Your browser doesn't support javascript.
loading
Enhancing production of herpes simplex virus type 1 in oral epithelial cells by co-infection with Aggregatibacter actinomycetemcomitans.
Wu, Ching-Yi; Yu, Zhu-Yun; Hsu, Yu-Chun; Hung, Shan-Ling.
Afiliación
  • Wu CY; Institute of Oral Biology, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Dentistry, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Stomatology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Yu ZY; Institute of Oral Biology, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Hsu YC; Institute of Oral Biology, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Hung SL; Institute of Oral Biology, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Dentistry, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Stomatology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Community Dentistry, Zhong-Xiao Branch, T
J Formos Med Assoc ; 121(9): 1841-1849, 2022 Sep.
Article en En | MEDLINE | ID: mdl-35144835
ABSTRACT
BACKGROUND/

PURPOSE:

The association between herpetic/bacterial co-infection and periodontal diseases has been reported. However, how interactions between herpesviruses and periodontal bacteria dampen periodontal inflammation is still unclear. This study determined effects of co-infection with oral bacteria, including Streptococcus sanguinis, Fusobacterium nucleatum or Aggregatibacter actinomycetemcomitans, in herpes simplex virus type 1 (HSV-1)-infected oral epithelial cells.

METHODS:

Cell viability was determined by detection the activity of mitochondrial dehydrogenase. Viral production was measured using the plaque assay. Levels of bacterial and viral DNA were determined by real-time polymerase chain reaction. Secretion of interleukin (IL)-6 and IL-8 was measured using the enzyme-linked immunosorbent assay.

RESULTS:

Viability was not further reduced by bacterial co-infection in HSV-1-infected cells. Co-infection with HSV-1 and S. sanguinis or F. nucleatum reduced the viral yield whereas co-infection with HSV-1 and A. actinomycetemcomitans significantly enhanced the viral yield in oral epithelial cells. The enhancing effect of A. actinomycetemcomitans was not affected by bacterial heat-inactivation. Co-infection with HSV-1/A. actinomycetemcomitans increased intracellular levels of both viral and bacterial DNA. Secretion of IL-6 and IL-8 stimulated by A. actinomycetemcomitans infection was partly reduced by co-infection with HSV-1 in oral epithelial cells.

CONCLUSION:

In contrast to S. sanguinis and F. nucleatum, A. actinomycetemcomitans enhanced the yield of HSV-1. Either HSV-1 or A. actinomycetemcomitans may be benefited from co-infection, in aspects of increases in production of viral and bacterial DNA as well as reductions in cytokine secretion. These findings echoed with previous clinical studies showing co-infection of HSV and A. actinomycetemcomitans in patients with aggressive periodontitis.
Asunto(s)
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Periodontitis Agresiva / Herpesvirus Humano 1 / Coinfección Idioma: En Revista: J Formos Med Assoc Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Periodontitis Agresiva / Herpesvirus Humano 1 / Coinfección Idioma: En Revista: J Formos Med Assoc Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article