Widespread Dissemination of Aminoglycoside Resistance Genes armA and rmtB in Klebsiella pneumoniae Isolates in Taiwan Producing CTX-M-Type Extended-Spectrum β-Lactamases

Author:

Ma Ling1,Lin Chi-Jan12,Chen Jiun-Han3,Fung Chang-Phone4,Chang Feng-Yee5,Lai Yiu-Kay2,Lin Jung-Chung5,Siu L. K.15

Affiliation:

1. Division of Clinical Research, National Health Research Institutes, Zhunan Town, Miaoli County

2. Department of Life Science and Institute of Biotechnology, National Tsing Hua University, Hsinchu

3. Department of Medical Laboratory Science and Biotechnology, Yuanpei University, Hsinchu

4. Department of Medicine, Chutung Veterans Hospital, and National Yang-Ming University, Taipei

5. Division of Infectious Disease and Tropical Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

Abstract

ABSTRACT Among 235 extended-spectrum β-lactamase-producing Klebsiella pneumoniae (ESBL) isolates collected from a nationwide surveillance performed in Taiwan, 102 (43.4%) were resistant to amikacin. Ninety-two of these 102 (90.2%) isolates were carrying CTX-M-type β-lactamases individually or concomitantly with SHV-type or CMY-2 β-lactamases. The armA and rmtB alleles were individually detected in 44 and 37 of these 92 isolates, respectively. One isolate contained both armA and rmtB . The coexistence of the aac(6′)-Il and rmtB genes was detected in three isolates. CTX-M-type β-lactamase genes belonging to either group 1 (CTX-M-3 and CTX-M-15) or group 9 (CTX-M-14) were found in all armA- or rmtB -bearing ESBL-producing K. pneumoniae isolates, and all were conjugatively transferable. All except one of the isolates bearing armA produced CTX-M enzymes of group 1, and the remaining isolate bearing armA produced a group 9 CTX-M-type β-lactamase. On the contrary, in the majority of rmtB carriers, the CTX-M-type β-lactamase belonged to group 9 (62.2%). Molecular typing revealed that the amikacin-resistant ESBL-producing K. pneumoniae isolates were epidemiologically unrelated, indicating that the acquisition of resistance was not through the spread of a resistant clone or a resistance plasmid. A tandem repeat or multiple copies of bla CTX-M-3 were found in some armA -bearing isolates. An IS Ecp1 insert was found in all CTX-M ESBL-producing K. pneumoniae isolates carrying armA or rmtB . In conclusion, the concomitant presence of a 16S rRNA methylase gene ( armA or rmtB ) and bla CTX-M among amikacin-resistant ESBL-producing K. pneumoniae isolates is widespread in Taiwan.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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