| Literature DB >> 33927462 |
Shiwam Dubey1, Ajeet Singh1, B T Naveen Kumar1, Niraj Kumar Singh2, Anuj Tyagi1.
Abstract
Among the various bacterial pathogens associated with the aquaculture environment, Vibrio parahaemolyticus the important one from shrimp and human health aspects. Though having been around for several decades, phage-based control of bacterial pathogens (phage therapy) has recently re-emerged as an attractive alternative due to the availability of modern phage characterization tools and the global emergence of antibiotic-resistant bacteria. In the present study, a total of 12 V. parahaemolyticus specific phages were isolated from 264 water samples collected from inland saline shrimp culture farms. During the host range analysis against standard/field isolates of V. parahaemolyticus and other bacterial species, lytic activity was observed against 2.3-45.5% of tested V. parahaemolyticus isolates. No lytic activity was observed against other bacterial species. For genomic characterization, high-quality phage nucleic acid with concentrations ranging from 7.66 to 220 ng/µl was isolated from 9 phages. After digestion treatments with DNase, RNase and S1 nuclease, the nature of phage nucleic acid was determined as ssDNA and dsDNA for 7 and 2 phages respectively. During transmission electron microscopy analysis of phage V5, it was found to have a filamentous shape making it a member of the family Inoviridae. During efficacy study of phage against V. parahaemolyticus in shrimp, 78.1% reduction in bacterial counts was observed within 1 h of phage application. These results indicate the potential of phage therapy for the control of V. parahaemoyticus in shrimp. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12088-021-00934-6. © Association of Microbiologists of India 2021.Entities:
Keywords: Bacteriophage; Genomic characterization; Host range; Shrimp; SsDNA; Vibrio parahaemolyticus
Year: 2021 PMID: 33927462 PMCID: PMC8039080 DOI: 10.1007/s12088-021-00934-6
Source DB: PubMed Journal: Indian J Microbiol ISSN: 0046-8991