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      Carriage of Mycoplasma pneumoniae in the Upper Respiratory Tract of Symptomatic and Asymptomatic Children: An Observational Study

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          Abstract

          In order to determine the possible asymptomatic carriage of Mycoplasma pneumoniae in the upper respiratory tracts of children, Emiel Spuesens and colleagues investigate the prevalence of M. pneumoniae in symptomatic and asymptomatic children at a hospital in The Netherlands.

          Please see later in the article for the Editors' Summary

          Abstract

          Background

          Mycoplasma pneumoniae is thought to be a common cause of respiratory tract infections (RTIs) in children. The diagnosis of M. pneumoniae RTIs currently relies on serological methods and/or the detection of bacterial DNA in the upper respiratory tract (URT). It is conceivable, however, that these diagnostic methods also yield positive results if M. pneumoniae is carried asymptomatically in the URT. Positive results from these tests may therefore not always be indicative of a symptomatic infection. The existence of asymptomatic carriage of M. pneumoniae has not been established. We hypothesized that asymptomatic carriage in children exists and investigated whether colonization and symptomatic infection could be differentiated by current diagnostic methods.

          Methods and Findings

          This study was conducted at the Erasmus MC–Sophia Children's Hospital and the after-hours General Practitioners Cooperative in Rotterdam, The Netherlands. Asymptomatic children ( n = 405) and children with RTI symptoms ( n = 321) aged 3 mo to 16 y were enrolled in a cross-sectional study from July 1, 2008, to November 30, 2011. Clinical data, pharyngeal and nasopharyngeal specimens, and serum samples were collected. The primary objective was to differentiate between colonization and symptomatic infection with M. pneumoniae by current diagnostic methods, especially real-time PCR. M. pneumoniae DNA was detected in 21.2% (95% CI 17.2%–25.2%) of the asymptomatic children and in 16.2% (95% CI 12.2%–20.2%) of the symptomatic children ( p = 0.11). Neither serology nor quantitative PCR nor culture differentiated asymptomatic carriage from infection. A total of 202 children were tested for the presence of other bacterial and viral pathogens. Two or more pathogens were found in 56% (63/112) of the asymptomatic children and in 55.5% (50/90) of the symptomatic children. Finally, longitudinal sampling showed persistence of M. pneumoniae in the URT for up to 4 mo. Fifteen of the 21 asymptomatic children with M. pneumoniae and 19 of the 22 symptomatic children with M. pneumoniae in this longitudinal follow-up tested negative after 1 mo.

          Conclusions

          Although our study has limitations, such as a single study site and limited sample size, our data indicate that the presence of M. pneumoniae in the URT is common in asymptomatic children. The current diagnostic tests for M. pneumoniae are unable to differentiate between asymptomatic carriage and symptomatic infection.

          Please see later in the article for the Editors' Summary

          Editors' Summary

          Background

          Pneumonia (a form of acute respiratory infection) is the single largest cause of death in children worldwide, killing an estimated 1.2 million children aged five and under every year, particularly in South Asia and sub-Saharan Africa. In these settings, bacterial infections with Streptococcus pneumoniae and Haemophilus influenzae are the most common causes of bacterial pneumonia. However, in high-income settings, bacterial infection with Mycoplasma pneumoniae is a major cause of upper and lower respiratory tract infections in children: over one-third of childhood cases of community-acquired pneumonia that require admission to a hospital are caused by M. pneumoniae. Currently, diagnosis of M. pneumoniae infections relies on the detection of antibodies against M. pneumoniae in the blood or detection of bacterial DNA in samples from the upper respiratory tract through polymerase chain reaction (PCR) tests.

          Why Was This Study Done?

          Other bacteria, such as Streptococcus pneumoniae, are commonly present in children without causing infection, a situation known as asymptomatic carriage. However, to date, it is unknown whether M. pneumoniae is also commonly carried in the upper respiratory tract of children without causing symptoms or leading to infection. The possibility of asymptomatic carriage of M. pneumoniae could have major implications for the interpretation of the results of diagnostic tests and also for clinical management. So in this study conducted in The Netherlands, the researchers investigated whether asymptomatic carriage of M. pneumoniae exists and also whether symptomatic infection could be differentiated from asymptomatic carriage by current diagnostic methods.

          What Did the Researchers Do and Find?

