Refine your search
Collections
Co-Authors
Journals
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Thakur, Sidharath Dev
- Rational Use of Antimicrobials in Animal Production:A Prerequisite to Stem the Tide of Antimicrobial Resistance
Abstract Views :259 |
PDF Views:66
Authors
Affiliations
1 Department of Veterinary Public Health and Epidemiology, Dr G. C. Negi College of Veterinary and Animal Sciences, Chaudhary Sarwan Kumar Himachal Pradesh Krishi Vishvavidyalaya, Palampur 176 062, IN
1 Department of Veterinary Public Health and Epidemiology, Dr G. C. Negi College of Veterinary and Animal Sciences, Chaudhary Sarwan Kumar Himachal Pradesh Krishi Vishvavidyalaya, Palampur 176 062, IN
Source
Current Science, Vol 113, No 10 (2017), Pagination: 1846-1857Abstract
Antimicrobial resistance (AMR) is a worldwide ‘One Health’ problem. The spread of AMR has limited the treatment options against infectious diseases. Inappropriate use of antimicrobials, is a major contributor for the development of AMR and its spread. In animal husbandry, antimicrobials are used for treating infectious diseases and in sub-therapeutic concentrations for growth promotion and disease prophylaxis. The use of antimicrobials in sub-therapeutic concentrations exerts selective pressure on bacteria and results in the emergence of bacterial strains resistant to one or more antimicrobials. The food animals raised on sub-optimal doses of antibiotics become reservoirs of resistant bacterial strains, transmitted subsequently to man and the environment. Various human, animal and environmental health agencies have decided to jointly address this problem. Establishment of integrated and harmonized AMR surveillance programmes, reduced use of antimicrobials in animal production, good governance of veterinary services, and development of new antimicrobials and their alternatives are some of the AMR management strategies in animals. Antibiotics are indispensable for human health; however, they should be totally banned in the food animals to preserve effectiveness of these drugs. In India, use of antimicrobials in food animals is limited for disease prophylaxis and growth promotion. However, absence of uniform regulations on the use of antimicrobials in animal production threatens the rationale use of these drugs in livestock.Keywords
Antibiotics, Food Animals, Growth Promoters, Surveillance, Veterinary Governance.References
- Organisation for Economic Co-operation and Development, Antimicrobial resistance–policy insights. 2016; https://www.oecd.org/health/health-systems/AMR-Policy-Insights-November2016. pdf (accessed on 11 April 2017).
- WHO, Antimicrobial resistance: global report on surveillance. World Health Organization, Geneva, Switzerland, 2014.
- da Costa, P. M., Loureiro, L. and Matos, A. J., Transfer of multidrug resistant bacteria between intermingled ecological niches: the interface between humans, animals and the environment. Int. J. Environ. Res. Public Health, 2013, 10, 278–294.
- WHO, Global action plan on antimicrobial resistance. World Health Organization, Geneva, Switzerland, 2015; http://www.wpro.who.int/entity/drug_resistance/resources/global_action_plan_eng.pdf (accessed on 11 April 2017).
- Food and Agriculture Organisation, World Organization for Animal Health and World Health Organization, High-level technical meeting to address health risks at the human–animal ecosystems interfaces. WHO Press, World Health Organization, Geneva, Switzerland, 2012; http://www.fao.org/docrep/017/i3119e/i3119e.pdf (accessed on 16 April 2017).
- CDDEP, State of the world’s antibiotics. Center for Disease Dynamics, Economics and Policy, Washington, DC, USA, 2015; https://cddep.org/sites/default/files/swa_2015_final.pdf (accessed on 11 April 2017).
- Angulo, F., Nargund, V. and Chiller, T., An evidence of an association between use of anti-microbial agents in food animals and anti-microbial resistance among bacteria isolated from humans and the human health consequences of such resistance. J. Vet. Med., 2004, 51, 374–379.
- Marshall, B. M. and Levy, S., Food animals and antimicrobials: impacts on human health. Clin. Microbiol. Rev., 2011, 24, 718–733.
- Price, L. B., Graham, J. P., Lackey, L. G., Roess, A., Vailes, R. and Silbergeld, E., Elevated risk of carrying gentamicin resistant Escherichia coli among U.S. poultry workers. Environ. Health Perspect., 2007, 115, 1738–1742.
- Zhang, X. Y., Ding, L. J. and Yue, J., Occurrence and characteristics of class 1 and class 2 integrons in resistant Escherichia coli isolates from animals and farm workers in Northeastern China. Microb. Drug Resist., 2009, 15, 223–228.
- Molbak, K., Human health consequences of antimicrobial drug-resistant Salmonella and other foodborne pathogens. Clin. Infect. Dis., 2005, 41, 1613–1620.
- Streit, J. M., Jones, R. N., Toleman, M. A., Stratchounski, L. S. and Fritsche, T. R., Prevalence and antimicrobial susceptibility patterns among gastroenteritis-causing pathogens recovered in Europe and Latin America and Salmonella isolates recovered from bloodstream infections in North America and Latin America: report from the SENTRY antimicrobial surveillance program (2003). Int. J. Antimicrob., 2006, 27, 367–375.
- Verraes, C. et al., Antimicrobial resistance in the food chain: a review. Int. J. Environ. Res. Public Health, 2013, 10, 2643–2669.
- Dutil, L. et al., Ceftiofur resistance in Salmonella enterica serovar Heidelberg from chicken meat and humans, Canada. Emerg. Infect. Dis., 2010, 16, 48–54.
- Daghrir, R. and Drogui, P., Tetracycline antibiotics in the environment: a review. Environ. Chem. Lett., 2013, 11, 209–227.
- Memish, Z., Venkatesh, S. and Shibl, A., Impact of travel on international spread of antimicrobial resistance. Int. J. Antimicrob., 2003, 21, 135–142.
- D’Costa, V. M. et al., Antibiotic resistance is ancient. Nature, 2011, 477, 457–461.
- Andersson, D. I. and Hughes, D., Evolution of antibiotic resistance at non-lethal drug concentrations. Drug Resist. Updates 2012, 15, 162–172.
- Martínez, J. L., Bottlenecks in the transferability of antibiotic resistance from natural ecosystems to human bacterial pathogens. Front. Microbiol., 2012, 2, 265.
- Finley, R. L. et al., The scourge of antibiotic resistance: the important role of the environment. Clin. Infect. Dis., 2013, 57, 704–710.
- Gibbons, A., Resistance to antibiotics found in isolated Amazonian tribe. Science, 2015, doi:10.1126/science.aab2509; http://www.sciencemag.org/news/2015/04/resistance-antibiotics-found-isolated-amazonian-tribe (accessed on 20 April 2017).
- Davies, J. E., Origins, acquisition and dissemination of antibiotic resistance determinants. Ciba Found. Symp., 1997, 207, 15–27.
- D’Costa, V. M., Mcgrann, K. M., Hughes, D. W. and Wright, G. D., Sampling the antibiotic resistome. Science, 2006, 311, 374–377.
- Aminov, R. I., The role of antibiotics and antibiotic resistance in nature. Environ. Microbiol., 2009, 11, 2970–2988.
- Poirel, L., Rodriguez-Martinez, J. M., Mammeri, H., Liard, A. and Nordmann, P., Origin of plasmid-mediated quinolone resistance determinant QnrA. Antimicrob. Agents Chemother., 2005, 49, 3523–3525.
- Wright, G. D., Antibiotic resistance in the environment: a link to the clinic? Curr. Opin. Microbiol., 2010, 13, 589–594.
- Livermore, D., Bacterial resistance: origins, epidemiology, and impact. Clin. Infect. Dis. (Suppl 1), 2003, 36, S11–S23.
- Jayaraman, R., Bacterial persistence: some new insights into an old phenomenon. J. Biosci., 2008, 33, 795–805.
