Publication:
Susceptibility of inbred mice to Rickettsia parkeri

dc.contributor.authorBritton J. Graspergeen_US
dc.contributor.authorKathryn E. Reifen_US
dc.contributor.authorTimothy D. Morganen_US
dc.contributor.authorPiyanate Sunyakumthornen_US
dc.contributor.authorJoseph Bynogen_US
dc.contributor.authorChristopher D. Paddocken_US
dc.contributor.authorKevin R. Macalusoen_US
dc.contributor.otherLSU School of Veterinary Medicineen_US
dc.contributor.otherWashington State University Pullmanen_US
dc.contributor.otherMississippi State Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherCenters for Disease Control and Preventionen_US
dc.date.accessioned2018-06-11T04:53:55Z
dc.date.available2018-06-11T04:53:55Z
dc.date.issued2012-05-01en_US
dc.description.abstractRickettsia parkeri, a member of the spotted fever group Rickettsia, is the causative agent of American boutonneuse fever in humans. Despite the increased recognition of human cases, limited information is available regarding the infection of invertebrate and vertebrate hosts for this emerging tick-borne disease. Toward the development of a viable transmission model and to further characterize the pathology associated with R. parkeri infection, inbred mouse strains (A/J, BALB/c, C3H/HeJ, and C3H/HeN) were intravenously and intradermally inoculated with 10 5 low-passage-number R. parkeri (Portsmouth strain), and infection, gross pathology, and histopathology were scored. Additionally, a quantitative real-time PCR (qPCR) was performed to estimate rickettsial load in heart, lung, spleen, and liver tissues of infected mice at 19 days postinoculation. Of the A/J, BALB/c, and C3H/ HeN mice, none displayed universal pathology consistent with sustained infection. Compared to age-matched control mice, the intravenously inoculated C3H/HeJ mice exhibited marked facial edema and marked splenomegaly upon gross examination, while the intradermally inoculated mice developed characteristic eschar-like lesions. The C3H/HeJ mice also exhibited the greatest concentrations of rickettsial DNA from heart, lung, liver, and spleen samples when examined by qPCR. The similarity of the pathology of human disease and sustained infection suggests that the C3H/HeJ strain of mice is a promising candidate for subsequent experiments to examine the tick transmission, dissemination, and pathology of R. parkeri rickettsiosis. © 2012, American Society for Microbiology.en_US
dc.identifier.citationInfection and Immunity. Vol.80, No.5 (2012), 1846-1852en_US
dc.identifier.doi10.1128/IAI.00109-12en_US
dc.identifier.issn10985522en_US
dc.identifier.issn00199567en_US
dc.identifier.other2-s2.0-84861123808en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/14329
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84861123808&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleSusceptibility of inbred mice to Rickettsia parkerien_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84861123808&origin=inwarden_US

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