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杜克雷嗜血杆菌可抑制U-937细胞(一种人巨噬细胞样细胞系)的吞噬作用。

Haemophilus ducreyi inhibits phagocytosis by U-937 cells, a human macrophage-like cell line.

作者信息

Wood G E, Dutro S M, Totten P A

机构信息

Department of Medicine, Division of Infectious Diseases, University of Washington, Seattle, Washington 98195, USA.

出版信息

Infect Immun. 2001 Aug;69(8):4726-33. doi: 10.1128/IAI.69.8.4726-4733.2001.

Abstract

Haemophilus ducreyi is a gram-negative obligate human pathogen that causes the genital ulcer disease chancroid. Chancroid lesions are deep necrotic ulcers with an immune cell infiltrate that includes macrophages. Despite the presence of these phagocytic cells, chancroid ulcers can persist for months and live H. ducreyi can be isolated from these lesions. To analyze the interaction of H. ducreyi with macrophages, we investigated the ability of H. ducreyi strain 35000 to adhere to, invade, and survive within U-937 cells, a human macrophage-like cell line. We found that although H. ducreyi strain 35000 adhered efficiently to U-937 cells, few bacteria were internalized, suggesting that H. ducreyi avoids phagocytosis by human macrophages. The few bacteria that were phagocytosed in these experiments were rapidly killed. We also found that H. ducreyi inhibits the phagocytosis of a secondary target (opsonized sheep red blood cells). Antiphagocytic activity was found in logarithmic, stationary-phase, and plate-grown cultures and was associated with whole, live bacteria but not with heat-killed cultures, sonicates, or culture supernatants. Phagocytosis was significantly inhibited after a 15-min exposure to H. ducreyi, and a multiplicity of infection of approximately 1 CFU per macrophage was sufficient to cause a significant reduction in phagocytosis by U-937 cells. Finally, all of nine H. ducreyi strains tested were antiphagocytic, suggesting that this is a common virulence mechanism for this organism. This finding suggests a mechanism by which H. ducreyi avoids killing and clearance by macrophages in chancroid lesions and inguinal lymph nodes.

摘要

杜克雷嗜血杆菌是一种革兰氏阴性专性人类病原体,可引起生殖器溃疡疾病软下疳。软下疳病变是伴有包括巨噬细胞在内的免疫细胞浸润的深部坏死性溃疡。尽管存在这些吞噬细胞,但软下疳溃疡可持续数月,并且可从这些病变中分离出活的杜克雷嗜血杆菌。为了分析杜克雷嗜血杆菌与巨噬细胞的相互作用,我们研究了杜克雷嗜血杆菌35000菌株黏附、侵入U-937细胞(一种人巨噬细胞样细胞系)并在其中存活的能力。我们发现,尽管杜克雷嗜血杆菌35000菌株能有效地黏附于U-937细胞,但很少有细菌被内化,这表明杜克雷嗜血杆菌可避免被人巨噬细胞吞噬。在这些实验中被吞噬的少数细菌会迅速被杀灭。我们还发现,杜克雷嗜血杆菌会抑制对第二个靶标(调理过的绵羊红细胞)的吞噬作用。在对数期、稳定期和平板培养的培养物中均发现了抗吞噬活性,且该活性与完整的活细菌有关,而与热灭活培养物、超声裂解物或培养上清液无关。暴露于杜克雷嗜血杆菌15分钟后,吞噬作用受到显著抑制,每个巨噬细胞约1 CFU的感染复数足以导致U-937细胞的吞噬作用显著降低。最后,所测试的9株杜克雷嗜血杆菌菌株均具有抗吞噬作用,这表明这是该病原体的一种常见毒力机制。这一发现提示了一种机制,通过该机制杜克雷嗜血杆菌可在软下疳病变和腹股沟淋巴结中避免被巨噬细胞杀灭和清除。

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本文引用的文献

1
Interaction between Salmonella typhimurium and phagocytic cells in cell culture.
J Infect Dis. 1958 Nov-Dec;103(3):272-7. doi: 10.1093/infdis/103.3.272.
3
DsrA-deficient mutant of Haemophilus ducreyi is impaired in its ability to infect human volunteers.
Infect Immun. 2001 Mar;69(3):1488-91. doi: 10.1128/IAI.69.3.1488-1491.2001.
5
Nonspecific adherence by Actinobacillus actinomycetemcomitans requires genes widespread in bacteria and archaea.
J Bacteriol. 2000 Nov;182(21):6169-76. doi: 10.1128/JB.182.21.6169-6176.2000.
6
Helicobacter pylori inhibits phagocytosis by professional phagocytes involving type IV secretion components.
Mol Microbiol. 2000 Sep;37(6):1389-404. doi: 10.1046/j.1365-2958.2000.02089.x.
7
Serum resistance in Haemophilus ducreyi requires outer membrane protein DsrA.
Infect Immun. 2000 Mar;68(3):1608-19. doi: 10.1128/IAI.68.3.1608-1619.2000.
8
Cytolethal distending toxin of Haemophilus ducreyi induces apoptotic death of Jurkat T cells.
Infect Immun. 1999 Dec;67(12):6394-402. doi: 10.1128/IAI.67.12.6394-6402.1999.
9
Characterization of a Haemophilus ducreyi mutant deficient in expression of cytolethal distending toxin.
Infect Immun. 1999 Aug;67(8):3900-8. doi: 10.1128/IAI.67.8.3900-3908.1999.
10
Target cell range of Haemophilus ducreyi hemolysin and its involvement in invasion of human epithelial cells.
Infect Immun. 1999 Aug;67(8):3740-9. doi: 10.1128/IAI.67.8.3740-3749.1999.

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