Incubation of Egg Contents Pools at an Elevated Temperature (42°C) Does Not Improve the Rapid Detection of Salmonella Enteritidis Phage Type 14b

2004 ◽  
Vol 67 (8) ◽  
pp. 1751-1754
Author(s):  
RICHARD K. GAST ◽  
PETER S. HOLT

Detecting internal Salmonella Enteritidis (SE) contamination in eggs is essential for protecting public health. Pooling together ≥10 eggs for sampling allows many eggs to be screened for contamination, but such pools must be incubated (usually at 25 to 37°C) to permit small numbers of SE to multiply before further testing. The present study determined whether incubating egg contents pools at an elevated temperature (42°C) could increase the rate of multiplication of a phage type 14b strain of SE sufficiently to support the detection of contamination by a rapid lateral flow immunodiffusion method within a single day. Pools of 10 eggs were contaminated with approximately 10 CFU of SE, supplemented with concentrated broth enrichment medium, and incubated at either 37 or 42°C. Incubation of contaminated egg pools at 42°C resulted in significantly higher SE levels after 6, 8, 10, and 12 h. However, incubation at 42°C could only generate a mean log SE concentration of4.21 CFU/ml within a single working day (8 h), inadequate to support efficient detection by most rapid assays. Detection of SE contamination in egg pools by a rapid lateral flow immunodiffusion test was not achieved at a high frequency until 12 h of incubation at 42°C.

1995 ◽  
Vol 58 (3) ◽  
pp. 268-272 ◽  
Author(s):  
RICHARD K. GAST ◽  
PETER S. HOLT

Direct-plating culture methods have been proposed for use in programs to test eggs for contamination by Salmonella enteritidis (SE) because of their speed and low cost, but direct plating has previously been observed to detect SE less frequently than more elaborate broth-enrichment culture methods. The present study used experimentally inoculated pools of egg contents to assess the comparative sensitivities of direct-plating and broth-enrichment culturing for detecting SE, to evaluate the ability of iron supplementation to increase the multiplication of SE during incubation of egg pools, and to determine whether iron supplementation could enhance the ability of direct plating to detect SE in egg pools that initially contained very few SE cells. Efficient detection of SE in egg pools was found to require an approximately 10,000-fold higher level of SE for direct plating than for broth-enrichment culturing. Iron supplementation of contaminated egg pools significantly (P < 0.005) increased the resulting final level of SE after 1 day of incubation at 37°C. Iron supplementation also significantly (P < 0.005) increased the percentage of 10-egg pools, initially inoculated with fewer than 10 SE cells each, that were identified as contaminated by direct plating after the pools had been incubated for 1 day at 37°C. Increasing the iron availability in incubating egg pools, therefore, increased the probability that a small initial number of SE cells would grow quickly to levels likely to be detected by direct plating.


1989 ◽  
Vol 103 (2) ◽  
pp. 243-248 ◽  
Author(s):  
J. A. Frost ◽  
L. R. Ward ◽  
B. Rowe

SUMMARYSalmonella enteritidisaccounted for 55% of the 27478 salmonellae isolated from humans in England and Wales during 1988. Within this serotype phage type 24 has increased from 24 isolations in 1987 to 201 in 1988. The high frequency of drug resistance in this phage type has been shown to be due to the presence of plasmids belonging to Inc N and coding for resistance to a range of antimicrobial drugs among which resistance to ampicillin, streptomycin, tetracycline (AST) and T predominate. These plasmids are phage-type determining and convert strains of phage type 4 to phage type 24.


2021 ◽  
Vol 22 (11) ◽  
pp. 6053
Author(s):  
Marziyeh Nazari ◽  
Abbas Amini ◽  
Nathan T. Eden ◽  
Mikel C. Duke ◽  
Chun Cheng ◽  
...  

Lead detection for biological environments, aqueous resources, and medicinal compounds, rely mainly on either utilizing bulky lab equipment such as ICP-OES or ready-made sensors, which are based on colorimetry with some limitations including selectivity and low interference. Remote, rapid and efficient detection of heavy metals in aqueous solutions at ppm and sub-ppm levels have faced significant challenges that requires novel compounds with such ability. Here, a UiO-66(Zr) metal-organic framework (MOF) functionalized with SO3H group (SO3H-UiO-66(Zr)) is deposited on the end-face of an optical fiber to detect lead cations (Pb2+) in water at 25.2, 43.5 and 64.0 ppm levels. The SO3H-UiO-66(Zr) system provides a Fabry–Perot sensor by which the lead ions are detected rapidly (milliseconds) at 25.2 ppm aqueous solution reflecting in the wavelength shifts in interference spectrum. The proposed removal mechanism is based on the adsorption of [Pb(OH2)6]2+ in water on SO3H-UiO-66(Zr) due to a strong affinity between functionalized MOF and lead. This is the first work that advances a multi-purpose optical fiber-coated functional MOF as an on-site remote chemical sensor for rapid detection of lead cations at extremely low concentrations in an aqueous system.


Author(s):  
Cheng Liu ◽  
Shuiqin Fang ◽  
Yachen Tian ◽  
Youxue Wu ◽  
Meijiao Wu ◽  
...  

Escherichia coli O157:H7 ( E. coli O157:H7) is a dangerous foodborne pathogen, mainly found in beef, milk, fruits, and their products, causing harm to human health or even death. Therefore, the detection of E. coli O157:H7 in food is particularly important. In this paper, we report a lateral flow immunoassay strip (LFIS) based on aggregation-induced emission (AIE) material labeling antigen as a fluorescent probe for the rapid detection of E. coli O157:H7. The detection sensitivity of the strip is 105 CFU/mL, which is 10 times higher than that of the colloidal gold test strip. This method has good specificity and stability and can be used to detect about 250 CFU of E. coli O157:H7 successfully in 25 g or 25 mL of beef, jelly, and milk. AIE-LFIS might be valuable in monitoring food pathogens for rapid detection.


Aquaculture ◽  
2021 ◽  
pp. 736756
Author(s):  
Jiaxin Liu ◽  
Xinyue Zhang ◽  
Jiaying Zheng ◽  
Yepin Yu ◽  
Xiaohong Huang ◽  
...  
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