Contrasted Patterns of Selection on MHC-Linked Microsatellites in Natural Populations of the Malagasy Plague Reservoir

Plague (Yersinia pestis infection) is a highly virulent rodent disease that persists in many natural ecosystems. The black rat (Rattus rattus) is the main host involved in the plague focus of the central highlands of Madagascar. Black rat populations from this area are highly resistant to plague, whereas those from areas in which the disease is absent (low altitude zones of Madagascar) are susceptible. Various lines of evidence suggest a role for the Major Histocompatibility Complex (MHC) in plague resistance. We therefore used the MHC region as a candidate for detecting signatures of plague-mediated selection in Malagasy black rats, by comparing population genetic structures for five MHC-linked microsatellites and neutral markers in two sampling designs. We first compared four pairs of populations, each pair including one population from the plague focus and one from the disease-free zone. Plague-mediated selection was expected to result in greater genetic differentiation between the two zones than expected under neutrality and this was observed for one MHC-class I-linked locus (D20Img2). For this marker as well as for four other MHC-linked loci, a geographic pattern of genetic structure was found at local scale within the plague focus. This pattern would be expected if plague selection pressures were spatially variable. Finally, another MHC-class I-linked locus (D20Rat21) showed evidences of balancing selection, but it seems more likely that this selection would be related to unknown pathogens more widely distributed in Madagascar than plague.

[1]  A. Shepherd,et al.  Experimental plague infection in South African wild rodents , 1986, Journal of Hygiene.

[2]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .

[3]  D. Heath,et al.  MHC genetic structure and divergence across populations of Chinook salmon (Oncorhynchus tshawytscha) , 2010, Heredity.

[4]  F. Jiggins,et al.  A screen for immunity genes evolving under positive selection in Drosophila , 2007, Journal of evolutionary biology.

[5]  S. Piertney,et al.  The evolutionary ecology of the major histocompatibility complex , 2006, Heredity.

[6]  A. Estoup,et al.  Microsatellite null alleles and estimation of population differentiation. , 2007, Molecular biology and evolution.

[7]  A. Jeffreys,et al.  Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex , 2001, Nature Genetics.

[8]  V. Loeschcke,et al.  Spatially and temporally fluctuating selection at non-MHC immune genes: evidence from TAP polymorphism in populations of brown trout (Salmo trutta, L.) , 2008, Heredity.

[9]  Jia Cao,et al.  Differential expression of genes associated with cell proliferation and apoptosis induced by okadaic acid during the transformation process of BALB/c 3T3 cells. , 2008, Toxicology in vitro : an international journal published in association with BIBRA.

[10]  E. Matisoo-Smith,et al.  Dating of divergences within the Rattus genus phylogeny using whole mitochondrial genomes. , 2008, Molecular phylogenetics and evolution.

[11]  D. Mabey,et al.  Neglected tropical diseases. , 2010, British medical bulletin.

[12]  R. Brubaker,et al.  Association between virulence of Yersinia pestis and suppression of gamma interferon and tumor necrosis factor alpha , 1993, Infection and immunity.

[13]  F. Rousset genepop’007: a complete re‐implementation of the genepop software for Windows and Linux , 2008, Molecular ecology resources.

[14]  C. Landry,et al.  MHC studies in nonmodel vertebrates: what have we learned about natural selection in 15 years? , 2003, Journal of evolutionary biology.

[15]  S. Chanteau,et al.  Epidemiological trends for human plague in Madagascar during the second half of the 20th century: a survey of 20 900 notified cases , 2006, Tropical medicine & international health : TM & IH.

[16]  Paul Keim,et al.  Phylogeography and Molecular Epidemiology of Yersinia pestis in Madagascar , 2011, PLoS neglected tropical diseases.

[17]  R. Stanyon,et al.  Black rat (Rattus rattus) genomic variability characterized by chromosome painting , 2002, Mammalian Genome.

