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      Antimicrobial Resistance in Food Animals and the Environment in Nigeria: A Review

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          Abstract

          Antimicrobial resistance (AMR) has emerged as a global health threat, which has elicited a high-level political declaration at the United Nations General Assembly, 2016. In response, member countries agreed to pay greater attention to the surveillance and implementation of antimicrobial stewardship. The Nigeria Centre for Disease Control called for a review of AMR in Nigeria using a “One Health approach”. As anecdotal evidence suggests that food animal health and production rely heavily on antimicrobials, it becomes imperative to understand AMR trends in food animals and the environment. We reviewed previous studies to curate data and evaluate the contributions of food animals and the environment (2000–2016) to the AMR burden in Nigeria using a Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flowchart focused on three areas: Antimicrobial resistance, residues, and antiseptics studies. Only one of the 48 antimicrobial studies did not report multidrug resistance. At least 18 bacterial spp. were found to be resistant to various locally available antimicrobials. All 16 residue studies reported high levels of drug residues either in the form of prevalence or concentration above the recommended international limit. Fourteen different “resistotypes” were found in some commonly used antiseptics. High levels of residues and AMR were found in food animals destined for the human food chain. High levels of residues and antimicrobials discharged into environments sustain the AMR pool. These had evolved into potential public health challenges that need attention. These findings constitute public health threats for Nigeria’s teeming population and require attention.

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          Novel classes of antibiotics or more of the same?

          The world is running out of antibiotics. Between 1940 and 1962, more than 20 new classes of antibiotics were marketed. Since then, only two new classes have reached the market. Analogue development kept pace with the emergence of resistant bacteria until 10-20 years ago. Now, not enough analogues are reaching the market to stem the tide of antibiotic resistance, particularly among gram-negative bacteria. This review examines the existing systemic antibiotic pipeline in the public domain, and reveals that 27 compounds are in clinical development, of which two are new classes, both of which are in Phase I clinical trials. In view of the high attrition rate of drugs in early clinical development, particularly new classes and the current regulatory hurdles, it does not seem likely that new classes will be marketed soon. This paper suggests that, if the world is to return to a situation in which there are enough antibiotics to cope with the inevitable ongoing emergence of bacterial resistance, we need to recreate the prolific antibiotic discovery period between 1940 and 1962, which produced 20 classes that served the world well for 60 years. If another 20 classes and their analogues, particularly targeting gram-negatives could be produced soon, they might last us for the next 60 years. How can this be achieved? Only a huge effort by governments in the form of finance, legislation and providing industry with real incentives will reverse this. Industry needs to re-enter the market on a much larger scale, and academia should rebuild its antibiotic discovery infrastructure to support this effort. The alternative is Medicine without effective antibiotics. © 2011 The Authors. British Journal of Pharmacology © 2011 The British Pharmacological Society.
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            Pattern of antimicrobial usage in livestock animals in south-western Nigeria: The need for alternative plans

            Resistance to antibiotics has continued to increase, placing future animal and human disease management in real danger. The developing countries characterised by widespread indiscriminate antibiotic use and in which ‘third-generation’ antibiotics are not readily available or affordable are the worst affected. A 3-year (2010–2012) retrospective survey of antibiotic usage in livestock production in three selected states of south-western Nigeria was conducted. Data obtained from eight purposively selected licensed veterinary pharmaceutical sales establishments in the area, based on keeping detailed sales records for the study period, were analysed using Stata Version 12. Results showed that tetracyclines (33.6%), fluoroquinolones (26.5%) and beta-lactams/aminoglycosides (20.4%) constituted the majority of the antibiotics used over the 3 years. The differences in the quantities of antibiotic types used within each antimicrobial class were statistically significant for tetracyclines (F = 59.87; p < 0.0001) and fluoroquinolones (F = 43.97; p < 0.0001) but not for beta-lactams/aminoglycosides (F = 3.21; p = 0.148). Furthermore, antibiotic consumption increased by 40.4% between 2010 and 2012. Although statistically insignificant (F = 0.277; p = 0.762), the increasing trend across the years was at rates of 23.5% between 2010 and 2011 and 13.8% between 2011 and 2012. In addition, the findings show a significantly higher consumption rate (t = 15.21; df = 5; p < 0.0001) during the rainy (52.5%) than the dry (47.5%) seasons. The current increasing trend in antibiotic usage holds a serious danger for the future and therefore calls for alternative plans to safeguard future livestock production, food security and human health. This becomes more imperative considering emerging resistance against tetracyclines and fluoroquinolones, the foremost remedies for livestock diseases in most developing countries.
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              Antimicrobial susceptibility and serovars of Salmonella from chickens and humans in Ibadan, Nigeria.

