<i>Staphylococcus aureus</i> Isolated from the Oral Cavity: Phage Susceptibility in Relation to Antibiotic Resistance

Nowadays, research on bacteriophage therapy and its potential use in combination with antibiotics has been gaining momentum. One hundred and ten oral <i>Staphylococcus aureus</i> isolates were phage-typed and their antibiotic resistance was determined by standard and molecular methods. T...

Full description

Bibliographic Details
Published in:Antibiotics
Main Authors: Katarzyna Garbacz, Ewa Kwapisz, Lidia Piechowicz, Maria Wierzbowska
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Subjects:
Online Access:https://www.mdpi.com/2079-6382/10/11/1329
Description
Summary:Nowadays, research on bacteriophage therapy and its potential use in combination with antibiotics has been gaining momentum. One hundred and ten oral <i>Staphylococcus aureus</i> isolates were phage-typed and their antibiotic resistance was determined by standard and molecular methods. The prevalence of MSSA and MRSA strains was 89.1% and 10.9%, respectively. Nearly all (91.8%) analyzed isolates, whether MSSA or MRSA, were susceptible to the phages used from the international set. The highest lytic activity showed phages 79 and 52 A from lytic group I. The predominant phage groups were mixed, the I+III group and a mixed group containing phages from at least three various lytic groups. <i>S. aureus</i> strains sensitive to phage group I were usually resistant to penicillin and susceptible to ciprofloxacin, whereas the strains typeable with group V or group V with the 95 phage were susceptible to most antibiotics. Epidemic CA-MRSA strains (SCC<i>mec</i>IV) of phage type 80/81 carried Panton–Valentine leucocidin genes. Considering the high sensitivity of oral <i>S. aureus</i> to the analyzed phages and the promising results of phage therapies reported by other authors, phage cocktails or phage-antibiotic combinations may potentially find applications in both the prevention and eradication of staphylococcal infections.
ISSN:2079-6382