IHU Méditerranée Infection, 13005 Marseille, France.
Aix-Marseille Université, IRD, APHM, MEPHI, 13005 Marseille, France.
Int J Mol Sci. 2022 May 13;23(10):5446. doi: 10.3390/ijms23105446.
The increased exploitation of microbial sequencing methods has shed light on the high diversity of new microorganisms named Candidate Phyla Radiation (CPR). CPR are mainly detected via 16S rRNA/metabarcoding analyses or metagenomics and are found to be abundant in all environments and present in different human microbiomes. These microbes, characterized by their symbiotic/epiparasitic lifestyle with bacteria, are directly exposed to competition with other microorganisms sharing the same ecological niche. Recently, a rich repertoire of enzymes with antibiotic resistance activity has been found in CPR genomes by using an in silico adapted screening strategy. This reservoir has shown a high prevalence of putative beta-lactamase-encoding genes. We expressed and purified five putative beta-lactamase sequences having the essential domains and functional motifs from class A and class B beta-lactamase. Their enzymatic activities were tested against various beta-lactam substrates using liquid chromatography-mass spectrometry (LC-MS) and showed some beta-lactamase activity even in the presence of a beta-lactamase inhibitor. In addition, ribonuclease activity was demonstrated against RNA that was not inhibited by sulbactam and EDTA. None of these proteins could degrade single- and double-stranded-DNA. This study is the first to express and test putative CPR beta-lactamase protein sequences in vitro. Our findings highlight that the reduced genomes of CPR members harbor sequences encoding for beta-lactamases known to be multifunction hydrolase enzymes.
微生物测序方法的广泛应用揭示了大量新的微生物,被命名为候选门辐射(CPR)。CPR 主要通过 16S rRNA/代谢组学分析或宏基因组学检测到,存在于所有环境中,并存在于不同的人类微生物组中。这些微生物的特点是与细菌共生/寄生生活方式,并直接暴露于与其他共享相同生态位的微生物的竞争中。最近,通过采用一种适应于计算机的筛选策略,在 CPR 基因组中发现了具有抗生素抗性活性的丰富酶 repertoire。该储库显示出高比例的假定β-内酰胺酶编码基因。我们表达和纯化了五个具有 A 类和 B 类β-内酰胺酶必需结构域和功能基序的假定β-内酰胺酶序列。使用液相色谱-质谱(LC-MS)对它们针对各种β-内酰胺底物的酶活性进行了测试,并在存在β-内酰胺酶抑制剂的情况下显示出一些β-内酰胺酶活性。此外,还证明了这些酶对不受 sulbactam 和 EDTA 抑制的 RNA 具有核糖核酸酶活性。这些蛋白质都不能降解单链和双链 DNA。本研究首次在体外表达和测试了假定的 CPRβ-内酰胺酶蛋白序列。我们的研究结果表明,CPR 成员的简化基因组编码了已知为多功能水解酶的β-内酰胺酶。