Literature DB >> 24934261

Repeated cycles of chemical and physical disinfection and their influence on Mycobacterium avium subsp. paratuberculosis viability measured by propidium monoazide F57 quantitative real time PCR.

Petr Kralik1, Vladimir Babak2, Radka Dziedzinska2.   

Abstract

Mycobacterium avium subsp. paratuberculosis (MAP) has a high degree of resistance to chemical and physical procedures frequently used for the elimination of other bacteria. Recently, a method for the determination of viability by exposure of MAP to propidium monoazide (PMA) and subsequent real time quantitative PCR (qPCR) was established and found to be comparable with culture. The aim of this study was to apply the PMA qPCR method to determine the impact of increasing concentration or time and repeated cycles of the application of selected disinfectants on MAP viability. Different MAP isolates responded to the same type of stress in different ways. The laboratory strain CAPM 6381 had the highest tolerance, while the 8819 low-passage field isolate was the most sensitive. Ultraviolet exposure caused only a partial reduction in MAP viability; all MAP isolates were relatively resistant to chlorine. Only the application of peracetic acid led to the total elimination of MAP. Repeated application of the treatments resulted in more significant decreases in MAP viability compared to single increases in the concentration or time of exposure to the disinfectant.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Disinfection; Mycobacterium avium subsp. paratuberculosis; Propidium monoazide quantitative PCR; Viability

Mesh:

Substances:

Year:  2014        PMID: 24934261     DOI: 10.1016/j.tvjl.2014.05.032

Source DB:  PubMed          Journal:  Vet J        ISSN: 1090-0233            Impact factor:   2.688


  6 in total

1.  Molecular Viability Testing of UV-Inactivated Bacteria.

Authors:  Kris M Weigel; Felicia K Nguyen; Moira R Kearney; John S Meschke; Gerard A Cangelosi
Journal:  Appl Environ Microbiol       Date:  2017-05-01       Impact factor: 4.792

2.  A Rapid Method for Quantifying Viable Mycobacterium avium subsp. paratuberculosis in Cellular Infection Assays.

Authors:  Hannah B Pooley; Kumudika de Silva; Auriol C Purdie; Douglas J Begg; Richard J Whittington; Karren M Plain
Journal:  Appl Environ Microbiol       Date:  2016-08-30       Impact factor: 4.792

3.  Improved Culture Medium (TiKa) for Mycobacterium avium Subspecies Paratuberculosis (MAP) Matches qPCR Sensitivity and Reveals Significant Proportions of Non-viable MAP in Lymphoid Tissue of Vaccinated MAP Challenged Animals.

Authors:  Tim J Bull; Tulika Munshi; Heidi Mikkelsen; Sofie B Hartmann; Maria R Sørensen; Joanna S Garcia; Paula M Lopez-Perez; Sven Hofmann; Kai Hilpert; Gregers Jungersen
Journal:  Front Microbiol       Date:  2017-01-04       Impact factor: 5.640

4.  The Impact of the Antimicrobial Compounds Produced by Lactic Acid Bacteria on the Growth Performance of Mycobacterium avium subsp. paratuberculosis.

Authors:  Petr Kralik; Vladimir Babak; Radka Dziedzinska
Journal:  Front Microbiol       Date:  2018-04-03       Impact factor: 5.640

5.  Modelling Bovine Granuloma Formation In Vitro upon Infection with Mycobacterium Avium Subspecies Paratuberculosis.

Authors:  J Hunter Rice; Margaret M McDaniel; Alyson Holland; Shigetoshi Eda
Journal:  Vet Sci       Date:  2019-10-12

6.  The bactericidal effect of two photoactivated chromophore for keratitis-corneal crosslinking protocols (standard vs. accelerated) on bacterial isolates associated with infectious keratitis in companion animals.

Authors:  Anja Suter; Sarah Schmitt; Ella Hübschke; Malwina Kowalska; Sonja Hartnack; Simon Pot
Journal:  BMC Vet Res       Date:  2022-08-17       Impact factor: 2.792

  6 in total

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