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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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 |
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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 |
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