Literature DB >> 9542943

Nested PCR assay for detection of granulocytic ehrlichiae.

R F Massung1, K Slater, J H Owens, W L Nicholson, T N Mather, V B Solberg, J G Olson.   

Abstract

A sensitive and specific nested PCR assay was developed for the detection of granulocytic ehrlichiae. The assay amplifies the 16S rRNA gene and was used to examine acute-phase EDTA-blood and serum samples obtained from seven humans with clinical presentations compatible with human granulocytic ehrlichiosis. Five of the seven suspected cases were positive by the PCR assay using DNA extracted from whole blood as the template, compared with a serologic assay that identified only one positive sample. The PCR assay using DNA extracted from the corresponding serum samples as the template identified three positive samples. The sensitivity of the assay on human samples was examined, and the limit of detection was shown to be fewer than 2 copies of the 16S rRNA gene. The application of the assay to nonhuman samples demonstrated products amplified from template DNA extracted from Ixodes scapularis ticks collected in Rhode Island and from EDTA-blood specimens obtained from white-tailed deer in Maryland. All PCR products were sequenced and identified as specific to granulocytic ehrlichiae. A putative variant granulocytic ehrlichia 16S rRNA gene sequence was detected among products amplified from both the ticks and the deer blood specimens.

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Year:  1998        PMID: 9542943      PMCID: PMC104695          DOI: 10.1128/JCM.36.4.1090-1095.1998

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  41 in total

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Journal:  Clin Infect Dis       Date:  1996-09       Impact factor: 9.079

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Authors:  R Heimer; A Van Andel; G P Wormser; M L Wilson
Journal:  J Clin Microbiol       Date:  1997-04       Impact factor: 5.948

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Authors:  B Greig; K M Asanovich; P J Armstrong; J S Dumler
Journal:  J Clin Microbiol       Date:  1996-01       Impact factor: 5.948

7.  Prevalence of granulocytic Ehrlichia infection among white-tailed deer in Wisconsin.

Authors:  E A Belongia; K D Reed; P D Mitchell; C P Kolbert; D H Persing; J S Gill; J J Kazmierczak
Journal:  J Clin Microbiol       Date:  1997-06       Impact factor: 5.948

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Authors:  J J Walls; B Greig; D F Neitzel; J S Dumler
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Authors:  J E Barlough; J E Madigan; E DeRock; J S Dumler; J S Bakken
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Authors:  L A Magnarelli; K C Stafford; T N Mather; M T Yeh; K D Horn; J S Dumler
Journal:  J Clin Microbiol       Date:  1995-10       Impact factor: 5.948

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  104 in total

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2.  Ecological factors characterizing the prevalence of bacterial tick-borne pathogens in Ixodes ricinus ticks in pastures and woodlands.

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5.  Cluster of cases of human Rickettsia felis infection from Southern Europe (Spain) diagnosed by PCR.

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6.  Prevalence of Borrelia burgdorferi s.l. and Anaplasma phagocytophilum in the wood tick Ixodes ricinus in the Province of Trento, Italy.

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7.  Sequence analysis of the msp4 gene of Anaplasma phagocytophilum strains.

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8.  Isolation and propagation of the Ap-Variant 1 strain of Anaplasma phagocytophilum in a tick cell line.

Authors:  Robert F Massung; Michael L Levin; Ulrike G Munderloh; David J Silverman; Meghan J Lynch; Jariyanart K Gaywee; Timothy J Kurtti
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9.  Comparison of PCR assays for detection of the agent of human granulocytic ehrlichiosis, Anaplasma phagocytophilum.

Authors:  Robert F Massung; Kimetha G Slater
Journal:  J Clin Microbiol       Date:  2003-02       Impact factor: 5.948

10.  Multiplex real-time PCR for detection of anaplasma phagocytophilum and Borrelia burgdorferi.

Authors:  Joshua W Courtney; Leah M Kostelnik; Nordin S Zeidner; Robert F Massung
Journal:  J Clin Microbiol       Date:  2004-07       Impact factor: 5.948

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