Diversity and transmission competence in lymphatic filariasis vectors in West Africa, and the implications for accelerated elimination of Anopheles-transmitted filariasis.
Identifieur interne : 001E72 ( PubMed/Curation ); précédent : 001E71; suivant : 001E73Diversity and transmission competence in lymphatic filariasis vectors in West Africa, and the implications for accelerated elimination of Anopheles-transmitted filariasis.
Auteurs : Dziedzom K. De Souza [Ghana] ; Benjamin Koudou ; Louise A. Kelly-Hope ; Michael D. Wilson ; Moses J. Bockarie ; Daniel A. BoakyeSource :
- Parasites & vectors [ 1756-3305 ] ; 2012.
Descripteurs français
- KwdFr :
- MESH :
- parasitologie : Anopheles.
- épidémiologie : Afrique de l'Ouest, Filariose lymphatique.
- Animaux, Anopheles, Filariose lymphatique, Résistance aux insecticides, Vecteurs insectes.
English descriptors
- KwdEn :
- MESH :
- geographic , epidemiology : Africa, Western.
- drug effects : Anopheles.
- epidemiology : Elephantiasis, Filarial.
- parasitology : Anopheles.
- prevention & control : Elephantiasis, Filarial.
- transmission : Elephantiasis, Filarial.
- Animals, Insect Vectors, Insecticide Resistance.
Abstract
Lymphatic Filariasis (LF) is targeted for elimination by the Global Programme for the Elimination of Lymphatic Filariasis (GPELF). The strategy adopted is based on the density dependent phenomenon of Facilitation, which hypothesizes that in an area where the vector species transmitting Wuchereria bancrofti are Anopheles mosquitoes, it is feasible to eliminate LF using Mass Drug Administration (MDA) because of the inability of Anopheles species to transmit low-density microfilaraemia. Even though earlier studies have shown Anopheles species can exhibit the process of Facilitation in West Africa, observations point towards the process of Limitation in certain areas, in which case vector control is recommended. Studies on Anopheles species in West Africa have also shown genetic differentiation, cryptic taxa and speciation, insecticide resistance and the existence of molecular and chromosomal forms, all of which could influence the vectorial capacity of the mosquitoes and ultimately the elimination goal. This paper outlines the uniqueness of LF vectors in West Africa and the challenges it poses to the 2020 elimination goal, based on the current MDA strategies.
DOI: 10.1186/1756-3305-5-259
PubMed: 23151383
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Boakye</name></author></analytic><series><title level="j">Parasites & vectors</title><idno type="eISSN">1756-3305</idno><imprint><date when="2012" type="published">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Africa, Western (epidemiology)</term><term>Animals</term><term>Anopheles (drug effects)</term><term>Anopheles (parasitology)</term><term>Elephantiasis, Filarial (epidemiology)</term><term>Elephantiasis, Filarial (prevention & control)</term><term>Elephantiasis, Filarial (transmission)</term><term>Insect Vectors</term><term>Insecticide Resistance</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Afrique de l'Ouest (épidémiologie)</term><term>Animaux</term><term>Anopheles ()</term><term>Anopheles (parasitologie)</term><term>Filariose lymphatique ()</term><term>Filariose lymphatique (transmission)</term><term>Filariose lymphatique (épidémiologie)</term><term>Résistance aux insecticides</term><term>Vecteurs insectes</term></keywords><keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en"><term>Africa, Western</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Anopheles</term></keywords><keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Elephantiasis, Filarial</term></keywords><keywords scheme="MESH" qualifier="parasitologie" xml:lang="fr"><term>Anopheles</term></keywords><keywords scheme="MESH" qualifier="parasitology" xml:lang="en"><term>Anopheles</term></keywords><keywords scheme="MESH" qualifier="prevention & control" xml:lang="en"><term>Elephantiasis, Filarial</term></keywords><keywords scheme="MESH" qualifier="transmission" xml:lang="en"><term>Elephantiasis, Filarial</term></keywords><keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr"><term>Afrique de l'Ouest</term><term>Filariose lymphatique</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Insect Vectors</term><term>Insecticide Resistance</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Anopheles</term><term>Filariose lymphatique</term><term>Résistance aux insecticides</term><term>Vecteurs insectes</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Lymphatic Filariasis (LF) is targeted for elimination by the Global Programme for