- Jayaraman, R., Antibiotic resistance: an overview of mechanisms and a paradigm shift. Curr. Sci., 2009, 96, 1475–1484.
- Nikaido, H., Multidrug resistance in bacteria. Annu. Rev. Biochem., 2009, 78, 119–146.
- Bennett, P. M., Plasmid encoded antibiotic resistance: acquisition and transfer of antibiotic resistance genes in bacteria. Br. J. Pharmacol. (Suppl. 1), 2008, 153, S347–S357.
- Mao, E. F., Lane, L., Lee, J. and Miller, J. H., Proliferation of mutators in a cell population. J. Bacteriol., 1997, 179, 417–422.
- Blake, D. P., Hilman, K., Fenlon, D. R. and Low, J. C., Transfer of antibiotic resistance between commensal and pathogenic members of the Enterobacteriaceae under ileal conditions. J. Appl. Microbiol., 2003, 95, 428–436.
- Leverstein-van Hall, M. A. et al., Dutch patients, retail chicken meat and poultry share the same ESBL genes, plasmids and strains. Clin. Microbiol. Infect., 2011, 17, 873–880.
- CDDEP, Antibiotic use and resistance in food animals. Current policy and recommendations. Center for Disease Dynamics, Economics and Policy, Washington, DC, USA, 2016; https://cddep.org/sites/default/files/india_abx_report.pdf (accessed on 11 April 2017).
- Jukes, T. H., Stokstad, E. L. R., Taylor, R. R., Cunha, T. J., Edwards, H. M. and Meadows, G. B., Growth promoting effect of aureomycin on pigs. Arch. Biochem., 1950, 26, 324–325.
- Aarestrup, F., Sustainable farming: Get pigs off antibiotics. Nature, 2012, 486, 465–466.
- Van Boeckel, T. P. et al., Global trends in antimicrobial use in food animals. Proc. Natl. Acad. Sci. USA, 2015, 112, 5649–5654.
- Teillant, A., Costs and benefits of antimicrobial use in livestock. AMR Control, 2015, 116–122; http://www.globalhealthdynamics.co.uk/wp-content/uploads/2015/05/19_Aude-Teillant.pdf (accessed on 18 April 2017).
- Silbergeld, E. K., Graham, J. and Price, L. B., Industrial food animal production, antimicrobial resistance, and human health. Annu. Rev. Public Health, 2008, 29, 151–169.
- Maron, D. F., Smith, T. J. and Nachman, K. E., Restrictions on antimicrobial use in food animal production: an international regulatory and economic survey. Global Health, 2013, 9, 48.
- WHO, Antimicrobial use in aquaculture and antimicrobial resistance. Report of a joint FAO/OIE/WHO expert consultation on antimicrobial use in aquaculture and antimicrobial resistance. World Health Organization, Geneva, Switzerland, 2006; http://www.who.int/topics/foodborne_diseases/aquaculture_rep_13_16june2006%20.pdf (accessed on 23 April 2017).
- Le, T. X., Munekage, Y. and Kato, S., Antibiotic resistance in bacteria from shrimp farming in mangrove areas. Sci. Total Environ., 2005, 349, 95–105.
- Cabello, F. C., Heavy use of prophylactic antibiotics in aquaculture: a growing problem for human and animal health and for the environment. Environ. Microbiol., 2006, 8, 1137–1144.
- Chantziaras, I., Boyen, F., Callens, B. and Dewulf, J., Correlation between veterinary antimicrobial use and antimicrobial resistance in food-producing animals: a report on seven countries. J. Antimicrob. Chemother., 2014, 69, 827–834.
- Elliott, K., Antibiotics on the farm: agriculture’s role in drug resistance. Policy Paper 059, Center for Global Development, Washington DC, USA 2015; https://www.cgdev.org/sites/default/files/CGD-Policy-Paper-59-Elliott-Antibiotics-Farm-Agriculture-Drug-Resistance.pdf (accessed on 20 April 2017).
- Frana, T. S. et al., Isolation and characterization of methicillinresistant Staphylococcus aureus from pork farms and visiting veterinary students. PLoS ONE, 2013, 8, e53738.
- Rinsky, J. L. et al., Livestock-associated methicillin and multidrug resistant Staphylococcus aureus is present among industrial, not antibiotic-free livestock operation workers in North Carolina. PLoS ONE, 2013, 8, e67641.
- Liu, Y. Y. et al., Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: a microbiological and molecular biological study. Lancet Infect. Dis., 2016, 16, 161–168.
- Price, L. B. et al., Staphylococcus aureus CC398: host adaptation and emergence of methicillin resistance in livestock. MBio, 2012, 3, pii, e00305–e00311.
- Diarra, M. S. et al., Impact of feed supplementation with antimicrobial agents on growth performance of broiler chickens, Clostridium perfringens and Enterococcus counts, and antibiotic resistance phenotypes and distribution of antimicrobial resistance determinants in Escherichia coli isolates. Appl. Environ. Microbiol., 2007, 73, 6566–6576.
- Halling-Sørensen, B., Nors Nielsen, S., Lanzky, P. F., Ingerslev, F., Holten Lutzhøft, H. C. and Jørgensen, S. E., Occurrence, fate and effects of pharmaceutical substances in the environment – a review. Chemosphere, 1998, 36, 357–393.
- Sarmah, A. K., Meyer, M. T. and Boxall, A. B., A global perspective on the use, sales, exposure pathways, occurrence, fate and effects of veterinary antibiotics (VAs) in the environment. Chemosphere, 2006, 65, 725–759.
- Lindberg, R., Wennberg, P., Johansson, M., Tysklind, M. and Andersson, B., Screening of human antibiotic substances and determination of weekly mass flows in five sewage treatment plants in Sweden. Environ. Sci. Technol., 2005, 39, 3421–3429.
- Wang, L., Oda, Y., Grewal, S., Morrison, M., Michel Jr, F. and Yu, Z., Persistence of resistance to erythromycin and tetracycline in swine manure during simulated composting and lagoon treatments. Microb. Ecol., 2012, 63, 32–40.
- Chagas, T., Seki, L., Cury, J., Oliveira, J., Dávila, A., Silva, D. and Asensi, M., Multi-resistance -lactamase-encoding genes and bacterial diversity in hospital wastewater in Rio de Janeiro, Brazil. J. Appl. Microbiol., 2011, 111, 572–581.
- Roe, M., Veja, E. and Pillai, S., Antimicrobial resistance markers of class 1 and class 2 integron-bearing Escherichia coli from irrigation water and sediments. Emerg. Infect. Dis., 2003, 9, 822–826.
- Johnston, L. and Jaykus, L., Antimicrobial resistance of Enterococcus species isolated from produce. Appl. Environ. Microbiol., 2004, 70, 3133–3137.
- Meena, V. D., Dotaniya, M. L., Saha, J. K. and Patra, A. K., Antibiotics and antibiotic resistant bacteria in wastewater: impact on environment, soil microbial activity and human health. Afr. J. Microbiol. Res., 2015, 9, 965–997.
- Gilbert, P. and McBain, A. J., Potential impact of increased use of biocides in consumer products on prevalence of antibiotic resistance. Clin. Microbiol. Rev., 2003, 16, 189–208.
- Buffet-Bataillon, S., Branger, B., Cormier, M., Bonnaure-Mallet, M. and Jolivet-Gougeon, A., Effect of higher minimum inhibitory concentrations of quaternary ammonium compounds in clinical E. coli isolates on antibiotic susceptibilities. J. Hosp. Infect., 2011, 79, 141–146.
- Whitehead, R. N., Overton, T. W., Kemp, C. L. and Webber, M. A., Exposure of Salmonella enterica serovar Typhimurium to high level biocide challenge can select multidrug resistant mutants in a single step. PLoS ONE, 2011, 6, e22833:1–e22833:9.
