Safety and efficacy of a phage cocktail on murine wound infections caused by carbapenem-resistant Klebsiella pneumoniae

肺炎克雷伯菌 微生物学 溶解循环 噬菌体疗法 细菌 伤口愈合 噬菌体 病菌 生物 病毒学 医学 免疫学 大肠杆菌 基因 病毒 生物化学 遗传学
作者
Yujie Feng,Qian Fang,Huibo Luo,Juan Li,Xin Yin,Zhiyong Zong
出处
期刊:International Journal of Antimicrobial Agents [Elsevier]
卷期号:63 (2): 107088-107088
标识
DOI:10.1016/j.ijantimicag.2024.107088
摘要

Carbapenem-resistant Klebsiella pneumoniae (CRKP) is a leading pathogen causing difficult-to-treat, healthcare-associated wound infections. Phages are an alternative approach against CRKP. This study established murine wound infection models with a CRKP clinical strain of sequence type 11 and capsular type KL64, which is the dominant type in China, carrying genes encoding KPC-2 and NDM-1 carbapenemases.A cocktail was made comprising three lytic phages of different viral families against the strain. The phage cocktail restricted bacterial growth for 10 hours in vitro. The efficacy and safety of the phage cocktail in treating a murine wound CRKP infection were then evaluated. Mice were randomly assigned into four groups (16 for each) comprising a phage treatment group, infected with bacteria and 30 minutes later with phages, and three control groups administered with PBS (negative control), bacteria (infection control), or phages (phage control) on the wound. Wound tissues were processed for counting bacterial loads on days 1, 3, and 7 post-infection and examined for histopathological change on days 3 and 7. Two remaining mice in each group were monitored for wound healing until day 14.Compared with the infection control group, the wound bacterial load in the phage treatment group decreased by 4.95 × 102 CFU/g (> 100-fold; P < 0.05) at day 7 post-treatment, and wounds healed on day 10, as opposed to day 14 in the infection control group. No adverse events associated with phages were observed.The phage cocktail significantly reduced the wound bacterial load and promoted wound healing with good safety.
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