Journals / Etlik Veteriner Mikrobiyoloji Dergisi / 2019 / Cilt: 30 - Sayı: 2

Development of qPCR Diagnostic Kit for Salmonella Gallinarum and Salmonella Pullorum

Salmonella Gallinarum ve Salmonella Pullorum için qPCR Tanı Kitinin Geliştirilmesi

Pages
137–142
Publication Date
2019-12-27
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The results showed that the developed qPCR method was able to detect Salmonella Gallinarum/Pullorum correctly.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Salmonella Gallinarum and Salmonella Pullorum cause important disease of chicken, the others are turkey, quail, pigeon, sparrow and parrot, which are host specific and biovars of each other.
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Key Findings & Data:Therefore, rapid and reliable meth-ods to detect these poultry-associated Salmonella serotypes are necessary for efficient control of Salmonella in poultry.
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Conclusion & Impact:The results showed that the developed qPCR method was able to detect Salmonella Gallinarum/Pullorum correctly.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Salmonella · qPCR · tanı

Abstract

Salmonella Gallinarum and Salmonella Pullorum cause important disease of chicken, the others are turkey, quail, pigeon, sparrow and parrot, which are host specific and biovars of each other. Therefore, rapid and reliable meth-ods to detect these poultry-associated Salmonella serotypes are necessary for efficient control of Salmonella in poultry. For this purpose, a rapid qPCR diagnostic kit including S. Gallinarum / Pullorum and internal control targeted reactions was developed simultaneously to detect and differentiate biovars. S. Gallinarum/Pullorum reference and S. Gallinarum strains that were developed from VKMAE Poultry Laboratory were performed using qPCR method. In this study, sensitivity and specificity of qPCR analysis were evaluated. The results showed that the developed qPCR method was able to detect Salmonella Gallinarum/Pullorum correctly. Since the ease of use, reliability, technically simple, full automation, specific, sensitive and fast, the qPCR method is thought to provide more advantages in the diagnosis and differentiation of these biovars.

Özet

Konak spesifik ve biovar olan Salmonella Gallinarum ve Salmonella Pullorum başta tavuk olmak üzere hindi, bıldırcın, güvercin, serçe ve papağanlarda önemli hastalıklara sebep olmaktadır. Bu nedenle kanatlı hayvanlarda bu serotipleri saptamak için hızlı ve güvenilir tanı yöntemleri hastalığın etkin kontrolü için gerekli olmaktadır. Bu amaçla biovarları saptamak ve birbirinden ayrımını sağlamak için eş zamanlı olarak S. Gallinarum/Pullorum ve internal kontrol hedefli reaksiyonları içeren hızlı qPCR tanı kiti geliştirildi. S. Gallinarum/Pullorum referans ve VKMAE Kanatlı Hastalıkları Laboratuvarı'ndan temin edilen S. Gallinarum suşlarına qPCR metodu uygulandı. Çalışmada qPCR analizinin duyarlılığı ve özgüllüğü değerlendirildi. Sonuçlar geliştirilen qPCR yönteminin S. Gallinarum/Pullorum'u kesin olarak saptayabildiğini gösterdi. qPCR yönteminin kullanım kolaylığı, güvenirliliği, teknik olarak basit, tam otomasyon, spesifik, hassas, hızlı olmasından dolayı bu biovarların teşhisi ve ayrımında daha fazla avantaj sağlayacağı sonucuna varıldı.

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Cite This Article

YAPICIER, Ö. Ş. (2019). Development of qPCR Diagnostic Kit for Salmonella Gallinarum and Salmonella Pullorum. Etlik Veteriner Mikrobiyoloji Dergisi, Cilt: 30 - Sayı: 2, 137–142. https://ajindex.com/articles/118519

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References (2)

  1. Akan M, (2008). Kanatlılarda Salmonella infeksiyonları ve kontrolünde temel prensipler. Mektup Ankara. 6, 3-4.2. Barrow PA, Freitas Neto OC, (2011). Pullorum disease and fowl typhoid–new thoughts on old diseases: a review. Avian Pathol. 40: 1-13.3. Berchieri JRA, Murphy CK, Marston K, Barrow PA, (2001). Observations on the persistence and vertical transmission of Salmonella enterica serovars Pullorum and Gallinarum in chickens: effect of bacterial and host genetic background. Avian Pathol. 30, 229-239. 4. Bohaychuk VM, Gensler GE, McFall ME, King RK, Render DG, (2007). A real-time PCR assay for the detection of Salmonella in a wide variety of food-animal matrices. J Food Prot. 70, 1080-1087.5. Christensen JP, Olsen JE, Hansen HC, Bisgaard M, (1992). Characterisation of Salmonella enterica serovar Gallinarum biovars Gallinarum and Pullorum by plasmid profiling and biochemical analysis. Avian Pathol. 21,461-470. 6. Christensen JP, Olsen JE, Bisgaard M,(1993). Ribotypes of Salmonella enterica serovar Gallinarum biovars Gallinarum and Pullorum. Avian Pathol. 22,725-738. 7. Çarlı KT, Ünal CB, Caner V, Eyigör A, (2001). Detection of Salmonella chicken feces by a combination of tetrathionate broth enrichment, capillary PCR, and capillary gel electrophoresis. J Clin Microbiol. 39, 1871-1876.8. Dorak TM, (2007).
  2. Real-Time PCR. New York, NY, USA: Taylor&Francis.9. Eyigor A, Carli KT,(2003). Rapid detection of Salmonella from poultry by real-time polymerase chain reaction with fluorescent hybridization probes. Avian Dis. 47, 380-386. 10. Eyigor A, Carli KT, (2007). A PCR-ELISA for the detection of Salmonella from chicken intestine. J Biol Environ Sci. 1, 45-49. 11. Ellingson JL, Anderson JL, Carlson Sa, Sharma VK, (2004). Twelve hour real-time PCR technique for the sensitive and specific detection of Salmonella in raw and ready-to-eat meat products. Mol Cell Prob. 18, 51-57. 12. Hein I, Flekna G, Krassnig M, Wagner M, (2006). Real-time PCR for the detection of Salmonella spp. in food: an alternative approach to a conventional PCR system suggested by the FOOD-PCR project. J Microbiol Methods. 66, 538–547.13. Hoorfar J, Cook N, Malorny B, Rådström P, De Medici D, Abdulmawjood A, Fach P, (2003). Diagnostic PCR: making internal amplification control mandatory. J Clin Microbiol. 41, 5835. 14. Feng Y, Johnston RN, Liu G, Liu S, (2013). Genomic comparison between Salmonella Gallinarum and Pullorum: differential pseudogene formation under common host restriction. PLoS ONE