Wu Y, McQuiston J H, Cox A, Pack T D, Inzana T J
Center for Molecular Medicine and Infectious Diseases, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
Infect Immun. 2000 Jan;68(1):310-9. doi: 10.1128/IAI.68.1.310-319.2000.
Haemophilus somnus undergoes antigenic and structural phase variation in its lipooligosaccharide (LOS). A gene (lob-1) containing repetitive 5'-CAAT-3' sequences that may, in part, contribute to phase variation was cloned and sequenced (T. J. Inzana et al., Infect. Immun. 65:4675-4681, 1997). We have now identified another putative gene (lob-2A) immediately upstream from lob-1. Lob-2A contained homology to several LOS biosynthesis proteins of the family Pasteurellaceae and the LgtB and LgtE galactosyltransferases of Neisseria meningitidis and N. gonorrhoeae. Unlike lob-1, lob-2A contained 18 to 20 5'-GA-3' repeats 141 bp upstream of the termination codon as determined by PCR amplification of DNA from individual colonies. Twenty repeats were most common, but when 19 5'-GA-3' repeats were present a stop codon would occur 1 bp after the last 5'-GA-3' repeat. A 630-bp SalI-BsgI fragment within lob-2A was deleted, and a kanamycin resistance (Km(r)) gene was inserted into this site to create pCAATDeltalob2A. Following electroporation of pCAATDeltalob2A into H. somnus 738, several allelic exchange mutants were isolated. The LOS electrophoretic profile of one mutant, strain 738-lob2A1::Km, was altered, and the phase variation rate was reduced but phase variation was not eliminated. A variant with 19 5'-GA-3' repeats in lob-2A had an LOS profile similar to that of 738-lob2A1::Km, suggesting that lob-2A was turned off in this phase. Nanoelectrospray mass spectrometry (nES-MS) and nuclear magnetic resonance spectroscopy showed that 738-lob2A1::Km was deficient in the terminal betaGal(1-3)betaGlcNAc residue present in parent strain 738. Mutant 738-lob2A1::Km was significantly more sensitive to the bactericidal action of normal bovine serum and was less virulent in mice than was parent strain 738. When H. somnus 129Pt was electrotransformed with shuttle vector pLS88 containing lob-2A, its LOS electrophoretic profile was modified and additional N-acetylhexosamine residues were present, as determined by nES-MS analysis. These results indicated that lob-2A may be an N-acetylglucosamine transferase involved in LOS biosynthesis and phase variation and that LOS structure is important to H. somnus virulence.
睡眠嗜血杆菌的脂寡糖(LOS)会发生抗原性和结构相变。一个含有重复的5'-CAAT-3'序列的基因(lob-1)被克隆并测序,该序列可能在一定程度上导致了相变(T. J. Inzana等人,《感染与免疫》65:4675 - 4681,1997)。我们现在在lob-1上游紧邻位置鉴定出了另一个假定基因(lob-2A)。Lob-2A与巴斯德菌科的几种LOS生物合成蛋白以及脑膜炎奈瑟菌和淋病奈瑟菌的LgtB和LgtE半乳糖基转移酶具有同源性。与lob-1不同,通过对单个菌落的DNA进行PCR扩增确定,lob-2A在终止密码子上游141 bp处含有18至20个5'-GA-3'重复序列。20个重复序列最为常见,但当存在19个5'-GA-3'重复序列时,在最后一个5'-GA-3'重复序列后1 bp处会出现一个终止密码子。删除了lob-2A内一个630 bp的SalI - BsgI片段,并将卡那霉素抗性(Km(r))基因插入该位点,构建了pCAATDeltalob2A。将pCAATDeltalob2A电穿孔导入睡眠嗜血杆菌738后,分离出了几个等位基因交换突变体。其中一个突变体菌株738-lob2A1::Km的LOS电泳图谱发生了改变,相变率降低,但相变并未消除。lob-2A中具有19个5'-GA-3'重复序列变体的LOS图谱与738-lob2A1::Km相似,表明在此相变阶段lob-2A处于关闭状态。纳米电喷雾质谱(nES-MS)和核磁共振光谱显示,738-lob2A1::Km缺乏亲本菌株738中存在的末端βGal(1-3)βGlcNAc残基。突变体738-lob2A1::Km对正常牛血清的杀菌作用明显更敏感,并且在小鼠中的毒力比亲本菌株738弱。当用含有lob-2A的穿梭载体pLS88对睡眠嗜血杆菌129Pt进行电转化时,其LOS电泳图谱发生了改变,并且通过nES-MS分析确定存在额外的N-乙酰己糖胺残基。这些结果表明,lob-2A可能是一种参与LOS生物合成和相变的N-乙酰葡糖胺转移酶,并且LOS结构对睡眠嗜血杆菌的毒力很重要。