Molecular and Cellular Biochemistry Department, Indiana University Bloomington, Bloomington, IN, 47405, USA.
Department of Genetics, Harvard Medical School, Boston, MA, 02115, USA.
Nat Microbiol. 2017 Dec;2(12):1648-1657. doi: 10.1038/s41564-017-0029-y. Epub 2017 Oct 3.
Modification of essential bacterial peptidoglycan (PG)-containing cell walls can lead to antibiotic resistance; for example, β-lactam resistance by L,D-transpeptidase activities. Predatory Bdellovibrio bacteriovorus are naturally antibacterial and combat infections by traversing, modifying and finally destroying walls of Gram-negative prey bacteria, modifying their own PG as they grow inside prey. Historically, these multi-enzymatic processes on two similar PG walls have proved challenging to elucidate. Here, with a PG-labelling approach utilizing timed pulses of multiple fluorescent D-amino acids, we illuminate dynamic changes that predator and prey walls go through during the different phases of bacteria:bacteria invasion. We show formation of a reinforced circular port-hole in the prey wall, L,D-transpeptidase-mediated D-amino acid modifications strengthening prey PG during Bdellovibrio invasion, and a zonal mode of predator elongation. This process is followed by unconventional, multi-point and synchronous septation of the intracellular Bdellovibrio, accommodating odd- and even-numbered progeny formation by non-binary division.
细菌肽聚糖(PG)细胞壁的基本修饰可导致抗生素耐药性;例如,L,D-转肽酶活性导致β-内酰胺耐药性。捕食性蛭弧菌(Bdellovibrio bacteriovorus)具有天然的抗菌性,通过穿透、修饰并最终破坏革兰氏阴性猎物细菌的细胞壁来对抗感染,在猎物内部生长时会修饰自身的 PG。从历史上看,在两个类似的 PG 壁上进行这些多酶过程一直具有挑战性。在这里,我们利用多重荧光 D-氨基酸的时间脉冲 PG 标记方法,阐明了捕食者和猎物壁在细菌:细菌入侵的不同阶段所经历的动态变化。我们显示了在猎物壁上形成一个加固的圆形舷窗,L,D-转肽酶介导的 D-氨基酸修饰在 Bdellovibrio 入侵过程中增强了猎物 PG 的强度,以及捕食者的带状伸长模式。然后是细胞内 Bdellovibrio 的非常规、多点和同步的分隔,通过非二进制分裂适应奇数和偶数后代的形成。