Major histocompatibility complex variation and the evolution of resistance to amphibian chytridiomycosis.

Abstract:

:Chytridiomycosis, caused by the fungal pathogen Batrachochytrium dendrobatidis (Bd), has been implicated in population declines and species extinctions of amphibians around the world. Susceptibility to the disease varies both within and among species, most likely attributable to heritable immunogenetic variation. Analyses of transcriptional expression in hosts following their infection by Bd reveal complex responses. Species resistant to Bd generally show evidence of stronger innate and adaptive immune system responses. Major histocompatibility complex (MHC) class I and class II genes of some susceptible species are up-regulated following host infection by Bd, but resistant species show no comparable changes in transcriptional expression. Bd-resistant species share similar pocket conformations within the MHC-II antigen-binding groove. Among susceptible species, survivors of epizootics bear alleles encoding these conformations. Individuals with homozygous resistance alleles appear to benefit by enhanced resistance, especially in environmental conditions that promote pathogen virulence. Subjects that are repeatedly infected and subsequently cleared of Bd can develop an acquired immune response to the pathogen. Strong directional selection for MHC alleles that encode resistance to Bd may deplete genetic variation necessary to respond to other pathogens. Resistance to chytridiomycosis incurs life-history costs that require further study.

journal_name

Immunogenetics

journal_title

Immunogenetics

authors

Fu M,Waldman B

doi

10.1007/s00251-017-1008-4

subject

Has Abstract

pub_date

2017-08-01 00:00:00

pages

529-536

issue

8-9

eissn

0093-7711

issn

1432-1211

pii

10.1007/s00251-017-1008-4

journal_volume

69

pub_type

杂志文章,评审
  • Allelic repertoire of the human MHC class I MICA gene.

    abstract::The hallmark of the classical major histocompatibility complex (MHC) class I molecules is their astonishing level of polymorphism, a characteristic not shared by the nonclassical MHC class I genes. A distinct family of MHC class I genes has been recently identified within the human MHC class I region. The MICA (MHC cl...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF02602779

    authors: Fodil N,Laloux L,Wanner V,Pellet P,Hauptmann G,Mizuki N,Inoko H,Spies T,Theodorou I,Bahram S

    更新日期:1996-01-01 00:00:00

  • Copy number variation and association over T-cell receptor genes--influence of DNA source.

    abstract::Genomic copy number variants (CNVs) are a common, heritable source of inter-individual differences in genomic sequence. Their influence on phenotypic variability and their involvement in the pathogenesis of several common diseases is well established and the object of many current studies. In the course of examining C...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-010-0459-7

    authors: Schwienbacher C,De Grandi A,Fuchsberger C,Facheris MF,Svaldi M,Wjst M,Pramstaller PP,Hicks AA

    更新日期:2010-08-01 00:00:00

  • An epitope on C4 beta light (L) chains detected by human anti-Rg; its relationship with beta chain polymorphism and MHC associations.

    abstract::Two out of ten Rg-specific antisera tested contain a third antibody specific for the beta chain of C4. Analysis of the beta chains of 66 unrelated individuals by sodium dodecyl sulfate polyacrylamide gel electrophoresis revealed that the epitope detected is located exclusively on the light (L) beta chain. A strong, bu...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF02425274

    authors: Robson T,Heard RN,Giles CM

    更新日期:1989-01-01 00:00:00

  • Leukemia-cell rejection due to T-region encoded antigens.

    abstract::The role of H-2- and T-region products in determining allogeneic cell rejection was evaluated in H-2 congenic and recombinant mice by transplanting A1ATH and A6ATL leukemia cell lines induced in A.TH and A.TL strains, respectively, by Moloney murine leukemia virus.--In K- or D-region incompatible hosts transplant fail...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF01561686

    authors: Biasi G,Collavo D,Zanovello P,Chieco-Bianchi L

    更新日期:1981-03-01 00:00:00

  • Polymorphisms in recent GWA identified asthma genes CA10, SGK493, and CTNNA3 are associated with disease severity and treatment response in childhood asthma.

    abstract::Recent genome-wide association studies (GWAs) have identified several new genetic risk factors for asthma; however, their influence on disease behavior and treatment response is still unclear. The aim of our study was the association analysis of the most significant single nucleotide polymorphisms (SNPs) recently repo...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-013-0755-0

    authors: Perin P,Potočnik U

    更新日期:2014-03-01 00:00:00

  • Evidence for an HLA-C-like locus in the orangutan Pongo pygmaeus.

