Decreased expression of femXAB genes and fnbp mediated biofilm pathways in OS-MRSA clinical isolates.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
05 11 2019
Historique:
received: 06 10 2018
accepted: 01 10 2019
entrez: 7 11 2019
pubmed: 7 11 2019
medline: 4 11 2020
Statut: epublish

Résumé

Methicillin-Resistant Staphylococcus aureus (MRSA) is a significant threat to human health. Additionally, biofilm forming bacteria becomes more tolerant to antibiotics and act as bacterial reservoir leading to chronic infection. In this study, we characterised the antibiotic susceptibility, biofilm production and sequence types (ST) of 74 randomly selected clinical isolates of S. aureus causing ocular infections. Antibiotic susceptibility revealed 74% of the isolates as resistant against one or two antibiotics, followed by 16% multidrug-resistant isolates (MDR), and 10% sensitive. The isolates were characterized as MRSA (n = 15), Methicillin-sensitive S. aureus (MSSA, n = 48) and oxacillin susceptible mecA positive S. aureus (OS-MRSA, n = 11) based on oxacillin susceptibility, mecA gene PCR and PBP2a agglutination test. All OS-MRSA would have been misclassified as MSSA on the basis of susceptibility test. Therefore, both phenotypic and genotypic tests should be included to prevent strain misrepresentation. In addition, in-depth studies for understanding the emerging OS-MRSA phenotype is required. The role of fem XAB gene family has been earlier reported in OS-MRSA phenotype. Sequence analysis of the fem XAB genes revealed mutations in fem × (K3R, H11N, N18H and I51V) and fem B (L410F) genes. The fem XAB genes were also found down-regulated in OS-MRSA isolates in comparison to MRSA. In OS-MRSA isolates, biofilm formation is regulated by fibronectin binding proteins A & B. Molecular typing of the isolates revealed genetic diversity. All the isolates produced biofilm, however, MRSA isolates with strong biofilm phenotype represent a worrisome situation and may even result in treatment failure.

Identifiants

pubmed: 31690794
doi: 10.1038/s41598-019-52557-z
pii: 10.1038/s41598-019-52557-z
pmc: PMC6831631
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bacterial Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

16028

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Auteurs

Umarani Brahma (U)

National Institute of Animal Biotechnology, Hyderabad, India.

Paresh Sharma (P)

National Institute of Animal Biotechnology, Hyderabad, India.

Shweta Murthy (S)

National Institute of Animal Biotechnology, Hyderabad, India.

Savitri Sharma (S)

L.V. Prasad Eye Institute, Hyderabad, India.

Shalini Chakraborty (S)

National Institute of Animal Biotechnology, Hyderabad, India.

Sundarapu Naga Appalaraju (SN)

National Institute of Animal Biotechnology, Hyderabad, India.

Vasundhra Bhandari (V)

National Institute of Animal Biotechnology, Hyderabad, India. vasundhra23@gmail.com.

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