Title: Application of PCR-based serogrouping of Salmonellaenterica serotypes isolated from the poultry in Egypt | ||||
| SVU-International Journal of Veterinary Sciences | ||||
| Volume 7, Issue 1 - Serial Number 19, March 2024, Page 62-70 PDF (237.71 K) | ||||
| Document Type: Research article | ||||
| DOI: 10.21608/svu.2024.236263.1295 | ||||
 View on SCiNiTO | ||||
| Authors | ||||
Mona A.A. AbdelRahman  1; Amany Adel1; Abdelhafez Samir1; Wafaa A. A. Ibrahim2; Heba M Hassan1
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| 1Reference Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Agricultural Research Center (ARC), Nadi El-Seid Street, Dokki P.O. Box 246, Giza 12618, Egypt. | ||||
| 2Biotechnology Department, Reference Laboratory for Veterinary Quality Control On Poultry Production, Animal Health Research Institute, Agricultural Research Center (ARC), Ismailia, Egypt | ||||
| Abstract | ||||
| Salmonella spp. remains a significant concern in poultry flocks due to its potential impact on both animal health and public health. In this study, a comprehensive approach to isolate, serotype, and identify Salmonella strains from poultry flocks was employed. A total of 350 samples were collected, including internal organs liver, lung and cecum, from poultry flocks. Salmonella isolates were isolated and characterized according to established protocols. Conventional serotyping was performed based on the Kauffman–White scheme using Salmonella antisera, and the results were classified into various serogroups. To enhance the efficiency of serotyping, a multiplex PCR assay targeting both O and H antigens was developed. DNA extraction from collected samples followed the boiling method the multiplex PCR assay used specific primers for various serogroups. Out of the 350 samples tested, approximately 14.2% were positive for Salmonella. A total of 50 Salmonella isolates were serotyped, and the strains were categorized into several serogroups including B, D1, E1, C1, and C3. The multiplex PCR assay successfully identified O and H antigens, revealing a prevalence of serogroup B (46%) and D1 (32%) strains. Interestingly, none of the Salmonella strains exhibited the Vi antigen. This investigation showcased the precision and effectiveness of the multiplex PCR technique in identifying Salmonella strains. Notably, the multiplex PCR yielded outcomes surpassing those of traditional serotyping using the Kaufmann White scheme, all within a notably reduced time frame. In conclusion, the study highlights and presents a rapid and reliable method for serotyping and identifying Salmonella strains using multiplex PCR. This approach has the potential to expedite the control and prevention of Salmonella transmission, contributing to improved poultry health and reduced public health risks associated with Salmonella infections. The rapidity and accuracy of the multiplex PCR method make it particularly suitable for international efforts to monitor and manage Salmonella outbreaks effectively. The study highlighted the precision and effectiveness of multiplex PCR in identifying Salmonella strains, surpassing traditional serotyping in speed and accuracy. In conclusion, the research introduced a rapid and reliable method for Salmonella serotyping and identification using multiplex PCR, with the potential to expedite Salmonella control, benefiting poultry health and public health. This advancement holds promise for enhancing food safety and safeguarding both animal and human health in the poultry industry. Key words: Serotyping; Salmonella, PCR, flagellar antigens | ||||
| Keywords | ||||
| Key words: Serotyping; Salmonella, PCR, flagellar antigens | ||||
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