McQuiston J H, McQuiston J R, Cox A D, Wu Y, Boyle S M, Inzana T J
Center for Molecular Medicine and Infectious Diseases, Virginia-Maryland Regional College of Veterinary Medicine, Blacksburg, VA 24061, USA.
Microb Pathog. 2000 May;28(5):301-12. doi: 10.1006/mpat.1999.0351.
Repetitive tetranucleotide sequences of 5'-(CAAT)(n)-3' have been identified at the 5' end of an open reading frame (ORF) named lob1 from Haemophilus somnus strain 738. Based on sequence analysis, lob1 has 59% DNA homology to lex2B, which is involved in lipooligosaccharide (LOS) biosynthesis in H. influenzae. We now report that the number of 5'-CAAT-3' repeats in lob1 varied from 31-35, but that 94% of colonies contained 33 repeats of 5'-CAAT-3' downstream of two potential start codons, as determined by DNA sequence analysis of the 5'-CAAT-3' region from individual colonies. If transcription began with the start codon closest to the 5'-CAAT-3' repeats, a protein of 34.5 kDa would be encoded when 33 repeats were present. However, we could not establish a correlation between the number of 5'-CAAT-3' repeats in lob1 with a specific LOS electrophoretic profile or reactivity with two LOS monoclonal antibodies, indicating multiple genes control LOS phase variation in H. somnus. Complementation of strain 129Pt with lob1 containing 33 5 '-CAAT-3' repeats in shuttle vector pLS88 resulted in transformants 129Pt(pLSlob1-33A) and 129Pt(pLSlob1-33B), both of which demonstrated the same altered LOS electrophoretic profile. Unlike strain 129Pt, both transformants underwent limited LOS phase variation, which correlated with variation in the number of 5'-CAAT-3' repeats in pLSlob1-33. Nanoelectrospray-mass spectrometry of O-deacylated LOS indicated that transformant 129Pt(pLSlob1-33A) LOS was composed of a different distribution of glycoforms than LOS of the parent strain. The ratio of glucose to galactose changed from 1:2 in strain 129Pt LOS to 2:1 in transformant 129Pt(pLSlob1-33A) LOS, as determined by gas chromatography-mass spectrometry. Nuclear magnetic resonance spectroscopy confirmed and extended these observations. Transformant 129Pt(pLSlob1-33A) was constitutively more reactive in colony immunoblotting to polyclonal antiserum made to purified strain 738 LOS, and was more susceptible to complement-mediated killing in the presence of anti-738 LOS serum than parent strain 129Pt. Based on these results, Lob1 appears to be a phase variable galactosyl transferase involved in LOS biosynthesis in H. somnus.
在嗜眠嗜血杆菌738菌株一个名为lob1的开放阅读框(ORF)的5'端,已鉴定出5'-(CAAT)(n)-3'的重复四核苷酸序列。基于序列分析,lob1与lex2B有59%的DNA同源性,lex2B参与流感嗜血杆菌的脂寡糖(LOS)生物合成。我们现在报告,lob1中5'-CAAT-3'重复序列的数量在31至35之间变化,但通过对单个菌落的5'-CAAT-3'区域进行DNA序列分析确定,94%的菌落含有两个潜在起始密码子下游的33个5'-CAAT-3'重复序列。如果转录从最接近5'-CAAT-3'重复序列的起始密码子开始,当存在33个重复序列时,将编码一个34.5 kDa的蛋白质。然而,我们无法在lob1中5'-CAAT-3'重复序列的数量与特定的LOS电泳图谱或与两种LOS单克隆抗体的反应性之间建立相关性,这表明多个基因控制嗜眠嗜血杆菌的LOS相变。用穿梭载体pLS88中含有33个5 '-CAAT-3'重复序列的lob1对129Pt菌株进行互补,产生了转化体129Pt(pLSlob1-33A)和129Pt(pLSlob1-33B),两者都表现出相同的改变的LOS电泳图谱。与129Pt菌株不同,两个转化体都经历了有限的LOS相变,这与pLSlob1-33中5'-CAAT-3'重复序列数量的变化相关。对O-脱酰化LOS的纳米电喷雾质谱分析表明,转化体129Pt(pLSlob1-33A)的LOS由与亲本菌株LOS不同的糖型分布组成。通过气相色谱-质谱分析确定,葡萄糖与半乳糖的比例从129Pt菌株LOS中的1:2变为转化体129Pt(pLSlob1-33A)LOS中的2:1。核磁共振光谱证实并扩展了这些观察结果。转化体129Pt(pLSlob1-33A)在菌落免疫印迹中对针对纯化的738菌株LOS制备的多克隆抗血清的反应性更强,并且在存在抗738 LOS血清的情况下比亲本菌株129Pt更容易受到补体介导的杀伤。基于这些结果,Lob1似乎是一种参与嗜眠嗜血杆菌LOS生物合成的相变可变半乳糖基转移酶。