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Dive into the research topics where J.J. Sheridan is active.

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Featured researches published by J.J. Sheridan.


Journal of Applied Microbiology | 1999

The‐survival‐characteristics‐of‐a‐non‐toxigenic‐strain‐of‐Escherichia‐coli‐O157:H7

Declan Bolton; Catriona Byrne; J.J. Sheridan; D.A. McDowell; and-I. S. Blair

The‐survival‐characteristics‐of‐a‐non‐toxigenic,‐antibiotic‐resistant‐strain‐of‐Escherichia‐coli‐O157:H7‐in‐bovine‐faeces‐were‐investigated.‐Faecal‐samples‐were‐inoculated‐with 108‐9‐cfu‐g−1‐of‐the‐organism‐and‐(i)‐stored‐in‐closed‐plastic‐containers‐at‐10 °C, (ii) stored in closed plastic containers placed outside or (iii) decanted onto the surface of grazing land. Recovery and enumeration on Sorbitol MacConkey Agar (SMAC) and Tryptic Soya Agar (TSA) revealed that the E. coli O157:H7 numbers in both enclosed samples (i and ii) had decreased by 4·5–5·5 log10 cfu g−1 within 99 d. Numbers in samples decanted onto grassland (iii) decreased by 4·0–5·0 log10 cfu g−1 within 50 d but the organism was still detectable in the surrounding soil for up to 99 d. Persistence of E. coli O157:H7 in bovine faeces and contaminated pastures may therefore be an important factor in the initial infection and re‐infection of cattle.


International Journal of Food Microbiology | 2000

The role of microbiological testing in systems for assuring the safety of beef

M.H. Brown; C.O. Gill; J. Hollingsworth; R. Nickelson; S. Seward; J.J. Sheridan; T. Stevenson; J.L. Sumner; D.M. Theno; W.R. Usborne; D. Zink

The use of microbiological testing in systems for assuring the safety of beef was considered at a meeting arranged by the International Livestock Educational Foundation as part of the International Livestock Congress, TX, USA, during February, 2000. The 11 invited participants from industry and government research organizations concurred in concluding that microbiological testing is necessary for the implementation and maintenance of effective Hazard Analysis Critical Control Point (HACCP) systems, which are the only means of assuring the microbiological safety of beef; that microbiological testing for HACCP purposes must involve the enumeration of indicator organisms rather than the detection of pathogens; that the efficacy of process control should be assessed against performance criteria and food safety objectives that refer to the numbers of indicator organisms in product; that sampling procedures should allow indicator organisms to be enumerated at very low numbers; and that food safety objectives and microbiological criteria are better related to variables, rather than attributes sampling plans.


Journal of Applied Microbiology | 2003

The prevalence and spread of Escherichia coli O157:H7 at a commercial beef abattoir

John McEvoy; Alice M. Doherty; J.J. Sheridan; F.M. Thomson-Carter; P. Garvey; Liam McGuire; I.S. Blair; D.A. McDowell

Aims: To investigate the prevalence and virulence characteristics of Escherichia coli O157:H7 after a number of beef process operations at a commercial Irish abattoir.


Letters in Applied Microbiology | 2000

The relationship between hide cleanliness and bacterial numbers on beef carcasses at a commercial abattoir

John McEvoy; Alice M. Doherty; M. Finnerty; J.J. Sheridan; Liam McGuire; I.S. Blair; D.A. McDowell; D. Harrington

Cattle were visually inspected in the lairage of a commercial abattoir and assigned to a category ranging from 1 (very clean) to 5 (very dirty) depending on the observed cleanliness of the hide. Animals from categories 2, 3 and 5 were slaughtered and total viable counts (TVCs) enumerated at five sites (hock, brisket, cranial back, bung and inside round) on the subsequent carcasses. The TVCs at the hock were significantly higher on category 5 than on category 2 carcasses (P < 0·05). Similarly, TVCs at the brisket were significantly higher on categories 3 and 5 than on category 2 carcasses (P < 0·05). There were no differences in counts among the categories at any of the other sites. The TVCs averaged over the five carcass sites were higher for category 5 than for category 2 carcasses (P < 0·05). The TVCs at the brisket were significantly higher than all other sites (P < 0·01). In general, carcasses from category 2 animals slaughtered in a batch with dirtier animals (categories 3 and 5) did not have higher TVCs than carcasses of category 2 animals slaughtered at the beginning of the day in the absence of dirtier animals. The introduction of improved hygienic practices during the dehiding of category 4 animals resulted in reduced TVCs at the brisket (P < 0·001).


Journal of Applied Microbiology | 2001

Antibiotic resistance among Listeria, including Listeria monocytogenes, in retail foods

D. Walsh; Geraldine Duffy; J.J. Sheridan; I.S. Blair; D.A. McDowell

Aims: In the past eight to 10 years, reports of antibiotic resistance in food‐borne isolates in many countries have increased, and this work examined the susceptibility of 1001 food isolates of Listeria species.


Journal of Applied Microbiology | 2002

Washing and chilling as critical control points in pork slaughter hazard analysis and critical control point (HACCP) systems

Declan Bolton; Rachel Pearce; J.J. Sheridan; I.S. Blair; D.A. McDowell; D. Harrington

Aims: The aim of this research was to examine the effects of preslaughter washing, pre‐evisceration washing, final carcass washing and chilling on final carcass quality and to evaluate these operations as possible critical control points (CCPs) within a pork slaughter hazard analysis and critical control point (HACCP) system.


