Turner Kelli L, Cahill Bethaney K, Dilello Sarah K, Gutel Dedra, Brunson Debra N, Albertí Sebastián, Ellis Terri N
Department of Biology, University of North Florida, Jacksonville, Florida, USA.
IUNICS, University of the Balearic Islands, Palma de Mallorca, Spain.
Antimicrob Agents Chemother. 2015 Dec 14;60(3):1360-9. doi: 10.1128/AAC.01627-15.
Antibiotic-resistant strains of Klebsiella pneumoniae often exhibit porin loss. In this study, we investigated how porin loss impacted the composition of secreted outer membrane vesicles as well as their ability to trigger proinflammatory cytokine secretion by macrophages. We hypothesize that porin loss associated with antibiotic resistance will directly impact both the composition of outer membrane vesicles and their interactions with phagocytic cells. Using clonally related clinical isolates of extended-spectrum beta-lactamase (ESBL)-positive Klebsiella pneumoniae with different patterns of porin expression, we demonstrated that altered expression of OmpK35 and OmpK36 results in broad alterations to the protein profile of secreted vesicles. Additionally, the level of OmpA incorporation was elevated in strains lacking a single porin. Porin loss significantly impacted macrophage inflammatory responses to purified vesicles. Outer membrane vesicles lacking both OmpK35 and OmpK36 elicited significantly lower levels of proinflammatory cytokine secretion than vesicles from strains expressing one or both porins. These data demonstrate that antibiotic resistance-associated porin loss has a broad and significant effect on both the composition of outer membrane vesicles and their interactions with phagocytic cells, which may impact bacterial survival and inflammatory reactions in the host.
肺炎克雷伯菌的抗生素耐药菌株常常表现出孔蛋白缺失。在本研究中,我们调查了孔蛋白缺失如何影响分泌性外膜囊泡的组成以及它们触发巨噬细胞分泌促炎细胞因子的能力。我们假设与抗生素耐药性相关的孔蛋白缺失将直接影响外膜囊泡的组成及其与吞噬细胞的相互作用。使用具有不同孔蛋白表达模式的超广谱β-内酰胺酶(ESBL)阳性肺炎克雷伯菌的克隆相关临床分离株,我们证明OmpK35和OmpK36表达的改变会导致分泌性囊泡的蛋白质谱发生广泛变化。此外,在缺乏单个孔蛋白的菌株中,OmpA掺入水平升高。孔蛋白缺失显著影响巨噬细胞对纯化囊泡的炎症反应。与表达一种或两种孔蛋白的菌株来源的囊泡相比,同时缺乏OmpK35和OmpK36的外膜囊泡引发的促炎细胞因子分泌水平显著降低。这些数据表明,与抗生素耐药性相关的孔蛋白缺失对外膜囊泡的组成及其与吞噬细胞的相互作用具有广泛而显著的影响,这可能会影响宿主中的细菌存活和炎症反应。