2009
DOI: 10.1111/j.1469-0691.2008.02140.x
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Detection of Rickettsia felis and Rickettsia typhi in an area of California endemic for murine typhus

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Cited by 35 publications
(43 citation statements)
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“…At the NML, genomic DNA was extracted from spleen samples (n = 678) using the NucleoSpin 96 Tissue Kit (Machery-Nagel, Bethlehem, USA) and the QIAxtractor (Qiagen, Toronto, Canada) and screened using a multiplexed qPCR assay for the detection of R. typhi and R. felis (Karpathy et al 2009). R. typhi, R. felis, and rat glial cells were used as positive controls.…”
Section: Methodsmentioning
confidence: 99%
“…At the NML, genomic DNA was extracted from spleen samples (n = 678) using the NucleoSpin 96 Tissue Kit (Machery-Nagel, Bethlehem, USA) and the QIAxtractor (Qiagen, Toronto, Canada) and screened using a multiplexed qPCR assay for the detection of R. typhi and R. felis (Karpathy et al 2009). R. typhi, R. felis, and rat glial cells were used as positive controls.…”
Section: Methodsmentioning
confidence: 99%
“…typhi DNA was conducted by using a TaqMan assay for the citrate synthase ( glt A) gene of Rickettsia spp. as described elsewhere ( 11 , 12 ). The reactions were conducted by using the Brilliant Q PCR core reagent kit (Stratagene, La Jolla, CA, USA) and run on an i Cycler (Bio-Rad, Hercules, CA, USA).…”
Section: Methodsmentioning
confidence: 99%
“…Consequently, it was proposed that a suburban cycle involving cats, opossums, and cat fleas was responsible for the human cases of murine typhus reported from the foothill areas (Adams et al 1970, Williams et al 1992, Sorvillo et al 1993. The presence of Rickettsia felis (formerly called ELB agent) was then discovered in cat fleas, Ctenocephilides felis (Williams et al 1992), and C. felis commonplace association and feeding on both cats and opossums was established (Williams et al 1992, Karpathy et al 2009, Reif and Macaluso 2009.…”
Section: Vector-borne and Zoonotic Diseasesmentioning
confidence: 96%
“…Species-specific probes, primers, and amplification conditions were used as described previously (Eremeeva et al 2008, Karpathy et al 2009). Data were analyzed using an iCycler real-time Polymerase chain reaction (PCR) thermocycler and software (BioRad, Richmond, CA).…”
Section: Polymerase Chain Reaction Cloning and Sequencingmentioning
confidence: 99%