- Kakkar, M. and Rogawski, L., Antibiotic use and residues in chicken meat and milk samples from Karnataka and Punjab, India: research scheme. Public Health Foundation, New Delhi, 2013, vol. 34.
- Kalambhe, D. G., Zade, N. N., Chaudhari, S. P., Shinde, S. V., Khan, W. and Patil, A. R., Isolation, antibiogram and pathogenicity of Salmonella spp. recovered from slaughtered food animals in Nagpur region of Central India. Vet. World, 2016, 9, 176–181.
- Preethirani, P. L. et al., Isolation, biochemical and molecular identification, and in vitro antimicrobial resistance patterns of bacteria isolated from bubaline subclinical mastitis in South India. PLoS ONE, 2015, 10, e0142717.
- Kar, D. et al., Molecular and phylogenetic characterization of multidrug resistant extended spectrum beta-lactamase producing Escherichia coli isolated from poultry and cattle in Odisha, India. Infect. Genet. Evol., 2015, 29, 82–90.
- Rasheed, M. U., Thajuddin, N., Ahamed, P., Teklemariam, Z. and Jamil, K., Antimicrobial drug resistance in strains of Escherichia coli isolated from food sources. Rev. Inst. Med. Trop. Sao Paulo, 2014, 56, 341–346.
- Wani, S. A., Hussain, I., Beg, S. A., Rather, M. A., Kabli, Z. A., Mir, M. A. and Nishikawa, Y., Diarrhoeagenic Escherichia coli and salmonellae in calves and lambs in Kashmir absence, prevalence and antibiogram. Rev. Sci. Technol., 2013, 32, 833–840.
- Ghatak, S. et al., Detection of New Delhi metallo-beta-lactamase and extended-spectrum beta-lactamase genes in Escherichia coli isolated from mastitic milk samples. Transbound. Emerg. Dis., 2013, 60, 385–389.
- Kumar, A., Verma, A. K., Sharma, A. K. and Rahal, A., Isolation and antibiotic sensitivity of Streptococcus pneumoniae infections with involvement of multiple organs in lambs. Pak. J. Biol. Sci., 2013, 16, 2021–2025.
- Mahanti, A. et al., Isolation, molecular characterization and antibiotic resistance of Shiga Toxin-Producing Escherichia coli (STEC) from buffalo in India. Lett. Appl. Microbiol., 2013, 56, 291–298.
- Bhatt, V. D. et al., Milk microbiome signatures of subclinical mastitis-affected cattle analysed by shotgun sequencing. J. Appl. Microbiol., 2012, 112, 639–650.
- Kumar, R., Yadav, B. R. and Singh, R. S., Antibiotic resistance and pathogenicity factors in Staphylococcus aureus isolated from mastitic Sahiwal cattle. J. Biosci., 2011, 36, 175–188.
- Kumar, R., Yadav, B. R., Anand, S. K. and Singh, R. S., Molecular surveillance of putative virulence factors and antibiotic resistance in Staphylococcus aureus isolates recovered from intramammary infections of river buffaloes. Microb. Pathog., 2011, 51, 31–38.
- Singh, B. R., Agarwal, M., Chandra, M., Verma, M., Sharma, G., Verma, J. C. and Singh, V. P., Plasmid profile and drug resistance pattern of zoonotic Salmonella isolates from Indian buffaloes. J. Infect. Dev. Ctries., 2010, 4, 477–483.
- Kumar, R., Yadav, B. R. and Singh, R. S., Genetic determinants of antibiotic resistance in Staphylococcus aureus isolates from milk of mastitic crossbred cattle. Curr. Microbiol., 2010, 60, 379–386.
- Kumar, P., Singh, V. P., Agrawal, R. K. and Singh, S., Identification of Pasteurella multocida isolates of ruminant origin using polymerase chain reaction and their antibiogram study. Trop. Anim. Health Prod., 2009, 41, 573–578.
- Dhanarani, T. S., Shankar, C., Park, J., Dexilin, M., Kumar, R. R. and Thamaraiselvi, K., Study on acquisition of bacterial antibiotic resistance determinants in poultry litter. Poult. Sci., 2009, 88, 1381–1387.
- Das, A., Saha, D. and Pal, J., Antimicrobial resistance and in vitro gene transfer in bacteria isolated from the ulcers of EUS-affected fish in India. Lett. Appl. Microbiol., 2009, 49, 497–502.
- Kumar, R., Surendran, P. K. and Thampuran, N., Analysis of antimicrobial resistance and plasmid profiles in Salmonella serovars associated with tropical seafood of India. Foodborne Pathog. Dis., 2009, 6, 621–625.
- Shahid, M., Sobia, F., Singh, A. and Khan, H. M., Concurrent occurrence of bla ampC families and bla CTX-M genogroups and association with mobile genetic elements ISEcp1, IS26, ISCR1, and sul1-type class 1 integrons in Escherichia coli and Klebsiella pneumoniae isolates originating from India. J. Clin. Microbiol., 2012, 50, 1779–1782.
- Arya, G., Roy, A., Choudhary, V., Yadav, M. M. and Joshi, C. G., Serogroups, atypical biochemical characters, colicinogeny and antibiotic resistance pattern of Shiga toxin-producing Escherichia coli isolated from diarrhoeic calves in Gujarat, India. Zoonoses Public Health, 2008, 55, 89–98.
- Tiwari, J. G. and Tiwari, H. K., Staphylococcal zoonosis on dairy farms in Assam and Meghalaya. Indian J. Public Health, 2007, 51, 97–100.
- CSE, Factsheet 03: use of antibiotics in animals. Center for Science and Environment, New Delhi, 2014.
- Global Antibiotic Resistance Partnership-India National Working Group. 2011. Situation analysis. Antibiotic Use and Resistance in India, 2011; http://www.cddep.org/sites/default/files/india-report-web_ 8.pdf (accessed on 12 April 2017).
- Chennai Declaration Team, Chennai Declaration: 5-year plan to tackle the challenge of anti-microbial resistance. Indian J. Med. Microbiol., 2014, 32, 221–228.
- Ganguly, N. K. et al., Rationalizing antibiotic use to limit antibiotic resistance in India. Indian J. Med. Res., 2011, 134, 281–294.
- WHO, Report on the consultative meeting on antimicrobial resistance for countries in the Eastern Mediterranean Region: from policies to action. World Health Organization, Regional Office for the Eastern Mediterranean, Cairo, Egypt, 2014; http://applications.emro.who.int/docs/IC_Meet_Rep_2014_EN_ 15210.pdf (accessed on 16 April 2017).
- Aarestrup, F. M., Wegener, H. C. and Collignon, P., Resistance in bacteria of the food chain: epidemiology and control strategies. Expert Rev. Anti-Infect. Ther., 2008, 6, 733–750.
- Adley, C. C., Dowling, A., Handschuh, H. and Ryan, M. P., Emerging policies on antimicrobial resistance, the consumption of antimicrobial agents and occurrence of antimicrobial resistance in bacteria from humans and food producing animals. In The Battle Against Microbial Pathogens: Basic Science, Technological Advances and Educational Programs (ed. Méndez-Vilas, A.), Formatex Research Centre, Badajoz, Spain, 2015, pp. 913–922.
- World Organization for Animal Health, Terrestrial Animal Health Code, 24th edn, World Organisation for Animal Health Paris, France, 2015; http://www.rr-africa.oie.int/docspdf/en/Codes/en_csat-vol1.pdf (accessed on 18 April 2016).
- World Organization for Animal Health, Aquatic Animal Health Code. World Organisation for Animal Health, Paris, France, 2015; http://www.oie.int/international-standard-setting/aquatic-code/ access-online/ (accessed on 18 April 2016).
