Related Experiment Video
Updated: May 16, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
[Ultra-late onset group B streptococcal disease--a report of two cases]
Aya Iwata1, Kousaku Matsubara, Hiroyuki Nigami
1Department of Pediatrics, Nishi-Kobe Medical Center.
Insights
Ultra-late onset Group B Streptococcus (GBS) disease is rare. This study found that host factors like preterm birth and low immunity, combined with virulent GBS strains, contribute to its development.
Area of Science:
- Neonatal Medicine
- Infectious Diseases
- Microbiology
Background:
- Group B Streptococcus (GBS) typically causes early-onset disease in infants.
- Ultra-late onset disease (ULOD), occurring after 90 days of life, is exceptionally rare.
Observation:
- Two cases of ULOD are presented: meningitis in a 99-day-old infant and urosepsis in a 7-month-old infant.
- Both infants had underlying risk factors including preterm birth and bilateral vesicoureteral reflux.
- Critically low serum anti-GBS serotype-specific immunoglobulin levels were observed in both patients.
Findings:
- Isolates were identified as serotype III GBS (ST-335) and serotype Ia GBS (ST-23).
- These sequence types (STs) are known invasive strains in Japan and globally.
- ULOD appears to result from a combination of host susceptibility, immunological deficits, and specific GBS strains.
Implications:
- Understanding the interplay of host and microbial factors is crucial for diagnosing and managing rare GBS infections.
- Further research with larger case numbers is necessary to elucidate the full etiology of ULOD.
- This study highlights the importance of considering GBS in late-onset infant infections, especially in vulnerable populations.
Abstract:
Group B Streptococcus (GBS) infection in infants aged over 90 days, known as ultra-late onset disease (ULOD), is extremely rare. We present 2 cases of ULOD and investigate etiology from both the host and microbiological aspects. Case 1, 99-day-old girl born in the late preterm, had a history of 6-hour fever. Bacterial meningitis was diagnosed and the patient was treated with intravenous ampicillin for 14 days. The isolate was serotype III GBS. Case 2, a 7-month-old girl with no medically significant history had an intermittent fever for 2 weeks before admission. Serotype Ia GBS was isolated from urine and blood, leading to a diagnosis of urosepsis. Intravenous cefotaxime was administered for 7 days. Both patients were discharged without any sequelae. We examined the host risk factors for ULOD development. (i) One subject had underlying preterm birth and the other had bilateral vesicoureteral reflux. (ii) Both had extremely low serum anti-serotype specific immunoglobulin levels, an important measure of protective immunity. The anti-type Ia antibody concentration was 0.24 microg/mL and the anti-type III IgG antibody concentration was 0.25 microg/mL. We employed multilocus sequence typing (MLST) to determine the genetic background of bacterial isolates. Sequence types (STs) of isolates were ST-335 (one allele variant of ST-19) and ST-23. ST-335 is an epidemic invasive GBS disease strain in Japan and is dominantly correlated with serotype III. ST-23 is highly associated with serotype Ia and is also a common invasive type in Europe, the United States and Japan. Our findings suggest that ULOD likely develops combined with underlying host disease, immunological factors and highly virulent strains. Continuous investigation of large numbers of cases is needed to better understand ULOD etiology.
Related Concept Videos
Acute Pyelonephritis II: Diagnostic Studies and Management
Bacterial Meningitis II: Pathophysiology
Bacterial Meningitis I: Introduction
Endocarditis II: Clinical Features of Infective Endocarditis
Urinary Tract Infection II: Pathophysiology
Staphylococcal Skin Infections