亚胺培南通过刺激 H-NS 抑制肺炎克雷伯氏菌中 CRISPR-Cas 对 DNA 的获取干扰。
Imipenem represses CRISPR-Cas interference of DNA acquisition through H-NS stimulation in Klebsiella pneumoniae.
机构信息
Department of Microbiology, National Taiwan University College of Medicine, Taipei, Taiwan.
Department of Microbiology, School of Medicine, China Medical University, Taichung, Taiwan.
出版信息
Sci Rep. 2016 Aug 17;6:31644. doi: 10.1038/srep31644.
Analysis of the genome of Klebsiella pneumoniae NTUH-K2044 strain revealed the presence of two clustered regularly interspaced short palindromic repeats (CRISPR) arrays separated with CRISPR-associated (cas) genes. Carbapenem-resistant K. pneumoniae isolates were observed to be less likely to have CRISPR-Cas than sensitive strains (5/85 vs. 22/132). Removal of the transcriptional repressor, H-NS, was shown to prevent the transformation of plasmids carrying a spacer and putative proto-spacer adjacent motif (PAM). The CRISPR-Cas system also decreased pUC-4K plasmid stability, resulting in plasmid loss from the bacteria with acquisition of new spacers. Analysis of the acquired proto-spacers in pUC-4K indicated that 5'-TTN-3' was the preferred PAM in K. pneumoniae. Treatment of cells by imipenem induced hns expression, thereby decreasing cas3 expression and consequently repressed CRISPR-Cas activity resulted in increase of plasmid stability. In conclusion, NTUH-K2044 CRISPR-Cas contributes to decrease of plasmid transformation and stability. Through repression of CRISPR-Cas activity by induced H-NS, bacteria might be more able to acquire DNA to confront the challenge of imipenem.
分析肺炎克雷伯菌 NTUH-K2044 菌株的基因组显示,存在两个簇状规则间隔短回文重复序列(CRISPR)阵列,由 CRISPR 相关(cas)基因分隔。与敏感株相比,耐碳青霉烯肺炎克雷伯菌分离株较少具有 CRISPR-Cas(5/85 比 22/132)。转录抑制剂 H-NS 的去除被证明可防止携带间隔区和假定原间隔相邻基序(PAM)的质粒的转化。CRISPR-Cas 系统还降低了 pUC-4K 质粒的稳定性,导致细菌获得新间隔区后丢失质粒。对 pUC-4K 中获得的原间隔区的分析表明,5'-TTN-3'是肺炎克雷伯菌中首选的 PAM。亚胺培南处理细胞诱导 hns 表达,从而降低 cas3 表达,从而抑制 CRISPR-Cas 活性,导致质粒稳定性增加。总之,NTUH-K2044 的 CRISPR-Cas 有助于降低质粒转化和稳定性。通过诱导 H-NS 抑制 CRISPR-Cas 活性,细菌可能更能够获得 DNA 来应对亚胺培南的挑战。