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Published on: November 4, 2016
Late-onset neonatal group B streptococcal disease associated with breast milk transmission: molecular typing using
Micaela Brandolini1, Marta Corbella1, Patrizia Cambieri1
1Microbiology and Virology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Insights
Group B Streptococcus (GBS) can cause late-onset neonatal infections. Molecular typing confirmed GBS transmission via breast milk in four out of five infant cases, with distinct bacterial strains.
Area of Science:
- Neonatal infections
- Bacterial pathogenesis
- Molecular epidemiology
Background:
- Group B Streptococcus (GBS) is a primary cause of neonatal sepsis and meningitis.
- Late-onset GBS infections, occurring 1 week to 3 months post-birth, are less common.
- While GBS transmission via breast milk is suspected, molecular confirmation is rare.
Purpose of the Study:
- To investigate the role of maternal milk in late-onset Group B Streptococcus disease.
- To confirm GBS transmission through breast milk using molecular techniques.
- To determine the epidemiological relatedness of late-onset GBS infections.
Main Methods:
- Case study of five infants with late-onset GBS disease.
- Utilized random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) for bacterial strain typing.
- Compared GBS isolates from infants and maternal milk.
Main Results:
- Maternal milk was confirmed as the source of GBS infection in four of the five cases.
- RAPD-PCR typing revealed distinct genotypes for each GBS isolate.
- The infections were not epidemiologically linked, indicating independent transmission events.
Conclusions:
- Breast milk is a significant, though infrequent, route for late-onset GBS transmission.
- Molecular typing is crucial for confirming GBS transmission pathways.
- Late-onset GBS cases in this study originated from different GBS clones.
Abstract:
Group B Streptococcus (GBS) is considered to be the major cause of neonatal sepsis and meningitis of bacterial origin. Late-onset GBS infection is infrequent and occurs between 1 week and 3 months of age. The transmission of GBS through the ingestion of breast milk is reported in the literature, but only a few of these cases have been confirmed by molecular techniques. In this article we report five cases of late-onset GBS disease: transmission through maternal milk was confirmed in four cases, using the random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) typing assay. In addition, the RAPD-PCR assay showed that each of the isolated clones belonged to a different RAPD genotype, thus revealing that the late-onset GBS infections were not epidemiologically related.
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