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1.
Diabetes Metab Res Rev ; 26(4): 261-70, 2010 May.
Article in English | MEDLINE | ID: mdl-20503258

ABSTRACT

BACKGROUND: Type 2 diabetes (T2D) is influenced by diverse environmental and genetic risk factors. Metabolic syndrome (MS) increases the risk of cardiovascular disease and diabetes. We analysed 14 cases of polymorphisms located in 10 candidate loci, in a sample of patients with T2D and controls from Mexico City. METHODS: We analysed the association of 14 polymorphisms located within 10 genes (TCF7L2, ENPP1, ADRB3, KCNJ11, LEPR, PPARgamma, FTO, CDKAL1, SIRT1 and HHEX) with T2D and MS. The analysis included 519 subjects with T2D defined according to the ADA criteria, 389 with MS defined according to the AHA/NHLBI criteria and 547 controls. Association was tested with the program ADMIXMAP including individual ancestry, age, sex, education and in some cases body mass index (BMI), in a logistic regression model. RESULTS: The two markers located within the TCF7L2 gene showed strong associations with T2D (rs7903146, T allele, odd ratio (OR) = 1.76, p = 0.001 and rs12255372, T allele, OR = 1.78, p = 0.002), but did not show significant association with MS. The non-synonymous rs4994 polymorphism of the ADRB3 gene was associated with T2D (Trp allele, OR = 0.62, p = 0.001) and MS (Trp allele, OR = 0.74, p = 0.018). Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS and the HHEX rs5015480 polymorphism. CONCLUSIONS: Variants located within the gene TCF7L2 are strongly associated with T2D but not with MS, providing support to previous evidence indicating that polymorphisms at the TCF7L2 gene increase T2D risk. In contrast, the non-synonymous ADRB3 rs4994 polymorphism is associated with T2D and MS.


Subject(s)
Diabetes Mellitus, Type 2/genetics , Metabolic Syndrome/genetics , Polymorphism, Genetic , Adult , Age Factors , Blood Glucose/metabolism , Blood Pressure/genetics , Body Mass Index , Body Weight/genetics , Cholesterol/blood , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Diabetes Mellitus, Type 2/ethnology , Educational Status , Female , Genetic Association Studies , Humans , Insulin/blood , Insulin Resistance/genetics , Male , Metabolic Syndrome/ethnology , Mexico , Middle Aged , Triglycerides/blood
2.
Mucosal Immunol ; 2(1): 43-53, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19079333

ABSTRACT

Expressed by squamous mucosal keratinocytes, calprotectin is a complex of two EF-hand calcium-binding proteins of the S100 subfamily (S100A8 and S100A9) with significant antimicrobial activity. Calprotectin-expressing cells resist invasion by Porphyromonas gingivalis, Listeria monocytogenes, and Salmonella enterica serovar Typhimurium (S. typhimurium). To understand the interactions between calprotectin and invasive bacteria, we studied the distribution of calprotectin in the cytoplasm of TR146 epithelial cells. In response to L. monocytogenes, calprotectin mobilized from a diffuse cytoplasmic distribution to a filamentous pattern and colocalized with the microtubule network. Listeria more frequently invaded cells with mobilized calprotectin. Calprotectin mobilization was listeriolysin O-dependent and required calcium (extracellular and intracellular) and an intact microtubule network. In the presence of preformed microtubules in vitro, the anti-Listeria activity of calprotectin was abrogated. To facilitate intraepithelial survival, therefore, Listeria mobilizes calprotectin to colocalize with cytoplasmic microtubules, subverting anti-Listeria activity and autonomous cellular immunity.


Subject(s)
Anti-Infective Agents/metabolism , Cytoplasm/immunology , Cytoplasm/metabolism , Epithelial Cells/immunology , Epithelial Cells/metabolism , Leukocyte L1 Antigen Complex/metabolism , Listeria monocytogenes/immunology , Calcium/pharmacology , Cell Line , Cytoplasm/drug effects , Humans , Protein Binding , Salmonella typhimurium/immunology , Tubulin/metabolism
3.
Insect Mol Biol ; 9(6): 661-73, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11122476