- World Organization for Animal Health, OIE list of antimicrobial agents of veterinary importance, World Organisation for Animal Health Paris, France, 2015; http://www.oie.int/fileadmin/Home/eng/Our_scientific_expertise/docs/pdf/Eng_OIE_List_antimicrobials_ May2015.pdf (accessed on 10 April 2016).
- World Organization for Animal Health, Antimicrobial resistance standards, recommendations and work of the World Organisation for Animal Health (OIE). World Organisation for Animal Health Paris, France, 2015; (http://www.oie.int/fileadmin/Home/eng/Media_Center/docs/foll-AMR-Chatham-v19115-sansphrase_Final. pdf (accessed on 14 April 2017).
- Codex Alimentarius Commission, Maximum residue limits for veterinary drugs in foods, 2015; http://www.codexalimentarius.org/standards/veterinary-drugs-mrls/en/ (accessed on 20 April 2016).
- WHO, The WHO Advisory Group on Integrated Surveillance of Antimicrobial Resistance (WHO-AGISAR), World Health Organization, Geneva, Switzerland, 2013; http://apps.who.int/iris/bitstream/10665/91778/1/9789241506311_eng.pdf (accessed on 20 April 2017).
- WHO, Critically important antimicrobials for human drug. World Health Organization, Geneva, Switzerland, 2011; http://www.who.int/topics/foodborne_diseases/aquaculture_rep_13_16june2006%20.pdf (accessed on 13 April 2017).
- Pagel, S. W. and Gautier, P., Use of antimicrobial agents in livestock. Rev. Sci. Technol., 2012, 31, 145–188.
- Anon., Part XVIII. Antibiotic and other pharmacologically active substances, The Prevention of Food Adulteration Act & Rules, 2004; http://dbtbiosafety.nic.in/act/PFA%20Acts%20and%20Rules. pdf (accessed on 16 April 2017).
- World Organization for Animal Health, Antimicrobial resistance. Fact sheets, 2015; http://www.oie.int/fileadmin/Home/eng/Media_Center/docs/pdf/Fact_sheets/ANTIBIO_EN.pdf (accessed on 16 April 2017).
- Bengtsson, B. and Wierup, M., Antimicrobial resistance in Scandinavia after ban of antimicrobial growth promoters. Anim. Biotechnol., 2006, 17, 147–156.
- Grave, K., Jensen, V. F., Odensvik, K., Wierup, M. and Bangen, M., Usage of veterinary therapeutic antimicrobials in Denmark, Norway and Sweden following termination of antimicrobial growth promoter use. Prev. Vet. Med., 2006, 75, 123–132.
- Cogliani, C., Goossens, H. and Greko, C., Restricting antimicrobial use in food animals: lessons from Europe. Microbes, 2011, 6, 274–279.
- Dritz, S. S., Tokach, M. D., Goodband, R. D. and Nelssen, J. L., Effects of administration of antimicrobials in feed on growth rate and feed efficiency of pigs in multisite production systems. J. Am. Vet. Med. Assoc., 2002, 220, 1690–1695.
- Graham, J. P., Boland, J. J. and Silbergeld, E., Growth promoting antimicrobials in food animal production: an economic analysis. Public Health Rep., 2007, 122, 79–87.
- Wierup, M., The Swedish experience of the 1986 year ban of antimicrobial growth promoters, with special reference to animal health, disease prevention, productivity, and usage of antimicrobials. Microb. Drug Resist., 2001, 7, 183–190.
- MacDonald, J. M. and Wang, S. L., Foregoing sub-therapeutic antimicrobials: the impact on broiler grow-out operations. Appl. Econ. Perspect. Policy, 2011, 33, 79–98.
- Key, N. and McBride, W.D., Sub-therapeutic antimicrobials and the efficiency of US hog farms. Am. J. Agric. Econ., 2014, 96, 831–850.
- Wright, G. D. and Sutherland, A. D., New strategies for combating multidrug-resistant bacteria. Trends Mol. Med., 2007, 13, 260–267.
- Baltz, R. H., Antibiotic discovery from actinomycetes: will a renaisssance follow the decline and fall? SIM News, 2005, 55, 186–196.
- Genilloud, O., The re-emerging role of microbial natural products in antibiotic discovery. Antonie Van Leeuwenhoek, 2014, 106, 173–188.
- Yi, H. Y., Chowdhury, M., Huang, Y. D. and Yu, X. Q., Insect antimicrobial peptides and their applications. Appl. Microbiol. Biotechnol., 2014, 98, 5807–5822.
- Singh, R. P., Kumari, P. and Reddy, C. R. Antimicrobial compounds from seaweeds-associated bacteria and fungi. Appl. Microbiol. Biotechnol., 2015, 99, 1571–1586.
- Borges, A., Saavedra, M. J. and Simões, M., Insights on antimicrobial resistance, biofilms and the use of phytochemicals as new antimicrobial agents. Curr. Med. Chem., 2015, 22, 2590–2614.
- Kang, H. K., Seo, C. H. and Park, Y., Marine peptides and their anti-infective activities. Mar. Drugs, 2015, 13, 618–654.
- Harrison, P. L., Abdel-Rahman, M. A., Miller, K. and Strong, P. N., Antimicrobial peptides from scorpion venoms. Toxicon, 2014, 88, 115–1137.
- Kalayci, S., Iyigundogdu, Z. U., Muge Yazici, M., Burcin Asutay, A., Demir, O. and Sahin, F., Evaluation of antimicrobial and antiviral activities of different venoms. Infect. Disord. Drug Targets, 2016, 16, 44–53.
- da Costa, J. P., Cova, M., Ferreira, R. and Vitorino, R., Antimicrobial peptides: an alternative for innovative medicines? Appl. Microbiol. Biotechnol., 2015, 99, 2023–2040.
- Esplugas, S., Bila, D. M., Krause, L. G. and Dezotti, M., Ozonation and advanced oxidation technologies to remove endocrine disrupting chemicals (EDCs) and pharmaceuticals and personal care products (PPCPs) in water effluents. J. Hazard. Mater., 2007, 149, 631–642.
- Wahlberg, C., Bjorlenius, B. and Paxéus, N., Fluxes of 13 selected pharmaceuticals in the water cycle of Stockholm, Sweden. Water Sci. Technol., 2011, 63, 1772–1780.
- Westly, E., India moves to tackle antibiotic resistance. Nature, 2012, 489, 192.
- Scrub typhus: an underestimated endemic disease of Northwestern Himalayas, India
Abstract Views :178 |
PDF Views:70
Authors
Affiliations
1 Department of Veterinary Public Health and Epidemiology, DGCN College of Veterinary and Animal Sciences, CSK-Himachal Pradesh Agriculture University, Palampur 176 062, India
1 Department of Veterinary Public Health and Epidemiology, DGCN College of Veterinary and Animal Sciences, CSK-Himachal Pradesh Agriculture University, Palampur 176 062, India
Source
Current Science, Vol 121, No 7 (2021), Pagination: 899-905Abstract
Scrub typhus is a vector-borne rickettsial zoonotic disease, endemic to South Eastern and Far Eastern Asian countries and northern Australia. It is an acute febrile illness, associated with rash and often an eschar, a black crust-like skin lesion. Orientia tsutsugamushi, etiological agent of scrub typhus infects the endothelial cells causing vasculitis, multiple organ dysfunction, life threatening complications and mortalities. Scrub typhus is endemic in Himalayan/sub-Himalayan regions. This review summarizes the status of scrub typhus in mountainous states of India, i.e. Himachal Pradesh, Uttarakhand and Jammu and Kashmir, located in Northwestern Himalayas. Scrub typhus is a major cause of acute febrile illness, fever of unknown origin and febrile jaundice in this region. Disease has been reported both as mono-infection and co-infections with dengue, leptospirosis, malaria and hepatitis from these states. Pediatric scrub typhus cases with neurological complications are common in this region. Agricultural or farming activities are the primary risk factors for the occurrence of scrub typhus in both rural and urban population. Early presentation of the cases and timely diagnosis and treatment of patients is crucial to prevent life threatening complications and deaths. Scrub typhus mimics epidemiology and clinical course of commonly reported infectious diseases and requires differential diagnosis. Therefore, it is imperative to make health workers aware about its manifestations for early diagnosis and treatment and accurate prevalence estimations.Keywords
Acute febrile illness, fever of unknown origin, Himachal Pradesh, meningitis, scrub typhus, UttarakhandReferences
- Xu, G., Walker, D. H., Jupiter, D., Melby, P. C. and Arcari, C. M., A review of the global epidemiology of scrub typhus. PLoS Negl. Trop. Dis., 2017, 11, e0006062; doi:10.1371/journal.pntd.0006062.
