TY - JOUR
T1 - Development and characterization of a bacteriophage cocktail with high lytic efficacy against field-isolated Salmonella enterica
AU - Aguilera, Matías
AU - Tobar-Calfucoy, Eduardo
AU - Rojas-Martínez, Victoria
AU - Norambuena, Rodrigo
AU - Serrano, María Jesús
AU - Cifuentes, Onix
AU - Zamudio, María Sofía
AU - San Martín, Daniel
AU - Lara, Pabla
AU - Sabag, Andrea
AU - Zabner, Marcela
AU - Tichy, Daniel
AU - Camejo, Pamela
AU - León, Luis
AU - Pino, Michael
AU - Ulloa, Soledad
AU - Rojas, Felipe
AU - Pieringer, Christian
AU - Muster, Cecilia
AU - Castillo, Daniel
AU - Ferreira, Nicolás
AU - Avendaño, Camilo
AU - Canaval, Mauro
AU - Pieringer, Hans
AU - Cifuentes, Pablo
AU - Cifuentes Muñoz, Nicolás
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/12
Y1 - 2023/12
N2 - Salmonella spp. is a prevalent pathogen that causes great public health concern worldwide. Bacteriophage-based cocktails have arisen as an alternative to antibiotics to inhibit the growth of Salmonella. However, the bactericidal effect of bacteriophage cocktails in vivo largely differs from their observed effect in vitro. This is partly because in vitro developments of cocktails do not always consider the bacterial diversity nor the environmental conditions where bacteriophages will have to replicate. Here, we isolated and sequenced 47 bacteriophages that showed variable degrees of lytic activity against 258 Salmonella isolates from a commercial broiler company in Brazil. Three of these bacteriophages were characterized and selected to assemble a cocktail. In vitro quantitative assays determined the cocktail to be highly effective against multiple serovars of Salmonella, including Minnesota and Heidelberg. Remarkably, the in vitro lytic activity of the cocktail was retained or improved in conditions that more closely resembled the chicken gut, such as anaerobiosis, 42°C, and Salmonella mono-strain biofilms. Analysis of bacterial cross-resistance between the 3 bacteriophages composing the cocktail revealed limited or no generation of cross-resistance. Our results highlight the relevance of an optimized flux of work to develop bacteriophage cocktails against Salmonella with high lytic efficacy and strong potential to be applied in vivo in commercial broiler farms.
AB - Salmonella spp. is a prevalent pathogen that causes great public health concern worldwide. Bacteriophage-based cocktails have arisen as an alternative to antibiotics to inhibit the growth of Salmonella. However, the bactericidal effect of bacteriophage cocktails in vivo largely differs from their observed effect in vitro. This is partly because in vitro developments of cocktails do not always consider the bacterial diversity nor the environmental conditions where bacteriophages will have to replicate. Here, we isolated and sequenced 47 bacteriophages that showed variable degrees of lytic activity against 258 Salmonella isolates from a commercial broiler company in Brazil. Three of these bacteriophages were characterized and selected to assemble a cocktail. In vitro quantitative assays determined the cocktail to be highly effective against multiple serovars of Salmonella, including Minnesota and Heidelberg. Remarkably, the in vitro lytic activity of the cocktail was retained or improved in conditions that more closely resembled the chicken gut, such as anaerobiosis, 42°C, and Salmonella mono-strain biofilms. Analysis of bacterial cross-resistance between the 3 bacteriophages composing the cocktail revealed limited or no generation of cross-resistance. Our results highlight the relevance of an optimized flux of work to develop bacteriophage cocktails against Salmonella with high lytic efficacy and strong potential to be applied in vivo in commercial broiler farms.
KW - bacteriophage
KW - cocktail
KW - poultry
KW - Salmonella
UR - http://www.scopus.com/inward/record.url?scp=85174675396&partnerID=8YFLogxK
U2 - 10.1016/j.psj.2023.103125
DO - 10.1016/j.psj.2023.103125
M3 - Article
C2 - 37879168
AN - SCOPUS:85174675396
SN - 0032-5791
VL - 102
JO - Poultry Science
JF - Poultry Science
IS - 12
M1 - 103125
ER -