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土壤疣微菌的检测与培养

Detection and cultivation of soil verrucomicrobia.

作者信息

Sangwan Parveen, Kovac Suzana, Davis Kathryn E R, Sait Michelle, Janssen Peter H

机构信息

Department of Microbiology and Immunology, University of Melbourne, Parkville, Victoria 3010, Australia.

出版信息

Appl Environ Microbiol. 2005 Dec;71(12):8402-10. doi: 10.1128/AEM.71.12.8402-8410.2005.

Abstract

Only one isolate each of the class "Spartobacteria" (subdivision 2 of the phylum Verrucomicrobia) and of subdivision 3 of Verrucomicrobia have previously been reported to grow in laboratory culture. Using media that had been used successfully in other studies to isolate members of diverse groups of soil bacteria, we generated a collection of over 1,200 isolates from soil from a pasture. An oligonucleotide probe that targets the 16S rRNA genes of verrucomicrobia was used to screen this collection, and 14 new verrucomicrobia were identified. Nine of these belonged to the class "Spartobacteria" and were related to "Chthoniobacter flavus." Five further isolates were members of subdivision 3 and were related to the only known isolate of this subdivision. The differences in the 16S rRNA gene sequences of the new isolates and previously described isolates, of up to 10%, indicated that the new isolates represent new species and genera. All but two of the verrucomicrobial isolates were from colonies that first became visible one or more months after inoculation of plates with soil, but subcultures grew more rapidly. Analysis of PCR-amplified 16S rRNA genes in the pasture soil showed that members of the class "Spartobacteria" were more numerous than members of subdivision 3. Isolates of subdivision 3 were only found on plates receiving an inoculum that yielded a mean of 29 colonies per plate, while members of the class "Spartobacteria" were only found on plates receiving a more dilute inoculum that resulted in a mean of five colonies per plate. This suggested that colony development by members of the class "Spartobacteria" was inhibited by other culturable bacteria.

摘要

此前仅有一株“斯巴达细菌”(疣微菌门第2亚群)和一株疣微菌门第3亚群的菌株被报道能够在实验室培养条件下生长。我们使用在其他研究中成功用于分离不同土壤细菌类群成员的培养基,从一片牧场的土壤中获得了1200多个菌株。用一种靶向疣微菌16S rRNA基因的寡核苷酸探针筛选该菌株库,鉴定出14株新的疣微菌。其中9株属于“斯巴达细菌”类群,与“黄栖泥杆菌”相关。另外5株菌株是第3亚群的成员,与该亚群唯一已知的菌株相关。新分离菌株与先前描述菌株的16S rRNA基因序列差异高达10%,表明这些新分离菌株代表新的物种和属。除两株外,所有疣微菌分离株均来自接种土壤后1个月或更长时间首次可见的菌落,但传代培养生长更快。对牧场土壤中PCR扩增的16S rRNA基因分析表明,“斯巴达细菌”类群的成员比第3亚群的成员更多。第3亚群的分离株仅在接种量平均每平板产生29个菌落的平板上发现,而“斯巴达细菌”类群的成员仅在接种量更稀、平均每平板产生5个菌落的平板上发现。这表明“斯巴达细菌”类群成员的菌落发育受到其他可培养细菌的抑制。

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