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霍乱弧菌溶细胞素可促进完整的人肠黏膜分泌氯化物。

The Vibrio cholerae cytolysin promotes chloride secretion from intact human intestinal mucosa.

作者信息

Debellis Lucantonio, Diana Anna, Arcidiacono Diletta, Fiorotto Romina, Portincasa Piero, Altomare Donato Francesco, Spirlì Carlo, de Bernard Marina

机构信息

Department of General and Environmental Physiology, University of Bari, Bari, Italy.

出版信息

PLoS One. 2009;4(3):e5074. doi: 10.1371/journal.pone.0005074. Epub 2009 Mar 31.

Abstract

BACKGROUND

The pathogenicity of the Vibrio cholerae strains belonging to serogroup O1 and O139 is due to the production of virulence factors such as cholera toxin (CT) and the toxin-coregulated pilus (TCP). The remaining serogroups, which mostly lack CT and TCP, are more frequently isolated from aquatic environmental sources than from clinical samples; nevertheless, these strains have been reported to cause human disease, such as sporadic outbreaks of watery diarrhoea and inflammatory enterocolitis. This evidence suggested the possibility that other virulence factor(s) than cholera toxin might be crucial in the pathogenesis of Vibrio cholerae-induced diarrhoea, but their nature remains unknown. VCC, the hemolysin produced by virtually all Vibrio cholerae strains, has been proposed as a possible candidate, though a clear-cut demonstration attesting VCC as crucial in the pathogenesis of Vibrio cholerae-induced diarrhoea is still lacking.

METHODOLOGY/PRINCIPAL FINDINGS: Electrophysiological parameters and paracellular permeability of stripped human healthy colon tissues, obtained at subtotal colectomy, mounted in Ussing chamber were studied in the presence or absence of VCC purified from culture supernatants of V. cholerae O1 El Tor strain. Short circuit current (I(SC)) and transepithelial resistance (R(T)) were measured by a computerized voltage clamp system. The exposure of sigmoid colon specimens to 1 nM VCC resulted in an increase of I(SC) by 20.7%, with respect to the basal values, while R(T) was reduced by 12.3%. Moreover, increase in I(SC) was abolished by bilateral Cl(-) reduction.

CONCLUSION/SIGNIFICANCE: Our results demonstrate that VCC, by forming anion channels on the apical membrane of enterocytes, triggers an outward transcellular flux of chloride. Such an ion movement, associated with the outward movement of Na(+) and water, might be responsible for the diarrhoea caused by the non-toxigenic strains of Vibrio cholerae.

摘要

背景

霍乱弧菌O1群和O139群菌株的致病性源于霍乱毒素(CT)和毒素协同调节菌毛(TCP)等毒力因子的产生。其余血清群大多缺乏CT和TCP,相较于临床样本,它们更常从水生环境来源中分离得到;然而,据报道这些菌株会引发人类疾病,如散发性水样腹泻和炎症性小肠结肠炎。这一证据表明,除霍乱毒素外,其他毒力因子可能在霍乱弧菌所致腹泻的发病机制中起关键作用,但其性质仍不清楚。尽管仍缺乏明确证据证明VCC(几乎所有霍乱弧菌菌株产生的溶血素)在霍乱弧菌所致腹泻的发病机制中起关键作用,但它已被提出作为一种可能的候选因子。

方法/主要发现:在有无从霍乱弧菌O1埃尔托生物型菌株培养上清液中纯化得到的VCC的情况下,研究了在乌斯辛克室中安装的、取自全结肠切除术的剥离人健康结肠组织的电生理参数和细胞旁通透性。通过计算机化电压钳系统测量短路电流(I(SC))和跨上皮电阻(R(T))。将乙状结肠标本暴露于1 nM VCC后,I(SC)相对于基础值增加了20.7%,而R(T)降低了12.3%。此外,双侧Cl(-)减少可消除I(SC)的增加。

结论/意义:我们的结果表明,VCC通过在肠上皮细胞顶端膜上形成阴离子通道,触发氯离子的外向跨细胞通量。这种离子运动与Na(+)和水的外向运动相关,可能是霍乱弧菌非产毒菌株所致腹泻的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c9d/2659442/925895ab136b/pone.0005074.g001.jpg

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