1. 广东工业大学 环境健康与污染控制研究院,广东,广州,510006
2. 广东工业大学 环境科学与工程学院,广东,广州,510006
3. 粤港澳污染物暴露与健康联合实验室,广东,广州,510006
4. 环境催化与健康风险控制重点实验室,广东,广州,510006
黄鸿飞(1999–),男,硕士研究生,主要研究方向为环境抗生素耐药性的传播与扩散等,E-mail:15015998642@163.com
李桂英(1971–),女,特聘教授、博士,广东省特支计划百千万领军人才,主要研究方向为生物气溶胶污染及健康效应,病原微生物耐药性形成机制、健康效应与控制,有机污染物环境健康效应,毒害有机物生物降解的应用基础与研发,E-mail:ligy1999@gdut.edu.cn
纸质出版:2026
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黄鸿飞, 蔡仪威, 李桂英, 等. 金黄色葡萄球菌暴露对秀丽隐杆线虫的毒性机制研究[J]. 广东工业大学学报, 2026, 43(4): 39-46.
黄鸿飞, 蔡仪威, 李桂英, 等. 金黄色葡萄球菌暴露对秀丽隐杆线虫的毒性机制研究[J]. 广东工业大学学报, 2026, 43(4): 39-46. DOI: 10.12052/gdutxb.250086.
致病菌引发的感染性疾病已成为全球公共卫生安全的重大威胁。现有研究主要集中于阐明典型野生型(Wild Type
WT)致病菌的急性毒力机制,但对活的不可培养(Viable But Non-culturable
VBNC) 状态致病菌的宿主感染方式、毒性大小及其致病机理等方面的研究仍比较缺乏。因此,本文以秀丽隐杆线虫(
Caenorhabditis elegans
C. elegans
) 为模式宿主,构建了金黄色葡萄球菌(包括VBNC状态)(
Staphylococcus aureus
S. aureus
)−秀丽隐杆线虫感染体系。感染后,通过裂解技术将暴露后的线虫体内的金黄色葡萄球菌释放出来。进一步观察线虫体内金黄色葡萄球菌的状态变化、毒力蛋白释放以及毒力基因表达等情况,并揭示金黄色葡萄球菌在不同状态下进入线虫后的感染机理。结果表明:野生型金黄色葡萄球菌在线虫体内会加速繁殖并定植于其肠道。同时野生型致病菌可释放大量毒力蛋白,引发线虫急性感染;而VBNC状态的金黄色葡萄球菌的繁殖能力、定植能力均较弱。值得注意的是,VBNC状态金黄色葡萄球菌能够在线虫体内适宜环境下发生复苏,复苏率高达到90.4%,是体外自然复苏效率的6倍。此外,野生型金黄色葡萄球菌通过大规模上调其毒力基因表达来突破宿主免疫防御;而VBNC状态金黄色葡萄球菌则表现出不同的致病模式。首先其毒力基因表达延迟,会优先激活生物膜形成相关基因以创造复苏条件,随后通过应激响应系统逐步恢复毒力基因表达,最终重建致病能力并引发线虫慢性感染。这种独特的毒力复苏机制使VBNC状态金黄色葡萄球菌能够在宿主免疫压力下实现长期定植。因此,很有必要对环境系统中典型致病菌及其VBNC状态的致病菌的毒性进行长期监测来避免潜在的健康风险。
Infectious diseases caused by pathogenic bacteria pose a critical threat to global public health security. However
existing research predominantly focuses on elucidating the acute virulence mechanisms of typical cultura
ble (Wild-Type
WT) pathogenic bacteria
whereas studies on the host infection modes
virulence levels
and pathogenic mechanisms of viable but non-culturable (VBNC) state pathogens are notably lacking. Therefore
this study established a
Staphylococcus aureus
(
S. aureus
) (including VBNC state) -
Caenorhabditis elegans
(
C. elegans
) infection system. Following infection
S. aureus
within exposed nematodes was released via lysis techniques to investigate bacterial state transitions
virulence protein secretion
and virulence gene expression patterns
aiming to elucidate infection mechanisms under distinct bacterial states. Findings of this research revealed that wild-type
S. aureus
exhibited accelerated proliferation and intestinal colonization in nematodes
accompanied by substantial virulence protein release
triggering acute infection. In contrast
VBNC-state
S. aureus
displayed significantly reduced reproductive and colonization capacities. Notably
VBNC-state
S. aureus
underwent resuscitation within the nematode host
achieving a resuscitation rate of 90.4%
representing a sixfold increase compared with natural resuscitation
in vitro
. Furthermore
wild-type
S. aureus
subverted host immune defenses through global upregulation of virulence gene expression. Conversely
VBNC-state
S. aureus
exhibited a distinct pathogenic pattern: delayed virulence gene expression
prioritized activation of biofilm formation-related genes to establish resuscitation conditions
followed by gradual restoration of virulence gene expression through stress response systems
ultimately re-establishing pathogenicity and inducing chronic infection. This unique virulence resuscitation mechanism facilitates VBNC-state
S. aureus
in maintaining long-term colonization under host immune pressure. Consequently
long-term monitoring of both typica
l pathogenic bacteria and their VBNC-state counterparts in environmental systems is imperative to prevent potential health risks.
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