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Isolation and Characterization of a Bacteriophage That Hosts on Avian-pathogenic Escherichia coli (APEC)

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dc.contributor.advisor Al-Razem, Fawzi
dc.contributor.author Fakhouri, Haya
dc.contributor.author Juneidi, Orjowan
dc.contributor.author Al Mohtaseb, Hana
dc.contributor.author Ishnaiwer, Murad
dc.date.accessioned 2019-10-08T11:04:00Z
dc.date.accessioned 2022-05-22T08:52:18Z
dc.date.available 2019-10-08T11:04:00Z
dc.date.available 2022-05-22T08:52:18Z
dc.date.issued 2019-04-15
dc.identifier.citation International Journal of Poultry Science 18(5): 232-230 (2019) en_US
dc.identifier.issn 1682-8356
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/8083
dc.description.abstract Background and Objective: Infectious Colibacillosis disease caused by Avian-pathogenic Escherichia coli (APEC) commonly threatens poultry flocks worldwide. It limits productivity and causes severe economic losses to poultry sector. In addition, the emergence of multidrug resistance among APEC is an increasing concern since these resistant bacteria can infect humans and develop mechanisms that enable them to resist the commonly used antibiotics. The use of phages in treating pathogenic bacteria is considered a possible alternative to the conventional use of antibiotics. The aim of this study was to isolate and characterize APEC E. coli bacteriophage and to determine its cyclic replication through double layer test and one step growth curve. Materials and Methods: Bacteriophage was isolated from poultry feces samples using soft agar overlay method and was detected through the formation of clear zones on a lawn culture of APEC host bacterium on Luria Bertani (LB) agar plates. The phage total proteins analysis was carried out using SDS-PAGE through which samples were electrophoresed on a 10% polyacrylamide gel. The quantification of infectious viruses in bacterial suspension was determined through a one-step growth curve analysis using double layer test. The host range of the bacteriophage was further explored by performing spot tests with four APEC bacterial strains. Results: An APEC E. coli Bacteriophage was isolated. It was found to possess an apparently 17 kb genome size. The SDS-PAGE showed two major visible protein bands of 30 and 50 KDa. The phage was capable of lysing four tested APEC strains, an indicative of wide host range for the isolated bacteriophage. One step growth curve showed a phage latent period of about 24 h, burst period of 70 h and a burst size of about 2.4×104 plaque forming units (PFU) per plaque. Conclusion: A bacteriophage targeting four APEC strains has been isolated. It could be used to eliminate or reduce the scope of APEC infection in poultry and possibly used as an alternative to antibiotics. en_US
dc.language.iso en_US en_US
dc.publisher ANSI en_US
dc.relation.ispartofseries ISSN 1682-8356;
dc.subject APEC Escherichia coli , bacteriophages, burst period, burst size, Colibacillosis , latent period, plaque forming unit en_US
dc.title Isolation and Characterization of a Bacteriophage That Hosts on Avian-pathogenic Escherichia coli (APEC) en_US
dc.type Article en_US


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