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A Precise Pathogen Delivery and Recovery System for Murine Models of Secondary Bacterial Pneumonia
Published on: September 21, 2019
Viral and bacterial pathogens identification in children hospitalised for severe pneumonia and parapneumonic empyema
Jean-Noel Telles1, Nathalie Richard2, Yves Gillet2
114Emerging Pathogens Laboratory, Fondation Mérieux, IFR128 BioSciences Lyon-Gerland, Lyon, France.
Insights
Viral co-infections in hospitalized children with severe pneumonia were more common, particularly in those with parapneumonic empyema. This suggests viruses may aggravate pneumonia severity.
Area of Science:
- Pediatric Infectious Diseases
- Respiratory Medicine
- Microbiology
Background:
- Pneumonia is a common childhood illness caused by bacteria and viruses.
- The role of viral co-infections in the severity of pediatric community-acquired pneumonia (CAP) is not well understood.
- Parapneumonic empyema (PPE) represents a severe form of CAP.
Purpose of the Study:
- To investigate the impact of respiratory pathogens, including viral co-infections, on the severity of pneumonia in hospitalized children.
- To compare the prevalence of viral and bacterial pathogens in children with CAP and those with CAP and PPE.
Main Methods:
- A cohort of 52 hospitalized children with CAP (with or without PPE) was studied between 2007 and 2009.
- Respiratory pathogens were identified in nasopharyngeal aspirates and pleural effusion samples using conventional and molecular assays (real-time multiplex PCR, antigen detection).
- Patients were divided into two groups: CAP (n=24) and CAP + PPE (n=28).
Main Results:
- *Streptococcus pneumoniae* was the primary bacterial agent identified in 76% of cases via molecular tests and BinaxNOW® in pleural fluid.
- Viral co-detection was significantly higher in nasopharyngeal aspirates from patients with CAP + PPE (35%) compared to CAP patients (5%).
- Commonly detected viruses included rhinovirus, parainfluenza viruses, human metapneumovirus, and respiratory syncytial virus.
Conclusions:
- Viral co-detection is more prevalent in children with severe pneumonia, suggesting a potential role in disease exacerbation.
- Molecular diagnostic techniques enhance pathogen detection in pneumonia and confirm findings from rapid antigen tests.
- The predominant *S. pneumoniae* serotypes in PPE cases were not covered by the heptavalent pneumococcal conjugate vaccine.
Abstract:
Pneumonia is caused by respiratory bacteria and/or viruses. Little is known if co-infections are an aggravating factor in hospitalised children with severe pneumonia. We studied the impact of respiratory pathogens on the severity of pneumonia. Between 2007 and 2009, 52 children hospitalised with a well-documented diagnosis of community-acquired pneumonia (CAP), with or without parapneumonic empyema (PPE), were enrolled in the study. The patients were classified into 2 groups: CAP + PPE (n = 28) and CAP (n = 24). The identification of respiratory viruses and bacteria in nasopharyngeal aspirates and pleural effusion samples were performed using conventional bacterial techniques and molecular assays. Using real-time multiplex PCR and antigen detection, Streptococcus pneumoniae was the main agent identified in 76% of the cases by molecular tests and BinaxNOW® in pleural fluid. A total of 8% of pleural fluid samples remained undiagnosed. In nasopharyngeal aspirates, rhinovirus, parainfluenza viruses, human metapneumovirus, and respiratory syncytial virus were detected in both CAP and CAP + PPE populations; however, the percentage of viral co-detection was significantly higher in nasopharyngeal aspirates from CAP + PPE patients (35%) compared with CAP patients (5%). In conclusion, viral co-detection was observed mainly in patients with more severe pneumonia. Molecular biology assays improved the pathogens detection in pneumonia and confirmed the S. pneumoniae detection by BinaxNOW® in pleural effusion samples. Interestingly, the main S. pneumoniae serotypes found in PPE are not the ones targeted by the heptavalent pneumococcal conjugate vaccine.
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