Laboratory Animal Medicine 2002
DOI: 10.1016/b978-012263951-7/50013-2
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Microbiological Quality Control for Laboratory Rodents and Lagomorphs

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Cited by 8 publications
(4 citation statements)
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“…Once exposed, a given sentinel rat is most likely to have diagnostic RRV lesions 8–12 weeks after the initial exposure. This period is longer than that required for other types of serologic and molecular testing in rats; seroconversion generally occurs to most agents within 2–3 weeks, 10 preceded by shedding and tissue infection, which can be detected by PCR. Thus, sentinel exposure periods for rats should be extended to be between 6 and 13 weeks, with 8–12 weeks being an optimal exposure duration.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Once exposed, a given sentinel rat is most likely to have diagnostic RRV lesions 8–12 weeks after the initial exposure. This period is longer than that required for other types of serologic and molecular testing in rats; seroconversion generally occurs to most agents within 2–3 weeks, 10 preceded by shedding and tissue infection, which can be detected by PCR. Thus, sentinel exposure periods for rats should be extended to be between 6 and 13 weeks, with 8–12 weeks being an optimal exposure duration.…”
Section: Discussionmentioning
confidence: 99%
“…We recommend that the Brown Norway rat NOT be used for histologic screening for RRV. Nonetheless, the dense lymphoid cuffs of RRV are not seen in the strain-related Brown Norway pneumonia 10.…”
mentioning
confidence: 91%
“…If an incoming agent was enzootic at the source institution, detection may take only a few days with suffi ciently broad testing. Bona fi de quarantine periods generally last at least 3-4 weeks, however, because 2-4 weeks is the commonly accepted time period for micro-organisms to proliferate to levels detectable using serology, bacterial culture or molecular diagnostics ( Rehg and Toth, 1998 ;Shek and Gaertner, 2002 ). Depending upon the agent, inoculum, host age, host genotype and other factors, the development of detectable serum antibodies may be variable, requiring longer quarantine periods -as has been shown in the case with mouse parvovirus ( Besselsen et al ., 2000 ).…”
Section: Sources Of Risk and Principles Of Preventionmentioning
confidence: 99%
“…All animals were free of Helicobacter spp., Lawsonia intracellularis, Clostridium piliforme, Sendai virus, pneumonia virus of mice, lymphocytic choriomeningitis virus, reovirus (1, 2 and 3), mouse adenovirus (1 and 2), and simian virus 5 as determined using a combination of serological and molecular screening techniques (i.e., multiplex fluorescent immunoassay, indirect fluorescent antibody and/or polymerase chain reaction). 19 Our challenge dose (i.e., 5.4 log 10 PFU/ mL) aimed to mimic a moderate-to-high ZIKV exposure. 20 In our first hamster experiment, 24 hamsters, three per group, were inoculated subcutaneously with 5.4 log 10 PFU/mL of ZIKV strain ArD 41525 (N = 12) or CPC-0740 (N = 12).…”
mentioning
confidence: 99%