Arking D, Tong Y, Stein D C
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland 20742, USA.
J Bacteriol. 2001 Feb;183(3):934-41. doi: 10.1128/JB.183.3.934-941.2001.
Neisserial lipooligosaccharide (LOS) contains three oligosaccharide chains, termed the alpha, beta, and gamma chains. We used Southern hybridization experiments on DNA isolated from various Neisseria spp. to determine if strains considered to be nonpathogenic possessed DNA sequences homologous with genes involved in the biosynthesis of these oligosaccharide chains. The presence or absence of specific genes was compared to the LOS profiles expressed by each strain, as characterized by their mobilities on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel and their reactivities with various LOS-specific monoclonal antibodies. A great deal of heterogeneity was seen with respect to the presence of genes encoding glycosyltransferases in Neisseria. All pathogenic species were found to possess DNA sequences homologous with the lgt gene cluster, a group of genes needed for the synthesis of the alpha chain. Some of these genes were also found to be present in strains considered to be nonpathogenic, such as Neisseria lactamica, N. subflava, and N. sicca. Some nonpathogenic Neisseria spp. were able to express high-molecular-mass LOS structures, even though they lacked the DNA sequences homologous with rfaF, a gene whose product must act before gonococcal and meningococcal LOS can be elongated. Using a PCR amplification strategy, in combination with DNA sequencing, we demonstrated that N. subflava 44 possessed lgtA, lgtB, and lgtE genes. The predicted amino acid sequence encoded by each of these genes suggested that they encoded functional proteins; however, structural analysis of LOS isolated from this strain indicated that the bulk of its LOS was not modified by these gene products. This suggests the existence of an additional regulatory mechanism that is responsible for the limited expression of these genes in this strain.
奈瑟氏菌脂寡糖(LOS)包含三条寡糖链,分别称为α、β和γ链。我们对从各种奈瑟氏菌属分离的DNA进行了Southern杂交实验,以确定被认为无致病性的菌株是否拥有与这些寡糖链生物合成相关基因同源的DNA序列。将特定基因的有无与每个菌株表达的LOS谱进行比较,LOS谱通过其在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳凝胶上的迁移率及其与各种LOS特异性单克隆抗体的反应性来表征。在奈瑟氏菌中,关于糖基转移酶编码基因的存在存在很大的异质性。发现所有致病菌种都拥有与lgt基因簇同源的DNA序列,lgt基因簇是合成α链所需的一组基因。还发现其中一些基因存在于被认为无致病性的菌株中,如乳酸奈瑟氏菌、微黄奈瑟氏菌和干燥奈瑟氏菌。一些无致病性的奈瑟氏菌属能够表达高分子量的LOS结构,尽管它们缺乏与rfaF同源的DNA序列,rfaF基因的产物必须在淋球菌和脑膜炎球菌LOS延长之前发挥作用。使用PCR扩增策略并结合DNA测序,我们证明微黄奈瑟氏菌44拥有lgtA、lgtB和lgtE基因。这些基因各自编码的预测氨基酸序列表明它们编码功能蛋白;然而,从该菌株分离的LOS的结构分析表明,其大部分LOS并未被这些基因产物修饰。这表明存在一种额外的调节机制,负责该菌株中这些基因的有限表达。