Brossay L, Paradis G, Fox R, Koomey M, Hébert J
Centre de Recherche en Inflammation, Immunologie et Rhumatologie, l'Université Laval, Sainte-Foy, Québec, Canada.
Infect Immun. 1994 Jun;62(6):2302-8. doi: 10.1128/iai.62.6.2302-2308.1994.
A monoclonal antibody (MAb) directed against a highly conserved protein of Neisseria gonorrhoeae with a molecular size of 40 kDa was isolated and characterized. The protein antigen detected by this MAb was detected by enzyme-linked immunosorbent assay and immunoblotting in all strains of N. gonorrhoeae tested across a wide range of serovars. The 40-kDa protein was found to be expressed at relatively low levels and localized to both the cytosolic and cytoplasmic membrane fractions. Screening of a lambda gt11 expression library derived from gonococcal genomic DNA with the anti-40-kDa MAb and DNA sequence analysis suggested that the 40-kDa protein and the product of the gonococcal pilT gene were identical. Immunoblotting analysis of gonococcal mutants carrying defined mutations in the pilT gene confirmed that the 40-kDa protein was indeed PilT. The N-terminal sequence derived by microsequencing of the protein purified from gonococci led to the correction of the previously published pilT gene sequence. Sequencing of the pilT gene from three different strains revealed an extremely high degree of conservation at both the amino acid and DNA levels.
分离并鉴定了一种针对淋病奈瑟菌分子大小为40 kDa的高度保守蛋白的单克隆抗体(MAb)。通过酶联免疫吸附测定和免疫印迹法在广泛血清型的所有测试淋病奈瑟菌菌株中检测到该单克隆抗体所检测的蛋白抗原。发现40 kDa蛋白表达水平相对较低,且定位于胞质和细胞质膜部分。用抗40 kDa单克隆抗体筛选来自淋球菌基因组DNA的λgt11表达文库并进行DNA序列分析表明,40 kDa蛋白与淋球菌pilT基因的产物相同。对pilT基因中携带特定突变的淋球菌突变体进行免疫印迹分析证实,40 kDa蛋白确实是PilT。对从淋球菌中纯化的蛋白进行微量测序得到的N端序列导致了先前发表的pilT基因序列的校正。对来自三个不同菌株的pilT基因进行测序揭示了在氨基酸和DNA水平上极高的保守程度。