- Watt, G. and Parola, P., Scrub typhus and tropical rickettsioses. Curr. Opin. Infect. Dis., 2003, 16, 429–436.
- Ahmad, S., Srivastava, S., Verma, S. K., Puri, P. and Shirazi, N., Scrub typhus in Uttarakhand, India: a common rickettsial disease in an uncommon geographical region. Trop. Doct., 2010, 40, 188–190.
- Luce-Fedrow, A. et al., A review of scrub typhus (Orientia tsutsugamushi and related organisms): then, now, and tomorrow. Trop. Med. Infect. Dis., 2018, 3, 8; doi:10.3390/tropicalmed3010008.
- Elliott, I., Pearson, I., Dahal, P., Thomas, N. V., Roberts, T. and Newton, P. N., Scrub typhus ecology: a systematic review of Orientia in vectors and hosts. Parasit. Vectors, 2019, 12, 513; doi: 10.1186/s13071-019-3751-x
- Traub, R. and Wisseman Jr, C. L., Current concepts of the ecology of chigger borne rickettsiosis (scrub typhus). Jpn. J. Med. Sci. Biol., 1974, 27, 1–5.
- Muul, I. and Chai, K. S., Distribution of rats infected with Rickettsia tsutsugamushi (scrub typhus) in an edge habitat. Southeast Asian J. Trop. Med. Public Health, 1978, 9, 489–593.
- Rajapakse, S., Rodrigo, C. and Fernando, D., Scrub typhus: pathophysiology, clinical manifestations and prognosis. Asian Pac. J. Trop. Med., 2012, 5, 261–264.
- Singh, P., Scrub Typhus, a case report: military and regional significance. Med. J. Armed Forces India, 2004, 60, 89–90.
- Park, J. I. et al., Outbreak of hepatitis by Orientia tsutsugamushi in the early years of the new millennium. Korean J. Hepatol., 2003, 9, 198–204.
- Mahajan, S. K. et al., Pattern of clinical presentation, laboratory findings and mortality risk among patients of scrub typhus in Western Himalayas. J. Assoc. Phys. India, 2016, 64, 26–30.
- Gaba, S., Gaba, N., Gupta, M. and Sharma, S., Hepatic and renal profile of scrub typhus patients at a tertiary care center in India. Cureus, 2020, 12, e7925; doi:10.7759/cureus.7925.
- Balcells, M. E. et al., Endemic scrub typhus-like illness, Chile. Emerg. Infect. Dis., 2011, 17, 1659–1663.
- Izzard, L. et al., Isolation of a novel Orientia species (O. chuto sp. nov.) from a patient infected in Dubai. J. Clin. Microbiol., 2010, 48, 4404–4409.
- Weitzel, T. et al., Endemic ccrub typhus in South America. N. Engl. J. Med., 2016, 375, 954–961.
- Mahajan, S. K. and Mahajan, S. K., Neuropsychiatric manifestations of scrub typhus. J. Neurosci. Rural Pract., 2017, 8, 421–426.
- Sharma, A., Mahajan, S., Gupta, M. L., Kanga, A. and Sharma, V., Investigation of an outbreak of scrub typhus in the Himalayan region of India. Jpn. J. Infect. Dis., 2005, 58, 208–210.
- Mahajan, S. K. et al., Scrub typhus in Himalayas. Emerg. Infect. Dis., 2006, 12, 1590–1592.
- Mittal, G., Ahmad, S., Agarwal, R. K., Dhar, M., Mittal, M. and Sharma, S., Aetiologies of acute undifferentiated febrile illness in adult patients – an experience from a tertiary care hospital in Northern India. J. Clin. Diagn. Res., 2015, 9, DC22–DC24; doi:10.7860/JCDR/2015/11168.6990.
- Singh, R., Singh, S. P. and Ahmad, N. A., Study of etiological pattern in an epidemic of acute febrile illness during monsoon in a tertiary health care institute of Uttarakhand, India. J. Clin. Diagn. Res., 2014, 8, MC01–MC03; doi:10.7860/JCDR/2014/8965.4435.
- Raina, S., Raina, R. K., Agarwala, N., Raina, S. K. and Sharma, R., Coinfections as an aetiology of acute undifferentiated febrile illness among adult patients in the sub-Himalayan region of north India. J. Vector Borne Dis., 2018, 55, 130–136.
- Sonthayanon, P. et al., Association of high Orientia tsutsugamushi DNA loads with disease of greater severity in adults with scrub typhus. J. Clin. Microbiol., 2009, 47, 430–434.
- Bhat, N. K. et al., Scrub typhus in children at a tertiary hospital in north India: clinical profile and complications. Iran J. Pediatr., 2014, 24, 387–392.
- Silpapojakul, K., Scrub typhus in the Western Pacific Region. Ann. Acad. Med. Singapore, 1997, 26, 794–800.
- Mahajan, S. K., Rolain, J. M., Sankhyan, N., Kaushal, R. K. and Raoult, D., Pediatric scrub typhus in Indian Himalayas. Indian J. Pediatr., 2008, 75, 947–949.
- Kaushik, R. M., Kaushik, R. and Bhargava, A., Multiple eschars in scrub typhus. Trop. Med. Health, 2014, 42, 65–66.
- Koraluru, M., Nandigam, M., Bairy, I., Vidyasagar, S. and Varma, M., Multiple eschars in scrub typhus: a case report. Trop. Doct., 2017, 47, 67–69.
- Mokta, J., Ranjan, A. and Mokta, K., Early clinical suspicion and early use of doxycycline reduces scrub typhus associated complications. J. Assoc. Phys. India, 2019, 67, 26–27.
- Kumar, R., Thakur, S., Bhawani, R., Kanga, A. and Ranjan, A., Clinical profile and complications of scrub typhus: hospital-based study in Sub-Himalayan region. J. Assoc. Phys. India, 2016, 64, 30–34.
- Wang, C. C., Liu, S. F., Liu, J. W., Chung, Y. H., Su, M. C. and Lin, M. C., Acute respiratory distress syndrome in scrub typhus. Am. J. Trop. Med. Hyg., 2007, 76, 1148–1152.
- Mahajan, S. K., Kaushik, M., Raina, R., Sharma, R. C., Thakur, P. and Sharma, B., Scrub typhus with visual hallucinations. J. Trop. Doct., 2015, 45, 146–147; doi:10.1177/0049475514565426.
- Viswanathan, S., Muthu, V., Iqbal, N., Remalayam, B. and George, T., Scrub typhus meningitis in South India – a retrospective study. PLoS ONE, 2013, 8, e66595; doi:10.1371/journal.pone.0066595.
- Kang, Ji-In., Kim, D. M. and Lee, J., Acute sensorineural hearing and severe otalgia due to scrub typhus. BMC Infect. Dis., 2009, 9, 173; doi:10.1186/1471-2334-9-173.
