Mucoid <i>Staphylococcus aureus</i> : A Clinical Trial of Its Prevalence and Association with Lung Function in People with Cystic Fibrosis

<b>Rationale:</b> The mucoid phenotype of <i>Staphylococcus aureus</i> is caused by adaptation. Excessive biofilm formation associated with a protective effect for mucoid <i>S. aureus</i> was observed in isolates from respiratory samples of people with cystic fibrosis (pwCF). <b>Objectives:</b> There is little knowledge about the prevalence of mucoid <i>S. aureus</i> in pwCF and a potential association with CF lung disease. <b>Methods:</b> A prospective multicenter study was conducted (cross-sectional and longitudinal). Specimens and case report forms were sent to the central study laboratory for characterization of <i>S. aureus</i> and analysis of clinical parameters. <b>Measurements and Main Results:</b> In the cross-sectional study, in 41 (9.1%) of 451 <i>S. aureus</i>-positive pwCF from 13 CF centers, mucoid <i>S. aureus</i> was cultured. In the longitudinal study, the distribution of <i>CFTR</i> genotypes and the number of pwCF with highly effective modulator therapy and coinfection with <i>Pseudomonas aeruginosa</i> were equivalent in the mucoid group (35 pwCF) versus the control group (only nonmucoid <i>S. aureus</i>; 36 pwCF). Although lung function did not differ between groups as a whole, a subgroup analysis revealed significantly worse lung function for female pwCF with mucoid <i>S. aureus</i> as well as for pwCF if <i>P. aeruginosa</i> coinfection was excluded. <b>Conclusions:</b> In the era of highly effective modulator therapy, worse lung function was associated with female and <i>P. aeruginosa</i>-negative pwCF with mucoid <i>S. aureus</i> compared with pwCF with only nonmucoid <i>S. aureus</i>. Therefore, appropriate culture conditions should be established to detect mucoid <i>S. aureus</i>. Further investigations are needed to elucidate the relationship between mucoid <i>S. aureus</i> and CF lung disease. Clinical trial registered with www.clinicaltrials.gov (NCT04171583).

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Journal
American Journal of Respiratory and Critical Care Medicine
Published
2025-02-07
DOI
https://doi.org/10.1164/rccm.202407-1474oc
Citations
4
Primary Topic
Cystic Fibrosis Research Advances
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article
Field-Weighted Citation Impact
6.07
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article

Mucoid Staphylococcus aureus : A Clinical Trial of Its Prevalence and Association with Lung Function in People with Cystic Fibrosis

Helge Hebestreit, J. Peters, C.H. Rumpf, Manfred Ballmann et al.
4 citations
American Journal of Respiratory and Critical Care Medicine
Cystic Fibrosis Research Advances
6.07
article

Mucoid Staphylococcus aureus : A Clinical Trial of Its Prevalence and Association with Lung Function in People with Cystic Fibrosis

Helge Hebestreit, J. Peters, C.H. Rumpf, Manfred Ballmann, C. Decker, Silke van Koningsbruggen-Rietschel, Ute Graepler-Mainka, R. Hait, Sivagurunathan Sutharsan, K. Romme, Susanne Nährig, Dennis Görlich, Anne Schlegtendal, B Wollschläger, Sabine Renner, Barbara C. Kahl, Christina Keßler, Sibylle Junge, Jörg Große-Onnebrink, Susanne Deiwick, Tom Schildberg, Angelika Dübbers, Florian Stehling, Holger Schültingkemper, Peter Küster, Timo Janssen, Schwartbeck Bianca, Corinna Czowalla
article en
4 citations

Abstract

<b>Rationale:</b> The mucoid phenotype of <i>Staphylococcus aureus</i> is caused by adaptation. Excessive biofilm formation associated with a protective effect for mucoid <i>S. aureus</i> was observed in isolates from respiratory samples of people with cystic fibrosis (pwCF). <b>Objectives:</b> There is little knowledge about the prevalence of mucoid <i>S. aureus</i> in pwCF and a potential association with CF lung disease. <b>Methods:</b> A prospective multicenter study was conducted (cross-sectional and longitudinal). Specimens and case report forms were sent to the central study laboratory for characterization of <i>S. aureus</i> and analysis of clinical parameters. <b>Measurements and Main Results:</b> In the cross-sectional study, in 41 (9.1%) of 451 <i>S. aureus</i>-positive pwCF from 13 CF centers, mucoid <i>S. aureus</i> was cultured. In the longitudinal study, the distribution of <i>CFTR</i> genotypes and the number of pwCF with highly effective modulator therapy and coinfection with <i>Pseudomonas aeruginosa</i> were equivalent in the mucoid group (35 pwCF) versus the control group (only nonmucoid <i>S. aureus</i>; 36 pwCF). Although lung function did not differ between groups as a whole, a subgroup analysis revealed significantly worse lung function for female pwCF with mucoid <i>S. aureus</i> as well as for pwCF if <i>P. aeruginosa</i> coinfection was excluded. <b>Conclusions:</b> In the era of highly effective modulator therapy, worse lung function was associated with female and <i>P. aeruginosa</i>-negative pwCF with mucoid <i>S. aureus</i> compared with pwCF with only nonmucoid <i>S. aureus</i>. Therefore, appropriate culture conditions should be established to detect mucoid <i>S. aureus</i>. Further investigations are needed to elucidate the relationship between mucoid <i>S. aureus</i> and CF lung disease. Clinical trial registered with www.clinicaltrials.gov (NCT04171583).

American Journal of Respiratory and Critical Care MedicineVol. 211(5)
University of Cologne (DE), University of Würzburg (DE), Medizinische Hochschule Hannover (DE), Hochschule Campus Wien (AT), Ruhrlandklinik (DE), University Hospital Münster (DE), Essen University Hospital (DE), University Children's Hospital Tübingen (DE), Universitätsklinikum Würzburg (DE), Clemenshospital Münster (DE), St. Josef-Hospital (DE), STZ eyetrial (DE), University Hospital in Halle (DE), University Hospital Cologne (DE), Institute for Medical Informatics and Biostatistics (CH), University of Rostock (DE), University of Duisburg-Essen (DE), Medical University of Vienna (AT), University of Tübingen (DE), Ludwig-Maximilians-Universität München (DE), Ruhr University Bochum (DE)
Good health and well-being
Openalex Percentile: Top 4%
Cystic Fibrosis Research Advances
6.07
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