Characterization of bacterial strains isolated from a beef-processing plant following cleaning and disinfection — Influence of isolated strains on biofilm formation by Sakaï and EDL 933 E. coli O157:H7

2009 ◽  
Vol 133 (1-2) ◽  
pp. 62-67 ◽  
Author(s):  
Nesrine Marouani-Gadri ◽  
Gladys Augier ◽  
Brigitte Carpentier
2014 ◽  
Vol 81 (2) ◽  
pp. 713-725 ◽  
Author(s):  
John W. Schmidt ◽  
Getahun E. Agga ◽  
Joseph M. Bosilevac ◽  
Dayna M. Brichta-Harhay ◽  
Steven D. Shackelford ◽  
...  

ABSTRACTSpecific concerns have been raised that third-generation cephalosporin-resistant (3GCr)Escherichia coli, trimethoprim-sulfamethoxazole-resistant (COTr)E. coli, 3GCrSalmonella enterica, and nalidixic acid-resistant (NALr)S. entericamay be present in cattle production environments, persist through beef processing, and contaminate final products. The prevalences and concentrations of these organisms were determined in feces and hides (at feedlot and processing plant), pre-evisceration carcasses, and final carcasses from three lots of fed cattle (n= 184). The prevalences and concentrations were further determined for strip loins from 103 of the carcasses. 3GCrSalmonellawas detected on 7.6% of hides during processing and was not detected on the final carcasses or strip loins. NALrS. entericawas detected on only one hide. 3GCrE. coliand COTrE. coliwere detected on 100.0% of hides during processing. Concentrations of 3GCrE. coliand COTrE. colion hides were correlated with pre-evisceration carcass contamination. 3GCrE. coliand COTrE. coliwere each detected on only 0.5% of final carcasses and were not detected on strip loins. Five hundred and 42 isolates were screened for extraintestinal pathogenicE. coli(ExPEC) virulence-associated markers. Only two COTrE. coliisolates from hides were ExPEC, indicating that fed cattle products are not a significant source of ExPEC causing human urinary tract infections. The very low prevalences of these organisms on final carcasses and their absence on strip loins demonstrate that current sanitary dressing procedures and processing interventions are effective against antimicrobial-resistant bacteria.


1970 ◽  
Vol 17 ◽  
pp. 71-76
Author(s):  
M Fakruddin ◽  
Reaz Mohammad Mazumder ◽  
Towhida Khanom Tania ◽  
Saiful Islam ◽  
Meher Nigad Nipa ◽  
...  

Context: Waste water containing Chromium (Cr6+) is by far the most important environmental challenge being faced. Objectives: The present study was planned on the isolation and characterization of chromate resistant and reducing bacterial strains in order to use them for detoxification of chromate.Materials and Methods: Water samples were collected to isolate microorganisms from tannery effluent of Baluchara, Chittagong and inoculated into Luria-Bertani medium with added Cr6+ as K2Cr2O7. The organisms have been identified and studied for Cr6+ reduction-ability in growth dependent manner.Results: A total of 35 isolates have been selected as potential organism belonging to the species of Moraxella (14.3%), Bacillus (11.43%), Streptococcus (25.72%), Staphylococcus (5.7%), Salmonella (12.3%), E. coli (13.3%), Enterobacter (11.3%), Hafnia alvei (2.45%) and Alcaligenes (3.5%). The selected isolates were able to tolerate at least 500 mg/l of Cr6+. The total Cr6+ concentration of the effluent sample analysed was found to be about 23.73 mg/l as determined by Atomic Absorption Spectrophotometry. Two of the isolates reduced 38% and 32% of Cr6+ added to the medium. Another 7 isolates showed Cr6+; reducing capability ranging from 18 to 22%.Conclusion: As the isolates have turned out to successfully reduce Cr6+ in this study, these can be used for the development of bioremediation process. Key words: Enzymatic reduction; Bioremediation; Chromium; Ecotoxicity; Tannery.DOI: 10.3329/jbs.v17i0.7104J. bio-sci. 17: 71-76, 2009


2016 ◽  
Vol 62 (11) ◽  
pp. 893-903 ◽  
Author(s):  
Siphathele Sibanda ◽  
Jacques Theron ◽  
Divine Y. Shyntum ◽  
Lucy N. Moleleki ◽  
Teresa A. Coutinho

Quorum sensing (QS) plays an important role in the regulation of bacteria–host interactions and ecological fitness in many bacteria. In this study, 2 luxI/R homologs, namely eanI/eanR and rhlI/rhlR, were identified in the genome sequence of Pantoea ananatis LMG 2665T. To determine a role for these luxI/R homologs in pathogenicity and biofilm formation, mutant bacterial strains lacking either eanI/R or rhlI/R and both of these homologs were generated. The results indicated that both the RhlI/R and EanI/R systems are required for pathogenicity and biofilm formation in strain LMG 2665T. This is the first study to characterize the biological significance of the RhlI/R QS system in P. ananatis.


2018 ◽  
Vol 78 (2) ◽  
pp. 375-387 ◽  
Author(s):  
Jeyachchandran Visvalingam ◽  
Peipei Zhang ◽  
Timothy C. Ells ◽  
Xianqin Yang

2019 ◽  
Vol 234 (10) ◽  
pp. 18272-18282 ◽  
Author(s):  
Seyyed Khalil Shokouhi Mostafavi ◽  
Shahin Najar‐Peerayeh ◽  
Ashraf Mohabbati Mobarez ◽  
Mehdi Kardoust Parizi

1975 ◽  
Vol 21 (8) ◽  
pp. 1217-1223 ◽  
Author(s):  
Christopher J. Pazoles ◽  
Charles F. Kulpa Jr.

