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rdf:type | |
lifeskim:mentions |
umls-concept:C0016228,
umls-concept:C0025663,
umls-concept:C0030657,
umls-concept:C0032064,
umls-concept:C0032520,
umls-concept:C0043408,
umls-concept:C0086022,
umls-concept:C0442335,
umls-concept:C0679932,
umls-concept:C0680844,
umls-concept:C0681916,
umls-concept:C0750572,
umls-concept:C1442989,
umls-concept:C1521828,
umls-concept:C1704970,
umls-concept:C1705099
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pubmed:issue |
5
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pubmed:dateCreated |
1998-6-1
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pubmed:abstractText |
The prevalence of infectivity within a vector population is a critical factor in arthropod-borne disease epidemiology but it is difficult to estimate. In the case of bubonic plague, infective flea vectors contain large numbers of Yersinia pestis within a bacterial mass that blocks the flea's foregut, and only such blocked fleas are important for biologic transmission. A bacterial quantitation method could therefore be used to assess the prevalence of plague-infective (blocked) fleas in a population. We developed a standard, curve-based, competitive polymerase chain reaction (PCR) procedure to quantitate Y. pestis in individual fleas. The quantitative PCR (Q-PCR) method equaled a colony count reference method in accuracy and precision when evaluated using mock samples and laboratory-infected fleas. The Q-PCR was more reliable than colony count, however, for field-collected fleas and for blocked fleas collected after their death. In a sample of fleas collected from a prairie dog colony in the aftermath of a plague epizootic, 48% were infected but less than 2% contained numbers of Y. pestis indicative of blockage. The method provides a means to monitor plague epizootics and associated risks of flea-borne transmission to humans, and is applicable to the study of other vector-borne diseases.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0002-9637
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
58
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
562-9
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:9598442-Animals,
pubmed-meshheading:9598442-Insect Vectors,
pubmed-meshheading:9598442-Plague,
pubmed-meshheading:9598442-Polymerase Chain Reaction,
pubmed-meshheading:9598442-Prevalence,
pubmed-meshheading:9598442-Sciuridae,
pubmed-meshheading:9598442-Siphonaptera,
pubmed-meshheading:9598442-Yersinia pestis
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pubmed:year |
1998
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pubmed:articleTitle |
Estimation of vector infectivity rates for plague by means of a standard curve-based competitive polymerase chain reaction method to quantify Yersinia pestis in fleas.
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pubmed:affiliation |
Laboratory of Microbial Structure and Function, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana 59840, USA. joe_hinnebusch@nih.gov
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pubmed:publicationType |
Journal Article
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