Quantitative assessment and genomic profiling of Campylobacter dynamics in poultry processing: a case study in the United Arab Emirates integrated abattoir system

In the United Arab Emirates, no previous research has investigated the dynamics of the foodborne pathogen <i>Campylobacter</i> in broiler abattoir processing. This study conducted in one of the largest poultry producers in the UAE, following each key slaughter stage-defeathering, evisceration, and final chilling-five broiler carcasses were collected from 10 slaughter batches over a year. Additionally, one caecum was obtained from 15 chickens in each slaughter batch to evaluate the flock colonization. In total, 300 samples (150 carcasses and 150 caeca) were collected and enumerated for <i>Campylobacter</i> using standard methods. <i>Campylobacter</i> was pervasive in caecal samples from all slaughter batches, with 86% of carcasses post-defeathering and evisceration stages and 94% post-chilling tested positive for <i>Campylobacter</i>. <i>Campylobacter coli</i> predominates in 55.2% of positive samples, followed by <i>Campylobacter jejuni</i> in 21%, with both species co-existing in 23.8% of the samples. <i>Campylobacter</i> counts in caecal contents ranged from 6.7 to 8.5 log<sub>10</sub> CFU/g, decreasing post-defeathering and evisceration to 3.5 log<sub>10</sub> CFU/g of neck skin and further to 3.2 log<sub>10</sub> CFU/g of neck skin post-evisceration. After chilling, 70% of carcasses exceeded 3 log<sub>10</sub> CFU/g of neck skin. Whole-genome sequencing (WGS) of 48 isolates unveiled diverse sequence types and clusters, with isolates sharing the same clusters (less than 20 single nucleotide polymorphisms) between different farms, different flocks within the same farm, as well as in consecutive slaughter batches, indicating cross-contamination. Multiple antimicrobial resistance genes and mutations in <i>gyrA</i> T86I (conferring fluoroquinolone resistance) and an RNA mutation (23S r.2075; conferring macrolide resistance) were widespread, with variations between <i>C. coli</i> and <i>C. jejuni</i>. WGS results revealed that selected virulence genes (<i>pglG, pseD, pseI, flaA, flaB, cdtA,</i> and <i>cdtC</i>) were significantly present in <i>C. jejuni</i> compared to <i>C. coli</i> isolates. This study offers the first insights into <i>Campylobacter</i> dynamics in poultry processing in the UAE. This work provides a base for future research to explore additional contributors to <i>Campylobacter</i> contamination in primary production. In conclusion, effective <i>Campylobacter</i> management demands a comprehensive approach addressing potential contamination sources at every production and processing stage, guided by continued microbiological surveillance and genomic analysis to safeguard public health and food safety.

Authors

Institutions

Publication Details

Journal
Frontiers in Microbiology
Published
2024-09-04
DOI
https://doi.org/10.3389/fmicb.2024.1439424
Citations
4
Primary Topic
Salmonella and Campylobacter epidemiology
Type
article
Field-Weighted Citation Impact
1.39

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Quantitative assessment and genomic profiling of Campylobacter dynamics in poultry processing: a case study in the United Arab Emirates integrated abattoir system

Hanan Sobhy Afifi, Mohamed-Yousif Ibrahim Mohamed, Akela Ghazawi, Afra Abdalla et al.
4 citations
Frontiers in Microbiology
Salmonella and Campylobacter epidemiology
1.39
article

Quantitative assessment and genomic profiling of Campylobacter dynamics in poultry processing: a case study in the United Arab Emirates integrated abattoir system

Hanan Sobhy Afifi, Mohamed-Yousif Ibrahim Mohamed, Akela Ghazawi, Afra Abdalla, Mohamed G. Shehata, Hassan Mohamed Al Marzooqi, Glindya Bhagya Lakshmi, Ihab Habib, Febin Anes, Mushtaq Ahmad Khan
article en
4 citations

Abstract

In the United Arab Emirates, no previous research has investigated the dynamics of the foodborne pathogen <i>Campylobacter</i> in broiler abattoir processing. This study conducted in one of the largest poultry producers in the UAE, following each key slaughter stage-defeathering, evisceration, and final chilling-five broiler carcasses were collected from 10 slaughter batches over a year. Additionally, one caecum was obtained from 15 chickens in each slaughter batch to evaluate the flock colonization. In total, 300 samples (150 carcasses and 150 caeca) were collected and enumerated for <i>Campylobacter</i> using standard methods. <i>Campylobacter</i> was pervasive in caecal samples from all slaughter batches, with 86% of carcasses post-defeathering and evisceration stages and 94% post-chilling tested positive for <i>Campylobacter</i>. <i>Campylobacter coli</i> predominates in 55.2% of positive samples, followed by <i>Campylobacter jejuni</i> in 21%, with both species co-existing in 23.8% of the samples. <i>Campylobacter</i> counts in caecal contents ranged from 6.7 to 8.5 log<sub>10</sub> CFU/g, decreasing post-defeathering and evisceration to 3.5 log<sub>10</sub> CFU/g of neck skin and further to 3.2 log<sub>10</sub> CFU/g of neck skin post-evisceration. After chilling, 70% of carcasses exceeded 3 log<sub>10</sub> CFU/g of neck skin. Whole-genome sequencing (WGS) of 48 isolates unveiled diverse sequence types and clusters, with isolates sharing the same clusters (less than 20 single nucleotide polymorphisms) between different farms, different flocks within the same farm, as well as in consecutive slaughter batches, indicating cross-contamination. Multiple antimicrobial resistance genes and mutations in <i>gyrA</i> T86I (conferring fluoroquinolone resistance) and an RNA mutation (23S r.2075; conferring macrolide resistance) were widespread, with variations between <i>C. coli</i> and <i>C. jejuni</i>. WGS results revealed that selected virulence genes (<i>pglG, pseD, pseI, flaA, flaB, cdtA,</i> and <i>cdtC</i>) were significantly present in <i>C. jejuni</i> compared to <i>C. coli</i> isolates. This study offers the first insights into <i>Campylobacter</i> dynamics in poultry processing in the UAE. This work provides a base for future research to explore additional contributors to <i>Campylobacter</i> contamination in primary production. In conclusion, effective <i>Campylobacter</i> management demands a comprehensive approach addressing potential contamination sources at every production and processing stage, guided by continued microbiological surveillance and genomic analysis to safeguard public health and food safety.

Frontiers in MicrobiologyVol. 15
United Arab Emirates University (AE), Abu Dhabi Health Services (AE), City of Scientific Research and Technological Applications (EG)
United Arab Emirates University
Openalex Percentile: Top 19%
Salmonella and Campylobacter epidemiology
1.39
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.