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Filarial Antigenemia and Loa loa Night Blood Microfilaremia in an Area Without Bancroftian Filariasis in the Democratic Republic of Congo

Identifieur interne : 002A85 ( Main/Exploration ); précédent : 002A84; suivant : 002A86

Filarial Antigenemia and Loa loa Night Blood Microfilaremia in an Area Without Bancroftian Filariasis in the Democratic Republic of Congo

Auteurs : Didier K. Bakajika ; Maurice M. Nigo ; Jean Pierre Lotsima ; Germain A. Masikini ; Kerstin Fischer ; Melanie M. Lloyd ; Gary J. Weil ; Peter U. Fischer

Source :

RBID : PMC:4257636

Descripteurs français

English descriptors

Abstract

Implementation of mass drug administration for lymphatic filariasis (LF) has been delayed in central Africa because of incomplete mapping and coendemic loiasis. We mapped two regions in eastern Democratic Republic of Congo that were suspected to have LF. Night blood samples were collected from 2,724 subjects in 30 villages. Filarial antigenemia rates by card test exceeded 1% in 28 villages (range = 0–14%). Prevalence rates for large sheathed microfilariae (Mf) ranged from 4% to 40%; Mansonella perstans rates ranged from 22% to 98%. Large Mf were exclusively Loa loa by microscopy, and only 1 of 337 samples tested by quantitative polymerase chain reaction (qPCR) was positive for Wuchereria bancrofti DNA. Filarial antigen positivity was strongly associated with high L. loa Mf counts. Periodicity studies revealed atypical patterns, with no significant diurnal periodicity in some individuals. Thus, methods routinely used for LF mapping may not be reliable in areas in central Africa that are highly endemic for loiasis.


Url:
DOI: 10.4269/ajtmh.14-0358
PubMed: 25223938
PubMed Central: 4257636


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Elephantiasis, Filarial (blood)</term>
<term>Elephantiasis, Filarial (epidemiology)</term>
<term>Elephantiasis, Filarial (immunology)</term>
<term>Humans</term>
<term>Loa (isolation & purification)</term>
<term>Loiasis (blood)</term>
<term>Loiasis (epidemiology)</term>
<term>Microfilariae (immunology)</term>
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<term>Animaux</term>
<term>Antigènes d'helminthe (sang)</term>
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<term>Filariose lymphatique (sang)</term>
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<term>Humains</term>
<term>Loa (isolement et purification)</term>
<term>Loase (sang)</term>
<term>Loase (épidémiologie)</term>
<term>Microfilaria (immunologie)</term>
<term>République démocratique du Congo (épidémiologie)</term>
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<p>Implementation of mass drug administration for lymphatic filariasis (LF) has been delayed in central Africa because of incomplete mapping and coendemic loiasis. We mapped two regions in eastern Democratic Republic of Congo that were suspected to have LF. Night blood samples were collected from 2,724 subjects in 30 villages. Filarial antigenemia rates by card test exceeded 1% in 28 villages (range = 0–14%). Prevalence rates for large sheathed microfilariae (Mf) ranged from 4% to 40%;
<italic>Mansonella perstans</italic>
rates ranged from 22% to 98%. Large Mf were exclusively
<italic>Loa loa</italic>
by microscopy, and only 1 of 337 samples tested by quantitative polymerase chain reaction (qPCR) was positive for
<italic>Wuchereria bancrofti</italic>
DNA. Filarial antigen positivity was strongly associated with high
<italic>L. loa</italic>
Mf counts. Periodicity studies revealed atypical patterns, with no significant diurnal periodicity in some individuals. Thus, methods routinely used for LF mapping may not be reliable in areas in central Africa that are highly endemic for loiasis.</p>
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<name sortKey="Fischer, Kerstin" sort="Fischer, Kerstin" uniqKey="Fischer K" first="Kerstin" last="Fischer">Kerstin Fischer</name>
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