A novel blaCTX-M-14 gene-harboring complex class 1 integron with an In4-like backbone structure from a clinical isolate of Escherichia coli

2008 ◽  
Vol 62 (3) ◽  
pp. 340-342 ◽  
Author(s):  
Il Kwon Bae ◽  
Yong Hwan Lee ◽  
Ho Joong Jeong ◽  
Seong Geun Hong ◽  
Sang Hee Lee ◽  
...  
2007 ◽  
Vol 51 (8) ◽  
pp. 3017-3019 ◽  
Author(s):  
Il Kwon Bae ◽  
You-Nae Lee ◽  
Wee Gyo Lee ◽  
Sang Hee Lee ◽  
Seok Hoon Jeong

ABSTRACT This work identifies an ISCR1-related bla CTX-M-14 gene, which has never been reported before, from a clinical isolate of Escherichia coli. The bla CTX-M-14 gene was preceded by an ISCR1 element that was followed by a class 1 integron containing three different insert gene cassettes, i.e., dfrA12, orfF, and aadA2.


2019 ◽  
Vol 10 ◽  
Author(s):  
Hong-Ngoc Le-Vo ◽  
Phuong Thi-Bich Tran ◽  
Lien Le ◽  
Yuki Matsumoto ◽  
Daisuke Motooka ◽  
...  

2016 ◽  
Vol 60 (11) ◽  
pp. 6937-6940 ◽  
Author(s):  
Jae Jin Lee ◽  
Mi-Na Kim ◽  
Kwang Seung Park ◽  
Jung Hun Lee ◽  
Asad Mustafa Karim ◽  
...  

ABSTRACTThe coexistence ofqnrB62andblaVIM-2was detected in aCitrobacterclinical isolate. The reduced fluoroquinolone susceptibility is attributable toqnrB62, mutations of quinolone-resistance-determining regions, and an efflux pump or pumps. The genetic context surrounding chromosomalqnrB62was a novel complex class 1 integron (In1184::ISCR1::qnrB62) containing a unique gene array (blaVIM-2-aacA4′-8-gucD). An 18-nucleotide deletion at the 3′ end of thepspAgene [pspA(Δ18)], upstream ofqnrB62, and an inverted repeat region (IRR2) were detected in In1184::ISCR1::qnrB62, indicating past transposition events.


2011 ◽  
Vol 55 (6) ◽  
pp. 2974-2975 ◽  
Author(s):  
Juwon Kim ◽  
Seong Geun Hong ◽  
Il Kwon Bae ◽  
Ji Roung Kang ◽  
Seok Hoon Jeong ◽  
...  

ABSTRACTEscherichia coliclinical isolate BD07372 of sequence type ST131 recovered from a bed sore specimen exhibited high-level resistance to ceftazidime and cefotaxime but exhibited susceptibility to imipenem and meropenem. The isolate harbored two β-lactamase genes, theblaCTX-M-15gene carried by an ∼250-kbp plasmid carrying the FIA and FIC replicons and theblaGES-5gene carried by a class 1 integron in the chromosome.


2002 ◽  
Vol 46 (8) ◽  
pp. 2656-2661 ◽  
Author(s):  
Montserrat Sabaté ◽  
Ferran Navarro ◽  
Elisenda Miró ◽  
Susana Campoy ◽  
Beatriz Mirelis ◽  
...  

ABSTRACT For the present report, a novel complex class 1 integron, In60, was characterized. Part of this integron includes the bla CTX-M-9 gene and its downstream nucleotide sequence, which shares 81% and 78% nucleotide identity with those of kluA-1 β-lactamase and orf3 of K. ascorbata, respectively. Furthermore, a new insertion sequence, IS3000, has been found in In60. PCR analysis indicates that integron In60 is present in 33 of 34 nonclonal enterobacterial isolates carrying the putative β-lactamase CTX-M-9.


2010 ◽  
Vol 59 (1) ◽  
pp. 132-134 ◽  
Author(s):  
Jae Seok Song ◽  
Seon Ju Jang ◽  
Il Kwon Bae ◽  
Hyun Ji Lee ◽  
Byeong Chul Jeong ◽  
...  

2011 ◽  
Vol 64 (3) ◽  
pp. 265-270 ◽  
Author(s):  
Caixia Sun ◽  
Zhaoliang Su ◽  
Chenglin Zhou ◽  
Yanfang Liu ◽  
Hongyan Yuan ◽  
...  

2018 ◽  
Vol 62 (5) ◽  
Author(s):  
Chang-Wei Lei ◽  
Yan-Peng Chen ◽  
Ling-Han Kong ◽  
Jin-Xin Zeng ◽  
Yong-Xiang Wang ◽  
...  

ABSTRACT A novel 61,578-bp genomic island named Proteus genomic island 2 (PGI2) was characterized in Proteus mirabilis of swine origin in China. The 23.85-kb backbone of PGI2 is related to those of Salmonella genomic island 1 and Acinetobacter genomic island 1. The multidrug resistance (MDR) region of PGI2 is a complex class 1 integron containing 14 different resistance genes. PGI2 was conjugally mobilized in trans to Escherichia coli in the presence of a conjugative IncC helper plasmid.


2010 ◽  
Vol 67 (2) ◽  
pp. 188-190 ◽  
Author(s):  
Sónia Ferreira ◽  
Ana Paradela ◽  
Jorge Velez ◽  
Elmano Ramalheira ◽  
Timothy R. Walsh ◽  
...  

2017 ◽  
Vol 62 (No. 3) ◽  
pp. 169-177 ◽  
Author(s):  
TH Chung ◽  
SW Yi ◽  
BS Kim ◽  
WI Kim ◽  
GW Shin

The present study sought to identify pathogens associated with septicaemia in the Chinese soft-shelled turtle (Pelodiscus sinensis) and to characterise antibiotic resistance in these pathogens. Twenty-three isolates recovered from the livers of diseased soft-shelled turtles were genetically identified as Aeromonas hydrophila (n = 8), A. veronii (n = 3), Citrobacter freundii (n = 4), Morganella morganii (n = 3), Edwardsiella tarda (n = 2), Wohlfahrtiimonas chitiniclastica (n = 1), Chryseobacterium sp. (n = 1), and Comamonas sp. (n = 1). Most isolates (n = 21) were resistant to ampicillin whereas a low percentage of isolates was susceptible to aminoglycosides (amikacin, gentamicin, and tobramycin). PCR assays and sequence analysis revealed the presence of the qnrS2 and bla<sub>TEM</sub> antibiotic resistance genes in all isolates. The bla<sub>DHA-1</sub>, bla<sub>CTX-M-14</sub> and bla<sub>CMY-2</sub> genes were harboured by 17.4% (n = 4), 13.5% (n = 3) and 8.7% (n = 2) of the strains, respectively. One or more tetracycline resistance genes were detected in 60.9% (n = 14) of the isolates. Four isolates (17.4%) harboured single or multiple class 1 integron cassettes. Collectively, a variety of bacterial pathogens were involved in the occurrence of septicaemia in Chinese soft-shelled turtles and most of the isolates had multi-antibiotic resistant phenotypes. To our knowledge, the present report is the first to identify W. chitiniclastica and Comamonas sp. as causes of septicaemia in soft-shelled turtles and the first to identify Aeromonas spp. with bla<sub>CTX-M-14</sub> and bla<sub>DHA-1</sub> resistance genes.


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