TY - JOUR
T1 - Repeated-Dose 28-Day Oral Toxicity Study of a Salmonella enterica Serovar Typhimurium Bacteriophage Cocktail (SE.PC) in BALB/c Mice
AU - Tan, Yee Fan
AU - Mutusamy, Prasanna
AU - Parimannan, Sivachandran
AU - Rajandas, Heera
AU - Subramani, Parasuraman
PY - 2026
Y1 - 2026
N2 - Background: Phage therapy is a promising alternative for drug-resistant Salmonella, but safety data for repeated doses are limited. This study investigated the sub-chronic safety of SE.PC, a candidate Salmonella enterica serovar Typhimurium phage cocktail, in a non-specific pathogen-free (non-SPF) model, which contains a naturally occurring microbiota, to evaluate systemic safety under physiologically relevant conditions. We tested a range of phage doses to determine if there are any differences in tolerance. Materials and Methods: During a 28-day repeated-dose oral toxicity study, SE.PC was administered via weekly gavage to male and female non-SPF BALB/c mice across three different phage doses (2.43 & times; 10(9), 4.85 & times; 10(9), and 9.70 & times; 10(9) plaque-forming units/mL). Clinical signs, body weight, hematology, biochemistry, and histopathology were assessed. Results: Across all three administered phage dose groups, no mortality was recorded, and all mice exhibited normal clinical signs and growth. Hematological and biochemical values remained within baseline ranges. Histopathology revealed no treatment-related lesions; isolated findings were deemed incidental or adaptive. Conclusion: Evidence supports that SE.PC is well tolerated. This study demonstrates a strong safety profile, supporting the advancement of SE.PC as a biocontrol agent.
AB - Background: Phage therapy is a promising alternative for drug-resistant Salmonella, but safety data for repeated doses are limited. This study investigated the sub-chronic safety of SE.PC, a candidate Salmonella enterica serovar Typhimurium phage cocktail, in a non-specific pathogen-free (non-SPF) model, which contains a naturally occurring microbiota, to evaluate systemic safety under physiologically relevant conditions. We tested a range of phage doses to determine if there are any differences in tolerance. Materials and Methods: During a 28-day repeated-dose oral toxicity study, SE.PC was administered via weekly gavage to male and female non-SPF BALB/c mice across three different phage doses (2.43 & times; 10(9), 4.85 & times; 10(9), and 9.70 & times; 10(9) plaque-forming units/mL). Clinical signs, body weight, hematology, biochemistry, and histopathology were assessed. Results: Across all three administered phage dose groups, no mortality was recorded, and all mice exhibited normal clinical signs and growth. Hematological and biochemical values remained within baseline ranges. Histopathology revealed no treatment-related lesions; isolated findings were deemed incidental or adaptive. Conclusion: Evidence supports that SE.PC is well tolerated. This study demonstrates a strong safety profile, supporting the advancement of SE.PC as a biocontrol agent.
KW - Salmonella enterica serovar Typhimurium
KW - Antimicrobial resistance
KW - Bacteriophage cocktail
KW - Phage therapy
KW - Preclinical safety
KW - Repeated-dose toxicity
U2 - 10.1177/26416549261448405
DO - 10.1177/26416549261448405
M3 - Journal article
SN - 2641-6530
VL - 7
SP - 178
EP - 186
JO - PHAGE: Therapy, Applications, and Research
JF - PHAGE: Therapy, Applications, and Research
IS - 3
ER -