Department of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Department of Microbial Control, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
mSystems. 2023 Apr 27;8(2):e0068222. doi: 10.1128/msystems.00682-22. Epub 2023 Mar 20.
Vibrio vulnificus is a bacterium that inhabits warm seawater or brackish water environments and causes foodborne diseases and wound infections. In severe cases, V. vulnificus invades the skeletal muscle tissue, where bacterial proliferation leads to septicemia and necrotizing fasciitis with high mortality. Despite this characteristic, information on metabolic changes in tissue infected with V. vulnificus is not available. Here, we elucidated the metabolic changes in V. vulnificus-infected mouse skeletal muscle using capillary electrophoresis time-of-flight mass spectrometry (CE-TOFMS). Metabolome analysis revealed changes in muscle catabolites and energy metabolites during V. vulnificus infection. In particular, succinic acid accumulated but fumaric acid decreased in the infected muscle. However, the virulence factor deletion mutant revealed that changes in metabolites and bacterial proliferation were abolished in skeletal muscle infected with a multifunctional-autoprocessing repeats-in-toxin (MARTX) mutant. On the other hand, mice that were immunosuppressed via cyclophosphamide (CPA) treatment exhibited a similar level of bacterial counts and metabolites between the wild type and MARTX mutant. Therefore, our data indicate that V. vulnificus induces metabolic changes in mouse skeletal muscle and proliferates by using the MARTX toxin to evade the host immune system. This study indicates a new correlation between V. vulnificus infections and metabolic changes that lead to severe reactions or damage to host skeletal muscle. V. vulnificus causes necrotizing skin and soft tissue infections (NSSTIs) in severe cases, with high mortality and sign of rapid deterioration. Despite the severity of the infection, the dysfunction of the host metabolism in skeletal muscle triggered by V. vulnificus is poorly understood. In this study, by using a mouse wound infection model, we revealed characteristic changes in muscle catabolism and energy metabolism in skeletal muscle associated with bacterial proliferation in the infected tissues. Understanding such metabolic changes in V. vulnificus-infected tissue may provide crucial information to identify the mechanism via which V. vulnificus induces severe infections. Moreover, our metabolite data may be useful for the recognition, identification, or detection of V. vulnificus infections in clinical studies.
创伤弧菌是一种栖息于温暖海水或半咸水环境中的细菌,可引起食源性疾病和伤口感染。在严重的情况下,创伤弧菌会侵入骨骼肌组织,细菌增殖会导致败血病和坏死性筋膜炎,死亡率很高。尽管有这种特征,但关于创伤弧菌感染组织的代谢变化的信息尚不清楚。在这里,我们使用毛细管电泳飞行时间质谱(CE-TOFMS)阐明了创伤弧菌感染小鼠骨骼肌的代谢变化。代谢组学分析显示,在创伤弧菌感染过程中,肌肉分解代谢物和能量代谢物发生变化。特别是,在感染的肌肉中,琥珀酸积累,但富马酸减少。然而,毒力因子缺失突变体表明,在多功能自加工重复毒素(MARTX)突变体感染的骨骼肌中,代谢物的变化和细菌增殖被消除。另一方面,通过环磷酰胺(CPA)处理使小鼠免疫抑制,在野生型和 MARTX 突变体之间观察到细菌计数和代谢物相似的水平。因此,我们的数据表明,创伤弧菌诱导小鼠骨骼肌的代谢变化,并通过使用 MARTX 毒素增殖来逃避宿主免疫系统。这项研究表明,创伤弧菌感染与代谢变化之间存在新的相关性,这些变化导致宿主骨骼肌发生严重反应或损伤。在严重的情况下,创伤弧菌会导致坏死性皮肤和软组织感染(NSSTIs),死亡率高,病情迅速恶化。尽管感染严重,但宿主骨骼肌代谢功能障碍的机制仍不清楚。在这项研究中,我们通过使用小鼠伤口感染模型,揭示了与感染组织中细菌增殖相关的骨骼肌分解代谢和能量代谢的特征变化。了解创伤弧菌感染组织中的这种代谢变化可能为确定创伤弧菌引起严重感染的机制提供关键信息。此外,我们的代谢物数据可能有助于在临床研究中识别、鉴定或检测创伤弧菌感染。