              This study determines the prevalence and antibiotic resistance of Salmonella serovars from humans and chickens in Ibadan, Nigeria, in 2004-2007. A total of 991 blood samples were collected from patients in 2004 to 2005 and 641 fecal samples were collected from poultry farms in 2007. All Salmonella isolates were serotyped and tested for antimicrobial susceptibility. Thirty-nine (4%) Salmonella isolates were obtained from human blood and 70 (11%) from chicken fecal samples. The human isolates revealed nine different serovars; 82% were non-typhoidal Salmonella and 18% were (S. Typhi). The majority of serovars from humans were S. Enteritidis (33%), S. Dublin (18%), and S. Typhimurium (18%). Resistance to chloramphenicol, sulfamethoxazole, trimethoprim, and ampicillin ranged from 36% to 59% for the human isolates. Eight different serovars were obtained from chickens; S. Virchow (71%) predominated. A high frequency (87%) of reduced susceptibility to ciprofloxacin was observed among the chicken isolates. A high frequency of resistance to tetracycline (93%), nalidixic acid (81%), and sulfamethoxazole (87%) was observed. Rare serovars such as S. Apapa, S. Mouschaui, S. Jukestown, S. Oritamerin, and S. Onireke were isolated from both humans and chickens. Identical serovars were not found among human and chicken isolates. This study indicates that chickens are not a reservoir of Salmonella causing bacteraemia among humans in Ibadan, Nigeria. Studies locating the reservoirs responsible for invasive salmonellosis in humans are needed. Controls and targeted interventions against S. Virchow and the frequent occurrence of antimicrobial resistance in chickens should be initiated to prevent the spread of this serovar.
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                Author and article information

                Journal
                Int J Environ Res Public Health
                Int J Environ Res Public Health
                ijerph
                International Journal of Environmental Research and Public Health
                MDPI
                1661-7827
                1660-4601
                17 June 2018
                June 2018
                : 15
                : 6
                : 1284
                Affiliations
                [1 ]Department of Production Animal Studies (Epidemiology section), Faculty of Veterinary Science, Onderstepoort Campus 0110, University of Pretoria, 0110, South Africa
                [2 ]Public Health Agency, Ministry of Health, Riyadh, 11176, Saudi Arabia; oloungbo@ 123456yahoo.com
                [3 ]Department of Medicine, Infectious Diseases and Immunology Unit, University of Maiduguri, PMB 1069, Maiduguri 600230, Borno State, Nigeria; musagarbati@ 123456gmail.com
                [4 ]Department of Microbiology, Faculty of Life Sciences, Ahmadu Bello University, Zaria 810241, Nigeria; olonisteve@ 123456yahoo.com
                [5 ]Department of Veterinary Public Health and Preventive Medicine, University of Ibadan, Ibadan 200284, Nigeria; emmafisayo@ 123456yahoo.com
                [6 ]Veterinary Drugs/Animal Welfare Branch, Quality Assurance and Standards Division, Department of Veterinary & Pests Control Services, Federal Min. of Agric. & Rural Dev. F.C.D.A, Area 11, Garki, Abuja 900001, Nigeria; mabelaworh@ 123456yahoo.com
                [7 ]Center for Clinical Care and Clinical Research, Plot 784, By Glimor Engineering, Off Life camp, Gwarimpa Express Way, Jabi, Abuja 240102, Nigeria; hadamu@ 123456cccr-nigeria.org
                [8 ]Department of Veterinary Public Health and Preventive Medicine, Faculty of Veterinary Medicine, University of Ilorin, Ilorin 240272, Kwara State, Nigeria; odetokun.ia@ 123456unilorin.edu.ng
                [9 ]Emergency Centre for Transboundary Diseases (ECTAD-FAO), Food and Agricultural Organization of the United Nation, Dar es Salaam 0701072, Tanzania
                Author notes
                [* ]Correspondence: nurudeenoloso@ 123456gmail.com (N.O.O.); daydupe2003@ 123456yahoo.co.uk (F.O.F.); Tel.: +234-80-5525-4702 or +27-83-529-2326 (N.O.O.); +255-686-132-852 (F.O.F.)
                Author information
                https://orcid.org/0000-0001-9499-949X
                https://orcid.org/0000-0002-5171-1895
                https://orcid.org/0000-0003-3088-8752
                Article
                ijerph-15-01284
                10.3390/ijerph15061284
                6025306
                29914203
                7a9279c9-5db1-4e94-8b5c-a97ef907fbff
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 04 April 2018
                : 14 June 2018
                Categories
                Article

                Public health
                antimicrobial resistance,antibiotics residue,food animals,environment,bacteria,nigeria
                Public health
                antimicrobial resistance, antibiotics residue, food animals, environment, bacteria, nigeria

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