    abstract::HLA-B and C are related class I genes which are believed to have arisen by duplication of a common ancestor. Previous study showed the presence of orthologues for both HLA-B and C in African apes but only for HLA-B in Asian apes. These observations suggested that the primate C locus evolved subsequent to the divergenc...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s002510050566

    authors: Adams EJ,Thomson G,Parham P

    更新日期:1999-09-01 00:00:00

  • The properties of the single chicken MHC classical class II alpha chain ( B-LA) gene indicate an ancient origin for the DR/E-like isotype of class II molecules.

    abstract::In mammals, there are MHC class II molecules with distinctive sequence features, such as the classical isotypes DR, DQ and DP. These particular isotypes have not been reported in non-mammalian vertebrates. We have isolated the class II (B-L) alpha chain from outbred chickens as the basis for the cloning and sequencing...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-003-0620-7

    authors: Salomonsen J,Marston D,Avila D,Bumstead N,Johansson B,Juul-Madsen H,Olesen GD,Riegert P,Skjødt K,Vainio O,Wiles MV,Kaufman J

    更新日期:2003-12-01 00:00:00

  • Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes.

    abstract::Human cDNA probes for 21-hydroxylase (21-OH) and for complement component C4 are used on restriction digests of the members of several families with interesting supratypes. The presence of two Taq I fragments of 3.7 kb and 3.2 kb in size with a 21-OH probe is confirmed in most individuals who show no evidence of C4 de...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00377968

    authors: Garlepp MJ,Wilton AN,Dawkins RL,White PC

    更新日期:1986-01-01 00:00:00

  • Identical genetic control of MLC reactivity to different MHC incompatibilities, independent of production of and response to IL-2.

    abstract::The inbred strain STS/A exhibits a higher proliferative response in the mixed lymphocyte culture (MLC) to stimulator cells of all 11 tested inbred mouse strains with 10 different major histocompatibility complex (MHC) haplotypes, as well as to stimulation with IL-2 than does the strain BALB/cHeA. However, alloantigen-...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF02602654

    authors: Holán V,Lipoldová M,Demant P

    更新日期:1996-01-01 00:00:00

  • Residue 81 confers a restricted C-terminal peptide binding motif in HLA-B*44:09.

    abstract::Knowledge about the magnitude of individual polymorphism is a critical part in understanding the complexity of comprehensive mismatching. HLA-B*44:09 differs from the highly frequent HLA-B*44:02 allele by amino acid exchanges at residues 77, 80, 81, 82 and 83. We aimed to identify the magnitude of these mismatches on ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-012-0625-1

    authors: Huyton T,Schumacher H,Blasczyk R,Bade-Doeding C

    更新日期:2012-09-01 00:00:00

  • New types of multiple and single gene deletions in the human IgCH locus.

    abstract::The locus for human immunoglobulin heavy chain constant region genes (IgCH) is characterized by a significant frequency of deleted or duplicated haplotypes, due to unequal crossing-over events. Four types of deletions and one duplication have been reported so far. We describe here a molecular study of four cases of Ig...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF02341612

    authors: Bottaro A,De Marchi M,De Lange G,Boccazzi C,Caldesi F,Gallina R,Carbonara AO

    更新日期:1989-01-01 00:00:00

  • Allelic variants of the human MHC class I chain-related B gene (MICB).

    abstract::The human major histocompatibility complex (MHC) is located within a 4 megabase segment on chromosome 6p21.3. Recently, a highly divergent MHC class I chain-related gene family, MIC was identified within the class I region. The MICA and MICB genes in this family have unique patterns of tissue expression. The MICA gene...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s002510050311

    authors: Ando H,Mizuki N,Ota M,Yamazaki M,Ohno S,Goto K,Miyata Y,Wakisaka K,Bahram S,Inoko H

    更新日期:1997-01-01 00:00:00

  • A genetic analysis of natural resistance to nonsyngeneic cells: the role of H-2.

    abstract::The genetic control of natural resistance in vivo to four natural killer (NK) cell-resistant H-2 homozygous lymphoid tumor cell lines was investigated by following the survival and organ distribution of cells prelabeled with radioactive iododeoxyuridine. Backcross mice derived from DBA/2J and CBA/J parents were inject...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00364210

    authors: Carlson GA,Taylor BA,Marshall ST,Greenberg AH

    更新日期:1984-01-01 00:00:00

  • The H2 haplotype regulates the distribution of B cells into B-1a, B-1b and B-2 subsets.

    abstract::The size of B-cell subsets appears to be under genetic control, but the mechanism of this regulation is unknown. By analyzing five congenic strains of mice that differ only in their H2 haplotype, we addressed the issue of whether the MHC genes are involved in the relative proportions of B-1a, B-1b and B-2 cells. Not o...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-002-0457-5

    authors: Pers JO,Jamin C,Lydyard PM,Charreire J,Youinou P

    更新日期:2002-06-01 00:00:00

  • Differential behavior of cytotoxic effector cells against HLA antigens in strong genetic linkage disequilibrium.