[18]  M. Parent,et al.  Gamma Interferon, Tumor Necrosis Factor Alpha, and Nitric Oxide Synthase 2, Key Elements of Cellular Immunity, Perform Critical Protective Functions during Humoral Defense against Lethal Pulmonary Yersinia pestis Infection , 2006, Infection and Immunity.

[19]  D. Charlesworth,et al.  The effect of subdivision on variation at multi-allelic loci under balancing selection. , 2000, Genetical research.

[20]  Edwin Cuppen,et al.  Haplotype Block Structure Is Conserved across Mammals , 2006, PLoS genetics.

[21]  L. Rahalison,et al.  Isolation and characterization of microsatellites in Rattus rattus , 2008, Molecular ecology resources.

[22]  L. Rahalison,et al.  Susceptibility to Yersinia pestis Experimental Infection in Wild Rattus rattus, Reservoir of Plague in Madagascar , 2010, EcoHealth.

[23]  L. Walter,et al.  Physical Map and Expression Profile of Genes of the Telomeric Class I Gene Region of the Rat MHC1 2 , 2001, The Journal of Immunology.

[24]  R. Sokal,et al.  Multiple regression and correlation extensions of the mantel test of matrix correspondence , 1986 .

[25]  J. Pemberton,et al.  A long-term genetic survey of an ungulate population reveals balancing selection acting on MHC through spatial and temporal fluctuations in selection , 2005, Heredity.

[26]  P. Taberlet,et al.  New generation sequencers as a tool for genotyping of highly polymorphic multilocus MHC system , 2009, Molecular ecology resources.

[27]  H. Himmelbauer,et al.  The genomic sequence and comparative analysis of the rat major histocompatibility complex. , 2004, Genome research.

[28]  S. Chanteau,et al.  Susceptibility to plague of the rodents in Antananarivo, Madagascar. , 2003, Advances in experimental medicine and biology.

[29]  J. Garza,et al.  A comparison of variability and population structure for major histocompatibility complex and microsatellite loci in California coastal steelhead (Oncorhynchus mykiss Walbaum) , 2006, Molecular ecology.

[30]  L. Excoffier,et al.  Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows , 2010, Molecular ecology resources.

[31]  B. Fraser,et al.  A program to compare genetic differentiation statistics across loci using resampling of individuals and loci , 2010, Molecular ecology resources.

[32]  J. Childs,et al.  Guidelines for Working with Rodents Potentially Infected with Hantavirus , 1995 .

[33]  D. Bekkevold,et al.  Gene flow, effective population size and selection at major histocompatibility complex genes: brown trout in the Hardanger Fjord, Norway , 2007, Molecular ecology.

[34]  R. Julliard,et al.  Diversifying selection on MHC class I in the house sparrow (Passer domesticus) , 2009, Molecular ecology.

[35]  SUSCEPTIBILITY TO YERSINIA PESTIS IN THE NORTHERN GRASSHOPPER MOUSE (ONYCHOMYS LEUCOGASTER) , 1988, Journal of wildlife diseases.

[36]  R. Vitalis DETSEL: an R-package to detect marker loci responding to selection. , 2012, Methods in molecular biology.

[37]  J. Tropea,et al.  Human cytolytic T cell recognition of Yersinia pestis virulence proteins that target innate immune responses. , 2006, The Journal of infectious diseases.

[38]  T. Reusch,et al.  New evidence for habitat-specific selection in Wadden Sea Zostera marina populations revealed by genome scanning using SNP and microsatellite markers , 2010 .

[39]  J. Bliska,et al.  Turning Yersinia pathogenesis outside in: subversion of macrophage function by intracellular yersiniae. , 2005, Clinical immunology.

[40]  L. Kruglyak,et al.  Patterns of linkage disequilibrium in the human genome , 2002, Nature Reviews Genetics.

[41]  M. Pabijan,et al.  Contrasting patterns of variation in MHC loci in the Alpine newt , 2008, Molecular ecology.

[42]  Hidde L. Ploegh,et al.  The known unknowns of antigen processing and presentation , 2008, Nature Reviews Immunology.