the Elimination of Lymphatic Filariasis (GPELF). The strategy adopted is based on the density dependent phenomenon of Facilitation, which hypothesizes that in an area where the vector species transmitting Wuchereria bancrofti are Anopheles mosquitoes, it is feasible to eliminate LF using Mass Drug Administration (MDA) because of the inability of Anopheles species to transmit low-density microfilaraemia. Even though earlier studies have shown Anopheles species can exhibit the process of Facilitation in West Africa, observations point towards the process of Limitation in certain areas, in which case vector control is recommended. Studies on Anopheles species in West Africa have also shown genetic differentiation, cryptic taxa and speciation, insecticide resistance and the existence of molecular and chromosomal forms, all of which could influence the vectorial capacity of the mosquitoes and ultimately the elimination goal. This paper outlines the uniqueness of LF vectors in West Africa and the challenges it poses to the 2020 elimination goal, based on the current MDA strategies.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23151383</PMID><DateCreated><Year>2013</Year><Month>01</Month><Day>01</Day></DateCreated><DateCompleted><Year>2013</Year><Month>06</Month><Day>07</Day></DateCompleted><DateRevised><Year>2017</Year><Month>09</Month><Day>02</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1756-3305</ISSN><JournalIssue CitedMedium="Internet"><Volume>5</Volume><PubDate><Year>2012</Year><Month>Nov</Month><Day>14</Day></PubDate></JournalIssue><Title>Parasites & vectors</Title><ISOAbbreviation>Parasit Vectors</ISOAbbreviation></Journal><ArticleTitle>Diversity and transmission competence in lymphatic filariasis vectors in West Africa, and the implications for accelerated elimination of Anopheles-transmitted filariasis.</ArticleTitle><Pagination><MedlinePgn>259</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1186/1756-3305-5-259</ELocationID><Abstract><AbstractText>Lymphatic Filariasis (LF) is targeted for elimination by the Global Programme for the Elimination of Lymphatic Filariasis (GPELF). The strategy adopted is based on the density dependent phenomenon of Facilitation, which hypothesizes that in an area where the vector species transmitting Wuchereria bancrofti are Anopheles mosquitoes, it is feasible to eliminate LF using Mass Drug Administration (MDA) because of the inability of Anopheles species to transmit low-density microfilaraemia. Even though earlier studies have shown Anopheles species can exhibit the process of Facilitation in West Africa, observations point towards the process of Limitation in certain areas, in which case vector control is recommended. Studies on Anopheles species in West Africa have also shown genetic differentiation, cryptic taxa and speciation, insecticide resistance and the existence of molecular and chromosomal forms, all of which could influence the vectorial capacity of the mosquitoes and ultimately the elimination goal. This paper outlines the uniqueness of LF vectors in West Africa and the challenges it poses to the 2020 elimination goal, based on the current MDA strategies.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>de Souza</LastName><ForeName>Dziedzom K</ForeName><Initials>DK</Initials><AffiliationInfo><Affiliation>Parasitology Department, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon-Accra, Ghana.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Koudou</LastName><ForeName>Benjamin</ForeName><Initials>B</Initials></Author><Author ValidYN="Y"><LastName>Kelly-Hope</LastName><ForeName>Louise A</ForeName><Initials>LA</Initials></Author><Author ValidYN="Y"><LastName>Wilson</LastName><ForeName>Michael D</ForeName><Initials>MD</Initials></Author><Author ValidYN="Y"><LastName>Bockarie</LastName><ForeName>Moses J</ForeName><Initials>MJ</Initials></Author><Author ValidYN="Y"><LastName>Boakye</LastName><ForeName>Daniel A</ForeName><Initials>DA</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>MRC_G1001337</GrantID><Agency>Medical Research Council</Agency><Country>United Kingdom</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>11</Month><Day>14</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Parasit Vectors</MedlineTA><NlmUniqueID>101462774</NlmUniqueID><ISSNLinking>1756-3305</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Med Vet Entomol. 2001 Sep;15(3):267-74</RefSource><PMID Version="1">11583443</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Trop Med Hyg. 1991 Aug;94(4):241-4</RefSource><PMID 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