    abstract::Five sets of cytotoxic effector cells were generated, using haplo-identical, first degree relatives in five different families, against the HLA-A3; B7 serological determinants combined with different DR antigens. When tested against a panel of cells bearing combinations of the HLA-A, -B and -DR antigens it was shown t...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00364495

    authors: Kim SJ,Christiansen FT,Silver DM,Dupont B

    更新日期:1981-01-01 00:00:00

  • Strain-dependent migration of lymphocytes to the vaginal mucosa after peripheral immunization.

    abstract::We have previously demonstrated a genetic predisposition among mice regarding their ability to be protected against vaginal candidiasis after peripheral immunization. Both BALB/c and (BALB/cx C57BL/6) F1 mice are protected against vaginal candidiasis after subcutaneous immunization with Candida albicans extract and C5...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s002510050581

    authors: Mulero-Marchese RD,Blank KJ,Sieck TG

    更新日期:1999-10-01 00:00:00

  • Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients.

    abstract::Human leucocyte antigen (HLA)-DRB1*15 is associated with predisposition to multiple sclerosis (MS), although conjecture surrounds the possible involvement of an alternate risk locus in the class I region of the HLA complex. We have shown previously that an alternate MS risk allele(s) may be encompassed by the telomeri...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-006-0183-5

    authors: Rubio JP,Bahlo M,Stankovich J,Burfoot RK,Johnson LJ,Huxtable S,Butzkueven H,Lin L,Taylor BV,Speed TP,Kilpatrick TJ,Mignot E,Foote SJ

    更新日期:2007-03-01 00:00:00

  • Gene duplication, allelic diversity, selection processes and adaptive value of MHC class II DRB genes of the bank vole, Clethrionomys glareolus.

    abstract::The generation and maintenance of allelic polymorphism in genes of the major histocompatibility complex (MHC) is a central issue in evolutionary genetics. Recently, the focus has changed from ex situ to in situ populations to understand the mechanisms that determine adaptive MHC polymorphism under natural selection. B...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-007-0205-y

    authors: Axtner J,Sommer S

    更新日期:2007-05-01 00:00:00

  • Accuracy and coverage assessment of Oryctolagus cuniculus (rabbit) genes encoding immunoglobulins in the whole genome sequence assembly (OryCun2.0) and localization of the IGH locus to chromosome 20.

    abstract::We report on the analyses of genes encoding immunoglobulin heavy and light chains in the rabbit 6.51× whole genome assembly. This OryCun2.0 assembly confirms previous mapping of the duplicated IGK1 and IGK2 loci to chromosome 2 and the IGL lambda light chain locus to chromosome 21. The most frequently rearranged and e...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-013-0722-9

    authors: Gertz EM,Schäffer AA,Agarwala R,Bonnet-Garnier A,Rogel-Gaillard C,Hayes H,Mage RG

    更新日期:2013-10-01 00:00:00

  • MICA, a new polymorphic HLA-related antigen, is expressed mainly by keratinocytes, endothelial cells, and monocytes.

    abstract::MICA is a new polymorphic gene in the HLA region expressed in epithelial cell lines and gastrointestinal epithelium. Little is yet known about the MICA protein, and the pattern of its expression by freshly isolated cells has not been established. In the present experiments, we used antibodies raised in rabbits against...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s002510050339

    authors: Zwirner NW,Fernández-Viña MA,Stastny P

    更新日期:1998-01-01 00:00:00

  • Proximity of the Mep-1 gene to H-2D on chromosome 17 in mice.

    abstract::The Mep-1 gene on chromosome 17 in mice controls the activity of meprin, a kidney brush border metalloendopeptidase. Most inbred mouse strains of the k haplotype (e.g., CBA, C3H, AKR) are markedly deficient in meprin activity; these mice carry the Mep-1b allele. Mouse strains in which meprin activity levels are normal...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00430310

    authors: Reckelhoff JF,Bond JS,Beynon RJ,Savarirayan S,David CS

    更新日期:1985-01-01 00:00:00

  • Extent of the mouse t complex and its inversions shown by in situ hybridization.

    abstract::Probes for loci situated near one end of the proximal (Tcp-1) and distal (Qa-2, 3) inversions of the mouse t complex have been hybridized to chromosomes of mice with and without t complexes and with morphologically distinguishable chromosome 17s. Both the probe for Tcp-1 and that for Qa-2, 3 hybridized to clearly diff...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00395134

    authors: Lyon MF,Zenthon J,Evans EP,Burtenshaw MD,Willison KR

    更新日期:1988-01-01 00:00:00

  • The same ELA class II risk factors confer equine insect bite hypersensitivity in two distinct populations.

