1992
DOI: 10.1093/infdis/165.3.569
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Analysis of DNA Restriction Fragment Length Polymorphism Extends the Evidence for Breast Milk Transmission in Streptococcus agalactiae Late-Onset Neonatal Infection

Abstract: Analysis of restriction fragment length polymorphism (RFLP) of total DNA and of ribosomal DNA (ribotyping) was used to document four cases of Streptococcus agalactiae mother-to-infant transmission potentially associated with ingestion of infected mother's milk. Twenty strains were analyzed. Ten strains were mother-baby pairs, five from the milk of five mothers, four from their neonates with late-onset infection, and one from a colonized neonate. All mothers had early postpartum mastitis. Ten unrelated strains … Show more

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Cited by 90 publications
(72 citation statements)
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“…The main phylogenetic groups (A, B1, B2, and D) were determined for all strains by using previously described PCR methods (11), and B2 strains were subgrouped by ribotyping with the restriction enzyme HindIII and with 16S and 23S rRNAs as the probes (1,(3)(4)(5).…”
Section: Methodsmentioning
confidence: 99%
“…The main phylogenetic groups (A, B1, B2, and D) were determined for all strains by using previously described PCR methods (11), and B2 strains were subgrouped by ribotyping with the restriction enzyme HindIII and with 16S and 23S rRNAs as the probes (1,(3)(4)(5).…”
Section: Methodsmentioning
confidence: 99%
“…The isolates were grown in 10 ml of nutrient broth (Sanofi Diagnostic Pasteur) for 18 h, and DNA was prepared from the bacterial pellet as previously described (2,3). DNA was digested with EcoRI (Boehringer, Mannheim, Germany) according to the manufacturer's instructions and analyzed by Southern blotting with a chemiluminescent ribosomal probe (2). Identification of genomovars was determined as previously described (20).…”
Section: Methodsmentioning
confidence: 99%
“…Other labelling molecules have been used. In our studies, 16S+23S rRNA from E. coli was cold labelled by random oligopriming, using a mixture of hexanucleotide primers and cloned mouse mammary leukemia virus reverse transcriptase (115) in the presence of deoxynucleotide triphosphates, including digoxigenin-11-dUTP (18) (Fig. 5).…”
Section: Introductionmentioning
confidence: 99%