1993
DOI: 10.1111/j.1472-765x.1993.tb01364.x
|View full text |Cite
|
Sign up to set email alerts
|

A rapid luminescent-phage based MPN method for the enumeration of Salmonella typhimurium in environmental samples

Abstract: Materials such as soils, waters, sewage sludges and foods can contain low numbers of salmonellas. A most‐probable‐number (MPN) method that utilized a bioluminescent‐bacteriophage is described that allowed the specific determination of as few as one Salmonella typhimurium cell/100 ml of material within 24 h. The method was developed with soil, lake water and sewage sludge inoculated with Salm. typhimurium and had an efficiency of 100% when tested against a traditional MPN method. The protocol is rapid, sensitiv… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
17
0
1

Year Published

1998
1998
2017
2017

Publication Types

Select...
6
3

Relationship

0
9

Authors

Journals

citations
Cited by 55 publications
(18 citation statements)
references
References 2 publications
(1 reference statement)
0
17
0
1
Order By: Relevance
“…12 Both these applications make use of the bacterial luciferase gene, luxAB, which requires aldehyde and NADH as substrates. NADH is present in viable cells, but the aldehyde is normally applied exogenously.…”
Section: Application Of Lrp In Other Generamentioning
confidence: 99%
See 1 more Smart Citation
“…12 Both these applications make use of the bacterial luciferase gene, luxAB, which requires aldehyde and NADH as substrates. NADH is present in viable cells, but the aldehyde is normally applied exogenously.…”
Section: Application Of Lrp In Other Generamentioning
confidence: 99%
“…3,7,10 Typically, detection technologies for Salmonella and other food-borne pathogens use the prokaryotic gene, 11,12 whereas systems for the detection of MTB use the ®re-¯y gene. 7 A mycobacteriophage, with a ®re-¯y luciferase gene (f¯ux) inserted within its genome, is used to infect MTB within a sample.…”
Section: Luciferase Reporter Phage Principlesmentioning
confidence: 99%
“…However, they are not always suited to pharmaceutical and medical devices due to the large difference in the number of contaminating microorganisms. Their procedures of detection may be direct, in which individual microorganisms or populations of organisms are directly observed, or indirect, whereby microbial metabolism, metabolites, or components can be Pettipher, 1983;Hutcheson et al, 1988;Rodrigues and Kroll, 1988;Rodrigues and Kroll, 1990;Diaper and Edwards, 1994;Nebe-von Caron et al, 1998;Newby, 2000;Van Poucke and Nelis, 2000;DeCory et al, 2005, electrical resistance Baynes et al, 1983Owens and WacherViveros, 1986;Silley and Forsythe, 1996;Newby, 2000 , enzyme monitoring Kroll andRodrigues, 1986;Watling and Leech, 1996;Newby, 2000 , Limulus amoebocyte lysate Jorgensen and Alexander, 1981;Bussey and Tsuji, 1984;Baines, 2000, nucleic acid probes Bauters et al, 1999Jordan, 2000;Newby, 2000;Dunsmoor et al, 2001;Jimenez et al, 2001;Serin et al, 2005;Chaieb et al, 2007;Zuluaga et al, 2009 , phage-interaction technology Wolber andGreen, 1990;Turpin et al, 1993;Stewart et al, 1996;Stewart et al, 1998;Mole et al, 1999;Wu et al, 2001 , andcarbon dioxide radiometry Cutler et al, 1989 . In addition to the methods summarized in Table 2, other techniques have been inve...…”
Section: Currently Available Rapid Methods and Their Brief Explanationmentioning
confidence: 99%
“…The specificity, sensitivity, discriminatory power and rapid replication of the bacteriophage makes the phage amplification technique an efficient way for a presumptive diagnostic (17,21,23). …”
Section: Introductionmentioning
confidence: 99%