Cargando…

Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri

BACKGROUND: Amblyomma maculatum is the primary vector for Rickettsia parkeri, a spotted fever group rickettsia (SFGR) and human pathogen. Cotton rats and quail are known hosts for larval and nymphal A. maculatum; however, the role of these hosts in the ecology of R. parkeri is unknown. METHODS: Cott...

Descripción completa

Detalles Bibliográficos
Autores principales: Moraru, Gail Miriam, Goddard, Jerome, Paddock, Christopher D, Varela-Stokes, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606396/
https://www.ncbi.nlm.nih.gov/pubmed/23497681
http://dx.doi.org/10.1186/1756-3305-6-70
_version_ 1782264002371387392
author Moraru, Gail Miriam
Goddard, Jerome
Paddock, Christopher D
Varela-Stokes, Andrea
author_facet Moraru, Gail Miriam
Goddard, Jerome
Paddock, Christopher D
Varela-Stokes, Andrea
author_sort Moraru, Gail Miriam
collection PubMed
description BACKGROUND: Amblyomma maculatum is the primary vector for Rickettsia parkeri, a spotted fever group rickettsia (SFGR) and human pathogen. Cotton rats and quail are known hosts for larval and nymphal A. maculatum; however, the role of these hosts in the ecology of R. parkeri is unknown. METHODS: Cotton rats and quail were inoculated with low or high doses of R. parkeri (strain Portsmouth) grown in Vero cells to evaluate infection by R. parkeri in these two hosts species. Animals were euthanized 2, 4, 7, 10, and 14 days post-injection (dpi) and blood, skin, and spleen samples were collected to analyze by Vero cell culture and polymerase chain reaction (PCR). In a second trial, cotton rats and quail were inoculated with R. parkeri and nymphal A. maculatum ticks were allowed to feed on animals. Animals were euthanized on 14, 20, 28, 31, and 38 dpi and blood and tissues were collected for serology and PCR assays. Fed ticks were tested for R. parkeri by PCR and Vero cell culture. RESULTS: Rickettsia parkeri was isolated in cell culture and detected by PCR in skin, blood, and spleen tissues of cotton rats in the initial trial 2, 4, and 7 dpi, but not in quail tissues. In the second trial, no ticks tested positive for R. parkeri by PCR or cell culture. CONCLUSIONS: These studies demonstrate that viable R. parkeri rickettsiae can persist in the tissues of cotton rats for at least 7 days following subcutaneous inoculation of these bacteria; however, quail are apparently resistant to infection. Rickettsia parkeri was not detected in nymphal ticks that fed on R. parkeri-inoculated cotton rats or quail, suggesting an alternate route of transmission to naïve ticks.
format Online
Article
Text
id pubmed-3606396
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-36063962013-03-24 Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri Moraru, Gail Miriam Goddard, Jerome Paddock, Christopher D Varela-Stokes, Andrea Parasit Vectors Research BACKGROUND: Amblyomma maculatum is the primary vector for Rickettsia parkeri, a spotted fever group rickettsia (SFGR) and human pathogen. Cotton rats and quail are known hosts for larval and nymphal A. maculatum; however, the role of these hosts in the ecology of R. parkeri is unknown. METHODS: Cotton rats and quail were inoculated with low or high doses of R. parkeri (strain Portsmouth) grown in Vero cells to evaluate infection by R. parkeri in these two hosts species. Animals were euthanized 2, 4, 7, 10, and 14 days post-injection (dpi) and blood, skin, and spleen samples were collected to analyze by Vero cell culture and polymerase chain reaction (PCR). In a second trial, cotton rats and quail were inoculated with R. parkeri and nymphal A. maculatum ticks were allowed to feed on animals. Animals were euthanized on 14, 20, 28, 31, and 38 dpi and blood and tissues were collected for serology and PCR assays. Fed ticks were tested for R. parkeri by PCR and Vero cell culture. RESULTS: Rickettsia parkeri was isolated in cell culture and detected by PCR in skin, blood, and spleen tissues of cotton rats in the initial trial 2, 4, and 7 dpi, but not in quail tissues. In the second trial, no ticks tested positive for R. parkeri by PCR or cell culture. CONCLUSIONS: These studies demonstrate that viable R. parkeri rickettsiae can persist in the tissues of cotton rats for at least 7 days following subcutaneous inoculation of these bacteria; however, quail are apparently resistant to infection. Rickettsia parkeri was not detected in nymphal ticks that fed on R. parkeri-inoculated cotton rats or quail, suggesting an alternate route of transmission to naïve ticks. BioMed Central 2013-03-15 /pmc/articles/PMC3606396/ /pubmed/23497681 http://dx.doi.org/10.1186/1756-3305-6-70 Text en Copyright ©2013 Moraru et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Moraru, Gail Miriam
Goddard, Jerome
Paddock, Christopher D
Varela-Stokes, Andrea
Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri
title Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri
title_full Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri
title_fullStr Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri
title_full_unstemmed Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri
title_short Experimental infection of cotton rats and bobwhite quail with Rickettsia parkeri
title_sort experimental infection of cotton rats and bobwhite quail with rickettsia parkeri
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606396/
https://www.ncbi.nlm.nih.gov/pubmed/23497681
http://dx.doi.org/10.1186/1756-3305-6-70
work_keys_str_mv AT morarugailmiriam experimentalinfectionofcottonratsandbobwhitequailwithrickettsiaparkeri
AT goddardjerome experimentalinfectionofcottonratsandbobwhitequailwithrickettsiaparkeri
AT paddockchristopherd experimentalinfectionofcottonratsandbobwhitequailwithrickettsiaparkeri
AT varelastokesandrea experimentalinfectionofcottonratsandbobwhitequailwithrickettsiaparkeri