[43]  J. Goudet FSTAT, a program to estimate and test gene diversities and fixation indices (version 2.9.3). Updated from Goudet (1995) , 2001 .

[44]  R. Nichols,et al.  Evidence for Directional Selection at a Novel Major Histocompatibility Class I Marker in Wild Common Frogs (Rana temporaria) Exposed to a Viral Pathogen (Ranavirus) , 2009, PloS one.

[45]  L. Bernatchez,et al.  CLINAL VARIATION IN MHC DIVERSITY WITH TEMPERATURE: EVIDENCE FOR THE ROLE OF HOST–PATHOGEN INTERACTION ON LOCAL ADAPTATION IN ATLANTIC SALMON , 2007, Evolution; international journal of organic evolution.

[46]  J. Piálek,et al.  Genetic structure and contrasting selection pattern at two major histocompatibility complex genes in wild house mouse populations , 2011, Heredity.

[47]  N. Stenseth,et al.  Plague: Past, Present, and Future , 2008, PLoS medicine.

[48]  H. Leirs,et al.  Phylogeography of the introduced species Rattus rattus in the western Indian Ocean, with special emphasis on the colonization history of Madagascar , 2010 .

[49]  M. Galan,et al.  Analysis of major histocompatibility complex class II gene in water voles using capillary electrophoresis‐single stranded conformation polymorphism , 2005 .

[50]  M. Galan,et al.  Density‐related changes in selection pattern for major histocompatibility complex genes in fluctuating populations of voles , 2007, Molecular ecology.

[51]  P. Boursot,et al.  Interpretation of variation across marker loci as evidence of selection. , 2001, Genetics.

[52]  R. Bontrop,et al.  A highly divergent microsatellite facilitating fast and accurate DRB haplotyping in humans and rhesus macaques , 2007, Proceedings of the National Academy of Sciences.

[53]  R. Tapping,et al.  The Resistance of BALB/cJ Mice to Yersinia pestis Maps to the Major Histocompatibility Complex of Chromosome 17 , 2008, Infection and Immunity.

[54]  Bruce T Lahn,et al.  Positive selection on the human genome. , 2004, Human molecular genetics.

[55]  H. Flick-Smith,et al.  Mechanisms of major histocompatibility complex class II‐restricted processing and presentation of the V antigen of Yersinia pestis , 2006, Immunology.

[56]  Gilles Caraux,et al.  A 454 multiplex sequencing method for rapid and reliable genotyping of highly polymorphic genes in large-scale studies , 2010, BMC Genomics.

[57]  J. Höglund,et al.  Spatial pattern of MHC class II variation in the great snipe (Gallinago media) , 2007, Molecular ecology.

[58]  N. Gratz,et al.  Plague manual--epidemiology, distribution, surveillance and control. , 1999, Releve epidemiologique hebdomadaire.

[59]  D. Lambracht-Washington,et al.  Structure and expression of MHC class Ib genes of the central M region in rat and mouse: M4, M5, and M6 , 2008, Immunogenetics.

[60]  Lewis G. Spurgin,et al.  How pathogens drive genetic diversity: MHC, mechanisms and misunderstandings , 2010, Proceedings of the Royal Society B: Biological Sciences.

[61]  S. Chanteau,et al.  Genetic structure of black rat populations in a rural plague focus in Madagascar , 2007 .

[62]  C. Oosterhout,et al.  Micro-Checker: Software for identifying and correcting genotyping errors in microsatellite data , 2004 .

[63]  G. Luikart,et al.  Candidate gene microsatellite variation is associated with parasitism in wild bighorn sheep , 2008, Biology Letters.

[64]  K. Ibrahim,et al.  Selection on MHC-linked microsatellite loci in sheep populations , 2007, Heredity.

[65]  Brygoo Er Epidémiologie de la peste à Madagascar , 1966 .

[66]  M. Beaumont,et al.  Evaluating loci for use in the genetic analysis of population structure , 1996, Proceedings of the Royal Society of London. Series B: Biological Sciences.