MacPhee D G, Krishnapillai V, Roantree R J, Stocker B A
J Gen Microbiol. 1975 Mar;87(1):1-10. doi: 10.1099/00221287-87-1-1.
Several mutants obtained from smooth Salmonella typhimurium strains by selection for resistance to Felix O (FO) phage [whose receptor site includes the N-acetylglucosamine branch of the lipopolysaccharide (LPS) core] were smooth in cultural properties, antigenic character and phage sensitivity pattern (except for their FO resistance). However, the affected genes of several such 'FOR' (FO-resistant) mutants were shown by transduction of map in the short cysE-pyrE segment, which includes nearly all known rfa genes responsible for synthesis of LPS core. All of seven FOR mutants differed from their parents, and resembled rfa mutants with defects in the deeper part of the LPS core, by increased sensitivity to various antibiotics. One FOR mutant was non-virulent (LD50 greater than 10-7, compared with smaller than 100 for its parent); LT7 derivatives given this FOR gene by co-transduction with cysE+ were likewise non-virulent. It is inferred that FOR mutations affect the assembly of the inner part of the LPS core, perhaps causing incomplete blocks in glycosyl transferase reactions.
通过选择对费利克斯O(FO)噬菌体(其受体位点包括脂多糖(LPS)核心的N - 乙酰葡糖胺分支)具有抗性,从光滑型鼠伤寒沙门氏菌菌株获得了几个突变体。这些突变体在培养特性、抗原特性和噬菌体敏感性模式方面均为光滑型(除了它们对FO的抗性)。然而,通过转导图谱显示,几个这样的“FOR”(FO抗性)突变体的受影响基因位于短的cysE - pyrE区段,该区段几乎包含所有已知的负责LPS核心合成的rfa基因。七个FOR突变体均与其亲本不同,并且通过对各种抗生素的敏感性增加,类似于在LPS核心较深部分存在缺陷的rfa突变体。一个FOR突变体无毒(LD50大于10^-7,而其亲本小于100);通过与cysE +共转导赋予该FOR基因的LT7衍生物同样无毒。据推测,FOR突变影响LPS核心内部的组装,可能导致糖基转移酶反应的不完全阻断。