- Premaratna, R., Chandrasena, T. G., Dassayake, A. S., Loftis, A. D., Dasch, G. A. and de Silva, H. J., Acute hearing loss due to scrub typhus: a forgotten complication of a reemerging disease. Clin. Infect. Dis., 2006, 26, 42, e6–e8; doi.org/10.1086/498747.
- Bhardwaj, B., Panda, P., Revannasiddaiah, S. and Bhardwaj, H., Abducens nerve palsy in a patient with scrub typhus: a case report. Trop. Biomed., 2013, 30, 706–709.
- Lee, Y. H., Yun, Y. J. and Jeong, S. H., Isolated abducens nerve palsy in a patient with scrub typhus. J. Am. Assoc. Pediatr. Opthalmol. Strabismus, 2010, 14, 460–461.
- Chauhan, V., Thakur, A. and Thakur, S., Eschar is associated with poor prognosis in scrub typhus. Indian J. Med. Res., 2017, 145, 693–696; doi:10.4103/ijmr.IJMR_1888_15.
- Deepak, N. A. and Patel, N. D., Differential diagnosis of acute liver failure in India. Ann. Hepatol., 2006, 5, 150–156.
- Mathai, E. et al., Outbreak of scrub typhus in southern India during the cooler months. Ann. N. Y. Acad. Sci., 2003, 990, 359–364.
- Ahmad, S. et al., A comparative hospital-based observational study of mono- and co-infections of malaria, dengue virus and scrub typhus causing acute undifferentiated fever. Eur. J. Clin. Microbiol. Infect.
- Dis., 2016, 35, 705–711.
- Bhargava, A. et al., Scrub typhus in Uttarakhand and adjoining Uttar Pradesh: Seasonality, clinical presentations and predictors of mortality. Indian J. Med. Res., 2016, 144, 901–909.
- Guleria, V. S., Sharda, C., Sood, A. K. and Kumar, V., Scrub typhus: atypical presentation in sub-Himalayan region. Med. J. Armed Forces India, 2018, 74, 180–182.
- Pathania, M., Amisha, Malik, P. and Rathaur, V. K., Scrub typhus: Overview of demographic variables, clinical profile, and diagnostic issues in the sub-Himalayan region of India and its comparison to other Indian and Asian studies. J. Family Med. Prim. Care, 2019, 8, 1189–1195.
- Bhat, N. K., Pandita, N. and Dhar, M., Scrub typhus eschar. Indian Pediatr., 2020, 57, 93.
- Varghese, G. M. et al., Scrub typhus among hospitalised patients with febrile illness in South India: magnitude and clinical predictors. J. Infect., 2006, 52, 56–60; doi:10.1016/j.jinf.2005.02.001. 46. Yen, T. H., Chang, C. T., Lin, J. L., Jiang, J. R. and Lee, K. F., Scrub typhus: a frequently overlooked cause of acute renal failure. Ren. Fail., 2003, 25, 397–410.
- Bhat, N. K., Jindal, R. and Dhar, M., Eschar of scrub typhus hidden in umbilicus. Indian J. Pediatr., 2018, 85, 247–248.
- Bhat, N. K. et al., Scrub Typhus: a clinico-laboratory differentiation of children with and without meningitis. J. Trop. Pediatr., 2016, 62, 194–199.
- Mahajan, S. K., Scrub typhus. J. Assoc. Phys. India, 2005, 53, 954–958.
- Kumar, R., Thakur, S., Bhawani, R., Kanga, A. and Ranjan, A., Factors for severe outcome in scrub typhus: a hospital based study in sub Himalayan region. J. Assoc. Phys. India, 2018, 66, 36–38.
- Sharma, R., Mahajan, S. K., Singh, B., Raina, R. and Kanga, A., Predictors of severity in scrub typhus. J. Assoc. Phys. India, 2019, 67, 35–38.
- Sinha, P., Gupta, S., Dawra, R. and Rijhawan, P., Recent outbreak of scrub typhus in North Western part of India. Indian. J. Med. Microbiol., 2014, 32, 247–250.
- Farhana, A., Bali, N., Kanth, F., Farooq, R., Haq, I. U. and Shah, P., Serological evidence of scrub typhus among cases of PUO in the Kashmir valley – a hospital based study. J. Clin. Diagn. Res., 2016, 10, DC24–DC26.
- Bhatia, M., Kumar, P., Gupta, P., Gupta, P. K., Dhar, M. and Kalita, D., Serological evidence of human leptospirosis in patients with acute undifferentiated febrile illness from Uttarakhand, India: A pilot study. J. Lab. Phys., 2019, 11, 11–16; doi:10.4103/JLP.JLP_ 121_18.
- Mahajan, S. K., Babu, S., Singh, D., Kanga, A. and Kaushal, S. S., Scrub typhus and leptospirosis co-infection in Himalayan region. Trop. Doct., 2012, 42, 176–177.
- Park, S. W. et al., Urbanization of scrub typhus disease in South Korea. PLoS Negl. Trop. Dis., 2015, 9, e0003814; doi:10.1371/journal.pntd.0003814; eCollection 2015.
- Thapliyal, D. C. and Thakur, S. D., Livestock diseases in Himalayan region: a public health perspective. In Proceedings of Livestock Production Systems for Sustainable Food Security and Livelihoods in Mountain Areas, Department of Animal Sciences, GB Pant University of Agriculture and Technology, Pantnagar,
- Uttrakhand, India, 2003, pp. 139–148.
- Kumar, K., Saxena, V. K., Thomas, T. G. and Shiv Lal, Outbreak investigation of scrub typhus in Himachal Pradesh (India). J. Commun. Dis., 2004, 36, 277–283.
- Rana, A., Mahajan, S. K., Sharma, A., Sharma, S., Verma, B. S. and Sharma, A., Neurological manifestations of scrub typhus in adults. Trop. Doct., 2017, 47, 22–25.
- Sood, S., Sharma, S. and Khanna, S., Role of advanced MRI brain sequences in diagnosing neurological complications of scrub typhus. J. Clin. Imaging Sci., 2015, 5, 11; doi:10.4103/2156-7514.152340.
- Mahajan, S. K. et al., Scrub typhus presenting as acute cerebellitis. J. Assoc. Phys. India, 2016, 64, 69–70.
- Himral, P., Sharma, K. N., Kudial, S. and Himral, S., Scrub meningitis complicated by multiple cranial nerve palsies and cerebellitis. J. Assoc. Phys. India, 2019, 67, 88–89.
- Mahajan, S. K. and Bakshi, D., Acute reversible hearing loss in scrub typhus. J. Assoc. Phys. India, 2007, 55, 512–514.
- Mahajan, S. K., Babu, S. N., Sharma, D., Singh, D., Kanga, A. and Kaushal, S. S., Scrub typhus presenting as acute abdomen. Trop. Doct., 2011, 41, 185–186.
- Mokta, J., Yadav, R., Mokta, K., Panda, P. and Ranjan, A., Scrub Typhus – the most common cause of febrile jaundice in a tertiary care hospital of Himalayan state. J. Assoc. Phys. India, 2017, 65,
- –50.
- Vikrant, S., Gupta, D. and Singh, M., Epidemiology and outcome of acute kidney injury from a tertiary care hospital in India. Saudi J. Kidney Dis. Transpl., 2018, 29, 956–966.
- Sood, A. K., Chauhan, L. and Gupta, H., CNS manifestations in Orientia tsutsugamushi disease (Scrub Typhus) in North India. Indian J. Pediatr., 2016, 83, 634–639.
- Mittal, G., Ahmad, S., Agarwal, R. K., Dhar, M., Mittal, M. and Sharma, S., Aetiologies of acute undifferentiated febrile illness in adult patients – an experience from a tertiary care hospital in Northern India. J. Clin. Diagn. Res., 2015, 9, DC22–DC24; doi:10.7860/JCDR/2015/11168.6990.
