Multireceptor phage cocktail against Salmonella enterica to circumvent phage resistance

Author:

Martinez-Soto Carlos E12,McClelland Michael3,Kropinski Andrew M4,Lin Janet T1,Khursigara Cezar M2ORCID,Anany Hany12

Affiliation:

1. Guelph Research and Development Centre, Agriculture and Agri-Food Canada , 93 Stone Rd W, N1G 5C9, Guelph, Ontario , Canada

2. Department of Molecular and Cellular Biology, College of Biological Science, University of Guelph , 50 Stone Rd E, N1G 2W1, Guelph, Ontario , Canada

3. Department of Microbiology and Molecular Genetics, School of Medicine, University of California, Irvine , 811 Health Sciences Road, CA 92614 , United States

4. Department of Pathobiology, Ontario Veterinary College, University of Guelph , Guelph, 419 Gordon St, Guelph, ON N1G 2W1 , Canada

Abstract

Abstract Non-Typhoidal Salmonella (NTS) is one of the most common food-borne pathogens worldwide, with poultry products being the major vehicle for pathogenesis in humans. The use of bacteriophage (phage) cocktails has recently emerged as a novel approach to enhancing food safety. Here, a multireceptor Salmonella phage cocktail of five phages was developed and characterized. The cocktail targets four receptors: O-antigen, BtuB, OmpC, and rough Salmonella strains. Structural analysis indicated that all five phages belong to unique families or subfamilies. Genome analysis of four of the phages showed they were devoid of known virulence or antimicrobial resistance factors, indicating enhanced safety. The phage cocktail broad antimicrobial spectrum against Salmonella, significantly inhibiting the growth of all 66 strains from 20 serovars tested in vitro. The average bacteriophage insensitive mutant (BIM) frequency against the cocktail was 6.22 × 10−6 in S. Enteritidis, significantly lower than that of each of the individual phages. The phage cocktail reduced the load of Salmonella in inoculated chicken skin by 3.5 log10 CFU/cm2 after 48 h at 25°C and 15°C, and 2.5 log10 CFU/cm2 at 4°C. A genome-wide transduction assay was used to investigate the transduction efficiency of the selected phage in the cocktail. Only one of the four phages tested could transduce the kanamycin resistance cassette at a low frequency comparable to that of phage P22. Overall, the results support the potential of cocktails of phage that each target different host receptors to achieve complementary infection and reduce the emergence of phage resistance during biocontrol applications.

Funder

Agriculture and Agri-Food Canada

Canadian Poultry Research Council

Natural Sciences and Engineering Research Council of Canada

National Institutes of Health

Publisher

Oxford University Press (OUP)

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