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      In vitro inactivation of Mycobacterium avium subsp. paratuberculosis (MAP) by use of copper ions

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          Abstract

          Background

          Mycobacterium avium subsp. paratuberculosis (MAP) is the causative agent of paratuberculosis, a contagious infectious disease that affects domestic and wild ruminants causing chronic inflammation of the intestine. MAP has proven to be very resistant to both physical and chemical processes, making it difficult to control this pathogen. Based on the recognized antimicrobial properties of copper, the objective of this study was to evaluate the effectiveness of copper ions to reduce MAP numbers and/or MAP viability in a fluid matrix. Besides, methicillin-resistant Staphylococcus aureus (MRSA), and Escherichia coli were used as controls of the effectiveness of copper ions. MAP-spiked PBS was subjected to copper ions treatment at 24 V for 5 min and the PBS suspensions were sampled before and after treatment. MAP viability and quantification were determined using three complementary techniques: a phage amplification assay, MGIT culture and qPCR.

          Results

          Moderate numbers (10 3 CFU ml −1) of the two control bacteria were completely eliminated by treatment with copper ions. For MAP, copper ions treatment reduced both the viability and numbers of this pathogen. Phage assay information quickly showed that copper ions (24 V for 5 min) resulted in a significant reduction in viable MAP. MGIT culture results over time showed statistically significant differences in time-to-detection (TTD) values between PRE and POST treatment. MAP genome equivalent estimates for PBS suspensions indicated that MAP numbers were lower in samples POST-treatment with copper ions than PRE-treatment.

          Conclusions

          The use of copper ions resulted in a significant reduction of MAP in a liquid matrix, although some MAP survival on some occasions was observed.

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          Most cited references28

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          Mycobacterium avium subsp. paratuberculosis in Veterinary Medicine.

          Mycobacterium avium subsp. paratuberculosis (basonym M. paratuberculosis) is the etiologic agent of a severe gastroenteritis in ruminants known as Johne's disease. Economic losses to the cattle industry in the United States are staggering, reaching $1.5 billion annually. A potential pathogenic role in humans in the etiology of Crohn's disease is under investigation. In this article, we review the epidemiology, pathogenesis, diagnostics, and disease control measures of this important veterinary pathogen. We emphasize molecular genetic aspects including the description of markers used for strain identification, diagnostics, and phylogenetic analysis. Recent important advances in the development of animal models and genetic systems to study M. paratuberculosis virulence determinants are also discussed. We conclude with proposals for the applications of these models and recombinant technology to the development of diagnostic, control, and therapeutic measures.
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            Bacterial killing by dry metallic copper surfaces.

            Metallic copper surfaces rapidly and efficiently kill bacteria. Cells exposed to copper surfaces accumulated large amounts of copper ions, and this copper uptake was faster from dry copper than from moist copper. Cells suffered extensive membrane damage within minutes of exposure to dry copper. Further, cells removed from copper showed loss of cell integrity. Acute contact with metallic copper surfaces did not result in increased mutation rates or DNA lesions. These findings are important first steps for revealing the molecular sensitive targets in cells lethally challenged by exposure to copper surfaces and provide a scientific explanation for the use of copper surfaces as antimicrobial agents for supporting public hygiene.
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              Potential use of copper surfaces to reduce survival of epidemic meticillin-resistant Staphylococcus aureus in the healthcare environment.

              Epidemic meticillin-resistant Staphylococcus aureus (EMRSA) emerged in the early 1980s with EMRSA-15 and -16 being the most prevalent strains within the UK. MRSA transmission between patients is largely via the hands of healthcare workers, and contamination of the hospital environment may occur. The objective of this study was to evaluate the effectiveness of copper and brass to reduce the viability of air-dried deposits of three MRSA strains [MRSA (NCTC 10442), EMRSA-1 (NCTC 11939) and EMRSA-16 (NCTC 13143)] compared with stainless steel. MRSA and EMRSA [10(7)colony-forming units (CFU)] were inoculated on to coupons (1 cm x 1 cm) of copper, brass or stainless steel and incubated at either 22 degrees C or 4 degrees C for various time periods. Viability was determined by resuspending removed CFUs and plating out on tryptone soy agar plates in addition to staining with the respiratory indicator fluorochrome 5-cyano-2,3-ditolyl tetrazolium. On pure copper surfaces, 10(7) MRSA, EMRSA-1 and EMRSA-16 were completely killed after 45, 60 and 90 min, respectively, at 22 degrees C. In contrast, viable organisms for all three strains were detected on stainless steel (grade 304) after 72 h at 22 degrees C. At 4 degrees C, complete kill was achieved on copper for all three strains within 6 h. The results demonstrate an antimicrobial effect of copper on MRSA, EMRSA-1 and -16 in contrast to stainless steel. Consequently, the contemporary application of stainless steel in hospital environments for work surfaces and door furniture is not recommended.
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                Author and article information

                Contributors
                pamelasteuer@gmail.com
                caro.avilez@hotmail.com
                carlostb81@gmail.com
                nicolas.goncid@gmail.com
                alfredoramirez@uach.cl
                fernando.ulloa.o@gmail.com
                arminmella@uach.cl
                i.grant@qub.ac.uk
                michael.t.collins@wisc.edu
                +56 63-2 444358 , miguelsalgado@uach.cl
                Journal
                BMC Microbiol
                BMC Microbiol
                BMC Microbiology
                BioMed Central (London )
                1471-2180
                1 November 2018
                1 November 2018
                2018
                : 18
                : 172
                Affiliations
                [1 ]ISNI 0000 0004 0487 459X, GRID grid.7119.e, Instituto de Medicina Preventiva Veterinaria, Facultad de Ciencias Veterinarias, , Universidad Austral de Chile, ; Saelzer Building 5° Floor, Campus Isla Teja, PO Box 567, Valdivia, Chile
                [2 ]ISNI 0000 0004 0487 459X, GRID grid.7119.e, Instituto de Ciencia Animal, , Universidad Austral de Chile, ; Valdivia, Chile
                [3 ]ISNI 0000 0004 0487 459X, GRID grid.7119.e, Escuela de Graduados, Facultad de Ciencias Veterinarias, , Universidad Austral de Chile, ; Valdivia, Chile
                [4 ]ISNI 0000 0004 0487 459X, GRID grid.7119.e, Instituto de Bioquímica y Microbiología, , Universidad Austral de Chile, ; Valdivia, Chile
                [5 ]ISNI 0000 0004 0374 7521, GRID grid.4777.3, Institute for Global Food Security, School of Biological Sciences, , Queen’s University Belfast, ; Belfast, Northern Ireland UK
                [6 ]ISNI 0000 0001 0701 8607, GRID grid.28803.31, Department of Pathobiological Sciences, School of Veterinary Medicine, , University of Wisconsin, ; Madison, USA
                Author information
                http://orcid.org/0000-0002-2144-7982
                Article
                1313
                10.1186/s12866-018-1313-6
                6211491
                30382823
                fa767859-27f6-4e8e-8812-c40d11001cdd
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 21 February 2018
                : 11 October 2018
                Funding
                Funded by: FONDECYT
                Award ID: 1161633
                Funded by: CONICYT
                Award ID: beca doctorado nacional
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Microbiology & Virology
                mycobacterium avium subsp. paratuberculosis,copper ions,phosphate buffered saline,mgit culture,phage amplification assay

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