Frequency and expression of genes involved in adhesion and biofilm formation in Staphylococcus aureus strains isolated from periodontal lesions.


Journal

Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi
ISSN: 1995-9133
Titre abrégé: J Microbiol Immunol Infect
Pays: England
ID NLM: 100956211

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 06 02 2019
revised: 09 04 2019
accepted: 29 05 2019
pubmed: 14 7 2019
medline: 8 10 2021
entrez: 14 7 2019
Statut: ppublish

Résumé

The aim of this study was to characterize the Staphylococcus aureus strains isolated from periodontal lesions of patients, to determine the expression of genes involved in cell adhesion upon their infection of human epithelial cells using an in vitro model, its biofilm formation, and its resistance to antibiotics. S. aureus was analysed by PCR, Kirby-Bauer, and pulsed-field gel electrophoresis (PFGE), measuring gene expression by real-time PCR after infection of human cells in vitro. S. aureus was identified in 18.6% (50/268) of the samples. All strains (n = 50) possessed the virulence genes spa (Staphylococcal protein A), coa (coagulase), and icaAB (intercellular adhesin); 96% (n = 48) possessed clfB (clumping factor B), and 88% (n = 44) possessed ebps (elastin-binding protein) and sdrD (serine aspartate repeat protein D). All strains were resistant to methicillin, ampicillin, dicloxacillin, cefotaxime, and penicillin, and were multidrug resistant to 6-12 antibiotics. PFGE analysis showed 37 different pulsed-field types and most strains (60.4%) had a unique pulsed-field type. Twenty-four distinct combinations of virulence genes and antibiotic-resistant phenotypes were identified. Although S. aureus has been considered a transient member of the oral microbiota, our results indicate a high-level expression of virulence genes and multidrug resistance in the strains isolated from periodontal lesions. These strains might complicate the successful treatment of the disease.

Sections du résumé

BACKGROUND/PURPOSE OBJECTIVE
The aim of this study was to characterize the Staphylococcus aureus strains isolated from periodontal lesions of patients, to determine the expression of genes involved in cell adhesion upon their infection of human epithelial cells using an in vitro model, its biofilm formation, and its resistance to antibiotics.
METHODS METHODS
S. aureus was analysed by PCR, Kirby-Bauer, and pulsed-field gel electrophoresis (PFGE), measuring gene expression by real-time PCR after infection of human cells in vitro.
RESULTS RESULTS
S. aureus was identified in 18.6% (50/268) of the samples. All strains (n = 50) possessed the virulence genes spa (Staphylococcal protein A), coa (coagulase), and icaAB (intercellular adhesin); 96% (n = 48) possessed clfB (clumping factor B), and 88% (n = 44) possessed ebps (elastin-binding protein) and sdrD (serine aspartate repeat protein D). All strains were resistant to methicillin, ampicillin, dicloxacillin, cefotaxime, and penicillin, and were multidrug resistant to 6-12 antibiotics. PFGE analysis showed 37 different pulsed-field types and most strains (60.4%) had a unique pulsed-field type. Twenty-four distinct combinations of virulence genes and antibiotic-resistant phenotypes were identified.
CONCLUSION CONCLUSIONS
Although S. aureus has been considered a transient member of the oral microbiota, our results indicate a high-level expression of virulence genes and multidrug resistance in the strains isolated from periodontal lesions. These strains might complicate the successful treatment of the disease.

Identifiants

pubmed: 31300301
pii: S1684-1182(19)30076-3
doi: 10.1016/j.jmii.2019.05.010
pii:
doi:

Substances chimiques

Adhesins, Bacterial 0
Anti-Bacterial Agents 0
Antigens, Bacterial 0
streptococcal protective antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

267-275

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Alina Uribe-García (A)

FES Iztacala, Universidad Nacional Autónoma de México, Mexico.

Gloria Luz Paniagua-Contreras (GL)

FES Iztacala, Universidad Nacional Autónoma de México, Mexico.

Eric Monroy-Pérez (E)

FES Iztacala, Universidad Nacional Autónoma de México, Mexico.

Jaime Bustos-Martínez (J)

Departamento de Atención a la Salud, Universidad Autónoma Metropolitana Xochimilco, Calzada del Hueso 1100, 04960, Ciudad de México, Mexico.

Aída Hamdan-Partida (A)

Departamento de Atención a la Salud, Universidad Autónoma Metropolitana Xochimilco, Calzada del Hueso 1100, 04960, Ciudad de México, Mexico.

Javier Garzón (J)

Clínica de Endoperiodontología, FES Iztacala, Universidad Nacional Autónoma de México, Mexico.

Jesica Alanís (J)

FES Iztacala, Universidad Nacional Autónoma de México, Mexico.

Rosalía Quezada (R)

FES Iztacala, Universidad Nacional Autónoma de México, Mexico.

Felipe Vaca-Paniagua (F)

Laboratorio Nacional en Salud, Diagnóstico Molecular y Efecto Ambiental en Enfermedades Crónico-Degenerativas, FES Iztacala, Universidad Nacional Autónoma de México México, Mexico; Instituto Nacional de Cancerología, CDMX 14080, Mexico; Unidad de Biomedicina, FES Iztacala, Universidad Nacional Autónoma de México, Mexico.

Sergio Vaca (S)

FES Iztacala, Universidad Nacional Autónoma de México, Mexico. Electronic address: vacasergio@gmail.com.

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Classifications MeSH