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牙龈卟啉单胞菌动物感染实验模型

Experimental model for Porphyromonas gingivalis infection in animals.

作者信息

Eke P I, Rotimi V O, Laughon B E

机构信息

Department of Periodontics, Emory University, School of Postgraduate Dentistry, Atlanta, Ga 30322, USA.

出版信息

Afr J Med Med Sci. 1996 Mar;25(1):31-9.

PMID:9110052
Abstract

A virulence model suitable for studying the dynamics of Porphyromonas gingivalis infection, including the pathogenicity of P. gingivalis in experimentally induced infections of multiple organs was developed using mouse and hamster. Virulence of P. gingivalis strains was expressed contrastingly in subcutaneous (sc) infection in the Murine abscess model (MAM) and the Hamsters abscess model (HAM). Subcutaneous infection in the MAM was characterized by a gravity abscess, spreading from the primary site of inoculation downwards, frequently erupting as a secondary lesion. In contract, s.c. P. gingivalis infection in HAM was characterized as a palpable localized abscess at the primary site of inoculation. When the Semi-Solid Agar (SSA) was added to the mono-culture of P. gingivalis, reproducibility of infection in both models was enhanced. P. gingivalis culture supplemented with haemin, or combined with oral Actinomyces viscosus had its virulence overtly enhanced and often fatal in the MAM. Menadione, Eh reducing agents and mixture with the Streptococcus or A. neaslundii did not potentiate virulence in either mode. Transtracheal challenge of the lungs of hamster with P. gingivalis initiated an early pneumonitis and later sequelae of necrosis and abscess formation. Also, abscess was induced by direct inoculation of P. gingivalis in the muscles, liver and testes, but did not induce intra-abdominal abscesses. In conclusion, the HAM applied with the SSA procedure caused a localized P. gingivalis tissue infection with practical advantages for quantitative and qualitative studies of P. gingivalis infections. This study also demonstrates the pathogenic potential of P. gingivalis by reproducing similar infections in multiple anatomical sites.

摘要

利用小鼠和仓鼠建立了一种适合研究牙龈卟啉单胞菌感染动态的毒力模型,包括牙龈卟啉单胞菌在实验诱导的多器官感染中的致病性。牙龈卟啉单胞菌菌株的毒力在小鼠脓肿模型(MAM)和仓鼠脓肿模型(HAM)的皮下(sc)感染中表现出差异。MAM中的皮下感染特征为重力性脓肿,从接种的原发部位向下扩散,常作为继发性病变破溃。相比之下,HAM中的牙龈卟啉单胞菌皮下感染特征为在接种的原发部位出现可触及的局限性脓肿。当向牙龈卟啉单胞菌单培养物中添加半固体琼脂(SSA)时,两种模型中感染的可重复性均得到提高。添加血红素或与口腔粘性放线菌联合培养的牙龈卟啉单胞菌在MAM中的毒力明显增强,且常导致死亡。甲萘醌、电子供体还原剂以及与链球菌或内氏放线菌混合均未在任何一种模型中增强毒力。用牙龈卟啉单胞菌经气管接种仓鼠肺部引发早期肺炎,随后出现坏死和脓肿形成的后遗症。此外,直接将牙龈卟啉单胞菌接种到肌肉、肝脏和睾丸中可诱导脓肿形成,但不会诱导腹腔内脓肿。总之,采用SSA程序的HAM导致牙龈卟啉单胞菌局部组织感染,对牙龈卟啉单胞菌感染的定量和定性研究具有实际优势。本研究还通过在多个解剖部位再现类似感染,证明了牙龈卟啉单胞菌的致病潜力。

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