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  1. Article: Host genetic variations in glutathione-S-transferases, superoxide dismutases and catalase genes influence susceptibility to malaria infection in an Indian population

    Fernandes, Rayzel C / Hasan, Marriyah / Gupta, Himanshu / Geetha, K / Rai, Padmalatha S / Hande, Manjunath H / D’Souza, Sydney C / Adhikari, Prabha / Brand, Angela / Satyamoorthy, Kapaettu

    Molecular genetics and genomics. 2015 June, v. 290, no. 3

    2015  

    Abstract: Antioxidant enzymes can contribute to disease susceptibility or determine response to therapy in individuals with malaria. Genetic variations due to polymorphisms in host genes encoding antioxidant enzymes such as glutathione S-transferases-theta, mu, pi ...

    Abstract Antioxidant enzymes can contribute to disease susceptibility or determine response to therapy in individuals with malaria. Genetic variations due to polymorphisms in host genes encoding antioxidant enzymes such as glutathione S-transferases-theta, mu, pi (GSTT, GSTM, GSTP), superoxide dismutases (SOD) and catalase (CAT), may therefore, influence inter-individual response to malaria pathology and propensity of infection caused by Plasmodium vivax (Pv) and Plasmodium falciparum (Pf). Therefore, using polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) and DNA sequencing, we investigated the association of deletions of GSTT1 and GSTM1, single nucleotide polymorphisms (SNPs) of GSTP1 (rs1695), SOD1 (rs2234694), SOD2 (rs4880, rs1141718), SOD3 (rs2536512) and CAT (rs1001179) in individuals infected with Pf (n = 100) and Pv (n = 100) against healthy controls (n = 150). Our data suggest a significant role for GSTM1 deletions in complicated Pv (p = 0.0007) malaria with ODDs ratio 3.8 [with 95 % confidence interval (CI) 1.9–7.4]. The results also indicated that polymorphisms present in GSTP1, SOD1 and CAT genes may be associated with malaria susceptibility (p < 0.05), whereas SOD3 polymorphism may play a role in malarial resistance (p < 0.05). In addition, we observed significant SNP–SNP interactions with synergistic genetic effects in SOD2, SOD3 and CAT genes for Pv and in SOD2 and SOD3 genes for Pf. In conclusion, our results provide convincing evidence for a relationship between polymorphisms in host antioxidant enzymes and susceptibility to malaria infection.
    Keywords Plasmodium falciparum ; Plasmodium vivax ; antioxidants ; catalase ; confidence interval ; disease resistance ; genes ; genetic variation ; glutathione transferase ; malaria ; odds ratio ; polymerase chain reaction ; restriction fragment length polymorphism ; sequence analysis ; single nucleotide polymorphism ; superoxide dismutase ; India
    Language English
    Dates of publication 2015-06
    Size p. 1155-1168.
    Publishing place Springer-Verlag
    Document type Article
    ISSN 1617-4615
    DOI 10.1007/s00438-014-0984-4
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Host genetic variations in glutathione-S-transferases, superoxide dismutases and catalase genes influence susceptibility to malaria infection in an Indian population.

    Fernandes, Rayzel C / Hasan, Marriyah / Gupta, Himanshu / Geetha, K / Rai, Padmalatha S / Hande, Manjunath H / D'Souza, Sydney C / Adhikari, Prabha / Brand, Angela / Satyamoorthy, Kapaettu

    Molecular genetics and genomics : MGG

    2015  Volume 290, Issue 3, Page(s) 1155–1168

    Abstract: Antioxidant enzymes can contribute to disease susceptibility or determine response to therapy in individuals with malaria. Genetic variations due to polymorphisms in host genes encoding antioxidant enzymes such as glutathione S-transferases-theta, mu, pi ...

    Abstract Antioxidant enzymes can contribute to disease susceptibility or determine response to therapy in individuals with malaria. Genetic variations due to polymorphisms in host genes encoding antioxidant enzymes such as glutathione S-transferases-theta, mu, pi (GSTT, GSTM, GSTP), superoxide dismutases (SOD) and catalase (CAT), may therefore, influence inter-individual response to malaria pathology and propensity of infection caused by Plasmodium vivax (Pv) and Plasmodium falciparum (Pf). Therefore, using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and DNA sequencing, we investigated the association of deletions of GSTT1 and GSTM1, single nucleotide polymorphisms (SNPs) of GSTP1 (rs1695), SOD1 (rs2234694), SOD2 (rs4880, rs1141718), SOD3 (rs2536512) and CAT (rs1001179) in individuals infected with Pf (n = 100) and Pv (n = 100) against healthy controls (n = 150). Our data suggest a significant role for GSTM1 deletions in complicated Pv (p = 0.0007) malaria with ODDs ratio 3.8 [with 95 % confidence interval (CI) 1.9-7.4]. The results also indicated that polymorphisms present in GSTP1, SOD1 and CAT genes may be associated with malaria susceptibility (p < 0.05), whereas SOD3 polymorphism may play a role in malarial resistance (p < 0.05). In addition, we observed significant SNP-SNP interactions with synergistic genetic effects in SOD2, SOD3 and CAT genes for Pv and in SOD2 and SOD3 genes for Pf. In conclusion, our results provide convincing evidence for a relationship between polymorphisms in host antioxidant enzymes and susceptibility to malaria infection.
    MeSH term(s) Adult ; Antioxidants/metabolism ; Asian Continental Ancestry Group/genetics ; Case-Control Studies ; Catalase/genetics ; Female ; Genetic Predisposition to Disease ; Genetic Variation ; Genotype ; Glutathione S-Transferase pi/genetics ; Glutathione Transferase/genetics ; Humans ; India ; Malaria/enzymology ; Malaria/genetics ; Male ; Middle Aged ; Polymorphism, Restriction Fragment Length ; Polymorphism, Single Nucleotide/genetics ; Risk Factors ; Superoxide Dismutase/genetics ; Young Adult
    Chemical Substances Antioxidants ; Catalase (EC 1.11.1.6) ; Superoxide Dismutase (EC 1.15.1.1) ; glutathione S-transferase T1 (EC 2.5.1.-) ; GSTP1 protein, human (EC 2.5.1.18) ; Glutathione S-Transferase pi (EC 2.5.1.18) ; Glutathione Transferase (EC 2.5.1.18) ; glutathione S-transferase M1 (EC 2.5.1.18)
    Language English
    Publishing date 2015-06
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 2044817-X
    ISSN 1617-4623 ; 1617-4615
    ISSN (online) 1617-4623
    ISSN 1617-4615
    DOI 10.1007/s00438-014-0984-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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