1933
DOI: 10.1002/path.1700370302
|View full text |Cite
|
Sign up to set email alerts
|

Anaerobic methods for the identification of hæmolytic streptococci

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
6
0

Year Published

1935
1935
1973
1973

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 33 publications
(8 citation statements)
references
References 3 publications
2
6
0
Order By: Relevance
“…Moreover, subcultures were made from colonies and not from single cells. The findings nevertheless are consistent with the observations of Howell (15), Todd (16), and Fry (17), that group A hemolytic streptococcus may give rise to non-hemolytic pathogenic forms. Such variants, unrecognized in the throat flora, furnish a reasonable explanation for the absence of hemolytic colonies from the cultures of children who appeared to be spreading contagion.…”
Section: Biological Characteristics Of Typical Forms Contrasted With supporting
confidence: 92%
“…Moreover, subcultures were made from colonies and not from single cells. The findings nevertheless are consistent with the observations of Howell (15), Todd (16), and Fry (17), that group A hemolytic streptococcus may give rise to non-hemolytic pathogenic forms. Such variants, unrecognized in the throat flora, furnish a reasonable explanation for the absence of hemolytic colonies from the cultures of children who appeared to be spreading contagion.…”
Section: Biological Characteristics Of Typical Forms Contrasted With supporting
confidence: 92%
“…Anaerobic conditions have been recommended for the isolation of betahaemolytic streptococci (Jones et al, 1941 ;Brumfitt and Masters, 1959), and are known to facilitate the development of easily recognisable haemolytic colonies (Fry, 1933). In the present study, the presence of 10 per cent.…”
Section: Discussionsupporting
confidence: 48%
“…The original cultures were made on horse blood agar plates and incubated anaerobically in a McIutosh and Ffldes jar for 16 hours (6,8). Any hemolytic colonies were fished and the cultures purified by plating.…”
Section: Isolation Of the Strainsmentioning
confidence: 99%