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Characterising co-infections with Plasmodium spp., Mansonella perstans or Loa loa in asymptomatic children, adults and elderly people living on Bioko Island using nucleic acids extracted from malaria rapid diagnostic tests
Regular and comprehensive epidemiological surveys of the filarial nematodes Mansonella perstans and Loa loa in children, adolescents and adults living across Bioko Island, Equatorial Guinea are lacking. We aimed to demonstrate that blood retained on malaria rapid diagnostic tests, commonly deployed...
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Published in: | PLoS neglected tropical diseases 2022-01, Vol.16 (1), p.e0009798-e0009798 |
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creator | Yoboue, Charlene Aya Hosch, Salome Donfack, Olivier Tresor Guirou, Etienne A Nlavo, Bonifacio Manguire Ayekaba, Mitoha Ondo'o Guerra, Carlos Phiri, Wonder P Garcia, Guillermo A Schindler, Tobias Daubenberger, Claudia A |
description | Regular and comprehensive epidemiological surveys of the filarial nematodes Mansonella perstans and Loa loa in children, adolescents and adults living across Bioko Island, Equatorial Guinea are lacking. We aimed to demonstrate that blood retained on malaria rapid diagnostic tests, commonly deployed for malaria surveys, could be used as a source of nucleic acids for molecular based detection of M. perstans and L. loa. We wanted to determine the positivity rate and distribution of filarial nematodes across different age groups and geographical areas as well as to understand level of co-infections with malaria in an asymptomatic population.
M. perstans, L. loa and Plasmodium spp. parasites were monitored by qPCR in a cross-sectional study using DNA extracted from a subset malaria rapid diagnostic tests (mRDTs) collected during the annual malaria indicator survey conducted on Bioko Island in 2018.
We identified DNA specific for the two filarial nematodes investigated among 8.2% (263) of the 3214 RDTs screened. Positivity rates of M. perstans and L. loa were 6.6% and 1.5%, respectively. M. perstans infection were more prominent in male (10.5%) compared to female (3.9%) survey participants. M. perstans parasite density and positivity rate was higher among older people and the population living in rural areas. The socio-economic status of participants strongly influenced the infection rate with people belonging to the lowest socio-economic quintile more than 3 and 5 times more likely to be L. loa and M. perstans infected, respectively. No increased risk of being co-infected with Plasmodium spp. parasites was observed among the different age groups.
We found otherwise asymptomatic individuals were infected with M. perstans and L. loa. Our study demonstrates that employing mRDTs probed with blood for malaria testing represents a promising, future tool to preserve and ship NAs at room temperature to laboratories for molecular, high-throughput diagnosis and genotyping of blood-dwelling nematode filarial infections. Using this approach, asymptomatic populations can be reached and surveyed for infectious diseases beyond malaria. |
doi_str_mv | 10.1371/journal.pntd.0009798 |
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M. perstans, L. loa and Plasmodium spp. parasites were monitored by qPCR in a cross-sectional study using DNA extracted from a subset malaria rapid diagnostic tests (mRDTs) collected during the annual malaria indicator survey conducted on Bioko Island in 2018.
We identified DNA specific for the two filarial nematodes investigated among 8.2% (263) of the 3214 RDTs screened. Positivity rates of M. perstans and L. loa were 6.6% and 1.5%, respectively. M. perstans infection were more prominent in male (10.5%) compared to female (3.9%) survey participants. M. perstans parasite density and positivity rate was higher among older people and the population living in rural areas. The socio-economic status of participants strongly influenced the infection rate with people belonging to the lowest socio-economic quintile more than 3 and 5 times more likely to be L. loa and M. perstans infected, respectively. No increased risk of being co-infected with Plasmodium spp. parasites was observed among the different age groups.
