1991
DOI: 10.1016/0168-1605(91)90131-8
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Collaborative study on the use of motility enrichment on modified semisolid Rappaport-Vassiliadis medium for the detection of Salmonella from foods

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Cited by 40 publications
(15 citation statements)
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“…Under field conditions, the culture of faecal samples is considered to have a sensitivity below 50% [2]. In a collaborative study [12], it has been shown that the relative sensitivity of MSRV is 96% in naturally contaminated food samples. In mesenteric lymph node samples and in faecal samples, the combination of MSRV (selecting the more motile serotypes) with RV (selecting the non-motile serotypes) had a high relative sensitivity (98.4%), as shown in preliminary experiments [21].…”
Section: Discussionmentioning
confidence: 99%
“…Under field conditions, the culture of faecal samples is considered to have a sensitivity below 50% [2]. In a collaborative study [12], it has been shown that the relative sensitivity of MSRV is 96% in naturally contaminated food samples. In mesenteric lymph node samples and in faecal samples, the combination of MSRV (selecting the more motile serotypes) with RV (selecting the non-motile serotypes) had a high relative sensitivity (98.4%), as shown in preliminary experiments [21].…”
Section: Discussionmentioning
confidence: 99%
“…The original formulation of Rappaport broth (1) containing malachite green as a selective agent was developed for incubation at 37 °C. A semisolid agar based upon Rappaport-Vassiliadis selective broth has meanwhile been developed commercially (6) and used for the isolation of salmonellae from food samples (7). However, Rappaport-Vassiliadis broth for selective enrichment has not been widely adopted in laboratories processing human faecal samples, probably due to its unsuitability for isolation of Salmonella typhi and the importance of using a sufficiently small inoculum so as not to interfere with selectivity.…”
Section: Improved Isolation Of Salmonellae From Faeces Using a Semisomentioning
confidence: 99%
“…Next, the homogenates were serially diluted in 0.1% peptone water and plated on Violet Red Bile Glucose Agar ( To determine the incidence of Salmonella spp., 0.1 ml of each intestinal homogenate was inoculated in duplicate into tubes containing 10 ml of Rappaport-Vassiliadis broth (Oxoid CM669, Oxoid Ltd) and was incubated at 42°C for 2 days, as previously recommended (Anonymous, 1989;Cloak et al, 1999). Brilliant Green Agar (Oxoid CM263, Oxoid Ltd) plates were inoculated with each of the RV broths after 24 to 48 h and were incubated for 18 to 24 h at 37°C, as previously described De Zutter et al, 1991). Suspected colonies were confirmed biochemically by inoculation into Triple Sugar Iron Agar (Oxoid CM277, Oxoid Ltd) and Lysine Iron Agar (Oxoid CM381, Oxoid Ltd) slopes incubated at 37°C for 24 h. Salmonella spp.…”
Section: Measurements and Analysismentioning
confidence: 99%