A DNA bacteriophage, designated CP13, was isolated against Escherichia coli J5, a UDP-galactose-4-epimeraseless mutant of E. coli 0111:B4. Bacteriophage CP13 appears to be specific for rough bacterial strains. Adsorption studies with E. coli J5 grown with galactose show that the bacteriophage will not adsorb when complete lipopolysaccharide is present in the cell membrane. This indicates that lipopolysaccharide may be directly or indirectly involved with the receptor site for bacteriophage CP13. The bacteriophage DNA has a G + C content of 52%.


2005 ◽  
Vol 68 (2) ◽  
pp. 265-272 ◽  
Author(s):  
JOSEPH M. BOSILEVAC ◽  
XIANGWU NOU ◽  
MATTHEW S. OSBORN ◽  
DELL M. ALLEN ◽  
MOHAMMAD KOOHMARAIE

The hides of cattle are the source of Escherichia coli O157:H7 that contaminates beef carcasses during commercial beef processing. Therefore, effective interventions that reduce hide contamination should reduce subsequent carcass contamination. The first objective of this study was to identify the most effective reagents for decontamination of beef hides. Cattle hides draped over barrels were used for in vitro experiments to compare the efficacy of washes using 1.6% sodium hydroxide, 4% trisodium phosphate, 4% chlorofoam, or 4% phosphoric acid, each followed by a rinse step using either water or acidified (pH 7.0) chlorine at 200 or 500 ppm. All treatments using a water rinse reduced hide coliform counts by 1.5 to 2.5 log CFU/100 cm2. Compared with water rinses, 200 and 500 ppm acidified chlorine rinses increased efficacy by approximately 1.0 and 2.0 log CFU/100 cm2, respectively. Vacuuming of the treated areas to remove excess liquid improved hide cleanliness by an average of an additional 1.0 log CFU/100 cm2. The second objective was to evaluate the use of an on-line hide-wash cabinet that used a sodium hydroxide wash and a chlorinated (1 ppm) water rinse. Hides sampled before entering and after exiting the cabinet had aerobic plate counts and Enterobacteriaceae counts that were reduced by 2.1 and 3.4 log CFU/100 cm2, respectively, and the prevalence of E. coli O157 on hides was reduced from 44 to 17% when the cabinet was in use. Preevisceration carcass aerobic plate counts and Enterobacteriaceae counts were both reduced by 0.8 log CFU/100 cm2, and the prevalence of E. coli O157 on preevisceration carcasses was reduced from 17 to 2% when the cabinet was in use. These results support decontamination of hides as an effective means to reduce pathogen contamination of cattle carcasses during processing.


2008 ◽  
Vol 71 (9) ◽  
pp. 1752-1760 ◽  
Author(s):  
TERRANCE M. ARTHUR ◽  
JOSEPH M. BOSILEVAC ◽  
DAYNA M. BRICHTA-HARHAY ◽  
NORASAK KALCHAYANAND ◽  
DAVID A. KING ◽  
...  

Transportation from the feedlot and lairage at the processing plant have been identified as potential sources of Escherichia coli O157:H7 and Salmonella hide contamination. The objective of this study was to perform a comprehensive tracking analysis of E. coli O157:H7 and Salmonella associated with beef cattle from the feedlot through processing. Cattle (n = 581) were sampled in a feedlot, then transported in multiple lots to three commercial, fed beef processing plants in the United States, where they were sampled again. Samples were collected from the tractor trailers prior to loading cattle and from the lairage environment spaces prior to entry of the study cattle. Pathogen prevalence on cattle hides increased on every lot of cattle between exiting the feedlot and beginning processing. Prior to loading cattle, E. coli O157:H7 was found in 9 (64%) of 14 tractor trailers. E. coli O157:H7 was detected in over 60% of the samples from each lairage environment area, while Salmonella was detected in over 70% of the samples from each lairage environment area. E. coli O157:H7 and Salmonella isolates (n 3,645) were analyzed using pulsed-field gel electrophoresis. The results of the pulsed-field gel electrophoresis tracking indicate that the transfer of bacteria onto cattle hides that occurs in the lairage environments of U.S beef processing plants accounts for a larger proportion of the hide and carcass contamination than does the initial bacterial population found on the cattle exiting the feedlot. Finally, the results of this study indicate that hide wash cabinets are effective in removing contamination derived from the lairage environment.


2020 ◽  
Author(s):  
Rene DEMBELE ◽  
Ali Konaté ◽  
Issiaka Soulama ◽  
Wendpoulomdé A. D. Kaboré ◽  
Assèta Kagambèga ◽  
...  

Abstract Background In recent years, Carbapenemase-producing Enterobacteriaceae (CPE) resistance to antibiotics has dramatically increased leading to limitations of their treatment options. In the present study, we investigated the occurrence of carbapenemase-producing Escherichia coli and Salmonella in rural Burkina Faso, using bacterial strains obtained from previous studies. Results Diarrheagenic Escherichia coli (DEC) strains was identified using 16-plex Polymerase Chain Reaction (PCR), whereas antibiotic susceptibility was realized using the disk diffusion method. Furthermore, multiplex PCR assays were used to characterize bla KPC, bla VIM and bla IMP genes in carbapenemase-producing E . coli and Salmonella . The study highlighted high resistance rates of the identified bacteria to common antibiotics. Likewise, two strains of E . coli were imipenem resistant with Carbapenemase-encoding genes. The genes detected were Klebsiella pneumoniae carbapenemase (KPC), Verona integrin-encoded metallo-β-lactamase (VIM) and Imipenemase (IMP-2) reaching a rate of 40% each. However, no Carbapenemase-encoding genes were detected in Salmonella isolates. Conclusions This study showed that for a real-time infection control and prompt application of antimicrobial chemotherapy, characterization of carbapenemase-producing Enterobacteriaceae in patients is crucial.


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