Combined Loop-Mediated Isothermal Amplification Assays for Rapid Detection and One-Step Differentiation of Campylobacter jejuni and Campylobacter coli in Meat Products

被引:10
作者
Kreitlow, Antonia [1 ]
Becker, Andre [1 ]
Ahmed, Marwa F. E. [2 ,3 ]
Kittler, Sophie [1 ]
Schotte, Ulrich [4 ]
Ploetz, Madeleine [1 ]
Abdulmawjood, Amir [1 ]
机构
[1] Univ Vet Med Hannover, Inst Food Qual & Food Safety, Hannover, Germany
[2] Univ Vet Med Hannover, Inst Anim Hyg Anim Welf & Farm Anim Behav, Hannover, Germany
[3] Mansoura Univ, Fac Vet Med, Dept Hyg & Zoonoses, Mansoura, Egypt
[4] Bundeswehr Med Serv Kiel, Cent Inst, Dept Vet Med A, Kronshagen, Germany
关键词
LAMP assay; rplD gene; cdtC gene; gyrA gene; Campylobacter; meat products; SENSITIVE DETECTION; CHICKEN MEAT; POULTRY; TIME; LAMP; PCR; CHILDREN; SURVIVAL; SPP; LARI;
D O I
10.3389/fmicb.2021.668824
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A loop-mediated isothermal amplification (LAMP) assay system was established, allowing rplD gene-based simultaneous detection of Campylobacter jejuni and Campylobacter coli in enriched meat products. Additionally, one-step differentiation of target species on agar plates was enabled by cdtC gene- and gyrA gene-based duplex LAMP. Both the rplD and cdtC-gyrA LAMP assays amplified the target sequences in all 62 C. jejuni and 27 C. coli strains used for determining inclusivity and revealed 100% exclusivity toward 85 tested non-target species. Throughout the entire experiments, C. jejuni and C. coli strains were 100% distinguishable by melting curves of cdtC and gyrA LAMP products. After 24-h enrichment, the rplD LAMP assay reliably detected initial inoculation levels of 10-100 CFU/g in artificially contaminated minced meat. Investigation of naturally contaminated meat samples revealed a diagnostic accuracy of 95% toward real-time PCR and 94.1% toward the standard culture method applying the 24-h incubation period. Diagnostic sensitivity and specificity, and positive and negative predictive values were 89.8, 100, 100, and 91.2%, respectively, when measured against real-time PCR, and 89.6, 98.1, 97.7, and 91.2%, respectively, when measured against the standard culture method. After 48-h enrichment, the detection limit of the rplD LAMP assay improved to initial inoculation levels of 1-10 CFU/g in artificially contaminated minced meat. Applying the 48-h incubation period on naturally contaminated meat samples resulted in 100% concordant results between rplD LAMP, real-time PCR, and the standard culture method. The established LAMP assay system was proved to be suitable for rapid meat sample screening. Furthermore, it constitutes a promising tool for investigating other Campylobacter sources and could therefore make a valuable contribution to protect consumers from foodborne illness.
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页数:14
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