金黄色葡萄球菌l型与原生质体的细胞融合。

Biken journal Pub Date : 1985-12-01
Y Hirachi, Y Kato, Y Toda, N Takemasa, S Kotani
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引用次数: 0

摘要

溶葡萄球菌原生质体和稳定的l型金黄色葡萄球菌具有不同的耐药标记物,用聚乙二醇(PEG)处理溶葡萄球菌原生质体和稳定的l型金黄色葡萄球菌的各种组合的混合物,以观察双耐药融合产物(融合体)的发展。为了恢复双抗性菌落的l型,将它们培养在含有青霉素G (PCG)的4.5% nacl -脑心输注(BHI)肉汤中进行富集培养,并在PCG-4.5% NaCl-BHI琼脂培养基中培养(方法1);为了恢复双抗性融合体的l型和球菌型,将它们培养在还原培养基(R培养基)上,使原生质体或融合体向亲本型细胞还原,然后在试验培养基(R培养基)上培养。BHI琼脂培养基或PCG-4.5% NaCl-BHI琼脂培养基(方法2)。在两种实验条件下,通过PEG处理携带氯霉素(CP)抗性质粒的原生质体对和l型染色体耐链霉素(SM)的原生质体,形成双抗性融合体为l型细胞。在相反的组合中,即原生质具有染色体sm抗性和l型细胞携带cp抗性质粒,第一种方法没有获得双抗性菌落。通过第二种方法,不需要在R培养基上进行富集培养,后一种组合可以获得双抗的融合体,包括l型、球菌型和混合型殖民地形式,而当peg处理的混合物在R培养基上进行富集培养时,在R培养基或BHI琼脂试验培养基上都可以获得单抗的球菌型融合体。两种方法对原生质体和l型体进行peg处理均未产生双耐药融合体菌落,两者均为染色体,但具有不同的耐药性。这些结果表明,与原生质体之间或l型之间的融合不同,peg诱导的原生质体与l型之间的细胞融合导致了由质粒控制的耐药性转移到融合产物上。方法1获得的融合体为l型,方法2获得的融合体为球菌型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell fusion between L-forms and protoplasts of Staphylococcus aureus.

Mixtures of various combinations of Lysostaphin protoplasts and stable L-forms of Staphylococcus aureus, which have different markers for drug resistance, were treated with polyethylene glycol (PEG) to examine the development of doubly resistant fusion products (fusants). To recover doubly resistant colonies as L-forms, they were incubated in 4.5% NaCl-brain heart infusion (BHI) broth containing penicillin G (PCG) for enrichment culture and cultured in PCG-4.5% NaCl-BHI agar medium (method 1), while to recover doubly resistant fusants as L-forms and coccal forms, they were grown on reversion medium (R medium) which causes reversion of protoplasts or fusants to parent type cells, and then cultured on assay media, i.e., R medium, BHI agar medium or PCG-4.5% NaCl-BHI agar medium (method 2). Under both experimental conditions, doubly resistant fusants developed as L-form cells by PEG treatment of pairs of protoplasts carrying the chloramphenicol (CP)-resistance plasmid and L-forms having chromosomal resistance to streptomycin (SM). In the reverse combinations, i.e., protoplasts showing chromosomal SM-resistance and L-form cells carrying the CP-resistance plasmid, the first method gave no doubly resistant colonies. By the second method, without enrichment culture on R medium, the latter combination gave doubly resistant fusants as L-form, coccal-type and mixed-type colonial forms, while when the PEG-treated mixture was enriched on R medium, fusants were obtained exclusively as the coccal type on either R medium or BHI agar assay medium. Neither of the methods yielded colonies of doubly resistant fusants on PEG-treatment of pairs of protoplasts and L-forms both of which were chromosomal, but with different drug resistances. These results show that PEG-induced cell fusion between protoplasts and L-forms of S. aureus, unlike the fusion between protoplasts or between L-forms, resulted in transfer of the drug resistance controlled by the plasmid to the fusion products. The fusants obtained were L-forms in method 1, and coccal type in the method 2.

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