Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood cultures

<em>Background</em>. The rapid identification of the etiology and the evaluation of the antimicrobial susceptibility of the bacteria causing bacteremia is of outmost relevance to set up an adequate treatment of sepsis. In this study we evaluated the microarray based method, Verigene Gram...

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Main Authors: Agnese Cellini, Maria Federica Pedna, Francesca Del Bianco, Vittorio Sambri
Format: Article
Language:English
Published: PAGEPress Publications 2015-06-01
Series:Microbiologia Medica
Subjects:
Online Access:http://www.pagepressjournals.org/index.php/mm/article/view/4945
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spelling doaj-21ad362ba6674094a599786cbb6263ca2020-11-25T03:50:16ZengPAGEPress PublicationsMicrobiologia Medica 2280-64232015-06-0130110.4081/mm.2015.49454330Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood culturesAgnese Cellini0Maria Federica Pedna1Francesca Del Bianco2Vittorio Sambri3Unit of Microbiology, The Greater Romagna Hub Laboratory, Pievesestina di CesenaUnit of Microbiology, The Greater Romagna Hub Laboratory, Pievesestina di CesenaUnit of Microbiology, The Greater Romagna Hub Laboratory, Pievesestina di CesenaUnit of Microbiology, The Greater Romagna Hub Laboratory, Pievesestina di Cesena<em>Background</em>. The rapid identification of the etiology and the evaluation of the antimicrobial susceptibility of the bacteria causing bacteremia is of outmost relevance to set up an adequate treatment of sepsis. In this study we evaluated the microarray based method, Verigene Gram-positive blood cultures (BC-GP) nucleic acid test (Nanosphere Inc., Northbrook, IL, USA) for the identification of Gram positive pathogens from positive blood cultures. The panel BC-GP is capable to identify 13 germs and 3 genes associated with antimicrobial resistance. <br /><em>Materials</em> <em>and</em> <em>Methods</em>. In this study a total of 100 positive, non replicated and monomicrobic blood cultures have been evaluated. For testing on the Verigene platform using the BC-GP assay, 350 L of blood culture media from a positive the blood culture bottle.<br /><em>Results</em>. A total of 100 positive blood cultures were tested by the Verigene BC-GP assay: out of these a total of 100 Gram-positive cocci were identified. The most frequent bacteria identified included staphylococci, streptococci and enterococci. Among staphylococci, <em>Staphylococcus</em> <em>aureus</em> accounted for 25% (15/60), with 38% of <em>S.</em> <em>epidermidis</em> 37% (23/60) and 37% (22/60) other CoNS. All the <em>S</em>. <em>aureus</em> isolates were correctly identified by BC-GP whereas in 2/45 cases (4%) BC-GP misidentified CoNS. In the case of enterococci 7/10 were <em>E</em>. <em>faecalis</em> and 3 <em>E</em>. <em>faecium</em>, all of these were correctly identified.<br /><em>Conclusions</em>. The overall agreement with the results obtained by standard procedure is quite elevated (88%) and as a consequence the BC-GP panel could be used as a rapid diagnostic tool to give a faster response in the case of bacteremia associated with sepsis.http://www.pagepressjournals.org/index.php/mm/article/view/4945Sepsis, Blood culture, Gram positive, Rapid identification
collection DOAJ
language English
format Article
sources DOAJ
author Agnese Cellini
Maria Federica Pedna
Francesca Del Bianco
Vittorio Sambri
spellingShingle Agnese Cellini
Maria Federica Pedna
Francesca Del Bianco
Vittorio Sambri
Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood cultures
Microbiologia Medica
Sepsis, Blood culture, Gram positive, Rapid identification
author_facet Agnese Cellini
Maria Federica Pedna
Francesca Del Bianco
Vittorio Sambri
author_sort Agnese Cellini
title Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood cultures
title_short Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood cultures
title_full Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood cultures
title_fullStr Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood cultures
title_full_unstemmed Evaluation of the Verigene® Blood Culture Nucleic Acid test for rapid identification of gram positive pathogens from positive blood cultures
title_sort evaluation of the verigene® blood culture nucleic acid test for rapid identification of gram positive pathogens from positive blood cultures
publisher PAGEPress Publications
series Microbiologia Medica
issn 2280-6423
publishDate 2015-06-01
description <em>Background</em>. The rapid identification of the etiology and the evaluation of the antimicrobial susceptibility of the bacteria causing bacteremia is of outmost relevance to set up an adequate treatment of sepsis. In this study we evaluated the microarray based method, Verigene Gram-positive blood cultures (BC-GP) nucleic acid test (Nanosphere Inc., Northbrook, IL, USA) for the identification of Gram positive pathogens from positive blood cultures. The panel BC-GP is capable to identify 13 germs and 3 genes associated with antimicrobial resistance. <br /><em>Materials</em> <em>and</em> <em>Methods</em>. In this study a total of 100 positive, non replicated and monomicrobic blood cultures have been evaluated. For testing on the Verigene platform using the BC-GP assay, 350 L of blood culture media from a positive the blood culture bottle.<br /><em>Results</em>. A total of 100 positive blood cultures were tested by the Verigene BC-GP assay: out of these a total of 100 Gram-positive cocci were identified. The most frequent bacteria identified included staphylococci, streptococci and enterococci. Among staphylococci, <em>Staphylococcus</em> <em>aureus</em> accounted for 25% (15/60), with 38% of <em>S.</em> <em>epidermidis</em> 37% (23/60) and 37% (22/60) other CoNS. All the <em>S</em>. <em>aureus</em> isolates were correctly identified by BC-GP whereas in 2/45 cases (4%) BC-GP misidentified CoNS. In the case of enterococci 7/10 were <em>E</em>. <em>faecalis</em> and 3 <em>E</em>. <em>faecium</em>, all of these were correctly identified.<br /><em>Conclusions</em>. The overall agreement with the results obtained by standard procedure is quite elevated (88%) and as a consequence the BC-GP panel could be used as a rapid diagnostic tool to give a faster response in the case of bacteremia associated with sepsis.
topic Sepsis, Blood culture, Gram positive, Rapid identification
url http://www.pagepressjournals.org/index.php/mm/article/view/4945
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