Open AccessHighly clonal relationship among Salmonella Enteritidis isolates in a commercial chicken production chain, Brazil
Author(s) -
Daniel F.M. Monte,
Cristiano Andrigheto,
Vinícius Buccelli Ribeiro,
Mariza Landgraf,
Maria Teresa Destro
Publication year - 2020
Publication title -
brazilian journal of microbiology
Language(s) - English
Resource type - Journals
eISSN - 1678-4405
pISSN - 1517-8382
DOI - 10.1007/s42770-020-00372-4
Subject(s) - subtyping , biology , ribotyping , pulsed field gel electrophoresis , microbiology and biotechnology , salmonella enteritidis , rapd , ampicillin , phage typing , antibiotic resistance , genotyping , salmonella , typing , genetics , polymerase chain reaction , antibiotics , genotype , gene , bacteria , population , demography , sociology , computer science , genetic diversity , programming language
In this study, we described the comparison among pulsed-field gel electrophoresis (PFGE), random amplified polymorphic DNA (RAPD), ribotyping, and PCR-ribotyping methods for subtyping Salmonella Enteritidis isolated from an industrial chicken production chain. One hundred and eight S. Enteritidis were isolated at all stages of poultry meat processing plant. These isolates were pheno- and genotypically characterized by using antimicrobial susceptibility test, phage typing, RAPD, PFGE, ribotyping, and PCR-ribotyping. The highest antibiotic resistance rates were observed for enrofloxacin (18.5%) followed by furazolidone (15.7%), cefoxitin (1.8%), ciprofloxacin, and ampicillin with 0.9% each one, while seven isolates (6.4%) were pan-susceptible. Most strains belonged to the globally disseminated phage type PT4 (n = 74; 69.2%). Additionally, we identified strains belonging to phage types PT1 (n = 19; 17.8%) and PT7a (n = 14; 13.1%). Moreover, our results showed that these four molecular methods indicate similar results showing high similarity (≥ 90%) among S. Enteritidis strains, suggesting that these isolates appear to be from a common ancestor being spread at all stages of the poultry production chain. In summary, the combined molecular approaches of these methods remain a suitable alternative to efficiently subtyping S. Enteritidis in the absence of high-resolution genotyping methods and these results may serve as a baseline study for development of mitigation strategies.