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2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates

BACKGROUND: Agr is a key regulator that controls expression of secreted exoproteins and surface protein in Staphylococcus aureus. It has been reported that mixed status of two different phenotypes including agr functional and nonfunctional subpopulations can coexist in vitro and in vivo. However, da...

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Autores principales: Bae, Seongman, Cho, Eunbeen, Yang, Eunmi, Seo, Hyeonji, Kim, Eun Sil, Sung, Heungsup, Kim, Mi-Na, Jung, Jiwon, Jae Kim, Min, Kim, Sung-Han, Lee, Sang-Oh, Choi, Sang-Ho, Woo, Jun Hee, Kim, Yang Soo, Chong, Yong Pil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810731/
http://dx.doi.org/10.1093/ofid/ofz360.2283
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author Bae, Seongman
Cho, Eunbeen
Yang, Eunmi
Seo, Hyeonji
Kim, Eun Sil
Sung, Heungsup
Kim, Mi-Na
Jung, Jiwon
Jae Kim, Min
Kim, Sung-Han
Lee, Sang-Oh
Choi, Sang-Ho
Woo, Jun Hee
Kim, Yang Soo
Chong, Yong Pil
author_facet Bae, Seongman
Cho, Eunbeen
Yang, Eunmi
Seo, Hyeonji
Kim, Eun Sil
Sung, Heungsup
Kim, Mi-Na
Jung, Jiwon
Jae Kim, Min
Kim, Sung-Han
Lee, Sang-Oh
Choi, Sang-Ho
Woo, Jun Hee
Kim, Yang Soo
Chong, Yong Pil
author_sort Bae, Seongman
collection PubMed
description BACKGROUND: Agr is a key regulator that controls expression of secreted exoproteins and surface protein in Staphylococcus aureus. It has been reported that mixed status of two different phenotypes including agr functional and nonfunctional subpopulations can coexist in vitro and in vivo. However, data on the natural course and clinical implication of the mixed agr status is limited. We thus investigated the frequency and characteristics of the mixed agr in clinical settings. METHODS: We evaluated isogenic paired MRSA isolates collected from patients with persistent S. aureus bacteremia (SAB) between October 2010 and April 2016, and then prospectively performed surveillance for the presence of mixed agr function in MRSA isolates from patients with SAB between May 2016 and December 2017. The mixed agr status was evaluated by single colony evaluation on sheep blood agar plate containing RN4220 supernatant (β-hemolysin) (Figure 1). Cross-streaking with RN4220 and RNAIII measurement were performed to confirm the agr functionality of each of hemolytic and non-hemolytic colonies, separately. The expression levels of RNAIII, hla, and saeS/saeR were measured by real-time reverse transcription polymerase chain reaction. RESULTS: A total of 161 first blood isolates were collected during study period, and 6 isolates (4%) displayed mixed phenotype by single colony test. The mixed hemolytic pattern was observed in 5 out of 52 ST72 isolates (10%) and 1 out of 82 ST5 isolates (1%) (Figure 1). No difference was found in the genotypes between hemolytic and non-hemolytic colonies from each isolate. Of the 6 isolates, three lost mixed hemolytic features in the follow-up blood cultures (Table 1). One ST72 and one ST5 isolate showed agr mixed pattern determined by different RNAIII levels, but remaining four ST72 isolates had mixed hemolytic pattern due to different expression of hla correlated with saeS/saeR expression (Figure 2). CONCLUSION: The mixture of agr function status among the clinical blood isolates of MRSA was rarely observed and isolates displaying heterogeneous hemolytic phenotype were largely due to differential expression of α-hemolysin. Further investigation is needed to unveil the clinical significance of mixture of different hemolytic phenotypes. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68107312019-10-28 2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates Bae, Seongman Cho, Eunbeen Yang, Eunmi Seo, Hyeonji Kim, Eun Sil Sung, Heungsup Kim, Mi-Na Jung, Jiwon Jae Kim, Min Kim, Sung-Han Lee, Sang-Oh Choi, Sang-Ho Woo, Jun Hee Kim, Yang Soo Chong, Yong Pil Open Forum Infect Dis Abstracts BACKGROUND: Agr is a key regulator that controls expression of secreted exoproteins and surface protein in Staphylococcus aureus. It has been reported that mixed status of two different phenotypes including agr functional and nonfunctional subpopulations can coexist in vitro and in vivo. However, data on the natural course and clinical implication of the mixed agr status is limited. We thus investigated the frequency and characteristics of the mixed agr in clinical settings. METHODS: We evaluated isogenic paired MRSA isolates collected from patients with persistent S. aureus bacteremia (SAB) between October 2010 and April 2016, and then prospectively performed surveillance for the presence of mixed agr function in MRSA isolates from patients with SAB between May 2016 and December 2017. The mixed agr status was evaluated by single colony evaluation on sheep blood agar plate containing RN4220 supernatant (β-hemolysin) (Figure 1). Cross-streaking with RN4220 and RNAIII measurement were performed to confirm the agr functionality of each of hemolytic and non-hemolytic colonies, separately. The expression levels of RNAIII, hla, and saeS/saeR were measured by real-time reverse transcription polymerase chain reaction. RESULTS: A total of 161 first blood isolates were collected during study period, and 6 isolates (4%) displayed mixed phenotype by single colony test. The mixed hemolytic pattern was observed in 5 out of 52 ST72 isolates (10%) and 1 out of 82 ST5 isolates (1%) (Figure 1). No difference was found in the genotypes between hemolytic and non-hemolytic colonies from each isolate. Of the 6 isolates, three lost mixed hemolytic features in the follow-up blood cultures (Table 1). One ST72 and one ST5 isolate showed agr mixed pattern determined by different RNAIII levels, but remaining four ST72 isolates had mixed hemolytic pattern due to different expression of hla correlated with saeS/saeR expression (Figure 2). CONCLUSION: The mixture of agr function status among the clinical blood isolates of MRSA was rarely observed and isolates displaying heterogeneous hemolytic phenotype were largely due to differential expression of α-hemolysin. Further investigation is needed to unveil the clinical significance of mixture of different hemolytic phenotypes. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6810731/ http://dx.doi.org/10.1093/ofid/ofz360.2283 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Bae, Seongman
Cho, Eunbeen
Yang, Eunmi
Seo, Hyeonji
Kim, Eun Sil
Sung, Heungsup
Kim, Mi-Na
Jung, Jiwon
Jae Kim, Min
Kim, Sung-Han
Lee, Sang-Oh
Choi, Sang-Ho
Woo, Jun Hee
Kim, Yang Soo
Chong, Yong Pil
2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates
title 2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates
title_full 2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates
title_fullStr 2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates
title_full_unstemmed 2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates
title_short 2605. Mixed Subpopulation of Hemolytic and Non-Hemolytic Phenotype in Clinical Staphylococcus aureus Blood Isolates
title_sort 2605. mixed subpopulation of hemolytic and non-hemolytic phenotype in clinical staphylococcus aureus blood isolates
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810731/
http://dx.doi.org/10.1093/ofid/ofz360.2283
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