The little brown bat, M. lucifugus, displays a highly diverse VH, DH and JH repertoire but little evidence of somatic hypermutation

被引:37
作者
Bratsch, Sara [2 ]
Wertz, Nancy [1 ]
Chaloner, Kathryn [3 ]
Kunz, Thomas H. [4 ]
Butler, John E. [1 ]
机构
[1] Univ Iowa Carver, Coll Med, Dept Microbiol, Iowa City, IA 52242 USA
[2] Univ Wisconsin, Dept Biol, River Falls, WI 54022 USA
[3] Univ Iowa, Coll Publ Hlth, Dept Biostat, Iowa City, IA USA
[4] Boston Univ, Dept Biol, Ctr Ecol & Conservat Biol, Boston, MA 02215 USA
关键词
Heavy chain variable region; Repertoire; Somatic hypermutation; Bats; Phylogeny; HEAVY-CHAIN LOCUS; B-CELL; NEONATAL PIGLETS; GENE CONVERSION; VARIABLE REGION; DEAMINASE AID; FETAL; MODEL; FAMILY; USAGE;
D O I
10.1016/j.dci.2010.06.004
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Myotis lucifugus populations in Northeastern US are being decimated by a fungal disease. Since almost nothing is known about the immune system of bats, we are characterizing the immunoglobulin genes of bats. We show that M. lucifugus has a diverse V-H gene repertoire comprised of five of the seven human V-H gene families and an estimated 236 V(H)3 genes. 95% of these germline VH3 genes differ in FR3. A comparison of 67 expressed V(H)3 genes with 75 germline V(H)3 genes revealed a mutation frequency similar to fetal piglets never exposed to environmental antigens. Analysis of CDR3 regions identified at least 13 putative J(H) segments and a large D-H repertoire. The low mutation frequency, highly diverse V-H. D-H, and J(H) germline repertoire suggests that this species may rely more on combinatorial and junctional diversity than on somatic hypermutation raising questions about the ability of M. lucifugus to respond rapidly to emerging pathogens. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:421 / 430
页数:10
相关论文
共 62 条
[1]   Requirement of the activation-induced deaminase (AID) gene for immunoglobulin gene conversion [J].
Arakawa, H ;
Hauschild, J ;
Buerstedde, JM .
SCIENCE, 2002, 295 (5558) :1301-1306
[2]   SOMATIC DIVERSIFICATION OF IMMUNOGLOBULIN HEAVY-CHAIN VDJ GENES - EVIDENCE FOR SOMATIC GENE CONVERSION IN RABBITS [J].
BECKER, RS ;
KNIGHT, KL .
CELL, 1990, 63 (05) :987-997
[3]   MUTATION DRIFT AND REPERTOIRE SHIFT IN THE MATURATION OF THE IMMUNE-RESPONSE [J].
BEREK, C ;
MILSTEIN, C .
IMMUNOLOGICAL REVIEWS, 1987, 96 :23-41
[4]   Use of a single V-H family and long CDR3s in the variable region of cattle Ig heavy chains [J].
Berens, SJ ;
Wylie, DE ;
Lopez, OJ .
INTERNATIONAL IMMUNOLOGY, 1997, 9 (01) :189-199
[5]  
BLEHERT DS, 2009, SCI EXP, V30
[6]   ESTIMATING THE NUMBER OF SPECIES - A REVIEW [J].
BUNGE, J ;
FITZPATRICK, M .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1993, 88 (421) :364-373
[7]   The isolator piglet: a model for studying the development of adaptive immunity [J].
Butler, J. E. ;
Sinkora, Marek .
IMMUNOLOGIC RESEARCH, 2007, 39 (1-3) :33-51
[8]   The piglet as a model for B cell and immune system development [J].
Butler, J. E. ;
Lager, K. M. ;
Splichal, I. ;
Francis, D. ;
Kacskovics, I. ;
Sinkora, M. ;
Wertz, N. ;
Sun, J. ;
Zhao, Y. ;
Brown, W. R. ;
DeWald, R. ;
Dierks, S. ;
Muyidermans, S. ;
Lunney, J. K. ;
McCray, P. B. ;
Rogers, C. S. ;
Welsh, M. J. ;
Navarro, P. ;
Klobasa, F. ;
Habe, F. ;
Ramsoondar, J. .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2009, 128 (1-3) :147-170
[9]   Preface - Why I agreed to do this [J].
Butler, JE .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2006, 30 (1-2) :1-17
[10]   Immunoglobulin gene organization and the mechanism of repertoire development [J].
Butler, JE .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1997, 45 (05) :455-462