» Articles » PMID: 19114530

Poultry-associated Salmonella Enterica Subsp. Enterica Serovar 4,12:d:- Reveals High Clonality and a Distinct Pathogenicity Gene Repertoire

Overview
Date 2008 Dec 31
PMID 19114530
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

A European baseline survey during the years 2005 and 2006 has revealed that the monophasic Salmonella enterica subsp. enterica serovar 4,12:d:- was, with a prevalence of 23.6%, the most frequently isolated serovar in German broiler flocks. In Denmark and the United Kingdom, its serovar prevalences were 15.15% and 2.8%, respectively. Although poultry is a major source of human salmonellosis, serovar 4,12:d:- is rarely isolated in humans (approximately 0.09% per year). Molecular typing studies using pulsed-field gel electrophoresis and DNA microarray analysis show that the serovar is highly clonal and lacks genes with known contributions to pathogenicity. In contrast to other poultry-associated serovars, all strains were susceptible to 17 antimicrobial agents tested and did not encode any resistance determinant. Furthermore, serovar 4,12:d:- lacked the genes involved in galactonate metabolism and in the glycolysis and glyconeogenesis important for energy production in the cells. The conclusion of the study is that serovar 4,12:d:- seems to be primarily adapted to broilers and therefore causes only rare infections in humans.

Citing Articles

Virulence and antimicrobial resistance factors in serotypes isolated from pigs and chickens in central Chile.

Retamal P, Gaspar J, Benavides M, Saenz L, Galarce N, Aravena T Front Vet Sci. 2022; 9:971246.

PMID: 36204291 PMC: 9530323. DOI: 10.3389/fvets.2022.971246.


Investigation of class 1 integrons and virulence genes in the emergent Salmonella serovar Infantis in Turkey.

Namli S, Soyer Y Int Microbiol. 2021; 25(2):259-265.

PMID: 34559352 DOI: 10.1007/s10123-021-00212-x.


Iron-Uptake Systems of Chicken-Associated Serovars and Their Role in Colonizing the Avian Host.

Wellawa D, Allan B, White A, Koster W Microorganisms. 2020; 8(8).

PMID: 32784620 PMC: 7465098. DOI: 10.3390/microorganisms8081203.


Microbial Diagnostic Microarrays for the Detection and Typing of Food- and Water-Borne (Bacterial) Pathogens.

Kostic T, Sessitsch A Microarrays (Basel). 2016; 1(1):3-24.

PMID: 27605332 PMC: 5007712. DOI: 10.3390/microarrays1010003.


Genome-wide methylation patterns in Salmonella enterica Subsp. enterica Serovars.

Pirone-Davies C, Hoffmann M, Roberts R, Muruvanda T, Timme R, Strain E PLoS One. 2015; 10(4):e0123639.

PMID: 25860355 PMC: 4393132. DOI: 10.1371/journal.pone.0123639.


References
1.
Carattoli A, Bertini A, Villa L, Falbo V, Hopkins K, Threlfall E . Identification of plasmids by PCR-based replicon typing. J Microbiol Methods. 2005; 63(3):219-28. DOI: 10.1016/j.mimet.2005.03.018. View

2.
Gillespie I, OBrien S, Adak G, Ward L, Smith H . Foodborne general outbreaks of Salmonella Enteritidis phage type 4 infection, England and Wales, 1992-2002: where are the risks?. Epidemiol Infect. 2005; 133(5):795-801. PMC: 2870308. DOI: 10.1017/S0950268805004474. View

3.
Yoshida C, Franklin K, Konczy P, McQuiston J, Fields P, Nash J . Methodologies towards the development of an oligonucleotide microarray for determination of Salmonella serotypes. J Microbiol Methods. 2007; 70(2):261-71. DOI: 10.1016/j.mimet.2007.04.018. View

4.
Boyd E, Hartl D . Salmonella virulence plasmid. Modular acquisition of the spv virulence region by an F-plasmid in Salmonella enterica subspecies I and insertion into the chromosome of subspecies II, IIIa, IV and VII isolates. Genetics. 1998; 149(3):1183-90. PMC: 1460215. DOI: 10.1093/genetics/149.3.1183. View

5.
Cooke F, Wain J, Fookes M, Ivens A, Thomson N, Brown D . Prophage sequences defining hot spots of genome variation in Salmonella enterica serovar Typhimurium can be used to discriminate between field isolates. J Clin Microbiol. 2007; 45(8):2590-8. PMC: 1951247. DOI: 10.1128/JCM.00729-07. View