-
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,
Language English Country United States
Document type Journal Article
- MeSH
- Acinetobacter baumannii classification drug effects genetics isolation & purification MeSH
- Anti-Bacterial Agents pharmacology MeSH
- Genes, Bacterial MeSH
- Bacterial Proteins genetics MeSH
- Electrophoresis, Polyacrylamide Gel MeSH
- Genotype MeSH
- Acinetobacter Infections microbiology MeSH
- Colistin pharmacology MeSH
- Humans MeSH
- Lipopolysaccharides analysis MeSH
- Microbial Sensitivity Tests MeSH
- Minisatellite Repeats MeSH
- Multilocus Sequence Typing MeSH
- Polymerase Chain Reaction MeSH
- Burns complications MeSH
- Transcription Factors genetics MeSH
- DNA Transposable Elements * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
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