- Rawat, V., Singh, R. K., Kumar, A., Saxena, S. R., Varshney, U. and Kumar, M., Epidemiological clinical and laboratory profile of scrub typhus cases detected by serology and RT-PCR in Kumaon,
- Uttarakhand: a hospital-based study. Trop. Doct., 2018, 48, 103–106.
- Mehta, V., Bhasi, A., Panda, P. K. and Gupta, P. A., Coinfection of severe leptospirosis and scrub typhus in Indian Himalayas. J. Family Med. Prim. Care, 2019, 8, 3416–3418.
- Menon, R. D., Padbidri, V. S. and Gupta, N. P., Sero-epidemiological survey of scrub typhus. J. Hyg. Epidemiol. Microbiol. Immunol., 1978, 22, 306–311.
- Watt, G., Jongsakul, K. and Suttinont, C., Possible scrub typhus coinfections in Thai agricultural workers hospitalized with leptospirosis. Am. J. Trop. Med. Hyg., 2003, 68, 89–91.
- Integrated Antibiotic Resistance Surveillance: Importance of Harmonization and Quality Assurance of Antibiotic Susceptibility Testing
Abstract Views :47 |
PDF Views:28
Authors
Affiliations
1 Department of Veterinary Public Health and Epidemiology, DGCN College of Veterinary and Animal Sciences, Chaudhary Sarwan Kumar Himachal Pradesh Krishi Vishvavidyalaya, Palampur 176 062, IN
1 Department of Veterinary Public Health and Epidemiology, DGCN College of Veterinary and Animal Sciences, Chaudhary Sarwan Kumar Himachal Pradesh Krishi Vishvavidyalaya, Palampur 176 062, IN
Source
Current Science, Vol 125, No 3 (2023), Pagination: 268-276Abstract
Antibiotic resistance (AR) is an underestimated emerging One Health problem. Surveillance systems are the core components of AR management programmes. Integrated harmonized surveillance programmes with active watchfulness on the use of antimicrobials and trends of resistance in bacteria of human, animal and environmental origin are required for exact estimation of the true burden of AR. Harmonized surveillance programmes follow uniformity in antibiotic susceptibility testing protocols, targeted bacterial species, tested antimicrobials, reporting clinical limits, susceptibility interpretation criteria and use of control strains. Harmonization of AR surveillance programmes is crucial for reliable data generation and comparison of AR data at regional, national and global levels. Data generated by such programmes can be used to formulate empirical treatment guidelines and policies for the effective management of AR. Standardization of antibiotic susceptibility testing by adopting quality assurance and quality control programmes is essential for generating valid and reliable data under AR surveillance programmes.Keywords
Antibiotic Resistance, One Health, Quality Control, Surveillance Systems.References
- Murray, C. L. (Antimicrobial Resistance Collaborators), Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet, 2022, 399, 629–655.
- Payumo, J. et al., Next generation of AMR network. Encyclopedia, 2021, 1, 871–892.
- World Health Organization, Antimicrobial resistance, 2023; https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance
- Larsson, D. G. J. and Flach, C. F., Antibiotic resistance in environment. Nat. Rev. Microbiol., 2022, 20, 257–269.
- Martínez, J. L., Bottlenecks in the transferability of antibiotic resistance from natural ecosystems to human bacterial pathogens. Front. Microbiol., 2012, 2, 265; doi:10.3389/fmicb.2011.00265
- Davies, J. E., Origins, acquisition and dissemination of antibiotic resistance determinants. Ciba Found. Symp., 1997, 207, 15–27.
- Munita, J. M. and Arias, C. A., Mechanisms of antibiotic resistance. Microbiol. Spectr., 2016, 4, 10.1128/microbiolspec.VMBF-0016-2015; 10.1128/microbiolspec.VMBF-0016-2015.
- Van Boeckel, T. P. et al., Reducing antimicrobial use in food animals. Science, 2017, 357, 1350–1352.
- Tiseo, K., Huber, L., Gilbert, M., Robinson, T. P. and Van Boeckel T. P., Global trends in antimicrobial use in food animals from 2017 to 2030. Antibiotics (Basel), 2020, 9, 918; doi:10.3390/antibiotics-9120918.10
- Pokharel, S., Shrestha, P. and Adhikari, B., Antimicrobial use in food animals and human health: time to implement ‘One Health’ approach. Antimicrob. Resist. Infect. Control, 2020, 9, 181; doi: 10.1186/s13756-020-00847-x
- Cycon, M., Mrozik, A. and Piotrowska-Seget, Z., Antibiotics in the soil environment – degradation and their impact on microbial activity and diversity. Front. Microbiol., 2019, 10, 338; doi:10.3389/fmicb.2019.00338
- Gullbeg, E. et al., Selection of resistant bacteria at very low antibiotic concentrations. PLoS Pathog., 2011, 7, e1002158; https://doi.org/10.1371/journal.ppat.1002158
- Checcucci, A. et al., Exploring the animal waste resistome: the spread of antimicrobial resistance genes through the use of livestock manure. Front. Microbiol., 2020, 11, 1416; doi:10.3389/fmicb.2020.01416
- Mladenovic-Antic, S. et al., Correlation between antimicrobial consumption and antimicrobial resistance of Pseudomonas aeruginosa in a hospital setting: a 10-year study. J. Clin. Pharm. Ther., 2016, 41, 532–537.
- Roux, D. et al., Fitness cost of antibiotic susceptibility during bacterial infection. Sci. Transl. Med., 2015, 7, 297ra114; doi:10.1126/scitranslmed.aab1621
- Thakur, S. D. and Panda, A. K., Rationale use of antimicrobials in animal production: a prerequisite to stem the tide of antimicrobial resistance. Curr. Sci., 2017, 113, 1846–1857.
- Van Boeckel, T. P. et al., Global trends in antimicrobial use in food animals. Proc. Natl. Acad. Sci. (USA), 2015, 112, 5649–5654.
- Dutescu, I. A. and Hillier, S. A., Encouraging the development of new antibiotics: are financial incentives the right way forward? A systematic review and case study. Infect. Drug Resist., 2021, 14, 415–434; doi:10.2147/IDR.S287792
- Klug, D. M. et al., There is no market for new antibiotics: this allows an open approach to research and development. Wellcome Open Res., 2021, 6, 146; doi:10.12688/wellcomeopenres.16847.1
- Bennet, M. F. and Young, T., The PASTEUR Act. 2021; https://www.bennet.senate.gov/public/_cache/files/c/2/c2068e9f-8440-4960-86f4-acdd13145430/513C16806B1E8526E9F919EA7A72A004.past-eur-act---one-pager-1-.pdf
- Gotham, D., Moja, L., van der Heijden, M., Paulin, S., Smith, I. and Beyer, P., Reimbursement models to tackle market failures for anti-microbials: approaches taken in France, Germany, Sweden, the United Kingdom, and the United States. Health Policy, 2021, 125, 296–306.
- Boluarte, T. and Schulze, U., The case for a subscription model to tackle antimicrobial resistance, 2022; https://www.bcg.com/publications/2022/model-for-tackling-antimicrobial-resistance
- World Health Organization, Antibacterial agents in clinical and preclinical development: an overview and analysis. World Health Organization, Geneva, 2022.
- Iskandar, K. et al., Surveillance of antimicrobial resistance in low-and middle-income countries: a scattered picture. Antimicrob. Resist. Infect. Control, 2021, 10, 63; doi:10.1186/s13756-021-00931-w
- Hay, S. I. et al., Measuring and mapping the global burden of anti-microbial resistance. BMC Med., 2018, 16, 78; doi:10.1186/s12916-018-1073-z
- Thrushfield, M. (ed.), Survillience. In Veterinary Epidemiology, Blackwell Science Ltd, Oxford, UK, 2007, pp. 168–186.
