• Something wrong with this record ?

Acquisition of Tn6018-3' CS regions increases colistin MICs against Acinetobacter baumannii isolates harboring new variants of AbaRs

M. Savari, A. Ekrami, S. Shoja, A. Bahador,

. 2017 ; 62 (5) : 373-379. [pub] 20170225

Language English Country United States

Document type Journal Article

Colistin is the last hope to treat extensively drug resistance (XDR) Acinetobacter baumannii (A. baumannii) infections, but resistance to colistin is currently reported in clinical centers all over the world. Here, we studied two colistin-resistant A. baumannii isolates with a difference in minimum inhibitory concentrations (MICs) that were isolated from a single burn patient during treatment in the hospitalization period. The international clonal (IC) lineage, multilocus sequence typing (MLST), and multiple loci variable number tandem repeat (VNTR) analysis (MLVA) typing were used to characterize the relatedness of A. baumannii isolates. Lipopolysaccharides (LPS) and PmrAB system analysis by PCR sequencing, polyacrylamide gel electrophoresis (PAGE), and real-time PCR were performed to determine the intactness and probable modifications of the LPS as the main resistance mechanisms to colistin. A combination of PCR, sequencing, and restriction fragment length polymorphism (RFLP) was used for A. baumannii resistance islands (AbaR) mapping as resistance-determinant reservoirs. Two isolates were identical at all MLST and VNTR marker loci that indicated the isolates were the same strain. In comparison to colistin-heteroresistant A. baumannii strain TEH267 (MIC = 1.5 mg/L), colistin-resistant A. baumannii strain TEH273 (MIC ≥256 mg/L) acquired two genomic regions including Tn6018-topA sequence and topA sequence-3' CS in its AbaR structure containing ispA and cadA genes which, it would appear, could be associated with eightfold increase in colistin MIC. Both isolates had new variants of AbaR-like structures which could be derivatives of the typical AbaR3. According to the results of this study, AbaRs could be associated with an increase in MIC to colistin.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18025582
003      
CZ-PrNML
005      
20180711114124.0
007      
ta
008      
180711s2017 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s12223-017-0507-x $2 doi
035    __
$a (PubMed)28238067
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Savari, Mohammad $u Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Keshavarz Blvd, 100 Poursina Ave, Tehran, 1416753955, Iran.
245    10
$a Acquisition of Tn6018-3' CS regions increases colistin MICs against Acinetobacter baumannii isolates harboring new variants of AbaRs / $c M. Savari, A. Ekrami, S. Shoja, A. Bahador,
520    9_
$a Colistin is the last hope to treat extensively drug resistance (XDR) Acinetobacter baumannii (A. baumannii) infections, but resistance to colistin is currently reported in clinical centers all over the world. Here, we studied two colistin-resistant A. baumannii isolates with a difference in minimum inhibitory concentrations (MICs) that were isolated from a single burn patient during treatment in the hospitalization period. The international clonal (IC) lineage, multilocus sequence typing (MLST), and multiple loci variable number tandem repeat (VNTR) analysis (MLVA) typing were used to characterize the relatedness of A. baumannii isolates. Lipopolysaccharides (LPS) and PmrAB system analysis by PCR sequencing, polyacrylamide gel electrophoresis (PAGE), and real-time PCR were performed to determine the intactness and probable modifications of the LPS as the main resistance mechanisms to colistin. A combination of PCR, sequencing, and restriction fragment length polymorphism (RFLP) was used for A. baumannii resistance islands (AbaR) mapping as resistance-determinant reservoirs. Two isolates were identical at all MLST and VNTR marker loci that indicated the isolates were the same strain. In comparison to colistin-heteroresistant A. baumannii strain TEH267 (MIC = 1.5 mg/L), colistin-resistant A. baumannii strain TEH273 (MIC ≥256 mg/L) acquired two genomic regions including Tn6018-topA sequence and topA sequence-3' CS in its AbaR structure containing ispA and cadA genes which, it would appear, could be associated with eightfold increase in colistin MIC. Both isolates had new variants of AbaR-like structures which could be derivatives of the typical AbaR3. According to the results of this study, AbaRs could be associated with an increase in MIC to colistin.
650    _2
$a infekce bakteriemi rodu Acinetobacter $x mikrobiologie $7 D000151
650    _2
$a Acinetobacter baumannii $x klasifikace $x účinky léků $x genetika $x izolace a purifikace $7 D040981
650    _2
$a antibakteriální látky $x farmakologie $7 D000900
650    _2
$a bakteriální proteiny $x genetika $7 D001426
650    _2
$a popálení $x komplikace $7 D002056
650    _2
$a kolistin $x farmakologie $7 D003091
650    12
$a transpozibilní elementy DNA $7 D004251
650    _2
$a elektroforéza v polyakrylamidovém gelu $7 D004591
650    _2
$a bakteriální geny $7 D005798
650    _2
$a genotyp $7 D005838
650    _2
$a lidé $7 D006801
650    _2
$a lipopolysacharidy $x analýza $7 D008070
650    _2
$a mikrobiální testy citlivosti $7 D008826
650    _2
$a minisatelitní repetice $7 D018598
650    _2
$a multilokusová sekvenční typizace $7 D058885
650    _2
$a polymerázová řetězová reakce $7 D016133
650    _2
$a transkripční faktory $x genetika $7 D014157
655    _2
$a časopisecké články $7 D016428
700    1_
$a Ekrami, Alireza $u Health Research Institute, Infectious and Tropical Disease Research Center, Ahvaz Jundishapour University of Medical Sciences, Ahvaz, Iran.
700    1_
$a Shoja, Saeed $u Infectious and Tropical Disease Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
700    1_
$a Bahador, Abbas $u Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Keshavarz Blvd, 100 Poursina Ave, Tehran, 1416753955, Iran. abahador@sina.tums.ac.ir. Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran. abahador@sina.tums.ac.ir. Laser Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran. abahador@sina.tums.ac.ir.
773    0_
$w MED00011005 $t Folia microbiologica $x 1874-9356 $g Roč. 62, č. 5 (2017), s. 373-379
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28238067 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180711 $b ABA008
991    __
$a 20180711114416 $b ABA008
999    __
$a ok $b bmc $g 1317845 $s 1022504
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 62 $c 5 $d 373-379 $e 20170225 $i 1874-9356 $m Folia microbiologica $n Folia microbiol. (Prague) $x MED00011005
LZP    __
$a Pubmed-20180711

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...