2014
DOI: 10.1644/13-mamm-a-120
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Interpopulation differences in parasite load and variable selective pressures on MHC genes inCtenomys talarum

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Cited by 13 publications
(16 citation statements)
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References 106 publications
(159 reference statements)
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“…This finding contrasts markedly with the positive correlation between ectoparasite burden and population density of a solitary subterranean rodent, the Talas tuco-tuco (Ctenomys talarum), in Argentina (Cutrera et al 2014). It suggests that density-dependent mechanisms are unlikely to explain the observed patterns although all ectoparasites collected in the current study are directly transmitted.…”
Section: Discussioncontrasting
confidence: 99%
“…This finding contrasts markedly with the positive correlation between ectoparasite burden and population density of a solitary subterranean rodent, the Talas tuco-tuco (Ctenomys talarum), in Argentina (Cutrera et al 2014). It suggests that density-dependent mechanisms are unlikely to explain the observed patterns although all ectoparasites collected in the current study are directly transmitted.…”
Section: Discussioncontrasting
confidence: 99%
“… Leucocyte profile was evaluated as G/L ratio (granulocyte/lymphocyte) in Kurtz et al (), as N/L ratio (neutrophil/lymphocyte) in Cutrera et al (), Cutrera et al (), as H/L ratio (heterophil/lymphocyte) in Lukasch et al (). Antibody production was evaluated against sheep red blood cell antigens (SRBC) in Bonneaud et al (), Cutrera et al (), Lukasch et al () and the present study, against diphtheria and tetanus toxoid antigens in Ekblom et al (), and against human serum albumin and tetanus toxoid antigens in the present study. …”
Section: Methodsmentioning
confidence: 99%
“… Details regarding MHC diversity: in Charbonnel et al () measured as heterozygosity at two different MHC loci (0/1, Dqa1 and Drb loci), and number of amino acid differences between alleles for both loci; in Cutrera et al (), Cutrera et al () measured as MHC heterozygosity (0/1); in Rodríguez et al () measured as the number of amino acid differences between MHC alleles; in Montano‐Frías et al () measured as the number of MHC loci present; in Lukasch et al () measured as the number of different functional MHC alleles (i.e., “supertypes,” based only on sites located within the PBR and characterized by physicochemical descriptors). Details regarding specific MHC alleles: in Cutrera et al (), Cutrera et al () presence/absence of MHC allele groups (groups defined according to their amino acid similarity); in Ekblom et al () presence/absence of specific allelic lineages (lineages defined according to their nucleotide similarity); in Rodríguez et al () presence/absence of MHC allele groups (two groups were defined based on the most frequent vs. infrequent alleles); in Montano‐Frías et al () presence/absence of specific MHC loci; in Sin et al () presence/absence of specific MHC alleles and haplotypes; in Lukasch et al () presence/absence of the most frequent functional MHC alleles (i.e., “supertypes,” based only on sites located within the PBR and characterized by physicochemical descriptors). …”
Section: Methodsmentioning
confidence: 99%
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“…Mate choice may be influenced by MHC diversity (high or intermediate), compatibility (high or intermediate diversity in offspring), and/or based on specific alleles or supertypes (Ejsmond, Radwan, & Wilson, 2014). Spatial or temporal differences in mate choice for MHC characteristics may also occur (fluctuating selection, Cutrera, Zenuto, & Lacey, 2014). In some systems, sexual selection may play a large role in maintaining MHC diversity.…”
mentioning
confidence: 99%