Literature DB >> 17850994

Necrotic enteritis-producing strains of Clostridium perfringens displace non-necrotic enteritis strains from the gut of chicks.

Angelique J Barbara1, Hien T Trinh, Robert D Glock, J Glenn Songer.   

Abstract

We inoculated broiler chicks with mixtures of Clostridium perfringens strains to investigate the single strain dominance observed in natural cases of necrotic enteritis (NE) [Nauerby, B., Pedersen, K., Madsen, M., 2003. Analysis by pulsed-field gel electrophoresis of the genetic diversity among Clostridium perfringens isolates from chickens. Vet. Microbiol. 94, 257-266]. Pre-inoculation bacteriologic culture of chick intestines yielded up to six pulsed-field gel electrophoresis (PFGE) types of C. perfringens. Birds developed typical NE lesions in response to administration (2x per day for 4 days) of a combined inoculum comprising one NE strain (JGS4143, PFGE pattern 8) and four non-NE strains (from piglet necrotizing enteritis, chicken normal flora, human gas gangrene, and bovine neonatal enteritis). After inoculation commenced, only the NE strain was recovered through the first post-inoculation day, in spite of intense efforts to recover pre-challenge flora strains and the other challenge strains. Thereafter, pre-inoculation and previously undetected PFGE types were found, and JGS4143 became undetectable. Birds inoculated simultaneously with five NE strains (from disease in chickens or turkeys, and including JGS4143) also developed lesions, but again only JGS4143 was recovered through the 1st day post-challenge. At that time, birds began to be repopulated with pre-challenge PFGE types. Two NE strains (JGS4143 and JGS4064) produced bacteriocins, which inhibited each other and normal flora strains (n=17), while normal flora strains inhibited neither NE strains nor each other. Thus, it appears that naturally occurring dominance of the gut by NE strains can be reproduced experimentally. Bacteriocins directed against normal flora could possibly provide the necessary advantage, although inhibition of one NE strain by another suggests that other factors may be partially or completely responsible for the dominance.

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Year:  2007        PMID: 17850994     DOI: 10.1016/j.vetmic.2007.07.019

Source DB:  PubMed          Journal:  Vet Microbiol        ISSN: 0378-1135            Impact factor:   3.293


  21 in total

1.  Identification of accessory genome regions in poultry Clostridium perfringens isolates carrying the netB plasmid.

Authors:  D Lepp; J Gong; J G Songer; P Boerlin; V R Parreira; J F Prescott
Journal:  J Bacteriol       Date:  2013-01-04       Impact factor: 3.490

2.  Conjugation-Mediated Horizontal Gene Transfer of Clostridium perfringens Plasmids in the Chicken Gastrointestinal Tract Results in the Formation of New Virulent Strains.

Authors:  Jake A Lacey; Anthony L Keyburn; Mark E Ford; Ricardo W Portela; Priscilla A Johanesen; Dena Lyras; Robert J Moore
Journal:  Appl Environ Microbiol       Date:  2017-12-01       Impact factor: 4.792

3.  Identification of novel pathogenicity loci in Clostridium perfringens strains that cause avian necrotic enteritis.

Authors:  Dion Lepp; Bryan Roxas; Valeria R Parreira; Pradeep R Marri; Everett L Rosey; Joshua Gong; J Glenn Songer; Gayatri Vedantam; John F Prescott
Journal:  PLoS One       Date:  2010-05-24       Impact factor: 3.240

4.  Recombinant attenuated Salmonella enterica serovar typhimurium expressing the carboxy-terminal domain of alpha toxin from Clostridium perfringens induces protective responses against necrotic enteritis in chickens.

Authors:  Bereket Zekarias; Hua Mo; Roy Curtiss
Journal:  Clin Vaccine Immunol       Date:  2008-03-12

5.  Clostridium perfringens type E virulence traits involved in gut colonization.

Authors:  Leandro M Redondo; Juan M Díaz Carrasco; Enzo A Redondo; Fernando Delgado; Mariano E Fernández Miyakawa
Journal:  PLoS One       Date:  2015-03-23       Impact factor: 3.240

6.  The mycotoxin deoxynivalenol predisposes for the development of Clostridium perfringens-induced necrotic enteritis in broiler chickens.

Authors:  Gunther Antonissen; Filip Van Immerseel; Frank Pasmans; Richard Ducatelle; Freddy Haesebrouck; Leen Timbermont; Marc Verlinden; Geert Paul Jules Janssens; Venessa Eeckhaut; Mia Eeckhout; Sarah De Saeger; Sabine Hessenberger; An Martel; Siska Croubels
Journal:  PLoS One       Date:  2014-09-30       Impact factor: 3.240

7.  Identification of the replication region in pBCNF5603, a bacteriocin-encoding plasmid, in the enterotoxigenic Clostridium perfringens strain F5603.

Authors:  Kazuaki Miyamoto; Soshi Seike; Teruhisa Takagishi; Kensuke Okui; Masataka Oda; Masaya Takehara; Masahiro Nagahama
Journal:  BMC Microbiol       Date:  2015-06-09       Impact factor: 3.605

Review 8.  Effects of Mycotoxins on mucosal microbial infection and related pathogenesis.

Authors:  Seong-Hwan Park; Dongwook Kim; Juil Kim; Yuseok Moon
Journal:  Toxins (Basel)       Date:  2015-10-30       Impact factor: 4.546

Review 9.  The impact of Fusarium mycotoxins on human and animal host susceptibility to infectious diseases.

Authors:  Gunther Antonissen; An Martel; Frank Pasmans; Richard Ducatelle; Elin Verbrugghe; Virginie Vandenbroucke; Shaoji Li; Freddy Haesebrouck; Filip Van Immerseel; Siska Croubels
Journal:  Toxins (Basel)       Date:  2014-01-28       Impact factor: 4.546

10.  Perfrin, a novel bacteriocin associated with netB positive Clostridium perfringens strains from broilers with necrotic enteritis.

Authors:  Leen Timbermont; Lina De Smet; Filip Van Nieuwerburgh; Valeria R Parreira; Gonzalez Van Driessche; Freddy Haesebrouck; Richard Ducatelle; John Prescott; Dieter Deforce; Bart Devreese; Filip Van Immerseel
Journal:  Vet Res       Date:  2014-04-05       Impact factor: 3.683

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