Fong Stephanie A, Bouras George, Houtak Ghais, Nepal Roshan, Feizi Sholeh, Morales Sandra, Psaltis Alkis J, Wormald Peter-John, Vreugde Sarah
Department of Surgery - Otolaryngology Head and Neck Surgery, University of Adelaide, Adelaide, Australia.
AmpliPhi Australia, Brookvale, New South Wales, Australia.
Microbiol Spectr. 2025 May 6;13(5):e0214924. doi: 10.1128/spectrum.02149-24. Epub 2025 Mar 31.
is an opportunistic pathogen that can cause sinus infections and pneumonia in cystic fibrosis (CF) patients. Bacteriophage therapy is being investigated as a treatment for antibiotic-resistant infections. Although virulent bacteriophages have shown promise in treating infections, the development of bacteriophage-insensitive mutants (BIMs) in the presence of bacteriophages has been described. The aim of this study was to examine the genetic changes associated with the BIM phenotype. Biofilms of three genetically distinct strains, including PAO1 (ATCC 15692), and two clinical respiratory isolates (one CF and one non-CF) were grown for 7 days and treated with either a cocktail of four bacteriophages or a vehicle control for 7 consecutive days. BIMs isolated from the biofilms were detected by streak assays, and resistance to the phage cocktail was confirmed using spot test assays. Comparison of whole genome sequencing between the recovered BIMs and their respective vehicle control-treated phage-sensitive isolates revealed structural variants in two strains, and several small variants in all three strains. These variations involved a TonB-dependent outer membrane receptor in one strain, and mutations in lipopolysaccharide synthesis genes in two strains. Prophage deletion and induction were also noted in two strains, as well as mutations in several genes associated with virulence factors. Mutations in genes involved in susceptibility to conventional antibiotics were also identified in BIMs, with both decreased and increased antibiotic sensitivity to various antibiotics being observed. These findings may have implications for future applications of lytic phage therapy.IMPORTANCELytic bacteriophages are viruses that infect and kill bacteria and can be used to treat difficult-to-treat bacterial infections, including biofilm-associated infections and multidrug-resistant bacteria. is a bacterium that can cause life-threatening infections. Lytic bacteriophage therapy has been trialed in the treatment of infections; however, sometimes bacteria develop resistance to the bacteriophages. This study sheds light on the genetic mechanisms of such resistance, and how this might be harnessed to restore the sensitivity of multidrug-resistant to conventional antibiotics.
是一种机会致病菌,可导致囊性纤维化(CF)患者发生鼻窦感染和肺炎。噬菌体疗法正在作为一种治疗耐抗生素感染的方法进行研究。尽管烈性噬菌体在治疗感染方面已显示出前景,但在噬菌体存在的情况下会出现噬菌体不敏感突变体(BIMs)。本研究的目的是检查与BIM表型相关的基因变化。将三种基因不同的菌株,包括PAO1(ATCC 15692)以及两种临床呼吸道分离株(一株CF和一株非CF)的生物膜培养7天,并连续7天用四种噬菌体混合物或载体对照进行处理。通过划线试验检测从生物膜中分离出的BIMs,并使用点滴试验确认对噬菌体混合物的抗性。对回收的BIMs与其各自载体对照处理的噬菌体敏感分离株之间的全基因组测序比较显示,两个菌株存在结构变异,所有三个菌株均存在几个小变异。这些变异涉及一个菌株中的TonB依赖性外膜受体,以及两个菌株中脂多糖合成基因的突变。在两个菌株中还发现了前噬菌体缺失和诱导,以及与毒力因子相关的几个基因的突变。在BIMs中还鉴定出了与对传统抗生素敏感性相关基因的突变,观察到对各种抗生素的敏感性既有降低也有增加。这些发现可能对裂解性噬菌体疗法的未来应用有影响。重要性裂解性噬菌体是感染并杀死细菌的病毒,可用于治疗难治性细菌感染,包括生物膜相关感染和多重耐药细菌。是一种可导致危及生命感染的细菌。裂解性噬菌体疗法已在感染治疗中进行了试验;然而,有时细菌会对噬菌体产生抗性。本研究揭示了这种抗性的遗传机制,以及如何利用这一点来恢复多重耐药菌对传统抗生素的敏感性。