We found otherwise asymptomatic individuals were infected with M. perstans and L. loa. Our study demonstrates that employing mRDTs probed with blood for malaria testing represents a promising, future tool to preserve and ship NAs at room temperature to laboratories for molecular, high-throughput diagnosis and genotyping of blood-dwelling nematode filarial infections. Using this approach, asymptomatic populations can be reached and surveyed for infectious diseases beyond malaria.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0009798</identifier><identifier>PMID: 35100277</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Adolescent ; Adolescents ; Adult ; Adults ; Age groups ; Analysis ; Animals ; Asymptomatic ; Biology and Life Sciences ; Blood ; Care and treatment ; Child ; Children ; Coinfection - epidemiology ; Coinfection - parasitology ; Comorbidity ; Cross-Sectional Studies ; Deoxyribonucleic acid ; Diagnosis ; Diagnostic tests ; DNA ; DNA, Helminth ; Earth Sciences ; Economics ; Epidemiology ; Equatorial Guinea - epidemiology ; Female ; Filariasis ; Genotyping ; Health risks ; Human diseases ; Humans ; Infections ; Infectious diseases ; Laboratories ; Loa - isolation & purification ; Loa loa ; Loiasis - blood ; Loiasis - epidemiology ; Malaria ; Malaria - blood ; Malaria - epidemiology ; Male ; Mansonella - isolation & purification ; Mansonella perstans ; Mansonelliasis - blood ; Mansonelliasis - epidemiology ; Medical tests ; Medicine and Health Sciences ; Middle Aged ; Nematodes ; Nucleic acids ; Older people ; Parasites ; Plasmodium ; Plasmodium - isolation & purification ; Polls & surveys ; Prevalence ; Pruritus ; Public health ; Risk factors ; Room temperature ; Rural areas ; Ships ; Socioeconomic aspects ; Socioeconomic Factors ; Socioeconomics ; Surveying ; Surveys ; Testing ; Tests ; Tropical diseases ; Vector-borne diseases</subject><ispartof>PLoS neglected tropical diseases, 2022-01, Vol.16 (1), p.e0009798-e0009798</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Yoboue et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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We aimed to demonstrate that blood retained on malaria rapid diagnostic tests, commonly deployed for malaria surveys, could be used as a source of nucleic acids for molecular based detection of M. perstans and L. loa. We wanted to determine the positivity rate and distribution of filarial nematodes across different age groups and geographical areas as well as to understand level of co-infections with malaria in an asymptomatic population.
M. perstans, L. loa and Plasmodium spp. parasites were monitored by qPCR in a cross-sectional study using DNA extracted from a subset malaria rapid diagnostic tests (mRDTs) collected during the annual malaria indicator survey conducted on Bioko Island in 2018.
We identified DNA specific for the two filarial nematodes investigated among 8.2% (263) of the 3214 RDTs screened. Positivity rates of M. perstans and L. loa were 6.6% and 1.5%, respectively. M. perstans infection were more prominent in male (10.5%) compared to female (3.9%) survey participants. M. perstans parasite density and positivity rate was higher among older people and the population living in rural areas. The socio-economic status of participants strongly influenced the infection rate with people belonging to the lowest socio-economic quintile more than 3 and 5 times more likely to be L. loa and M. perstans infected, respectively. No increased risk of being co-infected with Plasmodium spp. parasites was observed among the different age groups.
We found otherwise asymptomatic individuals were infected with M. perstans and L. loa. Our study demonstrates that employing mRDTs probed with blood for malaria testing represents a promising, future tool to preserve and ship NAs at room temperature to laboratories for molecular, high-throughput diagnosis and genotyping of blood-dwelling nematode filarial infections. Using this approach, asymptomatic populations can be reached and surveyed for infectious diseases beyond malaria.</description><subject>Acids</subject><subject>Adolescent</subject><subject>Adolescents</subject><subject>Adult</subject><subject>Adults</subject><subject>Age groups</subject><subject>Analysis</subject><subject>Animals</subject><subject>Asymptomatic</subject><subject>Biology and Life Sciences</subject><subject>Blood</subject><subject>Care and treatment</subject><subject>Child</subject><subject>Children</subject><subject>Coinfection - epidemiology</subject><subject>Coinfection - parasitology</subject><subject>Comorbidity</subject><subject>Cross-Sectional Studies</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>Diagnostic tests</subject><subject>DNA</subject><subject>DNA, Helminth</subject><subject>Earth Sciences</subject><subject>Economics</subject><subject>Epidemiology</subject><subject>Equatorial Guinea - epidemiology</subject><subject>Female</subject><subject>Filariasis</subject><subject>Genotyping</subject><subject>Health risks</subject><subject>Human diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Laboratories</subject><subject>Loa - isolation & purification</subject><subject>Loa loa</subject><subject>Loiasis - blood</subject><subject>Loiasis - epidemiology</subject><subject>Malaria</subject><subject>Malaria - blood</subject><subject>Malaria - epidemiology</subject><subject>Male</subject><subject>Mansonella - isolation & purification</subject><subject>Mansonella perstans</subject><subject>Mansonelliasis - blood</subject><subject>Mansonelliasis - epidemiology</subject><subject>Medical tests</subject><subject>Medicine and Health Sciences</subject><subject>Middle Aged</subject><subject>Nematodes</subject><subject>Nucleic acids</subject><subject>Older people</subject><subject>Parasites</subject><subject>Plasmodium</subject><subject>Plasmodium - isolation & purification</subject><subject>Polls & surveys</subject><subject>Prevalence</subject><subject>Pruritus</subject><subject>Public health</subject><subject>Risk factors</subject><subject>Room temperature</subject><subject>Rural areas</subject><subject>Ships</subject><subject>Socioeconomic aspects</subject><subject>Socioeconomic Factors</subject><subject>Socioeconomics</subject><subject>Surveying</subject><subject>Surveys</subject><subject>Testing</subject><subject>Tests</subject><subject>Tropical diseases</subject><subject>Vector-borne 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Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoboue, Charlene Aya</au><au>Hosch, Salome</au><au>Donfack, Olivier Tresor</au><au>Guirou, Etienne A</au><au>Nlavo, Bonifacio Manguire</au><au>Ayekaba, Mitoha Ondo'o</au><au>Guerra, Carlos</au><au>Phiri, Wonder P</au><au>Garcia, Guillermo A</au><au>Schindler, Tobias</au><au>Daubenberger, Claudia A</au><au>Bradbury, Richard Stewart</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterising co-infections with Plasmodium spp., Mansonella perstans or Loa loa in asymptomatic children, adults and elderly people living on Bioko Island using nucleic acids extracted from malaria rapid diagnostic tests</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2022-01-01</date><risdate>2022</risdate><volume>16</volume><issue>1</issue><spage>e0009798</spage><epage>e0009798</epage><pages>e0009798-e0009798</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Regular and comprehensive epidemiological surveys of the filarial nematodes Mansonella perstans and Loa loa in children, adolescents and adults living across Bioko Island, Equatorial Guinea are lacking. We aimed to demonstrate that blood retained on malaria rapid diagnostic tests, commonly deployed for malaria surveys, could be used as a source of nucleic acids for molecular based detection of M. perstans and L. loa. We wanted to determine the positivity rate and distribution of filarial nematodes across different age groups and geographical areas as well as to understand level of co-infections with malaria in an asymptomatic population.
