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Extracellular Polysaccharides Associated with Thin Aggregative Fimbriae of Salmonella enterica Serovar Enteritidis

机译:沙门氏菌肠炎沙门氏菌薄聚集菌毛相关的细胞外多糖

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摘要

Lipopolysaccharide (LPS) O polysaccharide was identified as the principle factor impeding intercellular formation of intact thin aggregative fimbriae (Tafi) in Salmonella enterica serovar Enteritidis. The extracellular nucleation-precipitation assembly pathway for these organelles was investigated by quantifying fimbrial formation between ΔagfA (AgfA recipient) and ΔagfB (AgfA donor) cells harboring mutations in LPS (galE::Tn10) and/or cellulose (ΔbcsA) synthesis. Intercellular complementation could be detected between ΔagfA and ΔagfB strains only when both possessed the galE mutation. LPS O polysaccharide appears to be an impenetrable barrier to AgfA assembly between cells but not within individual cells. The presence of cellulose did not restrict Tafi formation between cells. Transmission electron microscopy of w+ S. enterica serovar Enteritidis 3b cells revealed diffuse Tafi networks without discernible fine structure. In the absence of cellulose, however, individual Tafi fibers were clearly visible, appeared to be occasionally branched, and showed the generally distinctive appearance described for Escherichia coli K-12 curli. A third extracellular matrix component closely associated with cellulose and Tafi was detected on Western blots by using immune serum raised to whole, purified Tafi aggregates. Cellulose was required to tightly link this material to cells. Antigenically similar material was also detected in S. enterica serovar Typhimurium and one diarrheagenic E. coli isolate. Preliminary analysis indicated that this material represented an anionic, extracellular polysaccharide that was distinct from colanic acid. Therefore, Tafi in their native state appear to exist as a complex with cellulose and at least one other component.
机译:脂多糖(LPS)O多糖被认为是阻止肠炎沙门氏菌肠炎沙门氏菌完整薄集聚菌毛(Tafi)细胞间形成的主要因素。通过量化在LPS(galE :: Tn10)和/或纤维素(ΔbcsA)合成中具有突变的ΔagfA(AgfA受体)和ΔagfB(AgfA供体)细胞之间的纤维形成来研究这些细胞器的细胞外成核-沉淀组装途径。仅当两者都具有galE突变时,才能在ΔagfA和ΔagfB菌株之间检测到细胞间互补。 LPS O多糖似乎是细胞之间而不是单个细胞内AgfA组装的不可穿透的屏障。纤维素的存在并不限制细胞之间Tafi的形成。 w +肠炎沙门氏菌血清肠炎沙门氏菌3b细胞的透射电子显微镜显示无明显精细结构的弥散Tafi网络。然而,在不存在纤维素的情况下,单个的Tafi纤维清晰可见,似乎偶尔会分支,并显示出与大肠杆菌K-12 curli所述的总体独特外观。通过使用免疫血清培养完整的纯化Tafi聚集体,在Western印迹上检测到与纤维素和Tafi紧密相关的第三种细胞外基质成分。需要纤维素将这种材料紧密连接到细胞上。在肠炎链球菌血清鼠伤寒沙门氏菌和一种腹泻性大肠杆菌分离物中也检测到抗原相似的物质。初步分析表明,这种物质代表一种不同于可乐酸的阴离子细胞外多糖。因此,处于其天然状态的Tafi似乎与纤维素和至少一种其他组分形成复合物存在。

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