1965
DOI: 10.1111/j.1365-2672.1965.tb04540.x
|View full text |Cite
|
Sign up to set email alerts
|

Methods for the Recovery of Clostridia from Foods

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

1
7
0
1

Year Published

1970
1970
2017
2017

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 30 publications
(9 citation statements)
references
References 26 publications
1
7
0
1
Order By: Relevance
“…The high confirmation rates (92% in this study), rapid confirmation, unequivocal results (positive or negative), and the use of aerobic incubators were among the advantages. This experience is consistent with the report of Gibbs and Freame (12), who noted that the DRCM medium was sensitive for C. perfringens while maintaining selectivity against most other sulfite-reducing organisms.…”
Section: Downloaded Fromsupporting
confidence: 92%
“…The high confirmation rates (92% in this study), rapid confirmation, unequivocal results (positive or negative), and the use of aerobic incubators were among the advantages. This experience is consistent with the report of Gibbs and Freame (12), who noted that the DRCM medium was sensitive for C. perfringens while maintaining selectivity against most other sulfite-reducing organisms.…”
Section: Downloaded Fromsupporting
confidence: 92%
“…( 26 ) If positive, samples were further evaluated to determine the quantitative load of bacteria by the most probable number (MPN) technique ( 27 ) which is a counting method commonly used when low numbers of viable cells are anticipated. ( 28 ) C‐EnterNet data were the only Canadian data available to describe Salmonella concentration level at retail.…”
Section: Risk Assessmentmentioning
confidence: 99%
“…Enumeration of intestinal microflora Brucella blood agar [20], bifidobacteria iodoacetate medium-25 [21], and modified differential clostridial agar supplemented with polymyxin B sulfate (8.5 mg/L) [22] were obtained from Merck (Darmstadt, Germany) and were used to selectively identify anaerobes, bifidobacteria, and Clostridium perfringens, respectively, in an anaerobic chamber (H 2 /CO 2 /N 2 , 10 : 10 : 80). Plates were inoculated in triplicate and incubated at 37 8C for 3 d. To confirm the identity of the colonies, polymerase chain reactions were performed by using specific primers as described in Wang et al [23].…”
Section: Comet Assaymentioning
confidence: 99%