2003
DOI: 10.1128/jcm.41.12.5557-5562.2003
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Evidence ofBorrelia lonestariDNA inAmblyomma americanum(Acari: Ixodidae) Removed from Humans

Abstract: We used a nested PCR with

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Cited by 117 publications
(70 citation statements)
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“…34 The PCR were carried out in a total of 50 μL solution containing 1X PCR buffer minus Mg, 1.5 mM MgCl2, 0.2 mM dNTPs, 1 U of Platinum TaqDNA Polymerase, and 0.2 μM of each primer. For all PCR reactions, one positive control (DNA extracted from Borrelia anserina culture) and two negative controls (water) were included.…”
Section: Methodsmentioning
confidence: 99%
“…34 The PCR were carried out in a total of 50 μL solution containing 1X PCR buffer minus Mg, 1.5 mM MgCl2, 0.2 mM dNTPs, 1 U of Platinum TaqDNA Polymerase, and 0.2 μM of each primer. For all PCR reactions, one positive control (DNA extracted from Borrelia anserina culture) and two negative controls (water) were included.…”
Section: Methodsmentioning
confidence: 99%
“…In Europe and Asia especially, the development of a uniform approach for the serological evaluation of LB is complicated by the prevalence of organisms from the three or more genospecies of B. burgdorferi sensu lato and by significant antigenic variation between and within each genospecies (Wang et al, 1999). Moreover, in the USA 'Borrelia lonestari' exposure may confound serological results (Stromdahl et al, 2003).…”
Section: Introductionmentioning
confidence: 99%
“…20,23,25 Borrelia lonestari has additionally been identified in A. americanum ticks that were removed from humans, including patients from Kentucky. 26 Ehrlichia chaffeensis is a gram-negative obligate intracellular bacterium and the etiologic agent of human monocytotrophic ehrlichiosis. [27][28][29] Ehrlichia chaffeensis is maintained in a zoonotic cycle involving its principal reservoir, the white-tailed deer ( Odocoileus virginianus ) and A. americanum ticks.…”
Section: Introductionmentioning
confidence: 99%