Mwandagalirwa2, Antoinette Tshefu2, Ravi Dhar2, Bidyut K Das2, Irving Hoffman2, Francis Martinson2, Andreas Mårtensson2, David L Saunders2, Nirbhay Kumar2, Steven R Meshnick2.
Abstract
Polymorphisms within Plasmodium falciparum vaccine candidate antigens have the potential to compromise vaccine efficacy. Understanding the allele frequencies of polymorphisms in critical binding regions of antigens can help in the designing of strain-transcendent vaccines. Here, we adopt a pooled deep-sequencing approach, originally designed to study P. falciparum drug resistance mutations, to study the diversity of two leading transmission-blocking vaccine candidates, Pfs25 and Pfs48/45. We sequenced 329 P. falciparum field isolates from six different geographic regions. Pfs25 showed little diversity, with only one known polymorphism identified in the region associated with binding of transmission-blocking antibodies among our isolates. However, we identified four new mutations among eight non-synonymous mutations within the presumed antibody-binding region of Pfs48/45. Pooled deep sequencing provides a scalable and cost-effective approach for the targeted study of allele frequencies of P. falciparum candidate vaccine antigens. © The American Society of Tropical Medicine and Hygiene.Entities:
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Year: 2015 PMID: 26503281 PMCID: PMC4710419 DOI: 10.4269/ajtmh.15-0571
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345