Luo Hua, Ni Lijia, Chen Tongling, Huang Lisi, Zhang Xiaofan, Li Xuexue, Liao Xiaoyan, Shen Rui, Luo Zhaofan, Xie Xiaoying
Department of Clinical Laboratory, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, China.
Institution of Antibiotic, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, China.
BMC Infect Dis. 2024 Oct 1;24(1):1092. doi: 10.1186/s12879-024-10001-2.
The contribution of interspecies interactions between coinfecting pathogens to chronic refractory infection by affecting pathogenicity is well established. However, little is known about the impact of intraspecific interactions on infection relapse, despite the cross-talk of different strains within one species is more common in clinical infection. We reported a case of chronic refractory pulmonary infection relapse, caused by two methicillin-sensitive S. aureus (MSSA) strains (SA01 and SA02) and revealed a novel strategy for relapse via intraspecific cooperation.
The hemolytic ability, growth curve, biofilm formation, virulence genes and response of G. mellonella larvae to S. aureus infection were analysed to confirm this hypothesis.
SA02 hemolytic activity was inhibited by SA01, along with the expression of hemolysin genes and the virulence factor Hla. Additionally, SA01 significantly enhanced the biofilm formation of SA02. AIP-RNAIII may be a possible pathway for this interaction. Compared with mono-infection, a worse outcome (decreased larval survival and increased microbial burden) of the two MSSA strains coinfected with G. mellonella confirmed that intraspecific interactions indeed enhanced bacterial survival in vivo.
The intraspecific interaction of S. aureus could lead to chronic refractory infection via pathogenicity changes.
共感染病原体之间的种间相互作用通过影响致病性对慢性难治性感染的作用已得到充分证实。然而,尽管同一物种内不同菌株之间的相互作用在临床感染中更为常见,但关于种内相互作用对感染复发的影响却知之甚少。我们报告了一例由两种对甲氧西林敏感的金黄色葡萄球菌(MSSA)菌株(SA01和SA02)引起的慢性难治性肺部感染复发病例,并揭示了一种通过种内合作导致复发的新策略。
分析溶血能力、生长曲线、生物膜形成、毒力基因以及米氏蜜蜂幼虫对金黄色葡萄球菌感染的反应,以证实这一假设。
SA01抑制了SA02的溶血活性,同时抑制了溶血素基因和毒力因子Hla的表达。此外,SA01显著增强了SA02的生物膜形成。AIP-RNAIII可能是这种相互作用的一条潜在途径。与单一感染相比,米氏蜜蜂幼虫同时感染两种MSSA菌株的结果更差(幼虫存活率降低和微生物负荷增加),这证实了种内相互作用确实增强了细菌在体内的存活能力。
金黄色葡萄球菌的种内相互作用可通过致病性改变导致慢性难治性感染。