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在一家三级医疗中心检测产超广谱β-内酰胺酶的伤寒杆菌血清型

Detection of Extended Spectrum Beta-lactamase Producing Serotype Typhi in a Tertiary Care Centre.

作者信息

Ramachandran Aishwarya, Shanthi Mariappan, Sekar Uma

机构信息

Postgraduate, Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, Tamil Nadu, India.

Associate Professor, Department of Microbiology, Sri Ramachandra Medical College and Research Institute, Chennai, Tamil Nadu, India.

出版信息

J Clin Diagn Res. 2017 Sep;11(9):DC21-DC24. doi: 10.7860/JCDR/2017/30150.10637. Epub 2017 Sep 1.

Abstract

INTRODUCTION

Infections caused by are an important public health threat in tropical and subtropical countries. Due to the emergence of resistance to ampicillin, chloramphenicol and trimethoprim/sulfamethoxazole (multidrug resistant salmonellae) in the late 1980s, fluoroquinolones and extended spectrum cephalosporins became the drugs of choice. Resistance to cefotaxime and ceftriaxone due to the production of Extended Spectrum Beta-Lactamase (ESBL) and reduced susceptibility to ciprofloxacin have emerged resulting in treatment failure. The Cefotaximase (CTX-M) type ESBLs are the most widespread beta lactamase among Enterobacteriaceae including salmonellae.

AIM

To detect the presence of in salmonellae causing human infections. Detection of genes to identify the coexistence of and gene

MATERIALS AND METHODS

The study included 103 consecutive, non-repetitive salmonellae isolated from clinical specimens obtained from July 2015- June 2016 which were identified up to species level by conventional/automated methods. Susceptibility to various classes of antimicrobial agents was determined by disc diffusion method. Minimum Inhibitory Concentration (MIC) to cefotaxime and ceftriaxone was determined by agar dilution method. The results were interpreted in accordance with Clinical & Laboratory Standard Institute (CLSI) (guidelines 2015. Detection of the ESBL phenotype was performed by the combined disk method. Polymerase Chain Reaction (PCR) amplification of all isolates was performed using group specific primers to characterize the presence of and .

RESULT

Of the 103 study isolates two isolates of were resistant to cefotaxime and ceftriaxone and had a MIC of 128μg/ml. PCR amplification and sequencing detected the presence of in these two isolates. These two isolates exhibited resistance to ciprofloxacin in vitro but gene was not detected in these isolates.

CONCLUSION

Resistance to third generation cephalosporins among salmonellae is a cause for concern as it may lead to treatment failure. It is imperative to continuously monitor the susceptibility pattern as enteric fever is endemic in India.

摘要

引言

由[具体病原体未给出]引起的感染在热带和亚热带国家是重要的公共卫生威胁。由于20世纪80年代末氨苄西林、氯霉素和甲氧苄啶/磺胺甲恶唑(多重耐药沙门氏菌)出现耐药性,氟喹诺酮类和广谱头孢菌素成为首选药物。因产超广谱β-内酰胺酶(ESBL)导致对头孢噻肟和头孢曲松耐药以及对环丙沙星敏感性降低,已导致治疗失败。头孢噻肟酶(CTX-M)型ESBL是肠杆菌科(包括沙门氏菌)中最广泛存在的β-内酰胺酶。

目的

检测引起人类感染的沙门氏菌中[具体内容未明确]的存在。检测[相关基因未明确]基因以鉴定[相关内容未明确]和[相关基因未明确]基因的共存情况。

材料与方法

该研究纳入了2015年7月至2016年6月从临床标本中分离出的103株连续、非重复的沙门氏菌,通过传统/自动化方法鉴定到种水平。采用纸片扩散法测定对各类抗菌药物的敏感性。采用琼脂稀释法测定对头孢噻肟和头孢曲松的最低抑菌浓度(MIC)。结果按照临床和实验室标准协会(CLSI)(2015年指南)进行解释。采用联合纸片法检测ESBL表型。使用组特异性引物对所有分离株进行聚合酶链反应(PCR)扩增,以鉴定[相关内容未明确]和[相关基因未明确]的存在情况。

结果

在103株研究分离株中,两株[具体沙门氏菌未明确]对头孢噻肟和头孢曲松耐药,MIC为128μg/ml。PCR扩增和测序检测到这两株分离株中存在[相关内容未明确]。这两株分离株在体外对环丙沙星耐药,但未检测到[相关基因未明确]基因。

结论

沙门氏菌对第三代头孢菌素耐药令人担忧,因为这可能导致治疗失败。由于印度伤寒流行,持续监测药敏模式至关重要。

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