Antigenic variation and transmission fitness as drivers of bacterial strain structure

被引:21
作者
Palmer, Guy H. [1 ]
Brayton, Kelly A. [1 ]
机构
[1] Washington State Univ, Dept Vet Microbiol & Pathol, Paul G Allen Sch Global Anim Hlth, Pullman, WA 99164 USA
基金
英国惠康基金;
关键词
ANAPLASMA-MARGINALE STRAINS; SURFACE PROTEIN-2 VARIANTS; GENE CONVERSION; MAMMALIAN RESERVOIR; TICK TRANSMISSION; HIGH PREVALENCE; DIVERSITY; EXPRESSION; GENOME; MSP2;
D O I
10.1111/cmi.12182
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Shifts in microbial strain structure underlie both emergence of new pathogens and shifts in patterns of infection and disease of known agents. Understanding the selective pressures at a population level as well as the mechanisms at the molecular level represent significant gaps in our knowledge regarding microbial epidemiology. Highly antigenically variant pathogens, which are broadly represented among microbial taxa, are most commonly viewed through the mechanistic lens of how they evade immune clearance within the host. However, equally important are mechanisms that allow pathogens to evade immunity at the population level. The selective pressure of immunity at both the level of the individual host and the population is a driver of diversification within a pathogen strain. Using Anaplasma marginale as a model highly antigenically variable bacterial pathogen, we review how immunity selects for genetic diversification in alleles encoding outer membrane proteins both within and among strains. Importantly, genomic comparisons among strains isolated from diverse epidemiological settings elucidates the counterbalancing pressures for diversification and conservation, driven by immune escape and transmission fitness, respectively, and how these shape pathogen strain structure.
引用
收藏
页码:1969 / 1975
页数:7
相关论文
共 42 条
[1]   Anaplasma marginale major surface protein 2 CD4+-T-cell epitopes are evenly distributed in conserved and hypervariable regions (HVR), whereas linear B-cell epitopes are predominantly located in the HVR [J].
Abbott, JR ;
Palmer, GH ;
Howard, CJ ;
Hope, JC ;
Brown, WC .
INFECTION AND IMMUNITY, 2004, 72 (12) :7360-7366
[2]   Anaplasma marginale major surface protein 3 is encoded by a polymorphic, multigene family [J].
Alleman, AR ;
Palmer, GH ;
McGuire, TC ;
McElwain, TF ;
Perryman, LE ;
Barbet, AF .
INFECTION AND IMMUNITY, 1997, 65 (01) :156-163
[3]   Antigenic variation of Anaplasma marginale by expression of MSP2 mosaics [J].
Barbet, AF ;
Lundgren, A ;
Yi, J ;
Rurangirwa, FR ;
Palmer, GH .
INFECTION AND IMMUNITY, 2000, 68 (11) :6133-6138
[4]   Trypanosoma brucei homologous recombination is dependent on substrate length and homology, though displays a differential dependence on mismatch repair as substrate length decreases [J].
Barnes, Rebecca L. ;
McCulloch, Richard .
NUCLEIC ACIDS RESEARCH, 2007, 35 (10) :3478-3493
[5]   Complete genome sequencing of Anaplasma marginale reveals that the surface is skewed to two superfamilies of outer membrane proteins [J].
Brayton, KA ;
Kappmeyer, LS ;
Herndon, DR ;
Dark, MJ ;
Tibbals, DL ;
Palmer, GH ;
McGuire, TC ;
Knowles, DP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (03) :844-849
[6]   Simultaneous variation of the immunodominant outer membrane proteins, MSP2 and MSP3, during Anaplasma marginale persistence in vivo [J].
Brayton, KA ;
Meeus, PFM ;
Barbet, AF ;
Palmer, GH .
INFECTION AND IMMUNITY, 2003, 71 (11) :6627-6632
[7]   Antigenic variation of Anaplasma marginale msp2 occurs by combinatorial gene conversion [J].
Brayton, KA ;
Palmer, GH ;
Lundgren, A ;
Yi, J ;
Barbet, AF .
MOLECULAR MICROBIOLOGY, 2002, 43 (05) :1151-1159
[8]   Efficient use of a small genome to generate antigenic diversity in tick-borne ehrlichial pathogens [J].
Brayton, KA ;
Knowles, DP ;
McGuire, TC ;
Palmer, GH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (07) :4130-4135
[9]   Conservation in the face of diversity: multistrain analysis of an intracellular bacterium [J].
Dark, Michael J. ;
Herndon, David R. ;
Kappmeyer, Lowell S. ;
Gonzales, Mikel P. ;
Nordeen, Elizabeth ;
Palmer, Guy H. ;
Knowles, Donald P., Jr. ;
Brayton, Kelly A. .
BMC GENOMICS, 2009, 10
[10]   Genetic diversity and molecular phylogeny of Anaplasma marginale isolates from Minas Gerais, Brazil [J].
de la Fuente, J ;
Passos, LMF ;
Van Den Bussche, RA ;
Ribeiro, MFB ;
Facury-Filho, EJ ;
Kocan, KM .
VETERINARY PARASITOLOGY, 2004, 121 (3-4) :307-316