4.6 Article

Invasive Group B Streptococcal Disease in Neonates and Infants, Italy, Years 2015-2019

期刊

MICROORGANISMS
卷 9, 期 12, 页码 -

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MDPI
DOI: 10.3390/microorganisms9122579

关键词

group B streptococci; GBS; Streptococcus agalactiae; surveillance; multi-drug resistant CC17 sub-clone; neonatal invasive GBS infection

资金

  1. ISS intramural fund R919 (Infections by beta-haemolytic streptococci)

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Invasive infections by group B streptococci (iGBS) are the leading cause of sepsis and meningitis in neonates and infants. Research in Italy from 2015 to 2019 found that the main clinical manifestations were sepsis, meningitis, bacteremia, and septic shock, with GBS serotype III being predominant in early-onset disease (EOD) and late-onset disease (LOD). Resistance to clindamycin was significant, with MDR-CC17 causing healthcare-associated infections. Monitoring of iGBS characteristics is crucial for prevention strategies and GBS vaccine development.
Invasive infections by group B streptococci (iGBS) are the leading cause of sepsis and meningitis in the first three months of life worldwide. The clinical and microbiological characteristics of neonatal and infant iGBS in Italy during the years 2015-2019 were investigated. Voluntary-based surveillance reported 191 cases (67 early-onset (EOD) and 124 late-onset disease (LOD)) and 89 bacterial isolates were received. The main clinical manifestations were sepsis (59.2%) followed by meningitis (21.5%), bacteremia (12.0%) and septic shock (6.3%). Hospitalized preterm babies accounted for one third of iGBS and constituted the most fragile population in terms of mortality (8.2%) and brain damage (16.4%). GBS serotype III was predominant in EOD (56%) and caused almost all LOD (95%). The rate of resistance to clindamycin reached 28.8%. Most of clindamycin-resistant GBS strains (76%) were serotype III-ST17 and possessed the genetic markers of the emerging multidrug resistant (MDR) CC-17 sub-clone. Our data revealed that iGBS is changing since it is increasingly reported as a healthcare-associated infection (22.6%), mainly caused by MDR-CC17. Continuous monitoring of the clinical and microbiological characteristics of iGBS remains of primary importance and it represents, at present, the most effective tool to support prevention strategies and the research on the developing GBS vaccine.

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