Necrotizing pneumonia caused by nanC-carrying serotypes is associated with pneumococcal haemolytic uraemic syndrome in children

• Published in: Clinical microbiology and infection Vol. 19; no. 5; pp. 480 - 486
• Main Authors: Janapatla, R.-P., Hsu, M.-H., Hsieh, Y.-C., Lee, H.-Y., Lin, T.-Y., Chiu, C.-H.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Elsevier Ltd 01-05-2013; Blackwell Publishing Ltd; Elsevier Limited
• Subjects: Bacterial Proteins - genetics; Case-Control Studies; Child; Child, Preschool; Female; Genotype; Haemolytic uraemic syndrome; Hemolytic-Uremic Syndrome - epidemiology; Hemolytic-Uremic Syndrome - microbiology; Humans; Infant; invasive pneumococcal disease; Male; Mortality; Necrosis; necrotizing pneumonia; neuraminidase; Neuraminidase - genetics; Pneumonia; Pneumonia, Pneumococcal - complications; Pneumonia, Pneumococcal - microbiology; Pneumonia, Pneumococcal - pathology; Serotyping; Streptococcus infections; Streptococcus pneumoniae; Streptococcus pneumoniae - classification; Streptococcus pneumoniae - genetics; Streptococcus pneumoniae - isolation & purification; Thomsen–Friedenreich antigen; Haemolytic uraemic syndrome; necrotizing pneumonia; Thomsen–Friedenreich antigen; invasive pneumococcal disease; neuraminidase; Streptococcus pneumoniae
• DOI: 10.1111/j.1469-0691.2012.03894.x
• EISSN: 1469-0691
• ISSN: 1198-743X

Streptococcus pneumoniae infection is a leading cause of morbidity and mortality worldwide. One of the most severe complications of invasive pneumococcal disease (IPD) is haemolytic uraemic syndrome (HUS). This study was undertaken to determine the risk factors and role of pneumococcal neuraminidases in HUS in children with IPD. Eighteen cases of HUS and 54 patients with IPD without HUS were identified. The controls were patients with culture-confirmed IPD without HUS. Clinical and laboratory characteristics of the two groups of patients were compared. Bacterial isolates from both groups were serotyped, sequence typed and examined for their carriage of three neuraminidase genes. Necrotizing pneumonia and serotype 3 infection were significantly associated with HUS in children with IPD, suggesting that a severe pulmonary suppurating disease increase the risk of HUS. Serotype 14 was associated with necrotizing pneumonia but not HUS. Children with HUS were more likely to require surgery and had a longer duration of hospitalization. The study identified a significantly higher carriage of a neuraminidase gene, nanC, in the causative pneumococcal isolates from patients with HUS (89% versus 41%, p 0.001). The sensitivity and specificity of nanC to predict HUS were 89% and 59%, respectively. In conclusion, necrotizing pneumonia, serotype 3 infection and neuraminidase gene nanC were associated with HUS in children with IPD. The result suggests that NanC could provide an additive effect to NanA and NanB in the overall activity of pneumococcal neuraminidases to expose Thomsen–Friedenreich antigen on various cells in patients with HUS.