Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia

The small-colony variant (SCV) phenotype of Staphylococcus aureus is associated with intracellular persistence and reduced antimicrobial susceptibility, which can lead to therapeutic failure. Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is diffi...

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Veröffentlicht in:Microbial drug resistance (Larchmont, N.Y.) N.Y.), 2016-10, Vol.22 (7), p.538-544
Hauptverfasser: Kim, Nak-Hyun, Kang, Yu Min, Han, Woong Dae, Park, Kyoung Un, Park, Kay-Hyun, Yoo, Jae Il, Lee, Dong-Gun, Park, Chulmin, Song, Kyoung-Ho, Kim, Eu Suk, Park, Sang Won, Kim, Nam Joong, Oh, Myoung-don, Kim, Hong Bin
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container_end_page 544
container_issue 7
container_start_page 538
container_title Microbial drug resistance (Larchmont, N.Y.)
container_volume 22
creator Kim, Nak-Hyun
Kang, Yu Min
Han, Woong Dae
Park, Kyoung Un
Park, Kay-Hyun
Yoo, Jae Il
Lee, Dong-Gun
Park, Chulmin
Song, Kyoung-Ho
Kim, Eu Suk
Park, Sang Won
Kim, Nam Joong
Oh, Myoung-don
Kim, Hong Bin
description The small-colony variant (SCV) phenotype of Staphylococcus aureus is associated with intracellular persistence and reduced antimicrobial susceptibility, which can lead to therapeutic failure. Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is difficult. We have identified SCVs in two patients who presented with persistent methicillin-resistant Staphylococcus aureus (MRSA) bacteremia complicated by surgical site infections after cardiothoracic surgery. Nine blood isolates were collected from the two patients for species identification, antimicrobial susceptibility testing, and phenotypic and genotypic characterization. Colonies on Columbia blood agar were pinpoint, nonpigmented, nonhemolytic, and reverted to normal colonies after 48 hr of incubation on Schaedler agar. Auxotrophy assays revealed hemin dependence. Susceptibility to vancomycin (minimal inhibitory concentrations 1.0 μg/mL) was confirmed by E -test and broth microdilution test. All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the mec A, fem A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC mec type II, agr type II, and spa type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the relA gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. A high level of suspicion is required to detect SCVs, and although it is not common, the possibility of the SCV phenotype has to be considered in persistent S. aureus bacteremia.
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Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is difficult. We have identified SCVs in two patients who presented with persistent methicillin-resistant Staphylococcus aureus (MRSA) bacteremia complicated by surgical site infections after cardiothoracic surgery. Nine blood isolates were collected from the two patients for species identification, antimicrobial susceptibility testing, and phenotypic and genotypic characterization. Colonies on Columbia blood agar were pinpoint, nonpigmented, nonhemolytic, and reverted to normal colonies after 48 hr of incubation on Schaedler agar. Auxotrophy assays revealed hemin dependence. Susceptibility to vancomycin (minimal inhibitory concentrations 1.0 μg/mL) was confirmed by E -test and broth microdilution test. All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the mec A, fem A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC mec type II, agr type II, and spa type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the relA gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. 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All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the mec A, fem A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC mec type II, agr type II, and spa type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the relA gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. 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Since SCVs grow slowly and have a confusing morphology, the identification of infections due to SCV is difficult. We have identified SCVs in two patients who presented with persistent methicillin-resistant Staphylococcus aureus (MRSA) bacteremia complicated by surgical site infections after cardiothoracic surgery. Nine blood isolates were collected from the two patients for species identification, antimicrobial susceptibility testing, and phenotypic and genotypic characterization. Colonies on Columbia blood agar were pinpoint, nonpigmented, nonhemolytic, and reverted to normal colonies after 48 hr of incubation on Schaedler agar. Auxotrophy assays revealed hemin dependence. Susceptibility to vancomycin (minimal inhibitory concentrations 1.0 μg/mL) was confirmed by E -test and broth microdilution test. All the isolates were identified as MRSA by multiplex polymerase chain reaction specific for the mec A, fem A, and 16S rRNA genes, and all had the same genotype: Multilocus sequence typing ST5, SCC mec type II, agr type II, and spa type t2460. Moreover pulsed-field gel electrophoresis typing revealed that all nine isolates belonged to the same clone. Mutations in the relA gene were not found, and none of the isolates was identified as hVISA by population analysis profiling-AUC ratio. A high level of suspicion is required to detect SCVs, and although it is not common, the possibility of the SCV phenotype has to be considered in persistent S. aureus bacteremia.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>26982169</pmid><doi>10.1089/mdr.2015.0262</doi><tpages>7</tpages></addata></record>
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subjects Aged
Anti-Bacterial Agents - pharmacology
Bacteremia - drug therapy
Bacteremia - microbiology
Bacteremia - pathology
Bacteria
Bacterial Typing Techniques
Blood
Clone Cells
Drug therapy
Electrophoresis, Gel, Pulsed-Field
Genes, Bacterial
Genotype
Genotype & phenotype
Humans
Male
Mechanisms
Methicillin-Resistant Staphylococcus aureus - classification
Methicillin-Resistant Staphylococcus aureus - drug effects
Methicillin-Resistant Staphylococcus aureus - genetics
Methicillin-Resistant Staphylococcus aureus - isolation & purification
Multilocus Sequence Typing
Phenotype
Recurrence
Staphylococcal Infections - drug therapy
Staphylococcal Infections - microbiology
Staphylococcal Infections - pathology
Staphylococcus aureus
Staphylococcus infections
Surgical Wound Infection - drug therapy
Surgical Wound Infection - microbiology
Surgical Wound Infection - pathology
Vancomycin - pharmacology
title Small-Colony Variants in Persistent and Recurrent Staphylococcus aureus Bacteremia
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