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Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections

BACKGROUNDS: Observable emergence of Vancomycin-Non susceptible Coagulase-negative Staphylococci (VNS-CoNS) associated with skin and soft tissue infections spreading among the urban and rural populace is gradually intensifying severe complications. The isolated VNS-CoNS were evaluated with Matrix-as...

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Autores principales: Akinduti, Paul A., Obafemi, Yemisi Dorcas, Ugboko, Harriet, El-Ashker, Maged, Akinnola, Olayemi, Agunsoye, Chioma Jane, Oladotun, Abiola, Phiri, Bruno S. J., Oranusi, Solomon U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250237/
https://www.ncbi.nlm.nih.gov/pubmed/35778767
http://dx.doi.org/10.1186/s12941-022-00516-4
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author Akinduti, Paul A.
Obafemi, Yemisi Dorcas
Ugboko, Harriet
El-Ashker, Maged
Akinnola, Olayemi
Agunsoye, Chioma Jane
Oladotun, Abiola
Phiri, Bruno S. J.
Oranusi, Solomon U.
author_facet Akinduti, Paul A.
Obafemi, Yemisi Dorcas
Ugboko, Harriet
El-Ashker, Maged
Akinnola, Olayemi
Agunsoye, Chioma Jane
Oladotun, Abiola
Phiri, Bruno S. J.
Oranusi, Solomon U.
author_sort Akinduti, Paul A.
collection PubMed
description BACKGROUNDS: Observable emergence of Vancomycin-Non susceptible Coagulase-negative Staphylococci (VNS-CoNS) associated with skin and soft tissue infections spreading among the urban and rural populace is gradually intensifying severe complications. The isolated VNS-CoNS were evaluated with Matrix-assisted Laser Desorption/ionization Time of Flight Mass Spectrometry (MALDI ToF MS) for species characterization and pan-antimicrobial resistance pattern. METHODS: Out of 256 clinical samples collected including pus, abscess, ear swabs, eye swabs, and aspirates, 91 CoNS isolates were biotyped and further characterized with MALDI-TOF MS. Staphylococci marker genes, Vancomycin susceptibility, and biofilm assays were performed. RESULTS: Of 91 CoNS isolates, S.cohnii (2.3%), S.condimentii (3.4%), S. saprophyticus (6.7%), and S.scuri (21.1%) were characterized with MALDI-TOF with significant detection rate (99.4%; CI 95, 0.775–0.997, positive predictive values, 90.2%) compared to lower biotyping detection rate (p = 0.001). Hemolytic VNS-CoNS lacked nuc, pvl and spa genes from wound, ear, and aspirates of more 0.83 MARI clustered into a separate phylo-diverse group and were widely distributed in urban and peri-urban locations. MALDI TOF–MS yielded a high discriminatory potential of AUC-ROC score of 0.963 with true-positivity prediction. VNS-CoNS of MIC ≥ 16 µg/mL were observed among all the ages with significant resistance at 25th and 75th quartiles. More than 10.5% of CoNS expressed multi-antibiotic resistance with more than 8 µg/mL vancomycin cut-off values (p < 0.05). CONCLUSION: Antibiotic resistant CoNS should be considered significant pathogens rather than contaminant. Biofilm producing VNS-S. sciuri and S. condimentii are potential strains with high pathological tropism for skin, soft tissues and wound infections, and these strains require urgent surveillance in peri-urban and rural communities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-022-00516-4.
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spelling pubmed-92502372022-07-03 Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections Akinduti, Paul A. Obafemi, Yemisi Dorcas Ugboko, Harriet El-Ashker, Maged Akinnola, Olayemi Agunsoye, Chioma Jane Oladotun, Abiola Phiri, Bruno S. J. Oranusi, Solomon U. Ann Clin Microbiol Antimicrob Research BACKGROUNDS: Observable emergence of Vancomycin-Non susceptible Coagulase-negative Staphylococci (VNS-CoNS) associated with skin and soft tissue infections spreading among the urban and rural populace is gradually intensifying severe complications. The isolated VNS-CoNS were evaluated with Matrix-assisted Laser Desorption/ionization Time of Flight Mass Spectrometry (MALDI ToF MS) for species characterization and pan-antimicrobial resistance pattern. METHODS: Out of 256 clinical samples collected including pus, abscess, ear swabs, eye swabs, and aspirates, 91 CoNS isolates were biotyped and further characterized with MALDI-TOF MS. Staphylococci marker genes, Vancomycin susceptibility, and biofilm assays were performed. RESULTS: Of 91 CoNS isolates, S.cohnii (2.3%), S.condimentii (3.4%), S. saprophyticus (6.7%), and S.scuri (21.1%) were characterized with MALDI-TOF with significant detection rate (99.4%; CI 95, 0.775–0.997, positive predictive values, 90.2%) compared to lower biotyping detection rate (p = 0.001). Hemolytic VNS-CoNS lacked nuc, pvl and spa genes from wound, ear, and aspirates of more 0.83 MARI clustered into a separate phylo-diverse group and were widely distributed in urban and peri-urban locations. MALDI TOF–MS yielded a high discriminatory potential of AUC-ROC score of 0.963 with true-positivity prediction. VNS-CoNS of MIC ≥ 16 µg/mL were observed among all the ages with significant resistance at 25th and 75th quartiles. More than 10.5% of CoNS expressed multi-antibiotic resistance with more than 8 µg/mL vancomycin cut-off values (p < 0.05). CONCLUSION: Antibiotic resistant CoNS should be considered significant pathogens rather than contaminant. Biofilm producing VNS-S. sciuri and S. condimentii are potential strains with high pathological tropism for skin, soft tissues and wound infections, and these strains require urgent surveillance in peri-urban and rural communities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-022-00516-4. BioMed Central 2022-07-01 /pmc/articles/PMC9250237/ /pubmed/35778767 http://dx.doi.org/10.1186/s12941-022-00516-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Akinduti, Paul A.
Obafemi, Yemisi Dorcas
Ugboko, Harriet
El-Ashker, Maged
Akinnola, Olayemi
Agunsoye, Chioma Jane
Oladotun, Abiola
Phiri, Bruno S. J.
Oranusi, Solomon U.
Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections
title Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections
title_full Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections
title_fullStr Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections
title_full_unstemmed Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections
title_short Emerging vancomycin-non susceptible coagulase negative Staphylococci associated with skin and soft tissue infections
title_sort emerging vancomycin-non susceptible coagulase negative staphylococci associated with skin and soft tissue infections
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250237/
https://www.ncbi.nlm.nih.gov/pubmed/35778767
http://dx.doi.org/10.1186/s12941-022-00516-4
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