Combined Loop-Mediated Isothermal Amplification Assays for Rapid Detection and One-Step Differentiation of Campylobacter jejuni and Campylobacter coli in Meat Products
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- an...
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Veröffentlicht in: | Frontiers in microbiology 2021-06, Vol.12, p.668824-668824 |
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Zusammenfassung: | 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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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2021.668824 |