Please use this identifier to cite or link to this item: https://hdl.handle.net/1822/79424

TitleScreening and in silico characterization of prophages in Helicobacter pylori genomes
Author(s)Ferreira, Rute Vanessa Novais
Sousa, Cláudia Sofia Cunha
Presa, Eva
Pires, Diana Priscila Penso
Oleastro, Mónica
Azeredo, Joana
Figueiredo, Céu
Melo, Luís Daniel Rodrigues
KeywordsHelicobacter pylori
Prophage
Phage Therapy
Issue date22-Jul-2022
CitationFerreira, R.; Sousa, Cláudia; Presa, Eva; Pires, Diana P.; Oleastro, Mónica; Azeredo, Joana; Figueiredo, Céu; Melo, Luís Daniel Rodrigues, Screening and in silico characterization of prophages in Helicobacter pylori genomes. VOM 2022 - Virus of Microbes Conference. Guimarães, Portugal, July 18-22, 537, 2022.
Abstract(s)Temperate bacterio(phages) play an important role on the evolution of pathogenic bacteria. Nevertheless, information on their role in Helicobacter pylori (an important gastric pathogen bacterium) is scarce. The present study developed a workflow for the identification of prophages in Portuguese H. pylori clinical strains, proposing the use of a new PCR-based screening method. The genome of strains with different PCR profiles were then sequenced. In the fourteen genomes analysed, nine intact prophages were identified by PHASTER. These prophages were annotated by analogy with other identified phages, where seven contained the integrase gene, corroborating the results obtained in the PCR screening, with only one exception. Still, in PCR screening, the holin gene was identified in 75 % of the strains containing intact phages, but BLASTp homologies only recognized this gene in one of the prophages. Fifty-six percent are podovirus, while in 44 % it was not possible to assign any family, according to the VirFam tool. Using the Resistance Gene Identifier of CARD it was identified the Acinetobacter mutant Lpx gene conferring resistance to colistin in two intact prophages. The BLASTp search identified a putative ABC binding cassette transporter in one of the intact prophages. On the bacterial genomes, 71 % have the CRISPR-Cas system classified as evidence level 1 by CRISPRCasFinder, which typically indicate potentially invalid CRISPR arrays. The use of an initial PCR screening method increased the identification of intact prophage-containing strains from 20 % to 57 %. Furthermore, the few virulence factors identified in prophages, and the possible inactivity of CRISPR-Cas in the bacterial genomes, allow the choice of strains for the isolation of phages for future studies. Overall, our results represent a significant contribution to the knowledge of prophages in H. pylori, and provide valuable insights into their potential use in phage therapy.
TypePoster
URIhttps://hdl.handle.net/1822/79424
Publisher versionhttps://vom2022.org/
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Painéis em Conferências / Posters in Conferences

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