Characterization of a haemolytic phospholipase A sub(2) activity in clinical isolates of Campylobacter concisus

• Published in: Journal of medical microbiology Vol. 53; no. 6; pp. 483 - 493
• Main Authors: Istivan, T S, Coloe, P J, Fry, B N, Ward, P, Smith, S C
• Format: Journal Article
• Language: English
• Published: 01-06-2004
• Subjects: Campylobacter concisus
• ISSN: 0022-2615
• DOI: 10.1099/jmm.0.45554-0

A membrane-bound, haemolytic phospholipase A sub(2) (PLA sub(2)) activity was detected in clinical strains of Campylobacter concisus isolated from children with gastroenteritis. The clinical strains were assigned into two molecular groups (genomospecies) based on PCR amplification of their 23S rDNA. This calcium-dependent, heat-stable, haemolytic PLA sub(2) activity was detected in strains from both genomospecies. A crude haemolysin extract (CHE) was initially prepared from cellular outer-membrane proteins of these isolates and was further fractionated by ultrafiltration. The haemolytic activity of the extracted fraction (R30) was retained by ultrafiltration using a 30 kDa molecular mass cut-off filter, and was designated haemolysin extract (HE). Both CHE and HE had PLA sub(2) activity and caused stable vacuolating and cytolytic effects on Chinese hamster ovary cells in tissue culture. Primers for the conserved region of pldA gene (phospholipase A gene) from Campylobacter coli amplified a gene region of 460 bp in all tested isolates, confirming the presence of a homologous PLA gene sequence in C. concisus. The detection of haemolytic PLA sub(2) activity in C. concisus indicates the presence of a potential virulence factor in this species and supports the hypothesis that C. concisus is a possible opportunistic pathogen.