    abstract::Insect bite hypersensitivity (IBH) is a chronic allergic dermatitis common in horses. Affected horses mainly react against antigens present in the saliva from the biting midges, Culicoides ssp, and occasionally black flies, Simulium ssp. Because of this insect dependency, the disease is clearly seasonal and prevalence...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-011-0573-1

    authors: Andersson LS,Swinburne JE,Meadows JR,Broström H,Eriksson S,Fikse WF,Frey R,Sundquist M,Tseng CT,Mikko S,Lindgren G

    更新日期:2012-03-01 00:00:00

  • Genetics-squared: combining host and pathogen genetics in the analysis of innate immunity and bacterial virulence.

    abstract::The interaction of bacterial pathogens with their hosts' innate immune systems can be extremely complex and is often difficult to disentangle experimentally. Using mouse models of bacterial infections, several laboratories have successfully applied genetic approaches to identify novel host genes required for innate im...

    journal_title:Immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1007/s00251-007-0248-0

    authors: Persson J,Vance RE

    更新日期:2007-10-01 00:00:00

  • Genetic influences on spontaneous autoimmune thyroiditis in (CS X OS)F2 chickens.

    abstract::Genetic effects on spontaneous autoimmune thyroiditis in chickens were assessed by measuring phenotypic symptoms, the titer of circulating antibody to thyroglobulin, and the pathological change in the thyroids of young chicks. One or more loci within the B complex (the major histocompatibility complex of the chicken) ...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF01561675

    authors: Bacon LD,Polley CR,Cole RK,Rose NR

    更新日期:1981-01-01 00:00:00

  • Two novel HLA-DQ2.5-restricted gluten T cell epitopes in the DQ2.5-glia-γ4 epitope family.

    abstract::Celiac disease is a chronic inflammatory condition of the small intestine caused by aberrant adaptive immune response to gluten protein from wheat and related cereal plants. Over 90% of celiac disease patients carry the HLA-DQ2.5 allotype and HLA-DQ2.5 presents gluten peptides to gluten-reactive CD4+ T cells in celiac...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-019-01138-5

    authors: Qiao SW,Sollid LM

    更新日期:2019-11-01 00:00:00

  • Inheritance of a mutant histocompatibility gene and a new mammary tumor virus genome in the B6.KH-84 mouse strain.

    abstract::The potential association between integration or deletion of mouse mammary tumor virus (MMTV) retroviral sequences and the appearance of non-H-2 histocompatibility (H) antigen mutations was investigated. Genomic blots from inbred strains carrying 22 loss, gain-loss, and gain mutations on the BALB/c and C57BL/6 backgro...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00345461

    authors: Colombo MP,Melvold RW,Wettstein PJ

    更新日期:1987-01-01 00:00:00

  • Involvement of both HLA and Ig heavy chain haplotypes in human IgA deficiency.

    abstract::Immunoglobulin-A deficiency (IgA-D) is the most common human Ig class deficiency with an estimated frequency of approximately 1 in 500 in the Swedish population. We investigated the immunoglobulin heavy chain constant region gene segments (IGHC) in 103 individuals with IgA-D and the immunoglobulin heavy chain variable...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/BF00218046

    authors: Olsson PG,Hammarström L,Cox DW,Smith CI

    更新日期:1992-01-01 00:00:00

  • Characterization of MHC class I in a long-distance migrant shorebird suggests multiple transcribed genes and intergenic recombination.

    abstract::The major histocompatibility complex (MHC) includes highly polymorphic gene families encoding proteins crucial to the vertebrate acquired immune system. Classical MHC class I (MHCI) genes code for molecules expressed on the surfaces of most nucleated cells and are associated with defense against intracellular pathogen...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s00251-012-0669-2

    authors: Buehler DM,Verkuil YI,Tavares ES,Baker AJ

    更新日期:2013-03-01 00:00:00

  • CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group.

    abstract::Multiple sclerosis (MS) is a common disease of the central nervous system characterized by myelin loss and progressive neurological dysfunction. An underlying genetic susceptibility plays a clear role in the etiology of MS, likely acting in concert with an undefined environmental exposure. Full-genome screenings in mu...

    journal_title:Immunogenetics

    pub_type: 杂志文章

    doi:10.1007/s002510050621

    authors: Barcellos LF,Schito AM,Rimmler JB,Vittinghoff E,Shih A,Lincoln R,Callier S,Elkins MK,Goodkin DE,Haines JL,Pericak-Vance MA,Hauser SL,Oksenberg JR

    更新日期:2000-04-01 00:00:00