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首页> 外文期刊>Antimicrobial agents and chemotherapy. >IND-6, a highly divergent IND-type metallo-beta-lactamase from Chryseobacterium indologenes strain 597 isolated in Burkina Faso.
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IND-6, a highly divergent IND-type metallo-beta-lactamase from Chryseobacterium indologenes strain 597 isolated in Burkina Faso.

机译:IND-6,一种从布基纳法索分离出的Indologenes产水晶杆菌菌株597的高异型IND型金属β-内酰胺酶。

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摘要

The genus Chryseobacterium and other genera belonging to the family Flavobacteriaceae include organisms that can behave as human pathogens and are known to cause different kinds of infections. Several species of Flavobacteriaceae, including Chryseobacterium indologenes, are naturally resistant to beta-lactam antibiotics (including carbapenems), due to the production of a resident metallo-beta-lactamase. Although C. indologenes presently constitutes a limited clinical threat, the incidence of infections caused by this organism is increasing in some settings, where isolates that exhibit multidrug resistance phenotypes (including resistance to aminoglycosides and quinolones) have been detected. Here, we report the identification and characterization of a new IND-type variant from a C. indologenes isolate from Burkina Faso that is resistant to beta-lactams and aminoglycosides. The levels of sequence identity of the new variant to other IND-type metallo-beta-lactamases range between 72 and 90% (for IND-4 and IND-5, respectively). The purified enzyme exhibited N-terminal heterogeneity and a posttranslational modification consisting of the presence of a pyroglutamate residue at the N terminus. IND-6 shows a broad substrate profile, with overall higher turnover rates than IND-5 and higher activities than IND-2 and IND-5 against ceftazidime and cefepime.
机译:属于黄杆菌科的金黄色葡萄球菌属和其他属包括可以起人类病原体作用的生物,并已知会引起不同种类的感染。由于常驻金属β-内酰胺酶的产生,黄杆菌科的几种菌种,包括吲哚氏杆菌,对β-内酰胺类抗生素(包括碳青霉烯类)具有天然抗性。尽管目前Indologenes构成了有限的临床威胁,但是在某些情况下,由这种生物体引起的感染的发生率正在增加,在这种情况下,已检测出表现出多药耐药表型(包括对氨基糖苷和喹诺酮类药物的耐药性)的分离株。在这里,我们报道了从布基纳法索的C. indologenes分离株对β-内酰胺类和氨基糖苷类耐药的新IND型变体的鉴定和表征。新变体与其他IND型金属β-内酰胺酶的序列同一性水平在72%至90%之间(分别针对IND-4和IND-5)。纯化的酶表现出N末端异质性和翻译后修饰,其由在N末端存在焦谷氨酸残基组成。 IND-6显示出较宽的底物谱图,总体而言,其对抗头孢他啶和头孢吡肟的周转率高于IND-5,活性高于IND-2和IND-5。

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