Inhibition of Porphyromonas gulae and periodontal disease in dogs by a combination of clindamycin and interferon alpha.


Journal

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

Informations de publication

Date de publication:
20 02 2020
Historique:
received: 16 04 2019
accepted: 29 01 2020
entrez: 22 2 2020
pubmed: 23 2 2020
medline: 31 12 2020
Statut: epublish

Résumé

Porphyromonas gulae is a major periodontal pathogen in dogs, which can be transmitted to their owners. A major virulence factor of P. gulae consists of a 41-kDa filamentous appendage (FimA) on the cell surface, which is classified into three genotypes: A, B, and C. Thus far, inhibition of periodontal disease in dogs remains difficult. The present study assessed the inhibitory effects of a combination of clindamycin and interferon alpha (IFN-α) formulation against P. gulae and periodontal disease. Growth of P. gulae was significantly inhibited by clindamycin; this inhibition had a greater effect on type C P. gulae than on type A and B isolates. In contrast, the IFN-α formulation inhibited the expression of IL-1β and COX-2 elicited by type A and B isolates, but not that elicited by type C isolates. Furthermore, periodontal recovery was promoted by the administration of both clindamycin and IFN-α formulation to dogs undergoing periodontal treatment; moreover, this combined treatment reduced the number of FimA genotypes in oral specimens from treated dogs. These results suggest that a combination of clindamycin and IFN-α formulation inhibit P. gulae virulence and thus may be effective for the prevention of periodontal disease induced by P. gulae.

Identifiants

pubmed: 32080231
doi: 10.1038/s41598-020-59730-9
pii: 10.1038/s41598-020-59730-9
pmc: PMC7033253
doi:

Substances chimiques

Cytokines 0
Interferon-alpha 0
Virulence Factors 0
fimbrillin 0
Fimbriae Proteins 147680-16-8
Clindamycin 3U02EL437C

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3113

Commentaires et corrections

Type : ErratumIn

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Auteurs

Ryota Nomura (R)

Department of Pediatric Dentistry, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan. rnomura@dent.osaka-u.ac.jp.

Hiroaki Inaba (H)

Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Hidemi Yasuda (H)

Yasuda Veterinary Clinic, Meguro, Tokyo, Japan.

Mitsuyuki Shirai (M)

Department of Pharmacology, School of Veterinary Medicine, Azabu University, Sagamihara, Kanagawa, Japan.

Yukio Kato (Y)

Department of Veterinary Public Health II, School of Veterinary Medicine, Azabu University, Sagamihara, Kanagawa, Japan.

Masaru Murakami (M)

Department of Molecular Biology, School of Veterinary Medicine, Azabu University, Sagamihara, Kanagawa, Japan.

Naoki Iwashita (N)

Department of Pharmacology, School of Veterinary Medicine, Azabu University, Sagamihara, Kanagawa, Japan.

So Shirahata (S)

Primo Animal Hospital, Sagamihara, Kanagawa, Japan.

Sho Yoshida (S)

Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Saaya Matayoshi (S)

Department of Pediatric Dentistry, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.

Junya Yasuda (J)

Yasuda Veterinary Clinic, Meguro, Tokyo, Japan.

Nobuaki Arai (N)

Yasuda Veterinary Clinic, Meguro, Tokyo, Japan.

Fumitoshi Asai (F)

Department of Pharmacology, School of Veterinary Medicine, Azabu University, Sagamihara, Kanagawa, Japan.

Michiyo Matsumoto-Nakano (M)

Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Kazuhiko Nakano (K)

Department of Pediatric Dentistry, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.

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