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1.
Epidemiol Infect ; 144(13): 2719-27, 2016 10.
Article in English | MEDLINE | ID: mdl-26522501

ABSTRACT

In 2012 a US multistate outbreak of listeriosis was linked to ricotta salata imported from Italy, made from pasteurized sheep's milk. Sampling activities were conducted in Italy to trace the source of Listeria monocytogenes contamination. The cheese that caused the outbreak was produced in a plant in Apulia that processed semi-finished cheeses supplied by five plants in Sardinia. During an 'emergency sampling', 179 (23·6%) out of 758 end-products tested positive for L. monocytogenes, with concentrations from <10 c.f.u./g to 1·1 × 106 c.f.u./g. Positive processing environment samples were found in two out of four processing plants. A 'follow-up sampling' was conducted 8 months later, when environmental samples from three out of six plants tested positive for L. monocytogenes and for Listeria spp. PFGE subtyping showed 100% similarity between US clinical strains and isolates from ricotta salata, confirming the origin of the outbreak. The persistence of strains in environmental niches of processing plants was demonstrated, and is probably the cause of product contamination. Two PFGE profiles from clinical cases of listeriosis in Italy in 2011, stored in the MSS-TESSy database, were found to have 100% similarity to one PFGE profile from a US clinical case associated with the consumption of ricotta salata, according to the US epidemiological investigation (sample C, pulsotype 17). However, they had 87% similarity to the only PFGE profile found both in the US clinical case and in 14 ricotta cheese samples collected during the emergency sampling (sample B, pulsotype 1). Sharing of molecular data and availability of common characterization protocols were key elements that connected the detection of the US outbreak to the investigation of the food source in Italy. Simultaneous surveillance systems at both food and human levels are a necessity for the efficient rapid discovery of the source of an outbreak of L. monocytogenes.


Subject(s)
Cheese/microbiology , Disease Outbreaks , Food Handling , Food Microbiology , Listeria monocytogenes/isolation & purification , Listeriosis/epidemiology , Bacterial Proteins/genetics , Electrophoresis, Gel, Pulsed-Field , Italy , Listeria monocytogenes/classification , Listeriosis/microbiology , Phylogeny , Sequence Analysis, DNA , United States/epidemiology
2.
Int J Food Microbiol ; 45(3): 205-10, 1998 Dec 22.
Article in English | MEDLINE | ID: mdl-9926997

ABSTRACT

Two rapid methods for Salmonella detection, Vidas-ICS and modified semi-solid Rappaport-Vassiliadis (MSRV) were evaluated using contaminated poultry meat. The sensitivity and specificity of the methods were investigated on field samples and on artificially contaminated samples inoculated with mixtures of Salmonella and non-Salmonella competing strains. ICS-Vidas and MSRV yielded virtually identical results, in full agreement with the standard cultural method (SCM). The MSRV method showed better results with artificially contaminated samples, but was less sensitive than SCM when applied to field samples. The use of the MSRV and Vidas-ICS methods could be particularly advantageous in the application of HACCP.


Subject(s)
Meat/microbiology , Poultry/microbiology , Reagent Kits, Diagnostic , Salmonella/isolation & purification , Animals , Antibodies, Bacterial , Colony Count, Microbial , Sensitivity and Specificity
3.
Minerva Anestesiol ; 63(11): 365-70, 1997 Nov.
Article in Italian | MEDLINE | ID: mdl-9549279

ABSTRACT

BACKGROUND: Thermodilution cardiac output measurements are commonly obtained by a manual bolus technique with a pulmonary artery catheter. METHODS: A new thermodilution catheter has been developed which utilizes an integral thermal filament and provides semicontinuous online cardiac output. The response of this new device in 25 patients undergoing coronary artery bypass grafting was examined. A total of 250 data pairs was obtained; the cardiac outputs ranged from 2.2 to 11.9 lts.min. RESULTS: The linear regression is represented by the following equation: continuous thermodilution = 0.7196 bolus thermodilution +1.038. The correlation coefficient was 0.75; the mean bias was 0.493 +/- 1.034. CONCLUSIONS: The new technique provides acceptable accuracy in many clinical situations except when sudden haemodynamic changes occur.


Subject(s)
Cardiac Output , Thermodilution/methods , Evaluation Studies as Topic , Humans , Thermodilution/instrumentation
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