Literature DB >> 32938740

A Novel Real-Time PCR-Based Screening Test with Pooled Fecal Samples for Bovine Johne's Disease.

Satoko Kawaji1, Reiko Nagata2, Yasutaka Minegishi3, Yumi Saruyama4, Akiko Mita5, Shingo Kishizuka5, Masahiro Saito5, Yasuyuki Mori2.   

Abstract

Johne's disease (JD) is an economically important infectious disease in livestock farming caused by Mycobacterium avium subsp. paratuberculosis As an alternative to serological tests, which are used mainly for the screening of whole herds, we developed a novel ResoLight-based real-time PCR (RL-PCR) assay with pooled fecal samples for the detection of fecal shedders in cattle herds. The RL-PCR assay included an internal amplification control (IC) which was amplified using the same primer pair as the target molecule M. avium subsp. paratuberculosis IS900 and differentiated based on melting temperatures. Individual fecal suspensions were pooled and concentrated by centrifugation to avoid a loss of sensitivity by the dilution effect. Combined with a DNA extraction kit (Johne-PureSpin; FASMAC), no inhibition of PCR amplification was observed with up to 15 fecal samples in a pool. The detection limit of RL-PCR at a pool size of 10 was 10 M. avium subsp. paratuberculosis organisms per gram of feces, which was comparable to that of individual testing. A total of 2,654 animals in 12 infected herds were screened by individual antibody-enzyme-linked immunosorbent assay (ELISA) and the RL-PCR assay using pooled feces. Fifty animals were diagnosed with JD through the screening by RL-PCR, compared with only 5 by ELISA (which were also positive in RL-PCR). In 7 JD-free herds, the results of 4 out of 327 pools (1.2%) were invalid due to the lack of IC amplification, and then animals were confirmed negative individually. Our results suggest that implementation of herd screening by pooled RL-PCR would advance the monitoring and control of JD in cattle herds.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  Johne’s disease; internal control; pooled feces; real-time PCR; screening test

Year:  2020        PMID: 32938740      PMCID: PMC7685889          DOI: 10.1128/JCM.01761-20

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  33 in total

1.  Making internal amplification control mandatory for diagnostic PCR.

Authors:  Jeffrey Hoorfar; Nigel Cook; Burkhard Malorny; Martin Wagner; Dario De Medici; Amir Abdulmawjood; Patrick Fach
Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

Review 2.  Practical considerations in design of internal amplification controls for diagnostic PCR assays.

Authors:  J Hoorfar; B Malorny; A Abdulmawjood; N Cook; M Wagner; P Fach
Journal:  J Clin Microbiol       Date:  2004-05       Impact factor: 5.948

3.  A longitudinal study to evaluate the diagnostic potential of a direct faecal quantitative PCR test for Johne's disease in sheep.

Authors:  Satoko Kawaji; Douglas J Begg; Karren M Plain; Richard J Whittington
Journal:  Vet Microbiol       Date:  2010-08-05       Impact factor: 3.293

4.  Evaluation of fecal shedding and antibody response in dairy cattle infected with paratuberculosis using national surveillance data in Japan.

Authors:  Takehisa Yamamoto; Kiyokazu Murai; Yoko Hayama; Sota Kobayashi; Reiko Nagata; Satoko Kawaji; Makoto Osaki; Shin-Ichi Sakakibara; Toshiyuki Tsutsui
Journal:  Prev Vet Med       Date:  2017-11-11       Impact factor: 2.670

5.  Evaluation of five antibody detection tests for diagnosis of bovine paratuberculosis.

Authors:  Michael T Collins; Scott J Wells; Kristine R Petrini; James E Collins; Ronald D Schultz; Robert H Whitlock
Journal:  Clin Diagn Lab Immunol       Date:  2005-06

Review 6.  A review of bovine Johne's disease control activities in 6 endemically infected countries.

Authors:  Timothy Geraghty; David A Graham; Peter Mullowney; Simon J More
Journal:  Prev Vet Med       Date:  2014-06-19       Impact factor: 2.670

7.  High-resolution genotyping by amplicon melting analysis using LCGreen.

Authors:  Carl T Wittwer; Gudrun H Reed; Cameron N Gundry; Joshua G Vandersteen; Robert J Pryor
Journal:  Clin Chem       Date:  2003-06       Impact factor: 8.327

8.  Use of lambda phage DNA as a hybrid internal control in a PCR-enzyme immunoassay to detect Chlamydia pneumoniae.

Authors:  D G Pham; G E Madico; T C Quinn; M J Enzler; T F Smith; C A Gaydos
Journal:  J Clin Microbiol       Date:  1998-07       Impact factor: 5.948

9.  Calves shedding Mycobacterium avium subspecies paratuberculosis are common on infected dairy farms.

Authors:  Robert Wolf; Karin Orsel; Jeroen De Buck; Herman Wildrik Barkema
Journal:  Vet Res       Date:  2015-06-19       Impact factor: 3.683

10.  Comparison of fecal pooling methods and DNA extraction kits for the detection of Mycobacterium avium subspecies paratuberculosis.

Authors:  Akiko Mita; Yasuyuki Mori; Tetsuo Nakagawa; Tomoko Tasaki; Katsuo Utiyama; Hitomi Mori
Journal:  Microbiologyopen       Date:  2015-12-15       Impact factor: 3.139

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  1 in total

1.  Development and Validation of a Novel ELISA for the Specific Detection of Antibodies against Mycobacterium avium Subspecies paratuberculosis Based on a Chimeric Polyprotein.

Authors:  Roberto Damián Moyano; Magali Andrea Romero; María Alejandra Colombatti Olivieri; María Fiorella Alvarado Pinedo; Gabriel Eduardo Traveria; María Isabel Romano; María Natalia Alonso
Journal:  Vet Med Int       Date:  2021-12-29
  1 in total

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