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通过双重PCR检测对肠炎沙门氏菌肠炎亚种鸡伤寒血清型鸡伤寒生物变种和鸡白痢生物变种进行分子鉴定。

Molecular identification of Salmonella enterica subsp. enterica serovar Gallinarum biovars Gallinarum and Pullorum by a duplex PCR assay.

作者信息

Batista Diego Felipe Alves, de Freitas Neto Oliveiro Caetano, de Almeida Adriana Maria, Barrow Paul Andrew, de Oliveira Barbosa Fernanda, Berchieri Junior Angelo

机构信息

Faculty of Agriculture and Veterinary Sciences, São Paulo State University, Jaboticabal, São Paulo, Brazil (Batista, Almeida, Barbosa, Berchieri Jr)Agronomical Science Centre, Federal University of Paraíba, Campus II, Areia, Paraíba, Brazil (Freitas Neto)School of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, Leicestershire, United Kingdom (Barrow).

Faculty of Agriculture and Veterinary Sciences, São Paulo State University, Jaboticabal, São Paulo, Brazil (Batista, Almeida, Barbosa, Berchieri Jr)Agronomical Science Centre, Federal University of Paraíba, Campus II, Areia, Paraíba, Brazil (Freitas Neto)School of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, Leicestershire, United Kingdom (Barrow)

出版信息

J Vet Diagn Invest. 2016 Jul;28(4):419-22. doi: 10.1177/1040638716651466. Epub 2016 May 22.

Abstract

Salmonella enterica subsp. enterica serovar Gallinarum biovar Gallinarum (S Gallinarum) and biovar Pullorum (S Pullorum) are 2 poultry pathogens that cause major economic losses to the poultry industry worldwide. Control of both diseases mainly relies on the adoption of biosecurity programs, and success is dependent on accurate and fast detection. Based on this concept, we developed a duplex PCR assay, targeting 2 chromosomal sequences, which allowed us to precisely identify and differentiate S Gallinarum and S Pullorum field strains. This assay was validated by testing genomic DNA from 40 S Gallinarum and 29 S Pullorum field strains, 87 other Salmonella serovars, and 7 non-Salmonella strains. The serovar identifier region (SIR) primers produced a fragment only in S Gallinarum and S Pullorum strains, whereas the fragment from the ratA coding sequence, which was previously demonstrated to differentiate the 2 biovars, was also amplified from other Salmonella serovars. Our results showed that the combination of both SIR and ratA amplifications could be used to identify as well as to differentiate colonies of S Gallinarum and S Pullorum reliably. Thus, we believe this methodology can be a useful ancillary tool for routine veterinary diagnostic laboratories by providing rapid, accurate results.

摘要

肠炎沙门氏菌肠炎亚种鸡伤寒血清型鸡伤寒生物变种(鸡伤寒沙门氏菌)和鸡白痢生物变种(鸡白痢沙门氏菌)是两种家禽病原体,给全球家禽业造成重大经济损失。这两种疾病的控制主要依赖于实施生物安全计划,而成功与否取决于准确快速的检测。基于这一理念,我们开发了一种针对2个染色体序列的双重PCR检测方法,可让我们精确鉴定和区分鸡伤寒沙门氏菌和鸡白痢沙门氏菌的田间菌株。通过检测40株鸡伤寒沙门氏菌、29株鸡白痢沙门氏菌田间菌株、87株其他沙门氏菌血清型以及7株非沙门氏菌菌株的基因组DNA,对该检测方法进行了验证。血清型鉴定区域(SIR)引物仅在鸡伤寒沙门氏菌和鸡白痢沙门氏菌菌株中产生片段,而先前证明可区分这两个生物变种的ratA编码序列片段在其他沙门氏菌血清型中也能扩增出来。我们的结果表明,SIR和ratA扩增相结合可用于可靠地鉴定和区分鸡伤寒沙门氏菌和鸡白痢沙门氏菌的菌落。因此,我们认为这种方法通过提供快速、准确的结果,可成为常规兽医诊断实验室有用的辅助工具。

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