7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Genetic variability of Taenia solium cysticerci recovered from experimentally infected pigs and from naturally infected pigs using microsatellite markers

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The adult Taenia solium, the pork tapeworm, usually lives as a single worm in the small intestine of humans, its only known definitive host. Mechanisms of genetic variation in T. solium are poorly understood. Using three microsatellite markers previously reported [ 1], this study explored the genetic variability of T. solium from cysts recovered from experimentally infected pigs. It then explored the genetic epidemiology and transmission in naturally infected pigs and adult tapeworms recovered from human carriers from an endemic rural community in Peru. In an initial study on experimental infection, two groups of three piglets were each infected with proglottids from one of two genetically different tapeworms for each of the microsatellites. After 7 weeks, pigs were slaughtered and necropsy performed. Thirty-six (92.3%) out of 39 cysts originated from one tapeworm, and 27 (100%) out of 27 cysts from the other had exactly the same genotype as the parental tapeworm. This suggests that the microsatellite markers may be a useful tool for studying the transmission of T. solium. In the second study, we analyzed the genetic variation of T. solium in cysts recovered from eight naturally infected pigs, and from adult tapeworms recovered from four human carriers; they showed genetic variability. Four pigs had cysts with only one genotype, and four pigs had cysts with two different genotypes, suggesting that multiple infections of genetically distinct parental tapeworms are possible. Six pigs harbored cysts with a genotype corresponding to one of the identified tapeworms from the human carriers. In the dendrogram, cysts appeared to cluster within the corresponding pigs as well as with the geographical origin, but this association was not statistically significant. We conclude that genotyping of microsatellite size polymorphisms is a potentially important tool to trace the spread of infection and pinpoint sources of infection as pigs spread cysts with a shared parental genotype.

          Author summary

          Taenia solium, the pork tapeworm, is a major cause of epilepsy in developing countries. Although it has been deemed a potentially eradicable pathogen, it remains prevalent in rural communities. This two-part study aims to evaluate the utility of three microsatellite markers previously reported, to identify parasites and to establish relationships among them. In the first study, we evaluated the genetic variability of the progeny of two individual tapeworms by infecting two groups of three pigs each. We found variation of 8% and 0% in the two groups with respect to the parental tapeworm, indicating that the cysts source may be identifiable. Next, in the second study we described the genetic relationships among tapeworms obtained from four carriers and cysts obtained from eight naturally infected pigs in a rural community. We demonstrated that pigs can have two types of cysts, suggesting multiple infections. In addition, we found relatedness between 6 pigs and one tapeworm identified in the community. Our results indicate the potential for microsatellite markers to identify genetic relationships between parasites and thereby establish routes of transmission. It is likely that the limited number of microsatellites prevented us from establishing relatedness with more precision. Therefore, further evaluation of additional microsatellites is recommended.

          Related collections

          Most cited references37

          • Record: found
          • Abstract: found
          • Article: not found

          Pregnancy and pregnancy-associated hormones alter immune responses and disease pathogenesis.

          During pregnancy, it is evolutionarily advantageous for inflammatory immune responses that might lead to fetal rejection to be reduced and anti-inflammatory responses that promote transfer of maternal antibodies to the fetus to be increased. Hormones modulate the immunological shift that occurs during pregnancy. Estrogens, including estradiol and estriol, progesterone, and glucocorticoids increase over the course of pregnancy and affect transcriptional signaling of inflammatory immune responses at the maternal-fetal interface and systemically. During pregnancy, the reduced activity of natural killer cells, inflammatory macrophages, and helper T cell type 1 (Th1) cells and production of inflammatory cytokines, combined with the higher activity of regulatory T cells and production of anti-inflammatory cytokines, affects disease pathogenesis. The severity of diseases caused by inflammatory responses (e.g., multiple sclerosis) is reduced and the severity of diseases that are mitigated by inflammatory responses (e.g., influenza and malaria) is increased during pregnancy. For some infectious diseases, elevated inflammatory responses that are necessary to control and clear a pathogen have a negative consequence on the outcome of pregnancy. The bidirectional interactions between hormones and the immune system contribute to both the outcome of pregnancy and female susceptibility to disease. Copyright © 2012 Elsevier Inc. All rights reserved.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Microsatellites: genomic distribution, putative functions and mutational mechanisms: a review.

