Habib Ihab, Mohamed Mohamed-Yousif Ibrahim, Lakshmi Glindya Bhagya, Al Marzooqi Hassan Mohamed, Afifi Hanan Sobhy, Shehata Mohamed Gamal, Khan Mushtaq, Ghazawi Akela, Abdalla Afra, Anes Febin
Veterinary Public Health Research Laboratory, Department of Veterinary Medicine, College of Agriculture and Veterinary Medicine, United Arab Emirates University, Al Ain, United Arab Emirates.
ASPIRE Research Institute for Food Security in the Drylands (ARIFSID), United Arab Emirates University, Al Ain, United Arab Emirates.
Front Microbiol. 2024 Sep 4;15:1439424. doi: 10.3389/fmicb.2024.1439424. eCollection 2024.
In the United Arab Emirates, no previous research has investigated the dynamics of the foodborne pathogen 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 using standard methods. 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 . predominates in 55.2% of positive samples, followed by in 21%, with both species co-existing in 23.8% of the samples. counts in caecal contents ranged from 6.7 to 8.5 log CFU/g, decreasing post-defeathering and evisceration to 3.5 log CFU/g of neck skin and further to 3.2 log CFU/g of neck skin post-evisceration. After chilling, 70% of carcasses exceeded 3 log 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 T86I (conferring fluoroquinolone resistance) and an RNA mutation (23S r.2075; conferring macrolide resistance) were widespread, with variations between and . WGS results revealed that selected virulence genes ( and ) were significantly present in compared to isolates. This study offers the first insights into dynamics in poultry processing in the UAE. This work provides a base for future research to explore additional contributors to contamination in primary production. In conclusion, effective 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.
在阿拉伯联合酋长国,此前尚无研究调查过肉鸡屠宰场加工过程中食源性病原体的动态变化。本研究在阿联酋最大的家禽生产商之一开展,在一年时间里,从10个屠宰批次的每个关键屠宰阶段(脱毛、开膛和最终冷却)收集5只肉鸡胴体。此外,从每个屠宰批次的15只鸡中获取一个盲肠,以评估鸡群的定植情况。总共收集了300个样本(150个胴体和150个盲肠),并使用标准方法进行计数。在所有屠宰批次的盲肠样本中普遍存在,脱毛和开膛阶段后86%的胴体以及冷却后94%的胴体检测呈阳性。在55.2%的阳性样本中占主导地位,其次是在21%的样本中,两种菌在23.8%的样本中共存。盲肠内容物中的计数范围为6.7至8.5 log CFU/g,脱毛和开膛后降至颈部皮肤的3.5 log CFU/g,开膛后进一步降至颈部皮肤的3.2 log CFU/g。冷却后,70%的胴体颈部皮肤超过3 log CFU/g。对48株分离株进行全基因组测序(WGS)揭示了不同的序列类型和簇,不同农场、同一农场内不同鸡群以及连续屠宰批次之间的分离株共享相同的簇(单核苷酸多态性少于20个),表明存在交叉污染。多种抗菌抗性基因以及T86I(赋予氟喹诺酮抗性)中的突变和一个RNA突变(23S r.2075;赋予大环内酯抗性)广泛存在,和之间存在差异。WGS结果显示,与分离株相比,选定的毒力基因(和)在中显著存在。本研究首次深入了解了阿联酋家禽加工过程中的动态变化。这项工作为未来研究探索初级生产过程中污染的其他促成因素奠定了基础。总之,有效的管理需要一种全面的方法,在持续的微生物监测和基因组分析的指导下,应对每个生产和加工阶段的潜在污染源,以保障公众健康和食品安全。