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1.
Korean J Parasitol ; 59(4): 363-368, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34470087

ABSTRACT

Despite the synergistic effect of Opisthorchis viverrini and Helicobacter pylori co-infection on pathogenesis of severe hepatobiliary abnormalities (HBA) including advanced periductal fibrosis and replace with cholangiocarcinoma (CCA) have been established, the immune response to H. pylori in O. viverrini infected population has never been explored. Hence, this study aimed to investigate the antibody responses to 2 immunogenic H. pylori proteins in O. viverrini-infected patients with HBA and CCA. The risk analysis by multinomial logistic regression revealed that GroEL seropositivity was associated with higher risks of hepatobiliary abnormalities and CCA with adjusted odds ratios (95% confidence intervals) of 2.11 (95% CI=1.20-3.71, P=0.008) and 2.13 (95% CI=1.21-3.75, P=0.009), respectively. These findings indicate that GroEL seropositivity might be a biomarker for early detection of O. viverrini associated HBA and CCA.


Subject(s)
Bile Duct Neoplasms , Cholangiocarcinoma , Helicobacter pylori , Opisthorchiasis , Opisthorchis , Animals , Bile Ducts, Intrahepatic , Humans , Opisthorchiasis/complications
2.
Nucleic Acids Res ; 41(2): 1363-71, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23221644

ABSTRACT

Repairing damaged DNA is essential for an organism's survival. UV damage endonuclease (UVDE) is a DNA-repair enzyme that can recognize and incise different types of damaged DNA. We present the structure of Sulfolobus acidocaldarius UVDE on its own and in a pre-catalytic complex with UV-damaged DNA containing a 6-4 photoproduct showing a novel 'dual dinucleotide flip' mechanism for recognition of damaged dipyrimidines: the two purines opposite to the damaged pyrimidine bases are flipped into a dipurine-specific pocket, while the damaged bases are also flipped into another cleft.


Subject(s)
DNA Damage , DNA Repair Enzymes/chemistry , Endodeoxyribonucleases/chemistry , Amino Acid Sequence , DNA/chemistry , DNA Repair Enzymes/metabolism , Endodeoxyribonucleases/metabolism , Metals/chemistry , Models, Molecular , Molecular Sequence Data , Pyrimidine Dimers/metabolism , Sequence Alignment , Sulfolobus acidocaldarius/enzymology
3.
Parasitol Int ; 75: 102050, 2020 Apr.
Article in English | MEDLINE | ID: mdl-31901435

ABSTRACT

The carcinogenic liver fluke Opisthorchis viverrini (O. viverrini) is endemic in Thailand and neighboring countries including Laos PDR, Vietnam and Cambodia. Infections with O. viverrini lead to hepatobiliary abnormalities including bile duct cancer-cholangiocarcinoma (CCA). Despite decades of extensive studies, the underlying mechanisms of how this parasite survives in the bile duct and causes disease are still unclear. Therefore, this study aims to identify and characterize the most abundant protein secreted by the parasite. Proteomics and bioinformatics analysis revealed that the most abundant secretory protein is a metallopeptidase, named Ov-M60-like-1. This protein contains an N-terminal carbohydrate-binding domain and a C-terminal M60-like domain with a zinc metallopeptidase HEXXH motif. Further analysis by mass spectrometry revealed that Ov-M60-like-1 is N-glycosylated. Recombinant Ov-M60-like-1 (rOv-M60-like-1) expressed in Escherichia coli (E. coli) was able to digest bovine submaxillary mucin (BSM). The mucinase activity was inhibited by the ion chelating agent EDTA, confirming its metallopeptidase identity. The enzyme was active at temperatures ranging 25-37 °C in a broad pH range (pH 2-10). The identification of Ov-M60-like-1 mucinase as the major secretory protein of O. viverrini worms warrants further research into the role of this glycoprotein in the pathology induced by this carcinogenic worm.


Subject(s)
Helminth Proteins/genetics , Metalloproteases/genetics , Opisthorchis/genetics , Amino Acid Sequence , Animals , Helminth Proteins/chemistry , Helminth Proteins/metabolism , Metalloproteases/chemistry , Metalloproteases/metabolism , Opisthorchiasis/metabolism , Opisthorchis/enzymology , Phylogeny , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Sequence Alignment
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