Volume 17, Issue 1 pp. 114-119

Pleural fluid nucleic acid testing enhances pneumococcal surveillance in children

ROXANNE. E. STRACHAN

ROXANNE. E. STRACHAN

Department of Respiratory Medicine, Sydney Children's Hospital, Randwick

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ANITA CORNELIUS

ANITA CORNELIUS

Department of Respiratory Medicine, Sydney Children's Hospital, Randwick

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GWENDOLYN. L. GILBERT

GWENDOLYN. L. GILBERT

Centre for Infectious Diseases and Microbiology, Institute of Clinical Pathology and Medical Research, Westmead

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TANYA GULLIVER

TANYA GULLIVER

Paediatric/Respiratory Department, John Hunter Hospital, Newcastle

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ANDREW MARTIN

ANDREW MARTIN

Department of General Paediatrics, Princess Margaret Hospital for Children, Perth

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TIM MCDONALD

TIM MCDONALD

Department of Paediatrics and Child Health, The Canberra Hospital, Canberra

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GILLIAN NIXON

GILLIAN NIXON

Department of Respiratory and Sleep Medicine, Monash Medical Centre and Ritchie Centre for Baby Health Research, Monash Institute of Medical Research, Melbourne

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ROB ROSEBY

ROB ROSEBY

Department of Paediatrics, Alice Springs Hospital, Alice Springs

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SARATH RANGANATHAN

SARATH RANGANATHAN

Department of Respiratory Medicine, Royal Children's Hospital, Melbourne

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HIRAN SELVADURAI

HIRAN SELVADURAI

Department of Respiratory Medicine, Children's Hospital at Westmead, Sydney

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GREG SMITH

GREG SMITH

Department of Pulmonary Medicine, Women's and Children's Hospital, North Adelaide

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MANUEL SOTO-MARTINEZ

MANUEL SOTO-MARTINEZ

Department of Respiratory Medicine, Royal Children's Hospital, Melbourne

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SADASIVAM SURESH

SADASIVAM SURESH

Department of Respiratory/Sleep Medicine, Mater Children's Hospital, South Brisbane

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LAUREL TEOH

LAUREL TEOH

Department of Paediatrics and Child Health, The Canberra Hospital, Canberra

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KIRAN THAPA

KIRAN THAPA

Centre for Infectious Diseases and Microbiology, Institute of Clinical Pathology and Medical Research, Westmead

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CLAIRE E. WAINWRIGHT

CLAIRE E. WAINWRIGHT

Queensland Children's Medical Research Institute, University of Queensland, Brisbane

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ADAM JAFFÉ

Corresponding Author

ADAM JAFFÉ

Department of Respiratory Medicine, Sydney Children's Hospital, Randwick

School of Women's and Children's Health, University of New South Wales, Sydney, New South Wales, Australia

Adam Jaffe, Department of Respiratory Medicine, Sydney Children's Hospital, High Street, Randwick, Sydney NSW 2031, Australia. Email: [email protected]Search for more papers by this author
First published: 17 August 2011
Citations: 21

Conflict of Interest statement: This study was funded through an unrestricted grant from GlaxoSmithKline, Belgium.

ABSTRACT

Background and objective:  National surveillance of invasive pneumococcal disease (IPD) includes serotyping Streptococcus pneumoniae (SP) isolates from sterile site cultures. PCR is more sensitive and can identify more SP serotypes (STs) in culture-negative samples. The aim of this study was to determine whether enhanced surveillance of childhood empyema, using PCR, provides additional serotype information compared with conventional surveillance.

Methods:  Pleural fluid (PF) from children with empyema were cultured and tested by PCR to identify SP, targeting the autolysin gene (lytA). Multiplex PCR-based reverse line blot assay was used to identify SP STs. Corresponding IPD surveillance and serotype data were obtained from the National Notifiable Diseases Surveillance System (NNDSS).

Results:  Eighty-nine children with empyema, aged ≤16 years, were recruited between April 2008 and March 2009, inclusive. SP was isolated from 5/84 (5.9%) PF cultures and by PCR in 43/79 (54.4%) PF samples. Serotypes were unidentifiable in 15 samples. The frequency of six serotypes (or serotype pairs) identified in 28 samples, including one with two serotypes, were: ST1, n = 4/29 (13.8%); ST3, n = 9/29 (31.0%); ST19A, n = 12/29 (41.4%); ST7F/7A, n = 1/29 (3.4%); ST9V/9A, n = 1/29 (3.4%); ST22F/22A, n = 2/29 (6.9%). Over the same period, 361 IPD patients, aged 16 years or less, were notified to NNDSS. Among 331 serotypeable NNDSS isolates (71.5% from blood), the frequencies of ST1 and 3 were significantly lower than in PF samples: ST1, n = 8/331 (2.4%; P < 0.05); ST3, n = 13/331 (3.9%; P < 0.0001).

Conclusions:  The use of PCR to identify and serotype SP in culture-negative specimens provides additive information.

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