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Acinetobacter septicus sp. nov. Association with a Nosocomial Outbreak of Bacteremia in a Neonatal Intensive Care Unit

Acinetobacter species other than Acinetobacter baumannii have rarely been reported to be associated with nosocomial outbreaks of bloodstream infections. Within a period of 1 week, seven Acinetobacter-like isolates were recovered from peripheral blood and catheter specimens of five patients at a neon...

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Published in:Journal of Clinical Microbiology 2008-03, Vol.46 (3), p.902-908
Main Authors: Kilic, Abdullah, Li, Haijing, Mellmann, Alexander, Basustaoglu, Ahmet C, Kul, Mustafa, Senses, Zeynep, Aydogan, Hakan, Stratton, Charles W, Harmsen, Dag, Tang, Yi-Wei
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cites cdi_FETCH-LOGICAL-c492t-e88d37155ec68729bb1cf363dd068bcc185ebcb3b06741d00f53a78dc46398703
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creator Kilic, Abdullah
Li, Haijing
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Basustaoglu, Ahmet C
Kul, Mustafa
Senses, Zeynep
Aydogan, Hakan
Stratton, Charles W
Harmsen, Dag
Tang, Yi-Wei
description Acinetobacter species other than Acinetobacter baumannii have rarely been reported to be associated with nosocomial outbreaks of bloodstream infections. Within a period of 1 week, seven Acinetobacter-like isolates were recovered from peripheral blood and catheter specimens of five patients at a neonatal intensive care unit (NICU) in a tertiary hospital in Turkey. All five patients had placement of central venous catheters and had received total parenteral nutrition before the onset of bacteremia. Two of the five patients died. Medical devices, tap water, aerators, water samples, various surfaces, intravenous fluids, and the hands of health care workers in the NICU were sampled and were culture negative for the bacterium. All seven of the isolates had identical biochemical reactions, antimicrobial susceptibility results, and pulsed-field gel electrophoresis patterns, indicating a clonal nosocomial outbreak. A panel of standard biochemical reaction profiles and three phenotypic commercial identification systems failed to identify these isolates. Phenotypically, the isolate differed from Acinetobacter ursingii by its hemolysis on sheep blood agar and its negative citrate utilization. Sequences of the full 16S rRNA gene, which contained at least three different gene copies with polymorphic sequences between nucleotide positions 70 and 206, were determined from the first recovered isolate. The complete 1,529- to 1,531-bp 16S rRNA gene sequences and partial 801-bp rpoB gene sequences had similarities of 99.5% and 97.2%, respectively, to an A. ursingii isolate. The DNA-DNA similarities of the strain against the type strain of A. ursingii were 64.7 and 68.7%, which were lower than the recommended threshold value of 70% for the definition of bacterial species. These data indicate that a novel Acinetobacter organism caused the nosocomial outbreak of bacteremia in the NICU unit. We propose the designation of Acinetobacter septicus sp. nov. for these isolates, with isolate AK001 as the type strain.
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All five patients had placement of central venous catheters and had received total parenteral nutrition before the onset of bacteremia. Two of the five patients died. Medical devices, tap water, aerators, water samples, various surfaces, intravenous fluids, and the hands of health care workers in the NICU were sampled and were culture negative for the bacterium. All seven of the isolates had identical biochemical reactions, antimicrobial susceptibility results, and pulsed-field gel electrophoresis patterns, indicating a clonal nosocomial outbreak. A panel of standard biochemical reaction profiles and three phenotypic commercial identification systems failed to identify these isolates. Phenotypically, the isolate differed from Acinetobacter ursingii by its hemolysis on sheep blood agar and its negative citrate utilization. Sequences of the full 16S rRNA gene, which contained at least three different gene copies with polymorphic sequences between nucleotide positions 70 and 206, were determined from the first recovered isolate. The complete 1,529- to 1,531-bp 16S rRNA gene sequences and partial 801-bp rpoB gene sequences had similarities of 99.5% and 97.2%, respectively, to an A. ursingii isolate. The DNA-DNA similarities of the strain against the type strain of A. ursingii were 64.7 and 68.7%, which were lower than the recommended threshold value of 70% for the definition of bacterial species. These data indicate that a novel Acinetobacter organism caused the nosocomial outbreak of bacteremia in the NICU unit. 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Medical devices, tap water, aerators, water samples, various surfaces, intravenous fluids, and the hands of health care workers in the NICU were sampled and were culture negative for the bacterium. All seven of the isolates had identical biochemical reactions, antimicrobial susceptibility results, and pulsed-field gel electrophoresis patterns, indicating a clonal nosocomial outbreak. A panel of standard biochemical reaction profiles and three phenotypic commercial identification systems failed to identify these isolates. Phenotypically, the isolate differed from Acinetobacter ursingii by its hemolysis on sheep blood agar and its negative citrate utilization. Sequences of the full 16S rRNA gene, which contained at least three different gene copies with polymorphic sequences between nucleotide positions 70 and 206, were determined from the first recovered isolate. The complete 1,529- to 1,531-bp 16S rRNA gene sequences and partial 801-bp rpoB gene sequences had similarities of 99.5% and 97.2%, respectively, to an A. ursingii isolate. The DNA-DNA similarities of the strain against the type strain of A. ursingii were 64.7 and 68.7%, which were lower than the recommended threshold value of 70% for the definition of bacterial species. These data indicate that a novel Acinetobacter organism caused the nosocomial outbreak of bacteremia in the NICU unit. We propose the designation of Acinetobacter septicus sp. nov. for these isolates, with isolate AK001 as the type strain.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>18160455</pmid><doi>10.1128/JCM.01876-07</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source PubMed Central(OpenAccess); American Society for Microbiology Journals
subjects Acinetobacter
Acinetobacter - classification
Acinetobacter - genetics
Acinetobacter - isolation & purification
Acinetobacter baumannii
Acinetobacter Infections - epidemiology
Acinetobacter Infections - microbiology
Acinetobacter ursingii
Bacteremia - epidemiology
Bacteremia - microbiology
Bacterial diseases
Bacterial sepsis
Bacterial Typing Techniques
Bacteriology
Biological and medical sciences
Cross Infection - epidemiology
Cross Infection - microbiology
Disease Outbreaks
DNA-Directed RNA Polymerases - genetics
Electrophoresis, Gel, Pulsed-Field
Epidemiology
Female
Fundamental and applied biological sciences. Psychology
Human bacterial diseases
Humans
Infant, Low Birth Weight
Infant, Newborn
Infant, Premature, Diseases - epidemiology
Infant, Premature, Diseases - microbiology
Infant, Very Low Birth Weight
Infectious diseases
Intensive Care Units, Neonatal
Male
Medical sciences
Microbial Sensitivity Tests
Microbiology
Miscellaneous
Molecular Sequence Data
Nucleic Acid Hybridization
Phylogeny
RNA, Ribosomal, 16S - genetics
Sequence Analysis, DNA
Species Specificity
Turkey - epidemiology
title Acinetobacter septicus sp. nov. Association with a Nosocomial Outbreak of Bacteremia in a Neonatal Intensive Care Unit
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