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      Salmonellosis detection and evidence of antibiotic resistance in an urban raccoon population in a highly populated area, Costa Rica

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          Abstract

          Wild animals are involved in zoonotic disease transmission cycles. These are generally complex and poorly understood, especially among animals adapted to life in human ecosystems. Raccoons are reservoirs and effective carriers for infectious agents such as Salmonella throughout different environments and contribute to the transference of resistance genes. This study examined the presence of circulating Salmonella sp. in a population of raccoons in a tropical urban environment and evaluated resistance to antibiotics commonly used to treat salmonellosis. A total of 97 raccoons of different ages and sex were included in this study. 49% (38–60 CI) of the faecal samples were positive for Salmonella spp. The study identified 15 circulating serovars with the most prevalent being S. Hartford (7/15), S. Typhimurium (4/15) and S. Bovismorbificans (4/15). These serovars correspond to the serovars detected in humans with clinical symptoms in Costa Rica. 9.5% of the Salmonella strains recovered demonstrated ciprofloxacin resistance, and 7.1% showed resistance to nalidixic acid. This study provides evidence of multiple Salmonella serovars circulating in a population of urban raccoons in Costa Rica. Furthermore, the study confirms the existence of antimicrobial resistance to two antibiotics used to treat human salmonellosis. The findings emphasize the role of the raccoon as a reservoir of Salmonella in the Greater Metropolitan Area of Costa Rica (GAM) and stress the need for active monitoring of the presence and possible spread in antibiotic resistance due to this peri‐domestic carnivore.

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          Mechanism of Quinolone Action and Resistance

          Quinolones are one of the most commonly prescribed classes of antibacterials in the world and are used to treat a variety of bacterial infections in humans. Because of the wide use (and overuse) of these drugs, the number of quinolone-resistant bacterial strains has been growing steadily since the 1990s. As is the case with other antibacterial agents, the rise in quinolone resistance threatens the clinical utility of this important drug class. Quinolones act by converting their targets, gyrase and topoisomerase IV, into toxic enzymes that fragment the bacterial chromosome. This review describes the development of the quinolones as antibacterials, the structure and function of gyrase and topoisomerase IV, and the mechanistic basis for quinolone action against their enzyme targets. It will then discuss the following three mechanisms that decrease the sensitivity of bacterial cells to quinolones. Target-mediated resistance is the most common and clinically significant form of resistance. It is caused by specific mutations in gyrase and topoisomerase IV that weaken interactions between quinolones and these enzymes. Plasmid-mediated resistance results from extrachromosomal elements that encode proteins that disrupt quinolone–enzyme interactions, alter drug metabolism, or increase quinolone efflux. Chromosome-mediated resistance results from the underexpression of porins or the overexpression of cellular efflux pumps, both of which decrease cellular concentrations of quinolones. Finally, this review will discuss recent advancements in our understanding of how quinolones interact with gyrase and topoisomerase IV and how mutations in these enzymes cause resistance. These last findings suggest approaches to designing new drugs that display improved activity against resistant strains.
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            Identifying Reservoirs of Infection: A Conceptual and Practical Challenge

            (2002)
            Many infectious agents, especially those that cause emerging diseases, infect more than one host species. Managing reservoirs of multihost pathogens often plays a crucial role in effective disease control. However, reservoirs remain variously and loosely defined. We propose that reservoirs can only be understood with reference to defined target populations. Therefore, we define a reservoir as one or more epidemiologically connected populations or environments in which the pathogen can be permanently maintained and from which infection is transmitted to the defined target population. Existence of a reservoir is confirmed when infection within the target population cannot be sustained after all transmission between target and nontarget populations has been eliminated. When disease can be controlled solely by interventions within target populations, little knowledge of potentially complex reservoir infection dynamics is necessary for effective control. We discuss the practical value of different approaches that may be used to identify reservoirs in the field.
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              Urbanization and the ecology of wildlife diseases

              Urbanization is intensifying worldwide, with two-thirds of the human population expected to reside in cities within 30 years. The role of cities in human infectious disease is well established, but less is known about how urban landscapes influence wildlife–pathogen interactions. Here, we draw on recent advances in wildlife epidemiology to consider how environmental changes linked with urbanization can alter the biology of hosts, pathogens and vectors. Although urbanization reduces the abundance of many wildlife parasites, transmission can, in some cases, increase among urban-adapted hosts, with effects on rarer wildlife or those living beyond city limits. Continued rapid urbanization, together with risks posed by multi-host pathogens for humans and vulnerable wildlife populations, emphasize the need for future research on wildlife diseases in urban landscapes.
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                Author and article information

                Contributors
                mario.baldi.salas@una.ac.cr
                Journal
                Zoonoses Public Health
                Zoonoses Public Health
                10.1111/(ISSN)1863-2378
                ZPH
                Zoonoses and Public Health
                John Wiley and Sons Inc. (Hoboken )
                1863-1959
                1863-2378
                29 July 2019
                November 2019
                : 66
                : 7 ( doiID: 10.1111/zph.v66.7 )
                : 852-860
                Affiliations
                [ 1 ] Research Institute of Wildlife Ecology University of Veterinary Medicine Vienna Austria
                [ 2 ] Tropical Diseases Research Program, School of Veterinary Medicine National University Heredia Costa Rica
                [ 3 ] Institute of Veterinary Public Health University of Veterinary, Medicine Vienna Austria
                [ 4 ] National Animal Health Service (SENASA) Ministry of Agriculture and Livestock (MAG) Heredia Costa Rica
                [ 5 ] Wildlife Conservation Society Wildlife Health Program Bronx NY USA
                Author notes
                [*] [* ] Correspondence

                Mario Baldi, Research Institute of Wildlife Ecology, University of Veterinary Medicine, Vienna, Austria.

                Email: mario.baldi.salas@ 123456una.ac.cr

                Author information
                https://orcid.org/0000-0001-6109-4993
                https://orcid.org/0000-0003-4428-3340
                Article
                ZPH12635
                10.1111/zph.12635
                6852039
                31359623
                05db90e8-174c-445f-8b56-fc16d8fdfe96
                © 2019 The Authors. Zoonoses and Public Health published by Blackwell Verlag GmbH.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 09 January 2019
                : 20 May 2019
                : 30 June 2019
                Page count
                Figures: 1, Tables: 3, Pages: 9, Words: 6605
                Funding
                Funded by: Fondo Institucional de Desarrollo Académico‐2013‐Universidad Nacional‐Universidad de Costa Rica, Fondo del Sistema‐Consejo Nacional de Rectores
                Award ID: ACUERDO-VI-167-2013
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                November 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.1 mode:remove_FC converted:13.11.2019

                antibiotic resistance,procyon lotor,public health,salmonella sp,zoonosis

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