Hickey T E, McVeigh A L, Scott D A, Michielutti R E, Bixby A, Carroll S A, Bourgeois A L, Guerry P
Enteric Diseases Department, Naval Medical Research Center, Silver Spring, Maryland 20910, USA.
Infect Immun. 2000 Dec;68(12):6535-41. doi: 10.1128/IAI.68.12.6535-6541.2000.
Live cells of Campylobacter jejuni and Campylobacter coli can induce release of interleukin-8 (IL-8) from INT407 cells. Additionally, membrane fractions of C. jejuni 81-176, but not membrane fractions of C. coli strains, can also induce release of IL-8. Membrane preparations from 81-176 mutants defective in any of the three membrane-associated protein subunits of cytolethal distending toxin (CDT) were unable to induce IL-8. The presence of the three cdt genes on a shuttle plasmid in trans restored both CDT activity and the ability to release IL-8 to membrane fractions. However, CDT mutations did not affect the ability of 81-176 to induce IL-8 during adherence to or invasion of INT407 cells. When C. jejuni cdt genes were transferred on a shuttle plasmid into a C. coli strain lacking CDT, membrane preparations became positive in both CDT and IL-8 assays. Growth of C. jejuni in physiological levels of sodium deoxycholate released all three CDT proteins, as well as CDT activity and IL-8 activity, from membranes into supernatants. Antibodies against recombinant forms of each of the three CDT subunit proteins neutralized both CDT activity and the activity responsible for IL-8 release. The data suggest that C. jejuni can induce IL-8 release from INT407 cells by two independent mechanisms, one of which requires adherence and/or invasion and the second of which requires CDT.
空肠弯曲菌和大肠弯曲菌的活细胞可诱导INT407细胞释放白细胞介素-8(IL-8)。此外,空肠弯曲菌81-176的膜组分可诱导IL-8释放,而大肠弯曲菌菌株的膜组分则不能。细胞致死性扩张毒素(CDT)的三个膜相关蛋白亚基中任何一个有缺陷的81-176突变体的膜制剂都无法诱导IL-8释放。穿梭质粒上三个cdt基因的反式存在恢复了CDT活性以及膜组分释放IL-8的能力。然而,CDT突变并不影响81-176在粘附或侵入INT407细胞期间诱导IL-8的能力。当空肠弯曲菌cdt基因通过穿梭质粒转移到缺乏CDT的大肠弯曲菌菌株中时,膜制剂在CDT和IL-8检测中均呈阳性。空肠弯曲菌在生理水平的脱氧胆酸钠中生长会使所有三种CDT蛋白以及CDT活性和IL-8活性从膜释放到上清液中。针对三种CDT亚基蛋白各自重组形式的抗体中和了CDT活性和负责IL-8释放的活性。数据表明,空肠弯曲菌可通过两种独立机制诱导INT407细胞释放IL-8,其中一种机制需要粘附和/或侵入,另一种机制需要CDT。