<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ramatla T</submitter><funding>National Research Foundation</funding><pagination>458</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11117945</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(5)</volume><pubmed_abstract>Rapid growth in commercial poultry production is one of the major sources of &lt;i>Salmonella&lt;/i> infections that leads to human salmonellosis. The two main &lt;i>Salmonella enterica&lt;/i> serovars associated with human salmonellosis are enteritidis and typhimurium. The aim of this study was to determine the prevalence of &lt;i>S. enterica&lt;/i> serovars Enteritidis and &lt;i>S.&lt;/i> Typhimurium as well as their &lt;i>Salmonella&lt;/i> pathogenicity islands (SPI) and antibiotic resistance profiles in broiler chicken feces from slaughterhouses. A total of 480 fecal samples from broiler chickens that were grouped into 96 pooled samples were identified to have &lt;i>Salmonella&lt;/i> spp. using the &lt;i>invA&lt;/i> gene, whilst the &lt;i>Spy&lt;/i> and &lt;i>sdfI&lt;/i> genes were used to screen for the presence of &lt;i>S.&lt;/i> Enteritidis and &lt;i>S.&lt;/i> Typhimurium serovars, respectively, by polymerase chain reaction (PCR) assays. The isolates were also screened for the presence of &lt;i>Salmonella&lt;/i> pathogenicity islands (SPIs) using PCR. The disc diffusion assay was performed to determine the antibiotic resistance profiles of the isolates. A total of 36 isolates were confirmed as &lt;i>Salmonella&lt;/i> spp. through amplification of the &lt;i>invA&lt;/i> gene. Out of 36 confirmed &lt;i>Salmonella&lt;/i> spp. a total of 22 isolates were classified as &lt;i>S&lt;/i>. Enteritidis (n = 8) and were &lt;i>S.&lt;/i> Typhimurium (n = 14) serovars. All (n = 22) &lt;i>S.&lt;/i> Enteritidis and &lt;i>S.&lt;/i> Typhimurium isolates possessed the &lt;i>hilA&lt;/i> (SPI-1), &lt;i>ssrB&lt;/i> (SPI-2) and &lt;i>pagC&lt;/i> (SPI-11) pathogenicity islands genes. Amongst these serovars, 50% of the isolates (n = 11/22) were resistant to tetracycline and nalidixic acid. Only 22% of the isolates, &lt;i>S.&lt;/i> Typhimurium (13.6%) and &lt;i>S.&lt;/i> Enteritidis (9.1%) demonstrated resistance against three or more antibiotic classes. The most detected antibiotic resistance genes were &lt;i>tet&lt;/i>(&lt;i>K&lt;/i>), &lt;i>mcr-1&lt;/i>, &lt;i>sulI&lt;/i> and &lt;i>strA&lt;/i> with 13 (59.1%), 9 (40.9%), 9 (40.9%) and 7 (31.8%), respectively. The findings of this study revealed that &lt;i>S.&lt;/i> Typhimurium is the most prevalent serotype detected in chicken feces. To reduce the risk to human health posed by salmonellosis, a stringent public health and food safety policy is required.</pubmed_abstract><journal>Antibiotics (Basel, Switzerland)</journal><pubmed_title>Detection of &lt;i>Salmonella&lt;/i> Pathogenicity Islands and Antimicrobial-Resistant Genes in &lt;i>Salmonella enterica&lt;/i> Serovars Enteritidis and Typhimurium Isolated from Broiler Chickens.</pubmed_title><pmcid>PMC11117945</pmcid><funding_grant_id>118949</funding_grant_id><pubmed_authors>Mokgokong P</pubmed_authors><pubmed_authors>Ndou R</pubmed_authors><pubmed_authors>Ramaili T</pubmed_authors><pubmed_authors>Lekota K</pubmed_authors><pubmed_authors>Mlangeni LN</pubmed_authors><pubmed_authors>Thekisoe O</pubmed_authors><pubmed_authors>Nkhebenyane JS</pubmed_authors><pubmed_authors>Ramatla T</pubmed_authors><pubmed_authors>Khasapane NG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Detection of &lt;i>Salmonella&lt;/i> Pathogenicity Islands and Antimicrobial-Resistant Genes in &lt;i>Salmonella enterica&lt;/i> Serovars Enteritidis and Typhimurium Isolated from Broiler Chickens.</name><description>Rapid growth in commercial poultry production is one of the major sources of &lt;i>Salmonella&lt;/i> infections that leads to human salmonellosis. The two main &lt;i>Salmonella enterica&lt;/i> serovars associated with human salmonellosis are enteritidis and typhimurium. The aim of this study was to determine the prevalence of &lt;i>S. enterica&lt;/i> serovars Enteritidis and &lt;i>S.&lt;/i> Typhimurium as well as their &lt;i>Salmonella&lt;/i> pathogenicity islands (SPI) and antibiotic resistance profiles in broiler chicken feces from slaughterhouses. A total of 480 fecal samples from broiler chickens that were grouped into 96 pooled samples were identified to have &lt;i>Salmonella&lt;/i> spp. using the &lt;i>invA&lt;/i> gene, whilst the &lt;i>Spy&lt;/i> and &lt;i>sdfI&lt;/i> genes were used to screen for the presence of &lt;i>S.&lt;/i> Enteritidis and &lt;i>S.&lt;/i> Typhimurium serovars, respectively, by polymerase chain reaction (PCR) assays. The isolates were also screened for the presence of &lt;i>Salmonella&lt;/i> pathogenicity islands (SPIs) using PCR. The disc diffusion assay was performed to determine the antibiotic resistance profiles of the isolates. A total of 36 isolates were confirmed as &lt;i>Salmonella&lt;/i> spp. through amplification of the &lt;i>invA&lt;/i> gene. Out of 36 confirmed &lt;i>Salmonella&lt;/i> spp. a total of 22 isolates were classified as &lt;i>S&lt;/i>. Enteritidis (n = 8) and were &lt;i>S.&lt;/i> Typhimurium (n = 14) serovars. All (n = 22) &lt;i>S.&lt;/i> Enteritidis and &lt;i>S.&lt;/i> Typhimurium isolates possessed the &lt;i>hilA&lt;/i> (SPI-1), &lt;i>ssrB&lt;/i> (SPI-2) and &lt;i>pagC&lt;/i> (SPI-11) pathogenicity islands genes. Amongst these serovars, 50% of the isolates (n = 11/22) were resistant to tetracycline and nalidixic acid. Only 22% of the isolates, &lt;i>S.&lt;/i> Typhimurium (13.6%) and &lt;i>S.&lt;/i> Enteritidis (9.1%) demonstrated resistance against three or more antibiotic classes. The most detected antibiotic resistance genes were &lt;i>tet&lt;/i>(&lt;i>K&lt;/i>), &lt;i>mcr-1&lt;/i>, &lt;i>sulI&lt;/i> and &lt;i>strA&lt;/i> with 13 (59.1%), 9 (40.9%), 9 (40.9%) and 7 (31.8%), respectively. The findings of this study revealed that &lt;i>S.&lt;/i> Typhimurium is the most prevalent serotype detected in chicken feces. To reduce the risk to human health posed by salmonellosis, a stringent public health and food safety policy is required.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-04-16T03:22:22.889Z</modification><creation>2026-04-16T03:13:02.125Z</creation></dates><accession>S-EPMC11117945</accession><cross_references><pubmed>38786186</pubmed><doi>10.3390/antibiotics13050458</doi></cross_references></HashMap>