AI Article Synopsis

  • Phage therapy is gaining traction as an alternative to antibiotics in controlling bacterial pathogens affecting shrimp, due to rising antibiotic resistance.
  • In a study, 12 specific phages were isolated from shrimp culture water samples, showing lytic activity against a small percentage of bacterial isolates.
  • Phage V5, identified through electron microscopy, demonstrated a significant reduction (78.1%) in bacterial counts when tested against shrimp, highlighting its therapeutic potential.

Article Abstract

Unlabelled: Among the various bacterial pathogens associated with the aquaculture environment, 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  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 and other bacterial species, lytic activity was observed against 2.3-45.5% of tested 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 . During efficacy study of phage against 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 in shrimp.

Supplementary Information: The online version contains supplementary material available at 10.1007/s12088-021-00934-6.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8039080PMC
http://dx.doi.org/10.1007/s12088-021-00934-6DOI Listing

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