Diagnosis of Brugian Filariasis by Loop-Mediated Isothermal Amplification
Identifieur interne : 005466 ( Ncbi/Checkpoint ); précédent : 005465; suivant : 005467Diagnosis of Brugian Filariasis by Loop-Mediated Isothermal Amplification
Auteurs : Catherine B. Poole ; Nathan A. Tanner ; Yinhua Zhang ; Thomas C. Evans ; Clotilde K. S. CarlowSource :
- PLoS Neglected Tropical Diseases [ 1935-2727 ] ; 2012.
Abstract
In this study we developed and evaluated a
Url:
DOI: 10.1371/journal.pntd.0001948
PubMed: 23272258
PubMed Central: 3521703
Affiliations:
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Diagnosis of Brugian Filariasis by Loop-Mediated Isothermal Amplification</title>
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<author><name sortKey="Tanner, Nathan A" sort="Tanner, Nathan A" uniqKey="Tanner N" first="Nathan A." last="Tanner">Nathan A. Tanner</name>
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<author><name sortKey="Zhang, Yinhua" sort="Zhang, Yinhua" uniqKey="Zhang Y" first="Yinhua" last="Zhang">Yinhua Zhang</name>
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<series><title level="j">PLoS Neglected Tropical Diseases</title>
<idno type="ISSN">1935-2727</idno>
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<front><div type="abstract" xml:lang="en"><p>In this study we developed and evaluated a <italic>Brugia Hha</italic>
I repeat loop-mediated isothermal amplification (LAMP) assay for the rapid detection of <italic>Brugia</italic>
genomic DNA. Amplification was detected using turbidity or fluorescence as readouts. Reactions generated a turbidity threshold value or a clear visual positive within 30 minutes using purified genomic DNA equivalent to one microfilaria. Similar results were obtained using DNA isolated from blood samples containing <italic>B. malayi</italic>
microfilariae. Amplification was specific to <italic>B. malayi</italic>
and <italic>B. timori</italic>
, as no turbidity was observed using DNA from the related filarial parasites <italic>Wuchereria bancrofti</italic>
, <italic>Onchocerca volvulus</italic>
or <italic>Dirofilaria immitis</italic>
, or from human or mosquito. Furthermore, the assay was most robust using a new strand-displacing DNA polymerase termed <italic>Bst 2.0</italic>
compared to wild-type <italic>Bst</italic>
DNA polymerase, large fragment. The results indicate that the <italic>Brugia Hha</italic>
I repeat LAMP assay is rapid, sensitive and <italic>Brugia</italic>
-specific with the potential to be developed further as a field tool for diagnosis and mapping of brugian filariasis.</p>
</div>
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<tree><noCountry><name sortKey="Carlow, Clotilde K S" sort="Carlow, Clotilde K S" uniqKey="Carlow C" first="Clotilde K. S." last="Carlow">Clotilde K. S. Carlow</name>
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