ArticlePloS one2013
Genetic diversity of food-isolated Salmonella strains through Pulsed Field Gel Electrophoresis (PFGE) and Enterobacterial Repetitive Intergenic Consensus (ERIC-PCR).
Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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Who cites it
22 citing papers in PubMed.
- Serovars, Genetic Relatedness and Antimicrobial Resistance of Non-TyphoidalMicroorganisms · 2026Article
- From Phenotype to Genotype: A Clonal Perspective on Virulence and Biofilm Formation in Bloodstream-DerivedInfection and drug resistance · 2026Article
- Helicobacter pylori in Turkish Children with Dyspepsia: Diagnosis, Prevalence, Genotyping and Antibiotic Resistance.Indian journal of pediatrics · 2026Article
- Does Every Strain ofPathogens (Basel, Switzerland) · 2024Article
- Salmonella enterica serovars linked with poultry in India: antibiotic resistance profiles and carriage of virulence genes.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024Article
- Ecological prevalence, genetic diversity, and multidrug resistance of Salmonella enteritidis recovered from broiler and layer chicken farms.Poultry science · 2024Article
- Characterization of genotypes and antimicrobial resistance profiles of clinical isolates of Shigella from patients in the southern region of Iran.European journal of medical research · 2023Article
- A comprehensive study of Helicobacter pylori infection: molecular analysis, antibacterial susceptibility, and histopathological examination.Antonie van Leeuwenhoek · 2023Article
- The Impact of Chlorine Disinfection of Hospital Wastewater on Clonal Similarity and ESBL-Production in Selected Bacteria of the Family Enterobacteriaceae.International journal of environmental research and public health · 2022Article
- Molecular Epidemiology ofInternational journal of microbiology · 2022Article
- Molecular characterization of antimicrobial resistance and enterobacterial repetitive intergenic consensus-PCR as a molecular typing tool forVeterinary world · 2020Article
- Isolation, conventional and molecular characterization of Salmonella spp. from newly hatched broiler chicks.AMB Express · 2019Article
- Laboratory characterisation of Salmonella enterica serotype Typhi isolates from Zimbabwe, 2009-2017.BMC infectious diseases · 2019Article
- Analysis ofTropical life sciences research · 2019Article
- Genetic characterization of antibiotic-resistantSaudi journal of biological sciences · 2018Article
- Occurrence, antimicrobial susceptibility patterns and genotypic relatedness of Salmonella spp. isolates from captive wildlife, their caretakers, feed and water in India.Epidemiology and infection · 2018Article
- Isolation, Identification, Prevalence, and Genetic Diversity ofFrontiers in microbiology · 2018Article
- Detection and Characterization ofFrontiers in microbiology · 2018Article
- Screening and DetectingFrontiers in microbiology · 2017Article
- Diverse distribution of Toxin-Antitoxin II systems in Salmonella enterica serovars.Scientific reports · 2016Article
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
All over the world, the incidence of Salmonella spp contamination on different food sources like broilers, clams and cow milk has increased rapidly in recent years. The multifaceted properties of Salomnella serovars allow the microorganism to grow and multiply in various food matrices, even under adverse conditions. Therefore, methods are needed to detect and trace this pathogen along the entire food supply network. In the present work, PFGE and ERIC-PCR were used to subtype 45 Salmonella isolates belonging to different serovars and derived from different food origins. Among these isolates, S. Enteritidis and S. Kentucky were found to be the most predominant serovars. The Discrimination Index obtained by ERIC-PCR (0.85) was slightly below the acceptable confidence value. The best discriminatory ability was observed when PFGE typing method was used alone (DI = 0.94) or combined with ERIC-PCR (DI = 0.93). A wide variety of profiles was observed between the different serovars using PFGE or/and ERIC-PCR. This diversity is particularly important when the sample origins are varied and even within the same sampling origin.
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