ABSTRACT

Wolbachia are cytoplasmically inherited bacteria that induce a variety of effects with fitness consequences on host arthropods, including cytoplasmic incompatibility, parthenogenesis, male-killing and feminization. We report here the presence of Wolbachia in native South American populations of the fire ant Solenopsis invicta, but the apparent absence of the bacteria in introduced populations of this pest species in the USA. The Wolbachia strains in native S. invicta are of two divergent types (A and B), and the frequency of infection varies dramatically between geographical regions and social forms of this host. Survey data reveal that Wolbachia also are found in other native fire ant species within the Solenopsis saevissima species complex from South America, including S. richteri. This latter species also has been introduced in the USA, where it lacks Wolbachia. Sequence data reveal complete phylogenetic concordance between mtDNA haplotype in S. invicta and Wolbachia infection type (A or B). In addition, the mtDNA and associated group A Wolbachia strain in S. invicta are more closely related to the mtDNA and Wolbachia strain found in S. richteri than they are to the mtDNA and associated group B Wolbachia in S. invicta. These data are consistent with historical introgression of S. richteri cytoplasmic elements into S. invicta populations, resulting in enhanced infection and mtDNA polymorphisms in S. invicta. Wolbachia may have significant fitness effects on these hosts (either directly or by cytoplasmic incompatibility) and therefore these microbes potentially could be used in biological control programmes to suppress introduced fire ant populations.


Subject(s)
Ants/microbiology , Wolbachia/physiology , Animals , Ants/classification , Ants/genetics , Ants/growth & development , DNA, Bacterial , DNA, Mitochondrial , Genetic Variation , Phylogeny , South America , Species Specificity , United States , Wolbachia/classification , Wolbachia/genetics
4.
Genetics ; 145(4): 961-74, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9093850

ABSTRACT

The reproductive success of individual fire ant queens (Solenopsis invicta) previously has been shown to be strongly influenced by their genotype at a single enzyme-encoding gene, designated Pgm-3. This paper presents evidence that a second, tightly linked gene, designated Gp-9, is under similarly strong selection in these ants. Selection appears to act independently on the two genes and is detectable in only one of the two social forms of this species (the "polygyne" social form in which nests contain multiple fertile queens). Strong directional selection on Pgm-3 in this form, involves worker destruction of all queens with genotype Pgm-3AA before they reproduce. Selection on Gp-9 is more complex, involving both lethality of all Gp-9bb females and a strong or even complete survival advantage to reproductive queens with the heterozygous genotype Gp-9Bb. Pgm-3 and Gp-9 are tightly linked (rf = 0.0016) and exhibit strong gametic phase disequilibrium in introduced populations in the U.S. This disequilibrium seems not to have stemmed from the founder event associated with the introduction, because the same associations of alleles found in the U.S. apparently occur also in two native populations in Argentina. Rather, selection acting independently on Pgm-3 and Gp-9, in conjunction with gene flow from the alternate, "monogyne" social form (in which nests contain a single fertile queen), may explain the origin of disequilibrium between the two loci in polygyne fire ants.


Subject(s)
Ants/genetics , Evolution, Molecular , Animals , Argentina , Female , Gene Frequency , Genetic Linkage , Genotype , Haplotypes/genetics , Insect Proteins/genetics , Phosphoglucomutase/genetics , Polymorphism, Genetic , Population Dynamics , Recombination, Genetic , Selection, Genetic , Social Behavior , United States
5.
Genetics ; 135(3): 843-54, 1993 Nov.
Article in English | MEDLINE | ID: mdl-8293983

ABSTRACT

Effects of a recent founder event on genetic diversity in wild populations of the fire ant Solenopsis invicta were studied, with particular attention given to the genetic sex-determining system. Diploid males are far more common relative to haploid males in introduced populations than in native populations of fire ants, and queens that produce diploid males account for a significantly larger proportion of the mated queens in introduced than in native populations. Differences between native and introduced populations in attributes of the mating systems (i.e., queen mating frequency or level of inbreeding) can be excluded as factors contributing to these different levels of diploid male production. Thus, we conclude that diploid males have increased in frequency in introduced populations because of a loss of allelic diversity at the sex-determining locus (loci). This loss of sex alleles has generated a substantial increase in the estimated segregational genetic load associated with production of sterile diploid males in introduced populations over the load in native populations. The loss of allelic diversity in the sex-determining system in introduced S. invicta is paralleled by a loss of electrophoretically detectable rare alleles at protein-encoding loci. Such concordance between these different types of markers is predicted because each of the many sex alleles present in the native populations is expected to be rare. Estimates of expected heterozygosity (Hexp) based on 76 electrophoretic loci do not differ significantly between the native and introduced fire ant populations, illustrating the lack of sensitivity of this measure for detecting many types of bottlenecks.


Subject(s)
Ants/genetics , Genetic Variation , Sex Determination Analysis , Alleles , Animals , Argentina , Biological Evolution , Diploidy , Female , Genetic Markers , Genetics, Population , Haploidy , Heterozygote , Male , Proteins/genetics , United States
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