Literature DB >> 24879709

Rapid identification of Campylobacter jejuni from poultry carcasses and slaughtering environment samples by real-time PCR.

Mirena Ivanova1, Randhir Singh2, Muthu Dharmasena3, Chao Gong3, Albert Krastanov1, Xiuping Jiang4.   

Abstract

The objective of this study was to develop a real-time PCR assay for rapid identification of Campylobacter jejuni and to apply the method in analyzing samples from poultry processing. A C. jejuni-specific primer set targeting a portion of the C. jejuni hippuricase gene was developed. The specificity of the newly designed primer pair was verified using 5 C. jejuni strains and 20 other bacterial strains. Sensitivity was determined to be as low as 1 genome copy per reaction. A total of 73 samples were collected at different sites along the processing line during 2 visits to a poultry slaughterhouse and were examined by direct plating onto modified charcoal cefoperazone deoxycholate agar or after enrichment in Bolton broth followed by plating on modified charcoal cefoperazone deoxycholate agar. The newly developed real-time PCR assay was used to identify the presumptive colonies as belonging to C. jejuni. A real-time PCR assay targeting 16S ribosomal RNA was also applied to determine Campylobacter spp. prevalence. Results from the real-time PCR analysis indicated considerable variability in Campylobacter contamination, with incidence rates of 72.7 and 27.6% for sampling days A and B, respectively. Campylobacter was isolated from 100% of prescalded and preeviscerated carcasses on sampling day A. In contrast, on sampling day B, the highest number of Campylobacter-positive carcasses was recovered after evisceration (60%). The chilling process significantly reduced (P < 0.05) Campylobacter population, but the percentage of positive samples on sampling day A increased to 80%. All samples collected from the processing environment, except scalding tank 3 and the prechiller and chiller tanks, were 100% positive on day A, whereas no campylobacters were isolated from machinery on sampling day B. Our results revealed the widespread of C. jejuni in poultry processing and proved that the newly developed real-time PCR assay is a simple, specific, and inexpensive method for rapid C. jejuni identification. The newly developed PCR method can be easily used in laboratories for reliable and unambiguous identification of C. jejuni in poultry samples. Poultry Science Association Inc.

Entities:  

Keywords:  Campylobacter jejuni; hippuricase gene; poultry carcass; real-time PCR; slaughtering environment

Mesh:

Substances:

Year:  2014        PMID: 24879709     DOI: 10.3382/ps.2013-03736

Source DB:  PubMed          Journal:  Poult Sci        ISSN: 0032-5791            Impact factor:   3.352


  4 in total

1.  New Approaches on Quantification of Campylobacter jejuni in Poultry Samples: The Use of Digital PCR and Real-time PCR against the ISO Standard Plate Count Method.

Authors:  Bojan Papić; Mateja Pate; Urška Henigman; Urška Zajc; Igor Gruntar; Majda Biasizzo; Matjaž Ocepek; Darja Kušar
Journal:  Front Microbiol       Date:  2017-03-02       Impact factor: 5.640

2.  Characterization and Prevalence of Campylobacter spp. From Broiler Chicken Rearing Period to the Slaughtering Process in Eastern China.

Authors:  Yuanyue Tang; Qidong Jiang; Haiyan Tang; Zhenyu Wang; Yi Yin; Fangzhe Ren; Linghua Kong; Xinan Jiao; Jinlin Huang
Journal:  Front Vet Sci       Date:  2020-04-30

3.  Unravelling the reservoirs for colonisation of infants with Campylobacter spp. in rural Ethiopia: protocol for a longitudinal study during a global pandemic and political tensions.

Authors:  Arie H Havelaar; Mussie Brhane; Ibsa Abdusemed Ahmed; Jafer Kedir; Dehao Chen; Loic Deblais; Nigel French; Wondwossen A Gebreyes; Jemal Yousuf Hassen; Xiaolong Li; Mark J Manary; Zelealem Mekuria; Abdulmuen Mohammed Ibrahim; Bahar Mummed; Amanda Ojeda; Gireesh Rajashekara; Kedir Teji Roba; Cyrus Saleem; Nitya Singh; Ibsa Aliyi Usmane; Yang Yang; Getnet Yimer; Sarah McKune
Journal:  BMJ Open       Date:  2022-10-05       Impact factor: 3.006

4.  Establishment and Validation of a Non-Radioactive Method for In Vitro Transcription Assay Using Primer Extension and Quantitative Real Time PCR.

Authors:  Juan Wang; Shasha Zhao; Ying Zhou; Yun Wei; Wensheng Deng
Journal:  PLoS One       Date:  2015-08-07       Impact factor: 3.240

  4 in total

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