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一种从口腔微生物群中分离出的新型噬菌体溶素,靶向……

A New Phage Lysin Isolated from the Oral Microbiome Targeting .

作者信息

van der Kamp Imme, Draper Lorraine A, Smith Muireann K, Buttimer Colin, Ross R Paul, Hill Colin

机构信息

APC Microbiome Ireland, University College Cork, T12 YT20 Cork, Ireland.

School of Microbiology, University College Cork, T12 YN60 Cork, Ireland.

出版信息

Pharmaceuticals (Basel). 2020 Dec 19;13(12):478. doi: 10.3390/ph13120478.

Abstract

is highly pathogenic and causes several mucosal and invasive infections. Due to the rising number of multidrug-resistant (MDR) strains of , new antimicrobials with alternative mechanisms of action are urgently needed. In this study, we identified two new Streptococcal phages from the oral microbiome, 23TH and SA01. Their lysins, 23TH_48 and SA01_53, were recombinantly expressed, characterized and tested for their lethality. SA01_53 was found to only lyse its host strain of , while 23TH_48 was found to possess a broader lytic activity beyond its host strain of , with several isolates sensitive to its lytic activity. 23TH_48 at a concentration of five activity units per mL (U/mL) was found to reduce cell counts of DSM 24048 by 4 log colony forming units per mL (CFU/mL) within 1 h and effectively prevented and destroyed biofilms of R6 at concentrations of 228.8 ng/µL and 14.3 ng/µL, respectively. Given its high lytic activity, 23TH_48 could prove to be a promising candidate to help combat pneumococcal infections.

摘要

具有高致病性,可引起多种黏膜和侵袭性感染。由于肺炎链球菌多重耐药(MDR)菌株数量不断增加,迫切需要具有替代作用机制的新型抗菌药物。在本研究中,我们从口腔微生物群中鉴定出两种新型链球菌噬菌体,23TH和SA01。对它们的溶菌酶23TH_48和SA01_53进行了重组表达、表征,并测试了其致死性。发现SA01_53仅能裂解其肺炎链球菌宿主菌株,而23TH_48除了能裂解其肺炎链球菌宿主菌株外,还具有更广泛的裂解活性,有几种肺炎链球菌分离株对其裂解活性敏感。发现浓度为每毫升五个活性单位(U/mL)的23TH_48在1小时内可使肺炎链球菌DSM 24048的细胞计数每毫升减少4个对数集落形成单位(CFU/mL),并分别在浓度为228.8 ng/µL和14.3 ng/µL时有效预防和破坏肺炎链球菌R6的生物膜。鉴于其高裂解活性,23TH_48可能是帮助对抗肺炎球菌感染的有前途的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab7/7767030/70f41b84d2c6/pharmaceuticals-13-00478-g001.jpg

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