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Tn916-generated lipooligosaccharide mutants of Neisseria meningitidis and Neisseria gonorrhoeae.

机译:Tn916生成的脑膜炎奈瑟氏球菌和淋病奈瑟氏球菌的脂寡糖突变体。

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摘要

A library of Tn916-generated, tetracycline-resistant (Tc) mutants of the group B Neisseri meningitidis strain NMB was screened by using monoclonal antibodies (MAbs) that recognize structural differences in neisserial lipooligosaccharide (LOS). The LOS of parental strain NMB had a relative molecular mass of 4.5 kDa, reacted with MAbs 3F11 and 6B4 but not with MAb 4C4 or 6E4, and contained a lacto-N-neotetrose unit. Two phenotypically stable mutants, SS3 and R6, altered in LOS, were identified by colony immunoblots, electrophoresis, and Western immunoblots. The LOS of mutant SS3 was 3.4 kDa and reacted with MAbs 4C4 and 6E4 but not MAb 3E11 or 6B4. The LOS of mutant R6 was 3.1 to 3.2 kDa and reacted with MAb 6E4 but not MAb 3F11, 6B4, or 4C4. Thus, the LOSs of the R6 and SS3 mutants were predicted to contain different truncations of the core oligosaccharide. The LOS phenotype of each mutant was linked to Tc(r), as determined by transformation of the parent strain with DNA from the mutant. Southern hybridizations and single-specific-primer PCR revealed in each mutant a single truncated tn916 insertion which had lost genes required for mobilization. Tn916 mutagenesis was used to identify two distinct genetic sites in the meningococcal chromosome involved in biosynthesis of the oligosaccharide chain of LOS and to create genetically defined LOS mutants of N. meningitidis and Neisseria gonorrhoeae.
机译:使用识别奈瑟球状脂寡糖(LOS)结构差异的单克隆抗体(MAb)筛选Bn群脑膜炎奈瑟氏球菌NMB组Tn916产生的四环素抗性(Tc)突变体的文库。亲本菌株NMB的LOS具有4.5kDa的相对分子量,与MAbs 3F11和6B4反应,但不与MAb 4C4或6E4反应,并且含有乳酸-N-neottrose单元。通过菌落免疫印迹,电泳和Western免疫印迹鉴定了两个表型稳定的突变体SS3和R6,它们在LOS中发生了改变。突变体SS3的LOS为3.4kDa,并且与MAb 4C4和6E4反应,但不与MAb 3E11或6B4反应。突变体R6的LOS为3.1至3.2kDa,并且与MAb 6E4反应,但不与MAb 3F11、6B4或4C4反应。因此,预计R6和SS3突变体的LOS包含核心寡糖的不同截短。每个突变体的LOS表型都与Tc(r)相连,这是通过用来自突变体的DNA转化亲本菌株来确定的。 Southern杂交和单特异性引物PCR在每个突变体中揭示了单个截短的tn916插入,其已经丢失了动员所需的基因。 Tn916诱变用于鉴定脑膜炎球菌染色体中两个与LOS寡糖链生物合成有关的独特遗传位点,并创建脑膜炎奈瑟氏球菌和淋病奈瑟氏球菌的遗传定义LOS突变体。

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