International Journal of Food Microbiology | 2004

Studies to determine the critical control points in pork slaughter hazard analysis and critical control point systems.

R.A. Pearce; Declan Bolton; J.J. Sheridan; D.A. McDowell; I.S. Blair; D. Harrington

Aerobic mesophilic counts (AMC), coliform (CC) and coliform resuscitation counts (CRCs) were obtained by swabbing 50 cm(2) areas at three sites (ham, belly and neck) on pig carcasses, after each of seven stages of the slaughter/dressing process (bleeding, scalding, dehairing, singeing, polishing, evisceration and chilling). In most cases, there were no statistical differences (P>0.05) among the counts derived by these three methods. Reductions in counts at individual sites were observed after scalding (3.5 log(10) cfu cm(-2)), and singeing (2.5 log(10) cfu cm(-2)). Increases in counts at individual sites were observed after dehairing (2.0 log(10) cfu cm(-2)) and polishing (1.5 log(10) cfu cm(-2)). The incidence of Salmonella on pig carcasses was also obtained by swabbing the outside surfaces of 100 half carcasses. Information on the incidence of Salmonella in scald tank water (108 samples) was also investigated. Carcass swabs and scald tank water were examined for the presence of Salmonella using standard enrichment methods. Salmonella were detected on 31% of carcasses immediately after bleeding, 7% of carcasses immediately after dehairing and evisceration, and 1% of carcasses immediately after scalding. Serovars included Salmonella Typhimurium, Salmonella Hadar, Salmonella Infantis and Salmonella Derby. No Salmonella were recovered from samples of scald tank water. The impact of pig slaughter/dressing processes on carcass microbiology and their potential use as critical control points (CCPs) during pork production are discussed.


Journal of Food Protection | 1998

Survival of Escherichia coli O157:H7 during the manufacture of pepperoni.

D. C. R. Riordan; Geraldine Duffy; J.J. Sheridan; B. S. Eblen; Richard C. Whiting; I.S. Blair; D.A. McDowell

This study investigated the growth and survival of Escherichia coli O157:H7 during the manufacture of pepperoni to determine whether a 5-log10-unit decline in numbers, as recommended by the U.S. Food Safety and Inspection Service (FSIS), could be achieved. A range of pepperoni formulations with variations in salt (2.5 to 4.8%) and sodium nitrite (100 to 400 ppm) levels, and with pH (4.4 to 5.6) adjusted by manipulation of dextrose concentrations were prepared. The batters produced were inoculated with E. coli O157:H7 380-94 at a level of approximately 6.70 log10 CFU/g; changes in pathogen numbers, pH, titratable acidity, and sodium nitrite concentrations were monitored during fermentation and drying. With the standard commercial formulation (i.e., 2.5% salt, 100 ppm sodium nitrite, pH 4.8) E. coli O157:H7 numbers declined by approximately 0.41 log10 CFU/g during fermentation and a further 0.43 log10 CFU/g during subsequent drying (7 days). A regression equation was fitted to the data which showed significantly (P < 0.001) greater reductions in pathogen numbers in samples with increased salt and sodium nitrite contents and lowered pH. However declines were in all cases less than the target reduction of 5 log10 CFU/g.


Applied and Environmental Microbiology | 2000

Effects of Acid Adaptation, Product pH, and Heating on Survival of Escherichia coli O157:H7 in Pepperoni

Denise C. R. Riordan; Geraldine Duffy; J.J. Sheridan; Richard C. Whiting; I.S. Blair; D.A. McDowell

ABSTRACT The thermotolerance of E. coli O157:H7 cells (strain 380-94) heated in pepperoni is reported. Information on the pattern of thermal inactivation of E. coli O157:H7 in pepperoni was applied in the development of heating processes designed to reduceE. coli O157:H7 numbers therein by 5 log10units.


Letters in Applied Microbiology | 2000

The effects of preslaughter washing on the reduction of Escherichia coli O157:H7 transfer from cattle hides to carcasses during slaughter

Catriona Byrne; Declan Bolton; J.J. Sheridan; D.A. McDowell; I.S. Blair

C.M. BYRNE, D.J. BOLTON, J.J. SHERIDAN, D.A. MCDOWELL and I.S. BLAIR.2000. Fresh bovine faeces were inoculated with a non‐toxigenic, antibiotic resistant strain of Escherichia coli O157:H7, spread on the rump areas of 30 heifers and allowed to dry for 24 h. Ten of the cattle then entered the normal slaughter process without further treatment. The remaining cattle were washed with a powerhose for 1 min (10 animals) and 3 min (10 animals) before entering the normal slaughter process. Both washing treatments removed all visible faecal materials on the live animals although a significant reduction (P < 0·05) in E. coli O157:H7 levels on the hides was only observed on those animals which were powerhosed for 3 min. After slaughter, E. coli O157:H7 was detected on carcasses and on the knives and hands of operatives. Preslaughter washing for 3 min did not statistically reduce the numbers of E. coli O157:H7 transferred from the hide to the carcass during slaughter. However, the organism was not detected on three of the four areas of the carcass sampled, indicating that washing may be a suitable method of decontamination animal hides before slaughter and as such deserves further investigation.

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John McEvoy

North Dakota State University

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Francis Butler

University College Dublin

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