M. perstans, L. loa and Plasmodium spp. parasites were monitored by qPCR in a cross-sectional study using DNA extracted from a subset malaria rapid diagnostic tests (mRDTs) collected during the annual malaria indicator survey conducted on Bioko Island in 2018.
We identified DNA specific for the two filarial nematodes investigated among 8.2% (263) of the 3214 RDTs screened. Positivity rates of M. perstans and L. loa were 6.6% and 1.5%, respectively. M. perstans infection were more prominent in male (10.5%) compared to female (3.9%) survey participants. M. perstans parasite density and positivity rate was higher among older people and the population living in rural areas. The socio-economic status of participants strongly influenced the infection rate with people belonging to the lowest socio-economic quintile more than 3 and 5 times more likely to be L. loa and M. perstans infected, respectively. No increased risk of being co-infected with Plasmodium spp. parasites was observed among the different age groups.
We found otherwise asymptomatic individuals were infected with M. perstans and L. loa. Our study demonstrates that employing mRDTs probed with blood for malaria testing represents a promising, future tool to preserve and ship NAs at room temperature to laboratories for molecular, high-throughput diagnosis and genotyping of blood-dwelling nematode filarial infections. Using this approach, asymptomatic populations can be reached and surveyed for infectious diseases beyond malaria.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>35100277</pmid><doi>10.1371/journal.pntd.0009798</doi><orcidid>https://orcid.org/0000-0001-9290-3589</orcidid><orcidid>https://orcid.org/0000-0002-5961-095X</orcidid><orcidid>https://orcid.org/0000-0002-4069-9528</orcidid><orcidid>https://orcid.org/0000-0001-7136-0642</orcidid><orcidid>https://orcid.org/0000-0001-5554-8039</orcidid><orcidid>https://orcid.org/0000-0002-8576-328X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1935-2735 |
ispartof | PLoS neglected tropical diseases, 2022-01, Vol.16 (1), p.e0009798-e0009798 |
issn | 1935-2735 1935-2727 1935-2735 |
language | eng |
recordid | cdi_plos_journals_2762208237 |
source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | Acids Adolescent Adolescents Adult Adults Age groups Analysis Animals Asymptomatic Biology and Life Sciences Blood Care and treatment Child Children Coinfection - epidemiology Coinfection - parasitology Comorbidity Cross-Sectional Studies Deoxyribonucleic acid Diagnosis Diagnostic tests DNA DNA, Helminth Earth Sciences Economics Epidemiology Equatorial Guinea - epidemiology Female Filariasis Genotyping Health risks Human diseases Humans Infections Infectious diseases Laboratories Loa - isolation & purification Loa loa Loiasis - blood Loiasis - epidemiology Malaria Malaria - blood Malaria - epidemiology Male Mansonella - isolation & purification Mansonella perstans Mansonelliasis - blood Mansonelliasis - epidemiology Medical tests Medicine and Health Sciences Middle Aged Nematodes Nucleic acids Older people Parasites Plasmodium Plasmodium - isolation & purification Polls & surveys Prevalence Pruritus Public health Risk factors Room temperature Rural areas Ships Socioeconomic aspects Socioeconomic Factors Socioeconomics Surveying Surveys Testing Tests Tropical diseases Vector-borne diseases |
title | Characterising co-infections with Plasmodium spp., Mansonella perstans or Loa loa in asymptomatic children, adults and elderly people living on Bioko Island using nucleic acids extracted from malaria rapid diagnostic tests |
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