首页> 外文期刊>BMC research notes >First report of molecular detection of fluoroquinolone resistance-associated gyrA mutations in multidrug-resistant clinical Mycobacterium tuberculosis isolates in Kuwait
【24h】

First report of molecular detection of fluoroquinolone resistance-associated gyrA mutations in multidrug-resistant clinical Mycobacterium tuberculosis isolates in Kuwait

机译:在科威特具有多重耐药性的临床结核分枝杆菌菌株中氟喹诺酮耐药相关的gyrA突变的分子检测的首次报道

获取原文
           

摘要

Background Nearly 5% of all Mycobacterium tuberculosis strains worldwide are resistant at least to rifampicin and isoniazid (multidrug-resistant tuberculosis, MDR-TB). Inclusion of a fluoroquinolone and an injectable agent (kanamycin, amikacin or capreomycin) in multidrug therapy is crucial for proper treatment of MDR-TB. The incidence of MDR-TB in Kuwait is ~1%. MDR-TB strains additionally resistant to fluoroquinolones and injectable agents are defined as extensively drug-resistant (XDR-TB) strains and have been detected in >55 countries. Infections with XDR-TB strains have very poor prognosis. This study detected the occurrence of gyrA mutations associated with fluoroquinolone resistance among MDR-TB strains in Kuwait. Findings Direct DNA sequencing of quinolone resistance-determining region of gyrA gene was performed to detect fluoroquinolone resistance-associated mutations in 85 MDR-TB strains isolated from 55 TB patients and 25 pansusceptible M. tuberculosis strains. For isolates exhibiting gyrA mutations, 3'-end of rrs (16S rRNA ) was sequenced for the detection of XDR-TB. Fingerprinting of fluoroquinolone resistant MDR-TB strains was performed by detecting mutations in three (81 bp hot-spot, N-terminal and cluster II) regions of rpoB , katG codon 315 and inhA -regulatory region, polymorphisms at gyrA codon 95 and katG codon 463 by DNA sequencing and by double-repetitive-element PCR for determining strain relatedness. None of the pansusceptible but six of 85 MDR-TB strains contained gyrA mutations. Only gyrA codon 94 was mutated in all six (D94A in one and D94G in five) strains. Three of six mutant strains were recovered from the same patient while three other strains represented individual patient isolates. Fingerprinting studies identified all individual patient isolates as epidemiologically distinct strains. All six strains with a gyrA mutation contained wild-type rrs sequence. Conclusions Although fluoroquinolones are generally not used for chemotherapy of TB and drug susceptibility testing for second-line drugs is not carried out in Kuwait, four of 55 (7%) individual patient MDR-TB strains contained mutations in gyrA gene. The data advocate routine drug susceptibility testing for this important second-line drug for proper management of MDR-TB in Kuwait. Lack of mutations in 3'-end of rrs gene that confer resistance to injectable agents reduce the likelihood of occurrence of XDR-TB, at present, in Kuwait.
机译:背景技术全世界所有分枝杆菌菌株中几乎有5%对至少利福平和异烟肼(耐多药结核病,MDR-TB)耐药。在多药治疗中包括氟喹诺酮和注射剂(卡那霉素,丁胺卡那霉素或卡普霉素)对于正确治疗耐多药结核病至关重要。在科威特,耐多药结核病的发病率约为1%。对氟喹诺酮类和注射剂具有额外耐药性的MDR-TB菌株被定义为广泛耐药(XDR-TB)菌株,并已在超过55个国家中检测到。 XDR-TB菌株感染的预后很差。这项研究发现在科威特的MDR-TB菌株中发生了与氟喹诺酮耐药相关的gyrA突变。研究结果对gyrA基因的喹诺酮耐药性决定区进行了直接DNA测序,以检测从55 TB患者和25例易感性结核分枝杆菌菌株中分离出的85个MDR-TB菌株中与氟喹诺酮耐药性相关的突变。对于表现出gyrA突变的分离株,对rrs的3'-末端(16S rRNA)进行测序以检测XDR-TB。通过检测rpoB,katG密码子315和inhA调控区的三个(81 bp热点,N末端和簇II)区域的突变,对gyrA密码子95和katG密码子的多态性,对氟喹诺酮抗药性MDR-TB菌株进行了指纹分析。通过DNA测序和双重复元件PCR测定463以确定菌株的相关性。 85个耐多药结核病菌株中,只有6个包含gyrA突变。在所有六个菌株中,只有gyrA密码子94发生了突变(一个菌株中的D94A和五个菌株中的D94G)。从同一名患者中回收了六种突变株中的三株,而其他三株则代表了个别患者分离株。指纹研究确定了所有个体患者分离株为流行病学上不同的菌株。所有六个具有gyrA突变的菌株均包含野生型rrs序列。结论尽管在科威特,氟喹诺酮类药物通常不用于结核的化疗,二线药物的药敏试验未在科威特进行,但55例个体耐多药结核病菌株中有四个(7%)含有gyrA基因突变。数据提倡对这种重要的二线药物进行常规药敏试验,以正确管理科威特的耐多药结核病。目前,在科威特,由于缺少rrs基因3'端的突变而无法赋予注射剂抗药性,因此降低了XDR-TB发生的可能性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号