Characterization and complete genome sequence of highly lytic phage active against methicillin-resistant Staphylococcus aureus (MRSA) isolated from Egypt

dc.contributor.authorEl-Tawab, Abeer K. Abd
dc.contributor.authorOthman, B. A.
dc.contributor.authorSharaf, Abdoallah
dc.contributor.authorEl-Masry, Samar S.
dc.contributor.authorEl-Arabi, T.F.
dc.date.accessioned2024-11-20T11:07:22Z
dc.date.available2024-11-20T11:07:22Z
dc.date.issued2024-11-08
dc.description.abstractBackground Methicillin-Resistant Staphylococcus aureus (MRSA) is one of the most resistant bacteria to antibiotics. S. aureus is an important, widespread pathogen that can cause a variety of infectious diseases in humans and animals. Phages have been recognized as natural, safe, highly specific and effective alternatives agents to antibiotics for preventing and treating bacterial infections caused by MRSA. Therefore, this study aims at the characterization of a novel isolated lytic phage, vB_SauP_ASUmrsa123. Methods Isolates of Staphylococcus aureus MRSA were obtained on Mannitol Salt Agar and Baird Parker Agar plates and confirmed using VITEK 2. Sewage and clinical samples were used to isolate specific phages for S. aureus MRSA, and plaque assays were used for host range determination on Luria-Bertani (LB) media. The phage morphology of the isolated phage was determined by transmission electron microscopy. The phage’s whole genome sequencing was identified. Results A total of 25 isolates of Staphylococci were obtained from different clinical sources and showed typical colonies on Baird-Parker and Mannitol Salt Agar plates. The VITEK 2 automated system revealed that all 25 isolates were confirmed as S. aureus (MRSA). Two of the most antibiotics-resistant isolates were further confirmed using 16S ribosomal RNA sequencing. A lytic phage was detected against the MRSA isolates tested In Vitro, namely vB_SauP_ASUmrsa123. The phage belonged to Rountreeviridae family based on morphological properties observed by TEM and the host range of the isolated phage was tested on the 25 clinical MRSA isolates in Vitro. The one-step growth curve of the isolated phage showed that the latent period was about 55 min, and the burst size was estimated at 167 PFU. The whole genome sequencing and annotation of genes revealed that phage vB_SauP_ASUmrsa123 contained a linear dsDNA with a size of about 17,155 bp with predicted 24 ORFs. Analysis of its genome provides valuable information approximately the variety of phages belonging to the staphylococcal phages class I. Conclusion A lytic Podo Phage vB_SauP_ASUmrsa123 was identified against S. aureus MRSA isolates and its genome was sequenced. The phage was found to be eligible for potential application in biocontrol.
dc.description.versionpublisheddeu
dc.identifier.doi10.1186/s12985-024-02554-0
dc.identifier.ppn1910590371
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/71363
dc.language.isoeng
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectStaphylococcus aureus
dc.subjectMRSA
dc.subjectAntimicrobial resistance (AMR)
dc.subjectPhage
dc.subjectGenome sequencing
dc.subject.ddc570
dc.titleCharacterization and complete genome sequence of highly lytic phage active against methicillin-resistant Staphylococcus aureus (MRSA) isolated from Egypteng
dc.typeJOURNAL_ARTICLE
dspace.entity.typePublication
kops.citation.bibtex
@article{ElTawab2024-11-08Chara-71363,
  year={2024},
  doi={10.1186/s12985-024-02554-0},
  title={Characterization and complete genome sequence of highly lytic phage active against methicillin-resistant Staphylococcus aureus (MRSA) isolated from Egypt},
  number={1},
  volume={21},
  journal={Virology Journal},
  author={El-Tawab, Abeer K. Abd and Othman, B. A. and Sharaf, Abdoallah and El-Masry, Samar S. and El-Arabi, T.F.},
  note={Article Number: 284}
}
kops.citation.iso690EL-TAWAB, Abeer K. Abd, B. A. OTHMAN, Abdoallah SHARAF, Samar S. EL-MASRY, T.F. EL-ARABI, 2024. Characterization and complete genome sequence of highly lytic phage active against methicillin-resistant Staphylococcus aureus (MRSA) isolated from Egypt. In: Virology Journal. Springer. 2024, 21(1), 284. eISSN 1743-422X. Verfügbar unter: doi: 10.1186/s12985-024-02554-0deu
kops.citation.iso690EL-TAWAB, Abeer K. Abd, B. A. OTHMAN, Abdoallah SHARAF, Samar S. EL-MASRY, T.F. EL-ARABI, 2024. Characterization and complete genome sequence of highly lytic phage active against methicillin-resistant Staphylococcus aureus (MRSA) isolated from Egypt. In: Virology Journal. Springer. 2024, 21(1), 284. eISSN 1743-422X. Available under: doi: 10.1186/s12985-024-02554-0eng
kops.citation.rdf
<rdf:RDF
    xmlns:dcterms="http://purl.org/dc/terms/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
    xmlns:bibo="http://purl.org/ontology/bibo/"
    xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#"
    xmlns:foaf="http://xmlns.com/foaf/0.1/"
    xmlns:void="http://rdfs.org/ns/void#"
    xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > 
  <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/71363">
    <foaf:homepage rdf:resource="http://localhost:8080/"/>