          Between 2008 and 2011, the researchers recruited children aged between three months and 16 years attending a hospital in Rotterdam for an elective surgical procedure (asymptomatic group) or admitted with a respiratory tract infection (symptomatic group). All children had blood tests and respiratory samples (nasopharyngeal swab) taken on admission and were tested for other pathogens. The researchers invited children who tested positive for M. pneumoniae by PCR to attend for further follow-up and tested them monthly for the presence of M. pneumoniae DNA in the upper respiratory tract until the test was negative on two occasions. Using these methods, the researchers recruited 726 children over the study period—405 in the asymptomatic group and 321 in the symptomatic group. The researchers found that the prevalence of M. pneumoniae did not differ between the asymptomatic group and the symptomatic group, with prevalences of 21.2% and 16.2%, respectively (the prevalence of M. pneumoniae also did not differ significantly between those with lower versus upper respiratory infection). There were also no differences in prevalence in the asymptomatic and symptomatic groups when diagnosed using blood tests. The researchers found a high rate of multiple, coexisting bacterial and viral pathogens in both asymptomatic and symptomatic children: two or more pathogens were found in 56% (63/112) of the asymptomatic children and in 55.5% (50/90) of the symptomatic children. Furthermore, season and the year of enrollment affected the prevalence of M. pneumoniae in the asymptomatic group, ranging from 3% during the spring of 2009 to 58% during the summer of 2010. Finally, of the 21 children from the asymptomatic group who participated in the follow-up study, 15 (71%) tested negative within one month, and in the symptomatic group, 19 of 22 children (86%) tested negative after the first visit.

          What Do These Findings Mean?

          These findings show that M. pneumoniae is carried at high rates in the upper respiratory tracts of healthy children, and that this asymptomatic carriage cannot be differentiated from symptomatic respiratory tract infection by diagnostic tests (serology or PCR). As the prevalence of M. pneumoniae varied between year and season, carriage of M. pneumoniae may follow a cyclic epidemic pattern. This study is from a single study site in one city in The Netherlands, with a relatively small number of children, and so these findings may not be generalizable to other populations. However, as this study suggests that current diagnostic tests do not discriminate between carriage and infection, clinicians may need to reconsider the clinical significance of a positive test result. Future studies are needed to address this diagnostic challenge and also to investigate possible factors that may affect the progression of asymptomatic carriage of M. pneumoniae to symptomatic infection.

          Additional Information

          Please access these websites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.1001444.

          Related collections

          Most cited references24

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          The Management of Community-Acquired Pneumonia in Infants and Children Older Than 3 Months of Age: Clinical Practice Guidelines by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America

          Abstract Evidenced-based guidelines for management of infants and children with community-acquired pneumonia (CAP) were prepared by an expert panel comprising clinicians and investigators representing community pediatrics, public health, and the pediatric specialties of critical care, emergency medicine, hospital medicine, infectious diseases, pulmonology, and surgery. These guidelines are intended for use by primary care and subspecialty providers responsible for the management of otherwise healthy infants and children with CAP in both outpatient and inpatient settings. Site-of-care management, diagnosis, antimicrobial and adjunctive surgical therapy, and prevention are discussed. Areas that warrant future investigations are also highlighted.
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            Mycoplasma pneumoniae and its role as a human pathogen.

            Mycoplasma pneumoniae is a unique bacterium that does not always receive the attention it merits considering the number of illnesses it causes and the degree of morbidity associated with it in both children and adults. Serious infections requiring hospitalization, while rare, occur in both adults and children and may involve multiple organ systems. The severity of disease appears to be related to the degree to which the host immune response reacts to the infection. Extrapulmonary complications involving all of the major organ systems can occur in association with M. pneumoniae infection as a result of direct invasion and/or autoimmune response. The extrapulmonary manifestations are sometimes of greater severity and clinical importance than the primary respiratory infection. Evidence for this organism's contributory role in chronic lung conditions such as asthma is accumulating. Effective management of M. pneumoniae infections can usually be achieved with macrolides, tetracyclines, or fluoroquinolones. As more is learned about the pathogenesis and immune response elicited by M. pneumoniae, improvement in methods for diagnosis and prevention of disease due to this organism may occur.
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              British Thoracic Society guidelines for the management of community acquired pneumonia in children: update 2011.

