Riverbed Sediments as Reservoirs of Multiple Vibrio cholerae Virulence-Associated Genes: A Potential Trigger for Cholera Outbreaks in Developing Countries.
Akebe Luther King AbiaEunice Ubomba-JaswaMaggy Ndombo Benteke MombaPublished in: Journal of environmental and public health (2017)
Africa remains the most cholera stricken continent in the world as many people lacking access to safe drinking water rely mostly on polluted rivers as their main water sources. However, studies in these countries investigating the presence of Vibrio cholerae in aquatic environments have paid little attention to bed sediments. Also, information on the presence of virulence-associated genes (VAGs) in environmental ctx-negative V. cholerae strains in this region is lacking. Thus, we investigated the presence of V. cholerae VAGs in water and riverbed sediment of the Apies River, South Africa. Altogether, 120 samples (60 water and 60 sediment samples) collected from ten sites on the river (January and February 2014) were analysed using PCR. Of the 120 samples, 37 sediment and 31 water samples were positive for at least one of the genes investigated. The haemolysin gene (hlyA) was the most isolated gene. The cholera toxin (ctxAB) and non-O1 heat-stable (stn/sto) genes were not detected. Genes were frequently detected at sites influenced by human activities. Thus, identification of V. cholerae VAGs in sediments suggests the possible presence of V. cholerae and identifies sediments of the Apies River as a reservoir for potentially pathogenic V. cholerae with possible public health implications.
Keyphrases
- heavy metals
- genome wide
- genome wide identification
- drinking water
- polycyclic aromatic hydrocarbons
- health risk assessment
- bioinformatics analysis
- escherichia coli
- risk assessment
- health risk
- public health
- south africa
- organic matter
- genome wide analysis
- dna methylation
- pseudomonas aeruginosa
- staphylococcus aureus
- copy number
- water quality
- transcription factor
- healthcare
- endothelial cells
- hepatitis c virus
- atomic force microscopy
- mass spectrometry
- klebsiella pneumoniae
- induced pluripotent stem cells
- human immunodeficiency virus
- antiretroviral therapy