Bacteriophage therapy using novel Aeromonas phage PAS-1 can be an alternative method to control salmonid furunculosis caused by antibiotic-resistant Aeromonas salmonicida subsp. salmonicida

DC Field Value Language
dc.contributor.author 김지형 -
dc.contributor.author 강도형 -
dc.contributor.author 오철홍 -
dc.contributor.author 허수진 -
dc.contributor.author 박세창 -
dc.date.accessioned 2020-07-16T03:34:22Z -
dc.date.available 2020-07-16T03:34:22Z -
dc.date.created 2020-02-11 -
dc.date.issued 2014-10-01 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/25999 -
dc.description.abstract Aeromonas (A.) salmonicida subsp. salmonicida is the causative agent of furunculosis and bacterial septicemia in a broad variety of fish including salmonids, and is thus responsible for significant economic losses in the global aquaculture industry. Recently, the acquisitions of antibiotic resistance in the bacteria have been recognized as serious concerns. To search for the alternative biocontrol agents against this fish pathogen, the morphological, molecular and several biological characteristics of the lytic Aeromonas bacteriophage (phage) PAS-1 were investigated, and its therapeutic potential against A. salmonicida subsp. salmonicida infections were simultaneously evaluated. The phage showed broad host ranges to other subspecies of A. salmonicida as well as A. salmonicida subsp. salmonicida including antibiotic-resistant strains. The PAS-1 was morphologically classified as Myoviridae and possessed approximately 48 kb of ds DNA genome. And according to the genomic and proteomic analysis, the phage was closely related to other Myoviridae phages infecting enterobacteria or Aeromonas species. For the therapeutic applications of PAS-1, the phage was preferentially co-cultured with one virulent A. salmonicida subsp. salmonicida strain that possesses the type III secretion system (TTSS) related ascV gene, and strong bacteriolytic activity was observed against the bacteria. Administration of the phage in rainbow trout (Oindustry. Recently, the acquisitions of antibiotic resistance in the bacteria have been recognized as serious concerns. To search for the alternative biocontrol agents against this fish pathogen, the morphological, molecular and several biological characteristics of the lytic Aeromonas bacteriophage (phage) PAS-1 were investigated, and its therapeutic potential against A. salmonicida subsp. salmonicida infections were simultaneously evaluated. The phage showed broad host ranges to other subspecies of A. salmonicida as well as A. salmonicida subsp. salmonicida including antibiotic-resistant strains. The PAS-1 was morphologically classified as Myoviridae and possessed approximately 48 kb of ds DNA genome. And according to the genomic and proteomic analysis, the phage was closely related to other Myoviridae phages infecting enterobacteria or Aeromonas species. For the therapeutic applications of PAS-1, the phage was preferentially co-cultured with one virulent A. salmonicida subsp. salmonicida strain that possesses the type III secretion system (TTSS) related ascV gene, and strong bacteriolytic activity was observed against the bacteria. Administration of the phage in rainbow trout (O -
dc.description.uri 1 -
dc.language English -
dc.publisher THE KOREAN SOCIETY OF OCEANOGRAPHY -
dc.relation.isPartOf AMBS2014 -
dc.title Bacteriophage therapy using novel Aeromonas phage PAS-1 can be an alternative method to control salmonid furunculosis caused by antibiotic-resistant Aeromonas salmonicida subsp. salmonicida -
dc.type Conference -
dc.citation.conferencePlace KO -
dc.citation.endPage 253 -
dc.citation.startPage 253 -
dc.citation.title AMBS2014 -
dc.contributor.alternativeName 김지형 -
dc.contributor.alternativeName 강도형 -
dc.contributor.alternativeName 오철홍 -
dc.contributor.alternativeName 허수진 -
dc.identifier.bibliographicCitation AMBS2014, pp.253 -
dc.description.journalClass 1 -
Appears in Collections:
Jeju Research Institute > Jeju Bio Research Center > 2. Conference Papers
Jeju Research Institute > Tropical & Subtropical Research Center > 2. Conference Papers
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