Ghosh Dhritiman, Roy Krishnakali, Williamson Kurt E, White David C, Wommack K Eric, Sublette Kerry L, Radosevich Mark
Biosystems Engineering and Soil Science, University of Tennessee, Knoxville, Tennessee 37996-4531, USA.
Appl Environ Microbiol. 2008 Jan;74(2):495-502. doi: 10.1128/AEM.01435-07. Epub 2007 Nov 9.
Bacteriophages are very abundant in the biosphere, and viral infection is believed to affect the activity and genetic diversity of bacterial communities in aquatic environments. Lysogenic conversion, for example, can improve host fitness and lead to phage-mediated horizontal gene transfer. However, little is known about lysogeny and transduction in the soil environment. In this study we employed atrazine-impregnated Bio-Sep beads (a cell immobilization matrix) to sample active microbiota from soils with prior pesticide exposure history. Once recovered from soil, the bead communities were induced with mitomycin C (MC), and viral and bacterial abundances were determined to evaluate the incidence of inducible prophage in soil bacteria. The inducible fraction calculated within bead communities was high (ca. 85%) relative to other studies in aquatic and sedimentary environments. Moreover, the bacterial genes encoding 16S rRNA and trzN, a chlorohydrolase gene responsible for dehalogenation of atrazine, were detected by PCR in the viral DNA fraction purified from MC-induced bead communities. A diverse collection of actinobacterial 16S rRNA gene sequences occurred within the viral DNA fraction of induced, water-equilibrated beads. Similar results were observed in induced atrazine-equilibrated beads, where 77% of the cloned sequences were derived from actinobacterial lineages. Heterogeneous 16S rRNA gene sequences consisting of fragments from two different taxa were detected in the clone libraries. The results suggest that lysogeny is a prevalent reproductive strategy among soil bacteriophages and that the potential for horizontal gene transfer via transduction is significant in soil microbial communities.
噬菌体在生物圈中极为丰富,并且病毒感染被认为会影响水生环境中细菌群落的活性和遗传多样性。例如,溶原性转换可提高宿主适应性并导致噬菌体介导的水平基因转移。然而,对于土壤环境中的溶原性和转导作用却知之甚少。在本研究中,我们使用浸渍了阿特拉津的生物分离珠(一种细胞固定基质)从具有农药暴露史的土壤中采集活性微生物群。一旦从土壤中回收,用丝裂霉素C(MC)诱导珠粒群落,然后测定病毒和细菌丰度,以评估土壤细菌中可诱导原噬菌体的发生率。相对于水生和沉积环境中的其他研究,在珠粒群落中计算出的可诱导比例很高(约85%)。此外,通过PCR在从MC诱导的珠粒群落中纯化的病毒DNA组分中检测到编码16S rRNA的细菌基因和trzN(一种负责阿特拉津脱卤的氯水解酶基因)。在诱导的、水均衡的珠粒的病毒DNA组分中出现了多种放线菌16S rRNA基因序列。在诱导的阿特拉津均衡珠粒中也观察到了类似结果,其中77%的克隆序列来自放线菌谱系。在克隆文库中检测到由来自两个不同分类群的片段组成的异质16S rRNA基因序列。结果表明,溶原性是土壤噬菌体中一种普遍的繁殖策略,并且通过转导进行水平基因转移的潜力在土壤微生物群落中很大。