Literature DB >> 20704510

Development of an anti-Salmonella phage cocktail with increased host range.

Jiayi Zhang1, Brittany L Kraft, Yanying Pan, Samantha K Wall, Anthea C Saez, Paul D Ebner.   

Abstract

Salmonella shedding in many livestock species can increase significantly after transport and lairage. Preprocessing increases in shedding can amplify the amount of Salmonella that enters the processing facility and the likelihood of end-product contamination. We previously produced an anti-Salmonella phage cocktail that reduced colonization in swine when the pigs were exposed to an environment heavily contaminated with Salmonella, similar to what might be seen in a transport trailer or processing facility holding pen. The aim of this study was to increase the efficacy of the phage treatment by (1) expanding the host-range of the cocktail and (2) developing a more cost-effective microencapsulation technique. We collected samples from wastewater treatment facilities and isolated 20 distinct phages belonging to either the Siphoviridae or Myoviridae families. From this library we identified 10 phages that together lysed a mixed culture of Salmonella enterica Typhimurium, Enteriditis, and Kentucky--three serovars commonly associated with meat and poultry products. The phages were microencapsulated using two sodium-alginate-based methods that only reduced the cocktail titer by 1.0-1.5 logs (premicroencapsulation: 10.4 log(10) PFU/mL; postmicroencapsulation method one: 9.2 log(10) PFU/mL; postmicroencapsulation method two: 8.9 log(10) PFU/mL). Microencapsulated phages remained stable at both 4°C and 22°C for up to 14 days with no appreciable drop in titer (mean titer: 8.9 log(10) PFU/mL). These data indicate that phage cocktails with wider host ranges are possible and a cost-effective microencapsulation process can protect the phages over an extended period, making simultaneous treatment of large numbers of animals with feed- or water-based delivery possible.

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Year:  2010        PMID: 20704510     DOI: 10.1089/fpd.2010.0621

Source DB:  PubMed          Journal:  Foodborne Pathog Dis        ISSN: 1535-3141            Impact factor:   3.171


  10 in total

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2.  Characterization of a T5-like coliphage, SPC35, and differential development of resistance to SPC35 in Salmonella enterica serovar typhimurium and Escherichia coli.

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Journal:  Appl Environ Microbiol       Date:  2011-01-21       Impact factor: 4.792

3.  Optimizing the Timing and Composition of Therapeutic Phage Cocktails: A Control-Theoretic Approach.

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4.  Core lipopolysaccharide-specific phage SSU5 as an Auxiliary Component of a Phage Cocktail for Salmonella biocontrol.

Authors:  Minsik Kim; Sujin Kim; Bookyung Park; Sangryeol Ryu
Journal:  Appl Environ Microbiol       Date:  2013-11-22       Impact factor: 4.792

5.  A method for generation phage cocktail with great therapeutic potential.

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6.  Complete genome sequences of Aeromonas and Pseudomonas phages as a supportive tool for development of antibacterial treatment in aquaculture.

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Journal:  PLoS One       Date:  2012-08-21       Impact factor: 3.240

9.  Genome sequence of a salmonella phage used to control salmonella transmission in Swine.

Authors:  Jiayi Zhang; Yingying Hong; Nicholas J Harman; Archana Das; Paul D Ebner
Journal:  Genome Announc       Date:  2014-09-11

10.  Evaluation of the broad-spectrum lytic capability of bacteriophage cocktails against various Salmonella serovars and their effects on weaned pigs infected with Salmonella Typhimurium.

Authors:  Byoung-Joo Seo; Eu-Tteum Song; Kichan Lee; Jong-Won Kim; Chang-Gi Jeong; Sung-Hyun Moon; Jee Soo Son; Sang Hyeon Kang; Ho-Seong Cho; Byeong Yeal Jung; Won-Il Kim
Journal:  J Vet Med Sci       Date:  2018-04-04       Impact factor: 1.267

  10 in total

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