Development of a TaqMan-based multiplex real-time PCR for simultaneous detection of porcine epidemic diarrhea virus, Brachyspira hyodysenteriae, and Lawsonia intracellularis

被引:0
|
作者
Ren, Jing [1 ,2 ]
Li, Fujun [3 ]
Yu, Xue [1 ,2 ]
Li, Yang [3 ]
Li, Meng [1 ,2 ]
Sha, Yujie [1 ,2 ]
Li, Xiaowen [1 ,3 ]
机构
[1] Dezhou Univ, Shandong Engn Res Ctr Swine Hlth Data & Intelligen, Dezhou, Peoples R China
[2] Dezhou Univ, Inst Biophys, Shandong Prov Key Lab Biophys, Dezhou, Peoples R China
[3] Shandong New Hope Liuhe Co Ltd, Shandong Engn Res Ctr Pig & Poultry Hlth Breeding, Qingdao, Peoples R China
关键词
multiplex real-time PCR; PEDV; Brachyspira hyodysenteriae; Lawsonia intracellularis; porcine diarrheal diseases; PILOSICOLI;
D O I
10.3389/fvets.2024.1450066
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Introduction: PEDV, Brachyspira hyodysenteriae, and Lawsonia intracellularis, are highly contagious diarrheal pathogens that have caused significant harm to the global swine industry. Co-infections with multiple pathogens are common, making it challenging to identify the actual causative agents depending only on clinical information. It is crucial to develop a reliable method to simultaneously detect and differentiate these pathogens. Methods: Based on the conserved regions of the M gene of PEDV, NADH oxidase gene of B. hyodysenteriae, and the 16S rDNA gene of L. intracellularis, specific probes and primers for the multiplex real-time PCR assay were designed. The concentrations of primers and probes were optimized using a matrix method. Results: The approach demonstrated high specificity and no cross-reactivity with major pathogens related to diarrheal diseases. It showed high sensitivity with a detection limit of 10 copies/mu L for B. hyodysenteriae and L. intracellularis, and 100 copies/mu L for PEDV, respectively. It also demonstrated high reproducibility and stability with low coefficients of variation. Results from the multiplex real-time PCR method were in complete agreement with the commercial singleplex real-time PCR kit for detecting PEDV, B. hyodysenteriae and L. intracellularis. Clinical data revealed single infection rates of 31.46% for PEDV, 58.43% for B. hyodysenteriae, and 98.6% for L. intracellularis. The co-infection rates were 16.85% for PEDV + B. hyodysenteriae, 31.46% for PEDV + L. intracellularis, 57.86% for B. hyodysenteriae + L. intracellularis, and 16.85% for PEDV + B. hyodysenteriae + L. intracellularis, respectively. Discussion: The new multiplex real-time PCR method can simultaneously differentiate PEDV, B. hyodysenteriae and L. intracellularis, making it a valuable diagnostic tool for preventing and controlling infectious diseases, as well as aiding in epidemiological investigations.
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页数:8
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