- Lewis, D., Antimicrobial resistance surveillance: methods will depend on objectives. J. Antimicrob. Chemother., 2002, 49, 3–5.
- Diallo, O. O. et al., Antibiotic resistance surveillance systems: a review. J. Glob. Antimicrob. Resist., 2020, 23, 430–438.
- Dunne, E. F. et al., Emergence of domestically acquired ceftriax-one-resistant Salmonella infections associated with AmpC β-lactamase. JAMA, 2000, 284, 3151–3156.
- World Health Organization, Global antimicrobial resistance and use surveillance system (GLASS), 2022; https://www.who.int/initiatives/glass
- World Organization for Animal Health, Harmonisation of national antimicrobial resistance surveillance and monitoring programmes. In Terrestrial Animal Health Code, 2022; https://www.woah.org/fileadmin/Home/eng/Health_standards/tahc/current/chapitre_anti-bio_harmonisation.pdf
- World Health Organization, Surveillance standards for antimicrobial resistance. WHO/CDS/CSR/DRS/2001.5, 2002; http://apps.who.int/iris/bitstream/handle/10665/67426/WHO_CDS_CSR_DRS_2001;5.pdf;jsessionid=17B1B2F5C7F868F6AE97E4DA9B1900B1?sequence=1
- Queenan, K., Häsler, B. and Rushton J., A One Health approach to antimicrobial resistance surveillance: is there a business case for it? Int. J. Antimicrob. Agents, 2016, 48, 422–427.
- World Health Organization, Integrated surveillance of antimicrobial resistance in food borne bacteria: application of a one health approach: guidance from the WHO Advisory Group on Integrated Surveillance of Antimicrobial Resistance (AGISAR), World Health Organization, 2017; https://apps.who.int/iris/handle/10665/255747
- Zinsstag, J., Schelling, E., Waltner-Toews, D. and Tanner, M., From’ One Medicine’ to’ One Health’ and systemic approaches to health and well-being. Prev. Vet. Med., 2011, 101, 148–156.
- World Health Organization, Global action plan on antimicrobial resistance, 2015; file:///C:/Users/admin/Downloads/9789241509763_eng.pdf
- Clinical Laboratory Standards Institute, Performance standards for antimicrobial susceptibility testing. CLSI supplement M-100. Clinical and Laboratory Standards Institute, Wayne, Pennsylvania, USA, 2013, 30th edn.
- The European Committee on Antimicrobial Susceptibility Testing, Breakpoint tables for interpretation of MICs and zone diameters. Version 12.0, 2022; http://www.eucast.org
- Cusack, T. P. et al., Impact of CLSI and EUCAST breakpoint discrepancies on reporting of antimicrobial susceptibility and AMR surveillance. Clin. Microbiol. Infect., 2019, 25, 910–911.
- Kahlmeter, G. and Brown, D. F., Resistance surveillance studies-comparability of results and quality assurance of methods. J. Anti-microb. Chemother., 2002, 50, 775–777.
- Sawatzky, P. et al., Quality assurance for antimicrobial susceptibility testing of Neisseria gonorrhoeae in Canada, 2003 to 2012. J. Clin. Microbiol., 2015, 53, 3646–3649.
- Tenover, F. C., Mohammed, M. J., Stelling, J., O’Brien, T. and Williams, R., Ability of laboratories to detect emerging antimicrobial resistance: proficiency testing and quality control results from the World Health Organizations external quality assurance system for anti-microbial susceptibility testing. J. Clin. Microbiol., 2001, 39, 241–250.
- Chaitram, J. M., Jevitt, L. A., Lary, S., Tenover, F. C. and WHO Antimicrobial Resistance Group, The World Health Organizations external quality assurance system proficiency testing program has improved the accuracy of antimicrobial susceptibility testing and reporting among participating laboratories using NCCLS methods. J. Clin. Microbiol., 2003, 41, 2372–2377.
- Karatuna, O., Quality assurance in antimicrobial susceptibility testing. In Latest Research into Quality Control (ed. Akyar, I.), IntechOpen, 2012; https://www.intechopen.com/books/3276
- Bayot, M. L. and Bragg, B. N., Antimicrobial susceptibility testing. In StatPearls (Internet), 2022, Treasure Island (FL), StatPearls Publishing, Tampa, Florida, USA, 2022.
- Steers, E., Foly, E. L., Graves, B. S. and Leder, J., Inocula replicating apparatus for routine testing of bacterial susceptibility to anti-biotics. Antibiot. Chemother., 1959, 9, 307–311.
- King, A. and Brown, D. F., Quality assurance of antimicrobial susceptibility testing by disc diffusion. J. Antimicrob. Chemother., 2001, 48(Suppl. 1), 71–76.
- Unemo, M. et al., The novel 2016 WHO Neisseria gonorrhoeae reference strains for global quality assurance of laboratory investigations: phenotypic, genetic and reference genome characterization. J. Antimicrob. Chemother., 2016, 71, 3096–3108.
- Thorington, R. et al., Antimicrobial susceptibilities of Neisseria gonorrhoeae in Canada, 2020. Canada Communicable Disease Report, 2022, 48, 571–579.
- Dillon, J. R., Trecker, M. and Thakur, S. D., Two decades of gonococcal antimicrobial surveillance program in South America and the Caribbean. Sex. Transm. Infect., 2013, 89, iv36–iv41.
- Sawatzky, P. et al., Quality assurance for antimicrobial susceptibility testing of Neisseria gonorrhoeae in Latin American and Caribbean countries, 2013 to 2015. Sex. Transm. Infect., 2018, 94, 479–482.
- World Health Organization, Global Antimicrobial Resistance Surveillance System. 2023; https://www.who.int/initiatives/glass
- European Centre for Disease Prevention and Control, European Antimicrobial Resistance Surveillance Network (EARS-Net). 2023; https://www.ecdc.europa.eu/en/about-us/networks/disease-networks-and-laboratory-networks/ears-net-data
- World Health Organization, Central Asian and European Surveillance of Antimicrobial Resistance (CAESAR). 2023; https://www.who.int/europe/groups/central-asian-and-european-surveillance-of-antimicrobial-resistance-(caesar).
- Pan American Health Organization, Latin American and Caribbean Network for Antimicrobial Resistance Surveillance – ReLAVRA+. 2023; https://www.paho.org/en/topics/antimicrobial-resistance/latin-american-and-caribbean-network-antimicrobial-resistance
- Centers of Disease Control and Prevention, National Antimicrobial Resistance Monitoring System for Enteric Bacteria (NARMS), 2023; https://www.cdc.gov/narms/index.html
- Centers of Disease Control and Prevention, CDC’s Antimicrobial Resistance (AR) Laboratory Networks, 2021; https://www.cdc.gov/drugresistance/laboratories.html
- Otto, S. J. G., Haworth-Brockman, M., Miazga-Rodriguez, M., Wierzbowski, A. and Saxinger, L. M., Integrated surveillance of anti-microbial resistance and antimicrobial use: evaluation of the status in Canada (2014–2019). Can. J. Public Health, 2022, 113, 11–22.
- Walia, K. et al., Establishing antimicrobial resistance surveillance and research network in India: journey so far. Indian J. Med. Res., 2019, 149, 164–179.
- Indian Council of Medical Research, Antimicrobial resistance research and surveillance network. Annual report January 2021 to December 2021, 2022; https://main.icmr.nic.in/sites/default/files/upload_documents/AMR_Annual_Report_2 021.pdf
- Vijay, S. et al., An integrated surveillance network for antimicrobial resistance, India. Bull. World Health Organ., 2021, 99, 562–571.
- Rathore, G., Lal, K. K., Bhatia, R. and Jenna, J. K., INFAAR – a research platform for accelerating laboratory-based surveillance of antimicrobial resistance in fisheries and aquaculture in India. Curr. Sci., 2020, 119, 1884–1885.