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中间普氏菌与口腔放线菌属的共聚。

Coaggregation of Prevotella intermedia with oral Actinomyces species.

作者信息

Nesbitt W E, Fukushima H, Leung K P, Clark W B

机构信息

Periodontal Disease Research Center, College of Dentistry, University of Florida, Gainesville 32610.

出版信息

Infect Immun. 1993 May;61(5):2011-4. doi: 10.1128/iai.61.5.2011-2014.1993.

Abstract

Five strains of Prevotella intermedia were examined for their ability to coaggregate with various gram-positive and gram-negative species of oral bacteria. Two of the P. intermedia strains coaggregated with selected Actinomyces species, P. intermedia 27 with Actinomyces viscosus T14V and Actinomyces naeslundii ATCC 12104, PK606, PK984, and PK947, and P. intermedia 113 with Actinomyces odontolyticus WVU 1546 and Actinomyces israelii WVU 838. Exposure of both Prevotella strains but not the Actinomyces strains to heat, trypsin, or proteinase K abolished most coaggregations. All pairs were disaggregated by the addition of sodium dodecyl sulfate, but only those coaggregations involving P. intermedia 113 were reversed by the addition of 2.0 M urea. P. intermedia 27 was sensitive to periodate oxidation, whereas the partner strains were stable to this treatment. Most coaggregations occurred in the presence of saliva; however, reactions involving P. intermedia 27 were not as strong as those of buffer-suspended cells. Treatment of both P. intermedia 113 coaggregations pairs with proteinase K and the results obtained from suspensions of these pairs in saliva suggest that different surface molecules of this P. intermedia strain may mediate each of these coaggregations. These data suggest that all of these coaggregations involve either a protein or glycoprotein on the Prevotella strain, which may interact with carbohydrates or carbohydrate-containing molecules on the surface of the Actinomyces strain.

摘要

对五株中间普氏菌与各种革兰氏阳性和革兰氏阴性口腔细菌的共聚能力进行了检测。其中两株中间普氏菌与选定的放线菌属菌株发生共聚,中间普氏菌27与黏性放线菌T14V、内氏放线菌ATCC 12104、PK606、PK984和PK947共聚,中间普氏菌113与溶牙放线菌WVU 1546和衣氏放线菌WVU 838共聚。将两株普氏菌菌株而非放线菌菌株暴露于热、胰蛋白酶或蛋白酶K下,可消除大部分共聚反应。添加十二烷基硫酸钠可使所有配对解聚,但只有涉及中间普氏菌113的那些共聚反应可通过添加2.0 M尿素逆转。中间普氏菌27对高碘酸盐氧化敏感,而其配对菌株对此处理稳定。大多数共聚反应在唾液存在下发生;然而,涉及中间普氏菌27的反应不如缓冲液悬浮细胞的反应强烈。用蛋白酶K处理中间普氏菌113的两对共聚反应配对以及从这些配对在唾液中的悬浮液获得的结果表明,该中间普氏菌菌株的不同表面分子可能介导这些共聚反应中的每一种。这些数据表明,所有这些共聚反应都涉及普氏菌菌株上的一种蛋白质或糖蛋白,其可能与放线菌菌株表面的碳水化合物或含碳水化合物分子相互作用。

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