首页> 美国卫生研究院文献>Infection and Immunity >Helicobacter saguini a Novel Helicobacter Isolated from Cotton-Top Tamarins with Ulcerative Colitis Has Proinflammatory Properties and Induces Typhlocolitis and Dysplasia in Gnotobiotic IL-10−/− Mice
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Helicobacter saguini a Novel Helicobacter Isolated from Cotton-Top Tamarins with Ulcerative Colitis Has Proinflammatory Properties and Induces Typhlocolitis and Dysplasia in Gnotobiotic IL-10−/− Mice

机译:幽门螺杆菌是一种新型的幽门螺杆菌从患有溃疡性结肠炎的棉顶Ta猴中分离出来具有促炎特性并能诱导人源性IL-10-/-小鼠的淋巴炎和发育异常。

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摘要

A urease-negative, fusiform, novel bacterium named Helicobacter saguini was isolated from the intestines and feces of cotton-top tamarins (CTTs) with chronic colitis. Helicobacter sp. was detected in 69% of feces or intestinal samples from 116 CTTs. The draft genome sequence, obtained by Illumina MiSeq sequencing, for H. saguini isolate MIT 97-6194-5, consisting of ∼2.9 Mb with a G+C content of 35% and 2,704 genes, was annotated using the NCBI Prokaryotic Genomes Automatic Annotation Pipeline. H. saguini contains homologous genes of known virulence factors found in other enterohepatic helicobacter species (EHS) and H. pylori. These include flagellin, γ-glutamyl transpeptidase (ggt), collagenase, the secreted serine protease htrA, and components of a type VI secretion system, but the genome does not harbor genes for cytolethal distending toxin (cdt). H. saguini MIT 97-6194-5 induced significant levels of interleukin-8 (IL-8) in HT-29 cell culture supernatants by 4 h, which increased through 24 h. mRNAs for the proinflammatory cytokines IL-1β, tumor necrosis factor alpha (TNF-α), IL-10, and IL-6 and the chemokine CXCL1 were upregulated in cocultured HT-29 cells at 4 h compared to levels in control cells. At 3 months postinfection, all H. saguini-monoassociated gnotobiotic C57BL/129 IL-10−/− mice were colonized and had seroconverted to H. saguini antigen with a significant Th1-associated increase in IgG2c (P < 0.0001). H. saguini induced a significant typhlocolitis, associated epithelial defects, mucosa-associated lymphoid tissue (MALT) hyperplasia, and dysplasia. Inflammatory cytokines IL-22, IL-17a, IL-1β, gamma interferon (IFN-γ), and TNF-α, as well as inducible nitric oxide synthase (iNOS) were significantly upregulated in the cecal tissues of infected mice. The expression of the DNA damage response molecule γ-H2AX was significantly higher in the ceca of H. saguini-infected gnotobiotic mice than in the controls. This model using a nonhuman primate Helicobacter sp. can be used to study the pathogenic potential of EHS isolated from primates with naturally occurring inflammatory bowel disease (IBD) and colon cancer.
机译:从患有慢性结肠炎的棉顶猴(CTT)的肠和粪便中分离出一种脲酶阴性,梭状形式的新型细菌,称为萨基尼螺旋杆菌。幽门螺杆菌在116例CTT中,有69%的粪便或肠标本中检出了这种毒素。使用NCBI原核基因组自动注释法,通过Illumina MiSeq测序获得的Saguini分离株MIT 97-6194-5的基因组序列草稿由2.9 Mb的G + C含量为35%和2,704个基因组成。管道。 saguini菌含有在其他肠肝幽门螺杆菌(EHS)和幽门螺杆菌中发现的已知毒力因子的同源基因。这些包括鞭毛蛋白,γ-谷氨酰转肽酶(ggt),胶原酶,分泌的丝氨酸蛋白酶htrA和VI型分泌系统的成分,但基因组中没有细胞致死性扩张毒素(cdt)的基因。 H. saguini MIT 97-6194-5诱导HT-29细胞培养上清液中的白细胞介素8(IL-8)水平显着增加了4 h,并持续了24 h。与共培养的HT-29细胞相比,与对照细胞相比,促炎细胞因子IL-1β,肿瘤坏死因子α(TNF-α),IL-10和IL-6以及趋化因子CXCL1的mRNA在4 h共上调。感染后3个月,所有鼠尾草单链相关致病菌C57BL / 129 IL-10 -// 小鼠均定居,并血清转化为鼠尾草抗原,其Th1相关联的IgG2c显着增加(P <0.0001)。 H. saguini引起严重的淋巴炎,相关的上皮缺损,粘膜相关的淋巴样组织(MALT)增生和不典型增生。在感染小鼠的盲肠组织中,炎性细胞因子IL-22,IL-17a,IL-1β,γ干扰素(IFN-γ)和TNF-α以及诱导型一氧化氮合酶(iNOS)明显上调。 DNA损伤反应分子γ-H2AX的表达在感染沙哑菌的致生菌小鼠的盲肠中明显高于对照组。该模型使用非人类灵长类幽门螺杆菌。可用于研究从患有自然发炎性肠病(IBD)和结肠癌的灵长类动物中分离出的EHS的致病潜力。

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