Literature DB >> 18459302

Serovar-specific real-time quantitative detection of Salmonella enteritidis in the gastrointestinal tract of ducks after oral challenge.

Shu-Xuan Deng1, An-Chun Cheng, Ming-Shu Wang, Ping Cao.   

Abstract

The objective of this study was to identify and understand the regular distribution pattern and primary penetration site for Salmonella Enteritidis (SE) in the gastrointestinal tract of ducks. An assay based on the serovar-specific DNA sequence of SE from GenBank, a serovar-specific real-time, fluorescence-based quantitative polymerase chain reaction, was developed for the detection of SE. We used this assay to detect genomic DNA of SE in the blood and gastrointestinal tract, including duodenum, jejunum, ileum, cecum, rectum, esophagus, stomach muscularis, and stomach glandularis, from ducks after oral challenge at different time points. The results showed that SE was consistently detected in all segments of the gastrointestinal tract. The jejunum and ileum were positive 8 hr postinoculation (PI). The organism was detected in blood 12 hr PI, while the final organ to show a positive result was the stomach at 24 hr PI. The copy number of SE DNA in each tissue reached a peak at 24-36 hr PI, with the jejunum, ileum, and cecum containing high concentrations of SE, whereas the blood, duodenum, rectum, stomach, and esophagus had low concentrations. SE populations began to decrease and were not detectable at 2 days PI, but were still present up to 9 days PI in the jejunum, ileum, and cecum without causing apparent symptoms. By 3 days PI the cecum had significantly higher numbers of SE than any of the other areas (P < 0.01), and this appeared to reflect its function as a repository for SE. In conclusion, the results provided significant data for understanding the life cycle of SE in the gastrointestinal tract and showed that the jejunum, ileum, and cecum were the primary sites of invasion in normal ducks after oral challenge. This study will help to understand the mechanisms of action of SE infection in vivo.

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Year:  2008        PMID: 18459302     DOI: 10.1637/8102-090107-Reg

Source DB:  PubMed          Journal:  Avian Dis        ISSN: 0005-2086            Impact factor:   1.577


  10 in total

1.  Quantitative studies of the distribution pattern for Salmonella Enteritidis in the internal organs of chicken after oral challenge by a real-time PCR.

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2.  Spontaneous excision of the Salmonella enterica serovar Enteritidis-specific defective prophage-like element phiSE14.

Authors:  Carlos A Santiviago; Carlos J Blondel; Carolina P Quezada; Cecilia A Silva; Pia M Tobar; Steffen Porwollik; Michael McClelland; Helene L Andrews-Polymenis; Cecilia S Toro; Mercedes Zaldívar; Inés Contreras
Journal:  J Bacteriol       Date:  2010-02-19       Impact factor: 3.490

3.  Replication kinetics of Salmonella enteritidis in internal organs of ducklings after oral challenge: a quantitative time-course study using real-time PCR.

Authors:  S X Deng; A C Cheng; M S Wang; X R Li; B Yan
Journal:  Vet Res Commun       Date:  2008-09-09       Impact factor: 2.459

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5.  Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe.

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8.  Splenic microRNA Expression Profiles and Integration Analyses Involved in Host Responses to Salmonella enteritidis Infection in Chickens.

Authors:  Peng Li; Wenlei Fan; Qinghe Li; Jie Wang; Ranran Liu; Nadia Everaert; Jie Liu; Yonghong Zhang; Maiqing Zheng; Huanxian Cui; Guiping Zhao; Jie Wen
Journal:  Front Cell Infect Microbiol       Date:  2017-08-24       Impact factor: 5.293

9.  Effects of Salmonella enterica serovar Enteritidis infection on egg production and the immune response of the laying duck Anas platyrhynchos.

Authors:  Yu Zhang; Yang Chen; Tiantian Gu; Qi Xu; Guoqiang Zhu; Guohong Chen
Journal:  PeerJ       Date:  2019-01-25       Impact factor: 2.984

10.  Development and application of a reverse transcription loop-mediated isothermal amplification method for rapid detection of Duck hepatitis A virus type 1.

Authors:  Limin Yang; Jing Li; Yuhai Bi; Lei Xu; Wenjun Liu
Journal:  Virus Genes       Date:  2012-08-07       Impact factor: 2.332

  10 in total

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