Passerini de Rossi B N, Friedman L E, Darnaud S, de Torres R A, Franco M A
Cátedra de Microbiología, Facultad de Farmacia y Bioquímica, U.B.A., Argentina.
Rev Argent Microbiol. 1997 Apr-Jun;29(2):75-83.
Bordetella pertussis virulent strains (Bvg+) produce a wide array of virulence factors. The production of these factors is coordinately regulated by the locus bvg in response to environmental signals in a process known as antigenic modulation. Mutations in the bvg locus originate avirulent variants (Bvg-) that are unable to express virulence factors regardless of growth conditions. In this paper we have obtained spontaneous variants Bvg- of B. pertussis Tohama I and 10536, which would be useful for studying virulence markers, using the selective media Stainer-Scholte agar supplemented with 1% Casamino-acids (SSA-CAS) and Jones-Kendrick with 0.20 microgram of erythromycin per ml (JK-Ery). We have also studied the efficiency of plating of B. pertussis Tohama I, 10536 and 40103 cells (Bvg+ strains) and of Bvg- strain 347 (control of the avirulent phenotype) on SSA-CAS and Stainer-Scholte agar (SSA), and we have analyzed the phenotype of the cells recovered from these media. The bacterial phenotype was characterized by using the following virulence markers: hemolysis production, hemagglutinin production, and outer membrane protein (OMP) enriched profiles. The three Bvg+ strains showed different behaviour in these selective media. B. pertussis Tohama I and 10536 could not be recovered on SSA, whereas on SSA-CAS the efficiency of plating was poor, less than 0.001%, but nevertheless allowed the selection of stable Bvg- variants of Tohama I since the OMP profile of this stain did not change after subculture in Cyclodextrin liquid medium. By contrast, strain 10536 grown on SSA-CAS suffered the process of antigenic modulation since this strain recovered the virulent phenotype when it was subcultured in Bordet-Gengou. Stable Bvg- variants from Tohama I and 10536 were obtained on JK-Ery. On the other hand, Bvg+ strain 40103 showed a high efficiency of plating on SSA and SSA-CAS and retained the virulent phenotype in all the selective media. Bvg- strain 347, in spite of being an avirulen variant, showed a poor efficiency of plating in SSA and a scant growth in JK-Ery, in agreement with the findings of other investigators which suggest that not all avirulent strains posses the ability to grow on media that inhibit most of virulent strains.
百日咳博德特氏菌强毒株(Bvg+)可产生多种毒力因子。这些因子的产生受bvg位点的协同调控,以响应环境信号,这一过程称为抗原调制。bvg位点的突变会产生无毒变体(Bvg-),无论生长条件如何,这些变体都无法表达毒力因子。在本文中,我们使用添加了1%酪蛋白氨基酸的选择性培养基Stainer-Scholte琼脂(SSA-CAS)和每毫升含0.20微克红霉素的Jones-Kendrick培养基(JK-Ery),获得了百日咳博德特氏菌Tohama I和10536的自发变体Bvg-,这将有助于研究毒力标记。我们还研究了百日咳博德特氏菌Tohama I、10536和40103细胞(Bvg+菌株)以及Bvg-菌株347(无毒表型对照)在SSA-CAS和Stainer-Scholte琼脂(SSA)上的平板接种效率,并分析了从这些培养基中回收的细胞的表型。通过以下毒力标记来表征细菌表型:溶血产生、血凝素产生和外膜蛋白(OMP)富集谱。这三种Bvg+菌株在这些选择性培养基中表现出不同的行为。百日咳博德特氏菌Tohama I和10536在SSA上无法回收,而在SSA-CAS上平板接种效率很低,低于0.001%,但仍能筛选出Tohama I的稳定Bvg-变体,因为该菌株在环糊精液体培养基中继代培养后OMP谱没有变化。相比之下,在SSA-CAS上生长的10536菌株经历了抗原调制过程,因为该菌株在博德-冈培养基中继代培养时恢复了强毒表型。在JK-Ery上获得了来自Tohama I和10536的稳定Bvg-变体。另一方面,Bvg+菌株40103在SSA和SSA-CAS上显示出较高的平板接种效率,并在所有选择性培养基中保留了强毒表型。Bvg-菌株347尽管是无毒变体,但在SSA上平板接种效率很低,在JK-Ery中生长稀疏,这与其他研究者的发现一致,即并非所有无毒菌株都具有在抑制大多数强毒株生长的培养基上生长的能力。