PCR assay targeting virulence genes of Helicobacter pylori isolated from drinking water and clinical samples in Lahore metropolitan, Pakistan

• Published in: Journal of water and health Vol. 9; no. 1; pp. 208 - 216
• Main Authors: Samra, Zahoor Qadir, Javaid, Umber, Ghafoor, Sadia, Batool, Aleeza, Dar, Nadia, Athar, Muhammad Amin
• Format: Journal Article
• Language: English
• Published: England IWA Publishing 01.03.2011
• Subjects: Adenocarcinoma; Adult; Antibodies; Antigens, Bacterial - genetics; Bacterial Proteins - genetics; Biopsy; Catalase; Catalase - genetics; Chronic infection; Deoxyribonucleic acid; Detection; Developing Countries; DNA; DNA probes; Drinking water; Fluids; Gastritis; Gastritis - microbiology; Genes; Health Education; Helicobacter Infections - epidemiology; Helicobacter Infections - transmission; Helicobacter pylori; Helicobacter pylori - classification; Helicobacter pylori - genetics; Helicobacter pylori - isolation & purification; Helicobacter pylori - pathogenicity; Humans; LDCs; Middle Aged; Nucleotide sequence; Pakistan - epidemiology; Pathogens; Patients; PCR; Polymerase Chain Reaction; Probes; Public health; RNA, Ribosomal, 16S - genetics; rRNA 16S; Sanitation; Socioeconomic factors; Ulcers; Urease; Urease - genetics; Virulence; Vomiting; Waste disposal; Water analysis; Water Microbiology; Water sampling; Water Supply - analysis; Young Adult; Pakistan
• ISSN: 1477-8920; 1996-7829
• DOI: 10.2166/wh.2010.169

Helicobacter pylorus is considered for chronic gastritis, gastric ulcers and adenocarcinoma and its high infection rate is observed in overcrowded and lower socioeconomic groups in developing countries. This study was designed to identify the role of drinking water in the transmission and prevalence of H. pylori (HP). Selective HP medium was developed for enrichment and presumptive identification of H. pylori by urease, catalase and species specific 16S rRNA tests. The virulence genes (vacA 's' and 'm' regions and cagA) of H. pylori in 90 out of 225 H. pylori positive drinking water samples were present (40%). Ten out of 18 biopsies (55.55%) and 15 out of 50 vomiting fluids of gastric disease patients (30%) were also positive for virulence genes. Anti-H. pylori antibodies were also detected in 31 out of 50 patients' sera. The presence of virulence genes was also directly confirmed by hybridization studies using non-radioactive DNA probes of 16S rRNA, vacA and cagA genes. The presence of H. pylori in water is due to poor sanitary conditions, improper waste disposal and lack of public health education. PCR-based analysis and colony hybridization can be used for detection of H. pylori in clinical and environmental samples.