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Identification of the Lipopolysaccharide Core of Yersinia pestis and Yersinia pseudotuberculosis as the Receptor for Bacteriophage φA1122 ▿

机译:鼠疫耶尔森氏菌和假结核耶尔森氏菌脂多糖核心作为噬菌体φA1122受体的鉴定 ▿

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摘要

φA1122 is a T7-related bacteriophage infecting most isolates of Yersinia pestis, the etiologic agent of plague, and used by the CDC in the identification of Y. pestis. φA1122 infects Y. pestis grown both at 20°C and at 37°C. Wild-type Yersinia pseudotuberculosis strains are also infected but only when grown at 37°C. Since Y. pestis expresses rough lipopolysaccharide (LPS) missing the O-polysaccharide (O-PS) and expression of Y. pseudotuberculosis O-PS is largely suppressed at temperatures above 30°C, it has been assumed that the phage receptor is rough LPS. We present here several lines of evidence to support this. First, a rough derivative of Y. pseudotuberculosis was also φA1122 sensitive when grown at 22°C. Second, periodate treatment of bacteria, but not proteinase K treatment, inhibited the phage binding. Third, spontaneous φA1122 receptor mutants of Y. pestis and rough Y. pseudotuberculosis could not be isolated, indicating that the receptor was essential for bacterial growth under the applied experimental conditions. Fourth, heterologous expression of the Yersinia enterocolitica O:3 LPS outer core hexasaccharide in both Y. pestis and rough Y. pseudotuberculosis effectively blocked the phage adsorption. Fifth, a gradual truncation of the core oligosaccharide into the Hep/Glc (l-glycero-d-manno-heptose/d-glucopyranose)-Kdo/Ko (3-deoxy-d-manno-oct-2-ulopyranosonic acid/d-glycero-d-talo-oct-2-ulopyranosonic acid) region in a series of LPS mutants was accompanied by a decrease in phage adsorption, and finally, a waaA mutant expressing only lipid A, i.e., also missing the Kdo/Ko region, was fully φA1122 resistant. Our data thus conclusively demonstrated that the φA1122 receptor is the Hep/Glc-Kdo/Ko region of the LPS core, a common structure in Y. pestis and Y. pseudotuberculosis.
机译:φA1122是与T7相关的噬菌体,可感染鼠疫耶尔森氏菌(鼠疫的病原体)的大多数分离株,并由CDC用于鉴定鼠疫耶尔森氏菌。 φA1122感染在20°C和37°C均生长的鼠疫耶尔森氏菌。野生型耶尔森氏菌假结核菌株也被感染,但仅在37℃下生长。由于鼠疫耶尔森氏菌表达缺少O多糖(O-PS)的粗糙脂多糖(LPS)并且假结核耶尔森氏菌O-PS的表达在高于30°C的温度下受到很大抑制,因此可以认为噬菌体受体是粗糙LPS。 。我们在这里提出了几条证据来支持这一点。首先,假结核耶尔森氏菌的粗衍生物在22℃下生长时对φA1122也敏感。其次,细菌的高碘酸盐处理而不是蛋白酶K处理抑制了噬菌体结合。第三,无法分离出鼠疫耶尔森氏菌和粗糙性假结核耶尔森氏菌的自发φA1122受体突变体,表明该受体在应用的实验条件下对于细菌的生长是必不可少的。第四,小肠结肠炎耶尔森氏菌和粗糙性假结核耶尔森氏菌中小肠结肠炎耶尔森菌O:3 LPS外核心六糖的异源表达有效地阻断了噬菌体的吸附。第五,将核心寡糖逐渐截断为Hep / Glc(1-甘油-d-甘露聚糖-庚糖/ d-吡喃葡萄糖)-Kdo / Ko(3-脱氧-d-甘露糖-辛基-2-铀-吡喃磺酸/ d一系列LPS突变体中的-glycero-d-talo-oct-2-ulopyranosonic acid)区伴随着噬菌体吸附的减少,最后是仅表达脂质A的waaA突变体,即也缺少Kdo / Ko区,完全具有ΦA1122抵抗能力。因此,我们的数据最终证明了φA1122受体是LPS核心的Hep / Glc-Kdo / Ko区,这是鼠疫耶尔森氏菌和假结核耶尔森氏菌的常见结构。

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