PMID- 28534196 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200930 IS - 2193-9616 (Print) IS - 2193-9616 (Electronic) IS - 2193-9616 (Linking) VI - 5 IP - 1 DP - 2016 Dec TI - In silico analysis of Shiga toxins (Stxs) to identify new potential vaccine targets for Shiga toxin-producing Escherichia coli. PG - 2 LID - 10.1007/s40203-017-0022-4 [doi] LID - 2 AB - Shiga toxins belong to a family of structurally and functionally related toxins serving as the main virulence factors for pathogenicity of the Shiga toxin-producing Escherichia coli (STEC) associating with Hemolytic uremic syndrome (HUS). At present, there is no effective treatment or prevention for HUS. The aim of the present study was to find conserved regions within the amino acid sequences of Stx1, Stx2 (Shiga toxin) and their variants. In this regard, In-silico identification of conformational continuous B cell and T-cell epitopes was performed in order to introduce new potential vaccine candidates. 93-100% Homology was observed in Stx1 and its variants. In Stx2 and its variants, 69-100% homology was shown. By sequence alignment with Stx1 and Stx2, 54% homology was detected. T-cell epitope identification in Stx1A and Stx2A epitopes with highest binding affinity for each HLA (human leukocyte antigen) was demonstrated with 100% identity among all Stxs. B-cell epitope prediction was resulted in finding of four common epitopes between Stxs. In silico analysis of Stxs was resulted to identification of new peptide targets that could be used in development of new epitope vaccine candidates or in immunodiagnostic tests. FAU - Golshani, Maryam AU - Golshani M AD - Molecular Biology Department, Institute Pasteur of Iran, Pasteur Ave., Tehran, 13164, Iran. FAU - Oloomi, Mana AU - Oloomi M AD - Molecular Biology Department, Institute Pasteur of Iran, Pasteur Ave., Tehran, 13164, Iran. manaoloomi@yahoo.com. FAU - Bouzari, Saeid AU - Bouzari S AD - Molecular Biology Department, Institute Pasteur of Iran, Pasteur Ave., Tehran, 13164, Iran. LA - eng PT - Journal Article DEP - 20170522 PL - Germany TA - In Silico Pharmacol JT - In silico pharmacology JID - 101623954 PMC - PMC5440418 OTO - NOTNLM OT - B-cell epitope OT - EHEC OT - HUS OT - Protein analysis OT - T-cell epitope OT - Vaccine COIS- The authors do not have any conflict of interest. EDAT- 2017/05/24 06:00 MHDA- 2017/05/24 06:01 PMCR- 2017/05/22 CRDT- 2017/05/24 06:00 PHST- 2017/03/05 00:00 [received] PHST- 2017/05/14 00:00 [accepted] PHST- 2017/05/24 06:00 [entrez] PHST- 2017/05/24 06:00 [pubmed] PHST- 2017/05/24 06:01 [medline] PHST- 2017/05/22 00:00 [pmc-release] AID - 10.1007/s40203-017-0022-4 [pii] AID - 22 [pii] AID - 10.1007/s40203-017-0022-4 [doi] PST - ppublish SO - In Silico Pharmacol. 2016 Dec;5(1):2. doi: 10.1007/s40203-017-0022-4. Epub 2017 May 22.