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炭疽芽孢杆菌染色体包含四个保守的、切除功能正常的假定原噬菌体。

The Bacillus anthracis chromosome contains four conserved, excision-proficient, putative prophages.

作者信息

Sozhamannan Shanmuga, Chute Michael D, McAfee Farrell D, Fouts Derrick E, Akmal Arya, Galloway Darrell R, Mateczun Alfred, Baillie Leslie W, Read Timothy D

机构信息

Biological Defense Research Directorate, Naval Medical Research Center, 503 Robert Grant Avenue, Silver Spring, Maryland 20852, USA.

出版信息

BMC Microbiol. 2006 Apr 6;6:34. doi: 10.1186/1471-2180-6-34.

Abstract

BACKGROUND

Bacillus anthracis is considered to be a recently emerged clone within the Bacillus cereus sensu lato group. The B. anthracis genome sequence contains four putative lambdoid prophages. We undertook this study in order to understand whether the four prophages are unique to B. anthracis and whether they produce active phages.

RESULTS

More than 300 geographically and temporally divergent isolates of B. anthracis and its near neighbors were screened by PCR for the presence of specific DNA sequences from each prophage region. Every isolate of B. anthracis screened by PCR was found to produce all four phage-specific amplicons whereas none of the non-B. anthracis isolates, produced more than one phage-specific amplicon. Excision of prophages could be detected by a PCR based assay for attP sites on extra-chromosomal phage circles and for attB sites on phage-excised chromosomes. SYBR-green real-time PCR assays indicated that prophage excision occurs at very low frequencies (2 x 10(-5) - 8 x 10(-8)/cell). Induction with mitomycin C increased the frequency of excision of one of the prophages by approximately 250 fold. All four prophages appear to be defective since, mitomycin C induced culture did not release any viable phage particle or lyse the cells or reveal any phage particle under electron microscopic examination.

CONCLUSION

The retention of all four putative prophage regions across all tested strains of B. anthracis is further evidence of the very recent emergence of this lineage and the prophage regions may be useful for differentiating the B. anthracis chromosome from that of its neighbors. All four prophages can excise at low frequencies, but are apparently defective in phage production.

摘要

背景

炭疽芽孢杆菌被认为是蜡样芽孢杆菌广义组中最近出现的一个克隆。炭疽芽孢杆菌的基因组序列包含四个假定的λ样原噬菌体。我们开展这项研究是为了了解这四个原噬菌体是否为炭疽芽孢杆菌所特有,以及它们是否产生有活性的噬菌体。

结果

通过PCR对300多个来自不同地理区域和时间的炭疽芽孢杆菌及其近缘菌株进行筛选,以检测每个原噬菌体区域的特定DNA序列。通过PCR筛选的每一株炭疽芽孢杆菌都能产生所有四种噬菌体特异性扩增子,而所有非炭疽芽孢杆菌菌株均未产生超过一种噬菌体特异性扩增子。原噬菌体的切除可通过基于PCR的检测方法进行检测,该方法用于检测染色体外噬菌体环上的attP位点和噬菌体切除染色体上的attB位点。SYBR-绿实时PCR检测表明,原噬菌体切除的发生频率非常低(2×10⁻⁵ - 8×10⁻⁸/细胞)。用丝裂霉素C诱导可使其中一个原噬菌体的切除频率提高约250倍。所有四个原噬菌体似乎都有缺陷,因为丝裂霉素C诱导培养物未释放任何有活力的噬菌体颗粒,也未裂解细胞,在电子显微镜检查下也未发现任何噬菌体颗粒。

结论

在所有测试的炭疽芽孢杆菌菌株中都保留了所有四个假定的原噬菌体区域,这进一步证明了该谱系是最近才出现的,并且原噬菌体区域可能有助于将炭疽芽孢杆菌的染色体与其近缘菌株的染色体区分开来。所有四个原噬菌体都能以低频率切除,但在噬菌体产生方面显然存在缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d0c/1475869/b3bd7a870b34/1471-2180-6-34-1.jpg

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