异常多重耐药和高毒肺炎克雷伯菌</i>临床分离不含<i> rma <或& lt; i> rmpA2< / i>

Q4 Engineering
Zhien He, Liwen Cao, Yuanyuan Dai, Huaiwei Lu, Baolin Sun, Yujie Li
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引用次数: 0

摘要

& lt; i>克雷伯氏菌pneumoniae< / i>是一种臭名昭著的机会致病菌,毒性特别强<& lt; i> pneumoniae< / i>(hvKp)。幸运的是,大多数经典hvKp菌株对抗生素敏感。然而,近年来,关于耐多药hvKp (MDR-hvKp)的报告急剧增加,威胁着全世界人民的健康和安全。在这里,我们报告发现了耐多药hvkp,没有<i>rmpA</i>和& lt; i> rmpA2< / i>一位92岁的慢性阻塞性肺病患者。患者在住院第8天死亡。K</i>表型实验及全基因组测序。& lt; i> pneumoniae< / i>从患者痰液中分离出21072329。此外,21072329属于ST11-KL47 MDR-hvKp,该菌株对mellonella</i>具有高致死率。同时,21072329黏度较强,难以完全离心;21072329携带ESBL基因(<i>bla</i><sub>CTX-M-65</sub> < bla</i> SHV-158</ i><sub>TEM-1</sub>)和碳青霉烯酶基因(<i>bla</i>< KPC-2</sub>),对碳青霉烯类抗生素和第三代、第四代头孢菌素耐药。虽然21072329具有hvKp的特性,但<i>rmpA</i>和& lt; i> rmpA2< / i>在其基因组中找不到;它也只携带了一个铁载体的yersinabactin。这可能表明其他高毒力因子促进了hvKp的形成。耐多药- hvkp已经给全球医疗保健带来了巨大负担,而那些携带未知高毒力因子的人是新的威胁,因此迫切需要进行紧急预防和控制研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An abnormal multidrug-resistant and hypervirulent <i>Klebsiella pneumoniae</i> clinical isolate without <i>rmpA</i> or <i>rmpA2</i>
Klebsiella pneumoniae is a notorious opportunistic pathogen, especially hypervirulent K. pneumoniae (hvKp). Fortunately, most classical hvKp strains are antibiotic-susceptible. However, in recent years, reports of multidrug-resistant hvKp (MDR-hvKp) have increased dramatically, threatening the health and safety of people worldwide. Here, we report the discovery of MDR-hvKp without rmpA and rmpA2 in a 92-year-old patient with chronic obstructive pulmonary disease. The patient died on the eighth day of hospitalization. Phenotyping experiments and whole-genome sequencing of K. pneumoniae isolate 21072329 isolated from the patient’s sputum were performed. Moreover, 21072329 belongs to ST11-KL47 MDR-hvKp, which was highly lethal to Galleria mellonella. Meanwhile, 21072329 had a strong viscosity, and it was difficult to completely centrifuge it; 21072329 carried ESBL genes (blaCTX-M-65, blaSHV-158, and blaTEM-1) and a carbapenemase gene (blaKPC-2), and it was resistant to carbapenem antibiotics and third- and fourth-generation cephalosporins. Although 21072329 had the characteristics of hvKp, rmpA and rmpA2 could not be found in its genome; it also only carried a siderophore of yersiniabactin. This may indicate that other hypervirulence factors promote the formation of hvKp. MDR-hvKp has already brought an enormous burden to global medical care, and those carrying unknown hypervirulence factors are new threats, so urgent prevention and control with research are urgently needed.
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来源期刊
中国科学技术大学学报
中国科学技术大学学报 Engineering-Mechanical Engineering
CiteScore
0.40
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5692
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