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Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015
In Africa, control programs that target primarily Plasmodium falciparum are inadequate for eliminating malaria. To learn more about prevalence and genetic variability of P. malariae in Africa, we examined blood samples from 663 asymptomatic and 245 symptomatic persons from western Kenya during June–...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367407/ https://www.ncbi.nlm.nih.gov/pubmed/28322694 http://dx.doi.org/10.3201/eid2304.161245 |
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author | Lo, Eugenia Nguyen, Kristie Nguyen, Jennifer Hemming-Schroeder, Elizabeth Xu, Jiaobao Etemesi, Harrisone Githeko, Andrew Yan, Guiyun |
author_facet | Lo, Eugenia Nguyen, Kristie Nguyen, Jennifer Hemming-Schroeder, Elizabeth Xu, Jiaobao Etemesi, Harrisone Githeko, Andrew Yan, Guiyun |
author_sort | Lo, Eugenia |
collection | PubMed |
description | In Africa, control programs that target primarily Plasmodium falciparum are inadequate for eliminating malaria. To learn more about prevalence and genetic variability of P. malariae in Africa, we examined blood samples from 663 asymptomatic and 245 symptomatic persons from western Kenya during June–August of 2014 and 2015. P. malariae accounted for 5.3% (35/663) of asymptomatic infections and 3.3% (8/245) of clinical cases. Among asymptomatic persons, 71% (32/45) of P. malariae infections detected by PCR were undetected by microscopy. The low sensitivity of microscopy probably results from the significantly lower parasitemia of P. malariae. Analyses of P. malariae circumsporozoite protein gene sequences revealed high genetic diversity among P. malariae in Africa, but no clear differentiation among geographic populations was observed. Our findings suggest that P. malariae should be included in the malaria elimination strategy in Africa and highlight the need for sensitive and field-applicable methods to identify P. malariae in malaria-endemic areas. |
format | Online Article Text |
id | pubmed-5367407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-53674072017-04-07 Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015 Lo, Eugenia Nguyen, Kristie Nguyen, Jennifer Hemming-Schroeder, Elizabeth Xu, Jiaobao Etemesi, Harrisone Githeko, Andrew Yan, Guiyun Emerg Infect Dis Research In Africa, control programs that target primarily Plasmodium falciparum are inadequate for eliminating malaria. To learn more about prevalence and genetic variability of P. malariae in Africa, we examined blood samples from 663 asymptomatic and 245 symptomatic persons from western Kenya during June–August of 2014 and 2015. P. malariae accounted for 5.3% (35/663) of asymptomatic infections and 3.3% (8/245) of clinical cases. Among asymptomatic persons, 71% (32/45) of P. malariae infections detected by PCR were undetected by microscopy. The low sensitivity of microscopy probably results from the significantly lower parasitemia of P. malariae. Analyses of P. malariae circumsporozoite protein gene sequences revealed high genetic diversity among P. malariae in Africa, but no clear differentiation among geographic populations was observed. Our findings suggest that P. malariae should be included in the malaria elimination strategy in Africa and highlight the need for sensitive and field-applicable methods to identify P. malariae in malaria-endemic areas. Centers for Disease Control and Prevention 2017-04 /pmc/articles/PMC5367407/ /pubmed/28322694 http://dx.doi.org/10.3201/eid2304.161245 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Lo, Eugenia Nguyen, Kristie Nguyen, Jennifer Hemming-Schroeder, Elizabeth Xu, Jiaobao Etemesi, Harrisone Githeko, Andrew Yan, Guiyun Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015 |
title | Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015 |
title_full | Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015 |
title_fullStr | Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015 |
title_full_unstemmed | Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015 |
title_short | Plasmodium malariae Prevalence and csp Gene Diversity, Kenya, 2014 and 2015 |
title_sort | plasmodium malariae prevalence and csp gene diversity, kenya, 2014 and 2015 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367407/ https://www.ncbi.nlm.nih.gov/pubmed/28322694 http://dx.doi.org/10.3201/eid2304.161245 |
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