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Identification of Gram negative non-fermentative bacteria: How hard can it be?

INTRODUCTION: The prevalence of bacteremia caused by Gram negative non-fermentative (GNNF) bacteria has been increasing globally over the past decade. Many studies have investigated their epidemiology but focus on the common GNNF including Pseudomonas aeruginosa and Acinetobacter baumannii. Knowledg...

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Autores principales: Whistler, Toni, Sangwichian, Ornuma, Jorakate, Possawat, Sawatwong, Pongpun, Surin, Uraiwan, Piralam, Barameht, Thamthitiwat, Somsak, Promkong, Chidchanok, Peruski, Leonard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786646/
https://www.ncbi.nlm.nih.gov/pubmed/31568511
http://dx.doi.org/10.1371/journal.pntd.0007729
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author Whistler, Toni
Sangwichian, Ornuma
Jorakate, Possawat
Sawatwong, Pongpun
Surin, Uraiwan
Piralam, Barameht
Thamthitiwat, Somsak
Promkong, Chidchanok
Peruski, Leonard
author_facet Whistler, Toni
Sangwichian, Ornuma
Jorakate, Possawat
Sawatwong, Pongpun
Surin, Uraiwan
Piralam, Barameht
Thamthitiwat, Somsak
Promkong, Chidchanok
Peruski, Leonard
author_sort Whistler, Toni
collection PubMed
description INTRODUCTION: The prevalence of bacteremia caused by Gram negative non-fermentative (GNNF) bacteria has been increasing globally over the past decade. Many studies have investigated their epidemiology but focus on the common GNNF including Pseudomonas aeruginosa and Acinetobacter baumannii. Knowledge of the uncommon GNNF bacteremias is very limited. This study explores invasive bloodstream infection GNNF isolates that were initially unidentified after testing with standard microbiological techniques. All isolations were made during laboratory-based surveillance activities in two rural provinces of Thailand between 2006 and 2014. METHODS: A subset of GNNF clinical isolates (204/947), not identified by standard manual biochemical methodologies were run on the BD Phoenix automated identification and susceptibility testing system. If an organism was not identified (12/204) DNA was extracted for whole genome sequencing (WGS) on a MiSeq platform and data analysis performed using 3 web-based platforms: Taxonomer, CGE KmerFinder and One Codex. RESULTS: The BD Phoenix automated identification system recognized 92% (187/204) of the GNNF isolates, and because of their taxonomic complexity and high phenotypic similarity 37% (69/187) were only identified to the genus level. Five isolates grew too slowly for identification. Antimicrobial sensitivity (AST) data was not obtained for 93/187 (50%) identified isolates either because of their slow growth or their taxa were not in the AST database associated with the instrument. WGS identified the 12 remaining unknowns, four to genus level only. CONCLUSION: The GNNF bacteria are of increasing concern in the clinical setting, and our inability to identify these organisms and determine their AST profiles will impede treatment. Databases for automated identification systems and sequencing annotation need to be improved so that opportunistic organisms are better covered.
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spelling pubmed-67866462019-10-19 Identification of Gram negative non-fermentative bacteria: How hard can it be? Whistler, Toni Sangwichian, Ornuma Jorakate, Possawat Sawatwong, Pongpun Surin, Uraiwan Piralam, Barameht Thamthitiwat, Somsak Promkong, Chidchanok Peruski, Leonard PLoS Negl Trop Dis Research Article INTRODUCTION: The prevalence of bacteremia caused by Gram negative non-fermentative (GNNF) bacteria has been increasing globally over the past decade. Many studies have investigated their epidemiology but focus on the common GNNF including Pseudomonas aeruginosa and Acinetobacter baumannii. Knowledge of the uncommon GNNF bacteremias is very limited. This study explores invasive bloodstream infection GNNF isolates that were initially unidentified after testing with standard microbiological techniques. All isolations were made during laboratory-based surveillance activities in two rural provinces of Thailand between 2006 and 2014. METHODS: A subset of GNNF clinical isolates (204/947), not identified by standard manual biochemical methodologies were run on the BD Phoenix automated identification and susceptibility testing system. If an organism was not identified (12/204) DNA was extracted for whole genome sequencing (WGS) on a MiSeq platform and data analysis performed using 3 web-based platforms: Taxonomer, CGE KmerFinder and One Codex. RESULTS: The BD Phoenix automated identification system recognized 92% (187/204) of the GNNF isolates, and because of their taxonomic complexity and high phenotypic similarity 37% (69/187) were only identified to the genus level. Five isolates grew too slowly for identification. Antimicrobial sensitivity (AST) data was not obtained for 93/187 (50%) identified isolates either because of their slow growth or their taxa were not in the AST database associated with the instrument. WGS identified the 12 remaining unknowns, four to genus level only. CONCLUSION: The GNNF bacteria are of increasing concern in the clinical setting, and our inability to identify these organisms and determine their AST profiles will impede treatment. Databases for automated identification systems and sequencing annotation need to be improved so that opportunistic organisms are better covered. Public Library of Science 2019-09-30 /pmc/articles/PMC6786646/ /pubmed/31568511 http://dx.doi.org/10.1371/journal.pntd.0007729 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Whistler, Toni
Sangwichian, Ornuma
Jorakate, Possawat
Sawatwong, Pongpun
Surin, Uraiwan
Piralam, Barameht
Thamthitiwat, Somsak
Promkong, Chidchanok
Peruski, Leonard
Identification of Gram negative non-fermentative bacteria: How hard can it be?
title Identification of Gram negative non-fermentative bacteria: How hard can it be?
title_full Identification of Gram negative non-fermentative bacteria: How hard can it be?
title_fullStr Identification of Gram negative non-fermentative bacteria: How hard can it be?
title_full_unstemmed Identification of Gram negative non-fermentative bacteria: How hard can it be?
title_short Identification of Gram negative non-fermentative bacteria: How hard can it be?
title_sort identification of gram negative non-fermentative bacteria: how hard can it be?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786646/
https://www.ncbi.nlm.nih.gov/pubmed/31568511
http://dx.doi.org/10.1371/journal.pntd.0007729
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