Initially the bacterium can cause gastroenteritis, and then spread systemically throughout the blood (bacteremia) and cause septicaemia, meningitis, and other systemic infections [2]. Selleck ABT-737 Bovine genital campylobacteriosis is an Office International des Epizooties (OIE) notifiable disease considered to have socio-economic and public health implications, particularly with respect to the international trade of animals and animal products [4]. Although Campylobacter sub species have largely conserved genomes, sub species display variable virulence phenotypes in animal models and this phenotypic

virulence has been speculated to be due to hyper-variable antigenic diversity and immune evasion [1, 5]. Very few gene targets have been

identified for the differentiation of C. fetus subspecies, with members of the Selleck Wortmannin subspecies shown to be 86% similar based on PFGE-DNA profiles [6]. Diagnostic testing of C. fetus colonies from transport medium and the biochemical differentiation of the 2 subspecies venerealis and https://www.selleckchem.com/products/bv-6.html fetus is important for the diagnosis of bovine venereal disease in cattle. Cff and Cfv can be differentiated from each other using a range of biochemical assays including H2S, selenite reduction, growth at 42°C, susceptibility to metronidazole and cefoperazone, basic fuchsin, KMnO4 and glycine tolerance [6, 7]. Glycine tolerance is the OIE recommended assay. Celecoxib It is however difficult to isolate viable colonies from transport medium for biochemical

analysis due to prolonged transport, contaminant overgrowth and the fastidious nature of the bacteria [8–10]. In addition doubts in regard to the stability of these biochemical markers has been suggested based on evidence from phage transduction [6, 11–13]. The H2S test although described as differentiating Cff (positive) and Cfv (negative), a Cfv strain subsequently named Cfv biovar intermedius is positive in this assay [14]. Molecular typing methods such as amplified fragment length polymorphism (AFLP) and multilocus sequence typing have been developed to differentiate C. fetus isolates [11, 15], but these methods require the isolation of pure colonies which are impractical for diagnostic application. Specific polymerase chain reaction (PCR) assays have been designed and applied to detect Cfv [16–18], however it has been suggested that the gene targets are plasmid borne and that in some cases have not reliably detected all Cfv isolates [19]. A sensitive real time assay designed to target the parA gene originally targeted by the Hum et al (1997) PCR assay, identified a high prevalence of Cfv in Australia cattle not associated with venereal cases [4]. It was thus postulated that isolates of Cfv differ in virulence and that other methods may be required to confirm the presence of pathogenic Cfv in clinical samples. Genomic Campylobacter comparisons of C.