Hatten B A, Sulkin S E
Department of Microbiology, The University of Texas Southwestern Medical School, Dallas, Texas.
J Bacteriol. 1966 Jan;91(1):285-96. doi: 10.1128/jb.91.1.285-296.1966.
Hatten, Betty A. (The University of Texas Southwestern Medical School, Dallas), and S. Edward Sulkin. Intracellular production of Brucella L forms. I. Recovery of L forms from tissue culture cells infected with Brucella abortus. J. Bacteriol. 91:285-296. 1966.-Infectivity of virulent Brucella abortus strain 3183 was less for hamster macrophages after a 2-hr adsorption period than for an attenuated strain (S19) and its tissue culture variant (30). Both strains S19 and 30 were very toxic for the cells, but 3183 was not toxic. Two types of L forms were recovered from a large percentage of hamster kidney cell cultures when disintegration of infected cells was accelerated by tissue culture medium of high pH. One type grew in finely granular microcolonies, was isolated from cells infected for short periods of time, and often reverted to the bacterial form. The other type occurred in small irregularly shaped forms which later developed into round bodies. Both stained specifically with fluorescein-conjugated B. abortus antiserum. Semisolid media containing 0.7% agar provided optimal subsurface L-form growth. L forms also grew well in Thioglycollate Medium but grew poorly in other liquid media. Surface L-form growth was supported by several agar media, but CO(2) was required for optimal growth. Monolayers infected with strain 3183 and examined immediately after adsorption contained occasional small, round bodies. Bizarre forms increased in number with time and, after 24 to 72 hr, large pink-staining inclusions were often present which persisted for several days. Also appearing at about the same time were smaller, dark-staining forms which were first seen in clusters but later dispersed and finally occurred in chainlike configurations. Direct fluorescent-antibody stains of infected cells established that the intracellular forms were related to the infecting strain of B. abortus.
哈滕,贝蒂·A.(得克萨斯大学西南医学中心,达拉斯),以及S. 爱德华·苏尔金。布鲁氏菌L型的细胞内产生。I. 从感染流产布鲁氏菌的组织培养细胞中回收L型。《细菌学杂志》91:285 - 296。1966年。- 强毒流产布鲁氏菌菌株3183在吸附2小时后对仓鼠巨噬细胞的感染力低于减毒株(S19)及其组织培养变异株(30)。S19和30这两个菌株对细胞都具有很强的毒性,但3183没有毒性。当用高pH值的组织培养基加速感染细胞的解体时,从很大比例的仓鼠肾细胞培养物中回收了两种类型的L型。一种以细颗粒状微菌落生长,是从短时间感染的细胞中分离出来的,并且经常回复到细菌形态。另一种以小的不规则形状出现,后来发展成圆形体。两者都用荧光素结合的流产布鲁氏菌抗血清进行特异性染色。含有0.7%琼脂的半固体培养基为L型在表面下生长提供了最佳条件。L型在硫乙醇酸盐培养基中也生长良好,但在其他液体培养基中生长较差。几种琼脂培养基支持L型在表面生长,但最佳生长需要二氧化碳。用菌株3183感染并在吸附后立即检查的单层细胞偶尔含有小的圆形体。奇异形态的数量随时间增加,在24至72小时后,经常出现大的粉红色染色包涵体,持续数天。大约在同一时间也出现了较小的、深色染色的形态,最初呈簇状出现,但后来分散,最终呈链状排列。对感染细胞的直接荧光抗体染色证实细胞内形态与感染的流产布鲁氏菌菌株有关。