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1.
Infect Genet Evol ; 75: 104011, 2019 11.
Article in English | MEDLINE | ID: mdl-31446138

ABSTRACT

BACKGROUND: The use of human and viral genetic markers offers a novel way to study human migration in multiethnic populations of Latin America. OBJECTIVES: Our goal was to characterize the genetic diversity and geographical origins of JC Polyomavirus (JCPyV) and the genetic ancestry of mitochondrial DNA (mtDNA) in inhabitants from 25 de Mayo, Misiones-Argentina, a small village of largely German ancestry located close to the border with Brazil. We also evaluated the extent of agreement between viral and mtDNA markers for the different ancestry components of this population. STUDY DESIGN: 68 individuals were analyzed for JCPyV and mtDNA diversity. JCPyV detection and typing was conducted in urine samples by PCR amplification, sequencing and phylogenetic analysis of the VP1 gene. mtDNA ancestry was assessed through HVS1 sequencing, with the resulting haplotypes being classified into haplogroups of Amerindian, European and African origin. The distribution of JCPyV diversity and mtDNA ancestry in the population was statistically evaluated by Fisher exact test and the level of agreement of both markers at the individual level was evaluated by Cohen's kappa coefficient. RESULTS: Our analysis showed that 57.4% of the samples were positive for JCPyV. Of these, the 47.6% were Asian-American Type 2, 33.3% European Type 1 and 19.1% African Type 3 in origin. The mtDNA ancestry of the study participants was 33.3% Amerindian and 66.7% European. There was a significant difference among the distribution of JCPyV diversity and mtDNA ancestry (p = 0.009) and at the individual level there was no correlation between the distribution of the both markers (κ = 0.154, p = 0.297). CONCLUSION: The apparent incongruence between JCPyV diversity and mtDNA ancestry may reflect the original settlement process and more recent migration to 25 de Mayo, the latter involving viral spread through migrants from Brazil. Some potential limitations to our interpretations are also discussed.


Subject(s)
DNA, Mitochondrial , Genetic Variation , JC Virus/genetics , Polyomavirus Infections/genetics , Polyomavirus Infections/virology , Adult , Aged , Aged, 80 and over , Argentina , Biological Evolution , Female , Genotype , Haplotypes , Humans , JC Virus/classification , Male , Middle Aged , Phylogeny
2.
Exp Parasitol ; 166: 16-20, 2016 Jul.
Article in English | MEDLINE | ID: mdl-26968777

ABSTRACT

The aim of this study was to detect, isolate and genetically characterize Toxoplasma gondii from tissues obtained from free range chickens which were breed in farms from patients with toxoplasmic retinochoroiditis in Misiones, Argentina. Thirty three samples of head (refrigerated = 18 and frozen = 15) from free range chickens were processed. Refrigerated (n = 18) chicken central nervous systems (CNS) were bioassay in mice. DNA was obtained from all samples (n = 33) and PCR was performed using TOX5-TOX8 T. gondii specific primers. Positive PCR samples were characterized by nested-PCR and restriction fragment length polymorphism using the markers SAG2, BTUB, GRA6, SAG3, PK1, L358, C22-8, C29-2 and Apico. T. gondii DNA was amplified in 30.3% (10/33) of CNS samples. Isolates were obtained in 27.7% (5/18) of inoculated CNS samples (TgCk11-9Arg, TgCk13-5Arg, TgCk14-5Arg, TgCk14-6Arg and TgCk14-7Arg). Seven samples showed a restriction pattern to all markers and were identified as atypical with several alleles type III. Genotyping of T. gondii from samples of patients with retinochoroiditis in the same area could improve the understanding of the epidemiology of toxoplasmosis in the region.


Subject(s)
Chickens/parasitology , Chorioretinitis/parasitology , Toxoplasma/isolation & purification , Toxoplasmosis, Animal/parasitology , Toxoplasmosis, Ocular/parasitology , Animals , Biological Assay , Brain/parasitology , Chlorocebus aethiops , DNA, Protozoan/genetics , DNA, Protozoan/isolation & purification , Genotype , Genotyping Techniques , Humans , Mice , Mice, Inbred BALB C , Mice, Knockout , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Toxoplasma/classification , Toxoplasma/genetics , Vero Cells
3.
Parasite ; 20: 44, 2013.
Article in English | MEDLINE | ID: mdl-24225023

ABSTRACT

BACKGROUND: Reactivation of toxoplasmic retinochoroiditis is the most frequent form of uveitis in Misiones, Argentina. Fluctuations in the number of patients consulting with this type of uveitis were detected during the last decade. Since the province was consecutively exposed to rainy and dry periods over the last years, we decided to explore whether a relationship between reactivation of toxoplasmic retinochoroiditis and rain might be established according to the data registered during the 2004-2010 period. RESULTS: The frequency of toxoplasmic reactivation episodes increases when precipitation increases (mostly in second and fourth trimesters of each year). Analysis of the independent variables demonstrates that precipitation is a significant predictor of the frequency of reactivation episodes. Although registered toxoplasmic reactivations were more frequent during the third trimester of the year, the association between the third trimester and the reactivation episodes did not reach statistical significance. CONCLUSION: Prolonged and intense rainfall periods were significantly associated with the reactivation of toxoplasmic retinochoroiditis. Changes promoted by this climatic condition on both the parasite survival in the soil as well as a putative effect on the host immune response due to other comorbidities are discussed.


Subject(s)
Choroiditis/epidemiology , Rain , Retinitis/epidemiology , Toxoplasmosis, Ocular/epidemiology , Toxoplasmosis, Ocular/etiology , Adult , Argentina/epidemiology , Choroiditis/parasitology , El Nino-Southern Oscillation , Female , Humans , Male , Middle Aged , Recurrence , Retinitis/parasitology , Seasons , Young Adult
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