    <dcterms:issued>2024-11-08</dcterms:issued>
    <dc:creator>Othman, B. A.</dc:creator>
    <dc:creator>El-Masry, Samar S.</dc:creator>
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <dc:contributor>Othman, B. A.</dc:contributor>
    <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2024-11-20T11:07:22Z</dcterms:available>
    <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/71363/1/El-Tawab_2-yv9eeng5uu093.pdf"/>
    <dcterms:title>Characterization and complete genome sequence of highly lytic phage active against methicillin-resistant Staphylococcus aureus (MRSA) isolated from Egypt</dcterms:title>
    <dc:language>eng</dc:language>
    <dc:creator>El-Tawab, Abeer K. Abd</dc:creator>
    <dc:contributor>Sharaf, Abdoallah</dc:contributor>
    <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/71363"/>
    <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/71363/1/El-Tawab_2-yv9eeng5uu093.pdf"/>
    <dc:creator>Sharaf, Abdoallah</dc:creator>
    <dc:contributor>El-Tawab, Abeer K. Abd</dc:contributor>
    <dc:contributor>El-Masry, Samar S.</dc:contributor>
    <dc:creator>El-Arabi, T.F.</dc:creator>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2024-11-20T11:07:22Z</dc:date>
    <dc:rights>Attribution 4.0 International</dc:rights>
    <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
    <dcterms:abstract>Background 
Methicillin-Resistant Staphylococcus aureus (MRSA) is one of the most resistant bacteria to antibiotics. S. aureus is an important, widespread pathogen that can cause a variety of infectious diseases in humans and animals. Phages have been recognized as natural, safe, highly specific and effective alternatives agents to antibiotics for preventing and treating bacterial infections caused by MRSA. Therefore, this study aims at the characterization of a novel isolated lytic phage, vB_SauP_ASUmrsa123.
Methods          
Isolates of Staphylococcus aureus MRSA were obtained on Mannitol Salt Agar and Baird Parker Agar plates and confirmed using VITEK 2. Sewage and clinical samples were used to isolate specific phages for S. aureus MRSA, and plaque assays were used for host range determination on Luria-Bertani (LB) media. The phage morphology of the isolated phage was determined by transmission electron microscopy. The phage’s whole genome sequencing was identified.                  Results
A total of 25 isolates of Staphylococci were obtained from different clinical sources and showed typical colonies on Baird-Parker and Mannitol Salt Agar plates. The VITEK 2 automated system revealed that all 25 isolates were confirmed as S. aureus (MRSA). Two of the most antibiotics-resistant isolates were further confirmed using 16S ribosomal RNA sequencing. A lytic phage was detected against the MRSA isolates tested In Vitro, namely vB_SauP_ASUmrsa123. The phage belonged to Rountreeviridae family based on morphological properties observed by TEM and the host range of the isolated phage was tested on the 25 clinical MRSA isolates in Vitro. The one-step growth curve of the isolated phage showed that the latent period was about 55 min, and the burst size was estimated at 167 PFU. The whole genome sequencing and annotation of genes revealed that phage vB_SauP_ASUmrsa123 contained a linear dsDNA with a size of about 17,155 bp with predicted 24 ORFs. Analysis of its genome provides valuable information approximately the variety of phages belonging to the staphylococcal phages class I.
Conclusion          
A lytic Podo Phage vB_SauP_ASUmrsa123 was identified against S. aureus MRSA isolates and its genome was sequenced. The phage was found to be eligible for potential application in biocontrol.</dcterms:abstract>
    <dcterms:rights rdf:resource="http://creativecommons.org/licenses/by/4.0/"/>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <dc:contributor>El-Arabi, T.F.</dc:contributor>
  </rdf:Description>
</rdf:RDF>
kops.description.openAccessopenaccessgold
kops.flag.isPeerReviewedtrue
kops.flag.knbibliographytrue
kops.identifier.nbnurn:nbn:de:bsz:352-2-yv9eeng5uu093
kops.relation.coreFacilitysequencing-analysis-core-facility
kops.sourcefieldVirology Journal. Springer. 2024, <b>21</b>(1), 284. eISSN 1743-422X. Verfügbar unter: doi: 10.1186/s12985-024-02554-0deu
kops.sourcefield.plainVirology Journal. Springer. 2024, 21(1), 284. eISSN 1743-422X. Verfügbar unter: doi: 10.1186/s12985-024-02554-0deu
kops.sourcefield.plainVirology Journal. Springer. 2024, 21(1), 284. eISSN 1743-422X. Available under: doi: 10.1186/s12985-024-02554-0eng
relation.isAuthorOfPublication00b8d7ef-1542-4801-8eda-348c434cdb01
relation.isAuthorOfPublication.latestForDiscovery00b8d7ef-1542-4801-8eda-348c434cdb01
source.bibliographicInfo.articleNumber284
source.bibliographicInfo.issue1
source.bibliographicInfo.volume21
source.identifier.eissn1743-422X
source.periodicalTitleVirology Journal
source.publisherSpringer

Dateien

Originalbündel

Gerade angezeigt 1 - 1 von 1
Vorschaubild nicht verfügbar
Name:
El-Tawab_2-yv9eeng5uu093.pdf
Größe:
1.7 MB
Format:
Adobe Portable Document Format
El-Tawab_2-yv9eeng5uu093.pdf
El-Tawab_2-yv9eeng5uu093.pdfGröße: 1.7 MBDownloads: 71