              The British Thoracic Society first published management guidelines for community acquired pneumonia in children in 2002 and covered available evidence to early 2000. These updated guidelines represent a review of new evidence since then and consensus clinical opinion where evidence was not found. This document incorporates material from the 2002 guidelines and supersedes the previous guideline document.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS Med
                PLoS Med
                PLoS
                plosmed
                PLoS Medicine
                Public Library of Science (San Francisco, USA )
                1549-1277
                1549-1676
                May 2013
                May 2013
                14 May 2013
                : 10
                : 5
                : e1001444
                Affiliations
                [1 ]Department of Paediatric Infectious Diseases and Immunology, Erasmus MC–Sophia, Rotterdam, The Netherlands
                [2 ]Laboratory of Paediatrics, Erasmus MC–Sophia, Rotterdam, The Netherlands
                [3 ]Department of General Paediatrics, Erasmus MC–Sophia, Rotterdam, The Netherlands
                [4 ]Department of Virology, Erasmus MC, Rotterdam, The Netherlands
                [5 ]Department of Biostatistics, Erasmus MC, Rotterdam, The Netherlands
                [6 ]Department of Plastic Surgery, Erasmus MC, Rotterdam, The Netherlands
                [7 ]Department of Anaesthesiology, Erasmus MC, Rotterdam, The Netherlands
                [8 ]General Practitioners Cooperative, Rotterdam, The Netherlands
                [9 ]Department of General Practice, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
                [10 ]Department of Medical Microbiology and Infectious Diseases, Erasmus MC, Rotterdam, The Netherlands
                [11 ]Microbiology R&D, bioMérieux, La Balme-les-Grottes, France
                Emory University, United States of America
                Author notes

                At the time of the study, AB was a paid member on the Cepheid Scientific Advisory Board in which he is no longer taking part. After the study, AB joined bioMérieux, a company specializing in infectious disease' diagnostics. ADO is Head of the department of Virology of the Erasmus MC. He is involved in or with many initiatives within the virology field. This involvement ranges from expert advice to various international organisations involved in the area of general human and veterinary health to advising spin-out companies of the Erasmus University Medical Center Rotterdam that are endeavouring to bridge the gap between scientific discovery/knowledge and putting these to practical use in society. For purposes of transparency and to avoid of possible conflicts of interest, Professor Osterhaus discloses all his interests in matters related, directly or indirectly, to his position as head of the Department of Virology of Erasmus MC. Professor Osterhaus has share certificates in Viroclinics Biosciences B.V. AMR received fees for speaking from Abbott. AMR has received grants from the NutsOhra Foundation, The Netherlands, and the Thrasher Fund, USA. All other authors have declared that no competing interests exist.

                Conceived and designed the experiments: EBS PLF NGH CV AMR. Performed the experiments: EBS TH TRV MS SDP CV. Analyzed the data: EBS PF WCH AB MS ADO NGH CV AMR. Contributed reagents/materials/analysis tools: LNA FW AB MS ADO CV. Wrote the first draft of the manuscript: EBS CV AMR. Contributed to the writing of the manuscript: EBS PLF WCH HAM MYB AB MS ADO NGH CV AMR. ICMJE criteria for authorship read and met: EBS PLF EGV TH WCH LNA FW HAM BB MYB TR AB MS SDP ADO NGH CV AMR. Agree with manuscript results and conclusions: EBS PLF EGV TH WCH LNA FW HAM BB MYB TR AB MS SDP ADO NGH CV AMR. Facilitated data collection: LNA FW HAM BB MYB.

                Article
                PMEDICINE-D-12-02629
                10.1371/journal.pmed.1001444
                3653782
                23690754
                f889eb67-ad3a-4f0f-a568-c0e1e69880af
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 5 September 2012
                : 4 April 2013
                Page count
                Pages: 12
                Funding
                “Stichting Vrienden van het Sophia,” Rotterdam, The Netherlands ( www.vriendensophia.nl). AMR was supported for this study by an Erasmus MC Fellowship Award ( http://www.erasmusmc.nl/research), a Clinical Fellowship Award of The Netherlands Organisation for Health Research and Development ( http://www.zonmw.nl/en/), and a Fellowship Award of the European Society for Paediatric Infectious Diseases ( http://www.espid.org/award_content.aspx?Group=Awards&Page=Fellowship). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Medicine
                Infectious Diseases
                Bacterial Diseases
                Mycoplasma Pneumonia
                Pediatrics
                Pulmonology
                Respiratory Infections

                Medicine
                Medicine

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