            Microsatellites, or tandem simple sequence repeats (SSR), are abundant across genomes and show high levels of polymorphism. SSR genetic and evolutionary mechanisms remain controversial. Here we attempt to summarize the available data related to SSR distribution in coding and noncoding regions of genomes and SSR functional importance. Numerous lines of evidence demonstrate that SSR genomic distribution is nonrandom. Random expansions or contractions appear to be selected against for at least part of SSR loci, presumably because of their effect on chromatin organization, regulation of gene activity, recombination, DNA replication, cell cycle, mismatch repair system, etc. This review also discusses the role of two putative mutational mechanisms, replication slippage and recombination, and their interaction in SSR variation.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Slippage synthesis of simple sequence DNA.

              The analysis of slippage synthesis of simple sequence DNA in vitro sheds some light on the question of how simple sequences arise in vivo. We show that it is possible to synthesize all types of repetitious di- and trinucleotide motifs starting from short primers and a polymerase in vitro. The rate of this synthesis depends on a sequence specific slippage rate, but is independent of the length of the fragments being synthesized. This indicates that only the ends of the DNA fragments are involved in determining this rate and that slippage is accordingly a short range effect. Slippage synthesis occurs also on a fixed template where only one strand is free to move, a situation which resembles chromosome replication in vivo. It seems therefore likely that slippage during replication is the cause of the observed length polymorphism of simple sequence stretches between individuals of a population.
                Bookmark

                Author and article information

                Contributors
                Role: ConceptualizationRole: Formal analysisRole: InvestigationRole: MethodologyRole: SupervisionRole: Writing – original draftRole: Writing – review & editing
                Role: Data curationRole: Formal analysisRole: InvestigationRole: Writing – original draftRole: Writing – review & editing
                Role: Data curationRole: InvestigationRole: ValidationRole: Writing – review & editing
                Role: InvestigationRole: Writing – review & editing
                Role: Formal analysisRole: InvestigationRole: Writing – review & editing
                Role: InvestigationRole: Writing – review & editing
                Role: SupervisionRole: Writing – review & editing
                Role: MethodologyRole: ValidationRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: MethodologyRole: Writing – original draftRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: MethodologyRole: ResourcesRole: Writing – review & editing
                Role: MethodologyRole: SupervisionRole: Writing – review & editing
                Role: ConceptualizationRole: ResourcesRole: SupervisionRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS Negl Trop Dis
                PLoS Negl Trop Dis
                plos
                plosntds
                PLoS Neglected Tropical Diseases
                Public Library of Science (San Francisco, CA USA )
                1935-2727
                1935-2735
                28 December 2017
                December 2017
                : 11
                : 12
                : e0006087
                Affiliations
                [1 ] Laboratorio de Bioinformática y Biología Molecular, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima, Peru
                [2 ] Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, United States of America
                [3 ] School of Veterinary Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru
                [4 ] Center for Global Health, Universidad, Peruana Cayetano Heredia, Lima, Peru
                [5 ] Department of Microbiology, School of Science and Philosophy, Universidad Peruana Cayetano Heredia, Lima, Peru
                Ludwig-Maximilians-University, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                ¶ Membership of the Cysticercosis Working Group in Peru is provided in the Acknowledgments.

                Author information
                http://orcid.org/0000-0003-3662-2250
                Article
                PNTD-D-17-00760
                10.1371/journal.pntd.0006087
                5746202
                29284011
                daf948a7-22fc-4163-a6b2-4be678fbfc1a
                © 2017 Pajuelo et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 17 May 2017
                : 31 October 2017
                Page count
                Figures: 2, Tables: 5, Pages: 15
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: TW001140
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: D43TW006581
                Award Recipient :
                This study was partially supported by the National Institutes of Health (grant numbers D43TW001140 and D43TW006581). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Organisms
                Eukaryota
                Animals
                Vertebrates
                Amniotes
                Mammals
                Swine
                Biology and Life Sciences
                Genetics
                Gene Types
                Microsatellite Loci
                Biology and Life Sciences
                Evolutionary Biology
                Population Genetics
                Genetic Polymorphism
                Biology and Life Sciences
                Genetics
                Population Genetics
                Genetic Polymorphism
                Biology and Life Sciences
                Population Biology
                Population Genetics
                Genetic Polymorphism
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Genotyping
                Research and Analysis Methods
                Molecular Biology Techniques
                Genotyping
                Medicine and Health Sciences
                Parasitic Diseases
                Medicine and Health Sciences
                Epidemiology
                Genetic Epidemiology
                Biology and Life Sciences
                Genetics
                Heredity
                Biology and Life Sciences
                Anatomy
                Digestive System
                Mouth
                Tongue
                Medicine and Health Sciences
                Anatomy
                Digestive System
                Mouth
                Tongue
                Custom metadata
                All relevant data are within the paper and its Supporting Information files.

                Infectious disease & Microbiology
                Infectious disease & Microbiology

                Comments

                Comment on this article