Typing and surface charges of the variable loop regions of PorB from Neisseria meningitidis.
Typing and surface charges of the variable loop regions of PorB from Neisseria meningitidis.
复制标题
脑膜炎奈瑟菌 PorB 可变环区的分型和表面电荷。
DOI:
10.1002/iub.1508
复制
发表时间:
2016
期刊:
影响因子:
4.6
通讯作者:
and Massari P.
中科院分区:
文献类型:
--
作者:
Stefanelli P.;Neri A.;Tanabe M.;Fazio C.;and Massari P.
PorB is a pan‐Neisserial major outer membrane protein with a trimeric β‐barrel structure. Each monomer presents eight periplasmic turns and eight surface exposed loop regions with sequence variability. PorB induces activation of host cell responses via a TLR2‐dependent mechanism likely mediated by electrostatic interactions between TLR2 and PorB surface exposed loops. Variability in the loop amino acid sequence is known to influence cell responses to PorBin vitro, particularly for the residues in L5 and L7. In this work, the sequence of theporBgene and the electrostatic surface charges of PorB from 35 invasive meningococcal isolates belonging to the main clonal complexes identified in Italy and from five carriage genomes available on the website http://pubmlst.org/neisseria/ were examined. Analysis of theporBencoding regions from the invasive meningococci has identified four new alleles and a potential association betweenporBalleles, serogroup, and clonal complexes. Through computer‐based modeling and analysis of the electrostatic surface charges of PorB from these strains, loop charge segregation between PorB from invasive serogroups B and C was observed. Specifically, loops 1, 4, and 7 were negatively charged and L2 and L8 were mostly neutral in serogroup B isolates, while an overall homogeneous positive surface charge was present in PorB from invasive serogroup C strains. A higher PorB sequence variability was observed among carriage genomes, and a general prevalence of negative loop surface charges. The surface charge differences in PorB from serogroups B and C invasive and carriage strains may, in part, influence the outcomes ofNeisseriaeinteractions with host cells. © 2016 IUBMB Life, 68(6):488–495, 2016