2016
DOI: 10.1016/j.mimet.2016.03.009
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Detection of virulence, antibiotic resistance and toxin (VAT) genes in Campylobacter species using newly developed multiplex PCR assays

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Cited by 21 publications
(11 citation statements)
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“…Sequencing of the C. jejuni NCTC 11168 genome demonstrated the existence of genes that code some proteins with infectious potential. Despite numerous studies on the molecular genetics of Campylobacter spp., their mechanisms of pathogenicity and virulence remain poorly understood [ 37 ]. Although the bacteria are considered to be susceptible to stress associated with environmental conditions, in the course of evolution, they were able to develop some complex mechanisms of survival and virulence, as presented in Table 1 [ 38 , 39 ].…”
Section: Campylobacteriosismentioning
confidence: 99%
“…Sequencing of the C. jejuni NCTC 11168 genome demonstrated the existence of genes that code some proteins with infectious potential. Despite numerous studies on the molecular genetics of Campylobacter spp., their mechanisms of pathogenicity and virulence remain poorly understood [ 37 ]. Although the bacteria are considered to be susceptible to stress associated with environmental conditions, in the course of evolution, they were able to develop some complex mechanisms of survival and virulence, as presented in Table 1 [ 38 , 39 ].…”
Section: Campylobacteriosismentioning
confidence: 99%
“…However, resistance to these empirical drugs has been reported in many countries [12,15,16]. High-level tetracycline resistance is usually associated with the tetO gene, while mutation of the gryA or parC gene triggers resistance to fluoroquinolones [14,17]. Resistance to macrolides frequently occurs due to mutations at positions 2074 or 2075 of domain V in the rrn gene which encodes the 23S rRNA gene [14].…”
Section: Introductionmentioning
confidence: 99%
“…In addition to typing, PCR can be used to identify bacterial pathogens based on specific virulence factors such as toxins, adhesins, or capsules. As in PCR-based genotyping, species-specific virulence genes are assessed as PCR primer targets and amplified for the characterization of a pathogen in a sample (68)(69)(70). Traditional PCR detection of virulence genes has the disadvantage of being able to identify only one gene or species per reaction, which limits its use in high-throughput outbreak analyses.…”
Section: Amplification-based Typing Technologiesmentioning
confidence: 99%