Community-acquired pneumonia due to pandemic A(H1N1)2009 influenzavirus and methicillin resistant Staphylococcus aureus co-infection

Bacterial pneumonia is a well described complication of influenza. In recent years, community-onset methicillin-resistant Staphylococcus aureus (cMRSA) infection has emerged as a contributor to morbidity and mortality in patients with influenza. Since the emergence and rapid dissemination of pandemi...

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Veröffentlicht in:PloS one 2010-01, Vol.5 (1), p.e8705-e8705
Hauptverfasser: Murray, Ronan J, Robinson, James O, White, Jodi N, Hughes, Frank, Coombs, Geoffrey W, Pearson, Julie C, Tan, Hui-Leen, Chidlow, Glenys, Williams, Simon, Christiansen, Keryn J, Smith, David W
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container_start_page e8705
container_title PloS one
container_volume 5
creator Murray, Ronan J
Robinson, James O
White, Jodi N
Hughes, Frank
Coombs, Geoffrey W
Pearson, Julie C
Tan, Hui-Leen
Chidlow, Glenys
Williams, Simon
Christiansen, Keryn J
Smith, David W
description Bacterial pneumonia is a well described complication of influenza. In recent years, community-onset methicillin-resistant Staphylococcus aureus (cMRSA) infection has emerged as a contributor to morbidity and mortality in patients with influenza. Since the emergence and rapid dissemination of pandemic A(H1N1)2009 influenzavirus in April 2009, initial descriptions of the clinical features of patients hospitalized with pneumonia have contained few details of patients with bacterial co-infection. Patients with community-acquired pneumonia (CAP) caused by co-infection with pandemic A(H1N1)2009 influenzavirus and cMRSA were prospectively identified at two tertiary hospitals in one Australian city during July to September 2009, the period of intense influenza activity in our region. Detailed characterization of the cMRSA isolates was performed. 252 patients with pandemic A(H1N1)2009 influenzavirus infection were admitted at the two sites during the period of study. Three cases of CAP due to pandemic A(H1N1)2009/cMRSA co-infection were identified. The clinical features of these patients were typical of those with S. aureus co-infection or sequential infection following influenza. The 3 patients received appropriate empiric therapy for influenza, but inappropriate empiric therapy for cMRSA infection; all 3 survived. In addition, 2 fatal cases of CAP caused by pandemic A(H1N1)2009/cMRSA co-infection were identified on post-mortem examination. The cMRSA infections were caused by three different cMRSA clones, only one of which contained genes for Panton-Valentine Leukocidin (PVL). Clinicians managing patients with pandemic A(H1N1)2009 influenzavirus infection should be alert to the possibility of co-infection or sequential infection with virulent, antimicrobial-resistant bacterial pathogens such as cMRSA. PVL toxin is not necessary for the development of cMRSA pneumonia in the setting of pandemic A( H1N1) 2009 influenzavirus co-infection.
doi_str_mv 10.1371/journal.pone.0008705
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In recent years, community-onset methicillin-resistant Staphylococcus aureus (cMRSA) infection has emerged as a contributor to morbidity and mortality in patients with influenza. Since the emergence and rapid dissemination of pandemic A(H1N1)2009 influenzavirus in April 2009, initial descriptions of the clinical features of patients hospitalized with pneumonia have contained few details of patients with bacterial co-infection. Patients with community-acquired pneumonia (CAP) caused by co-infection with pandemic A(H1N1)2009 influenzavirus and cMRSA were prospectively identified at two tertiary hospitals in one Australian city during July to September 2009, the period of intense influenza activity in our region. Detailed characterization of the cMRSA isolates was performed. 252 patients with pandemic A(H1N1)2009 influenzavirus infection were admitted at the two sites during the period of study. Three cases of CAP due to pandemic A(H1N1)2009/cMRSA co-infection were identified. The clinical features of these patients were typical of those with S. aureus co-infection or sequential infection following influenza. The 3 patients received appropriate empiric therapy for influenza, but inappropriate empiric therapy for cMRSA infection; all 3 survived. In addition, 2 fatal cases of CAP caused by pandemic A(H1N1)2009/cMRSA co-infection were identified on post-mortem examination. The cMRSA infections were caused by three different cMRSA clones, only one of which contained genes for Panton-Valentine Leukocidin (PVL). Clinicians managing patients with pandemic A(H1N1)2009 influenzavirus infection should be alert to the possibility of co-infection or sequential infection with virulent, antimicrobial-resistant bacterial pathogens such as cMRSA. PVL toxin is not necessary for the development of cMRSA pneumonia in the setting of pandemic A( H1N1) 2009 influenzavirus co-infection.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>20090931</pmid><doi>10.1371/journal.pone.0008705</doi><oa>free_for_read</oa></addata></record>
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subjects Antibiotics
Australia - epidemiology
Avian flu
Bacteria
Communities
Community-Acquired Infections - complications
Community-Acquired Infections - epidemiology
Deoxyribonucleic acid
DNA
Drug resistance
Forensic pathology
Hospitals
Humans
Infections
Infectious Diseases
Infectious Diseases/Antimicrobials and Drug Resistance
Infectious Diseases/Bacterial Infections
Infectious Diseases/Respiratory Infections
Infectious Diseases/Viral Infections
Influenza
Influenza A Virus, H1N1 Subtype - isolation & purification
Influenza, Human - complications
Influenza, Human - epidemiology
Influenza, Human - virology
Laboratories
Leukocidin
Medicine
Methicillin
Methicillin-Resistant Staphylococcus aureus - isolation & purification
Morbidity
Mortality
Pandemics
Patients
Pattern recognition
Pneumonia
Pneumonia, Bacterial - complications
Pneumonia, Bacterial - epidemiology
Polymerase chain reaction
Staphylococcal Infections - complications
Staphylococcal Infections - epidemiology
Staphylococcal Infections - microbiology
Staphylococcus aureus
Staphylococcus infections
Therapy
title Community-acquired pneumonia due to pandemic A(H1N1)2009 influenzavirus and methicillin resistant Staphylococcus aureus co-infection
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