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Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study

Published: April 5, 2024
By: Ajit Poudel 1,2; Shreeya Sharma 1; Kavya Dhital 1; Shova Bhandari 2; Pragun Gopal Rajbhandari 2; Rajindra Napit 1,2; Dhiraj Puri 1; Dibesh B. Karmacharya 1,2,3 / 1 One Health Division, Biovac Nepal, Nala, Nepal; 2 One Health Division, Center for Molecular Dynamics Nepal, Kathmandu, Nepal; 3 Department of Biological Sciences, University of Queensland, Brisbane, Australia.
Introduction
Nepal’s poultry industry has seen a significant and rapid growth in the last decade, contributing more than 4% to the national gross domestic product (GDP) [1, 2]. Majority of the poultry products are supplied by numerous commercial farms (54% of total poultry production) scattered throughout the country. Backyard poultry also accounts for significant proportion of the total poultry production (46%); poultry meat and eggs are an easy source for protein and livelihood [1, 3]. Rapidly expanding commercial poultry is reared in 64 out of 77 districts of Nepal and has an annual growth rate of over 18% [1, 4]. According to the latest poultry census by the Nepal Central Bureau of Statistics [5], majority of chickens reared in Nepal are broilers (87%), with only small number of farms keeping layer chickens (11%). Almost half of the poultry production (46%) comes from the central region of the country. Chitwan, Kathmandu, and Kaski districts account for more than 85% of total meat and eggs production.
In Nepal, in spite of burgeoning poultry industry, proper biosecurity measures are often overlooked [6]. Backyard poultry farmers often feel the burden of maintaining biosecurity due to lack of knowledge and perceived additional cost [7]. Biosafety encompasses measures to prevent transmission of infectious diseases, and biosecurity measures are meant to prevent introduction and spread of pathogens in farms. By implementing a proper biological containment (and exclusion) along with traffic control, segregation, and sanitation- an effective biosafety and biosecurity can be maintained [8]. Keeping healthy flocks not only guarantees financial security for the farmers, it can also prevent outbreaks of zoonotic diseases such as highly pathogenic avian influenza (HPAI) [2, 9]. With increased commercial poultry production, maintaining biosecurity and biosafety measures in farms have been challenging [6]. Lack of government initiatives (and efforts), both in developing and developed countries alike, to raise awareness and implement regulations on biosecurity and biosafety have also grossly undermined proper safe farming practices [10]. Although Veterinary Standards and Drug Administration Office (VSDAO) in Nepal has developed a manual for proper poultry management including biosecurity guidelines, it isn’t properly enforced and is often overlooked by farmers [11]. Poultry productions that are primarily focused on profitability, with compromised biosafety and biosecurity practices for cost saving, will eventually face production loss and increased health risks to both birds as well as humans (and other animals) [8].
Despite increasing occurrence of disease outbreaks such as Avian Influenza (AI) in poultry farms, many farmers in Nepal are unaware of the importance of biosecurity measures and their practices [7]. This lack of awareness, along with inadequate enforcement of biosecurity regulations, is exacerbating the risk of AI transmission in the country [12]. Poor farm management practices resulting in AI infection in poultry and use of their unprocessed poultry waste in vegetable cultivation can contribute to the spread of AI [13]. Lack of information available to farmers regarding safe poultry management or diseases is not an issue in Nepal. The government uses variety of media outlets to disseminate information pertaining to public health and pandemic preparedness guidelines and additionally, farmers and entire communities share their information and knowledge among each other regarding diseases and their transmission dynamics [14]. As aforementioned, a guideline on poultry biosafety and biosecurity has also been developed by the Veterinary Standards and Drug Administration Office (VSDAO) [11]. The issue seems to be either lack of knowledge or disregard of preventative measures that can be implemented to prevent poultry diseases. A knowledge, attitude, and practice study conducted in Nepal in 100 poultry farms stated although the farmers were aware of the contagious properties of AI, only half of them thought that it could be prevented [14]. Similar trend was observed in another study that analyzed commercial poultry in 10 districts of Nepal, in which, only 10% of the farms had comprehensive biosafety protection for the farmers. They were aware of the need for biosafety and biosecurity measures on a farm and had some form of personal protective equipment (PPE) and disinfecting agents but were inadequate [15].
Disease outbreaks in poultry farms due to bacterial pathogens such as Mycoplasma gallisepticum (Mg), Mycoplasma synoviae (Ms), Escherichia Coli (E. coli) and Salmonella also occur due to lapses in biosafety and biosecurity. Rampant and haphazard use of antibiotics in poultry farms in Nepal is a leading cause of antimicrobial resistance (AMR) and a looming threat to human health [16]. There is a need to reduce and promote responsible use of antibiotics in the poultry industry in Nepal [17, 18]. Antimicrobial stewardship, which is a coordinated program that promotes the appropriate use of antimicrobials (including antibiotics), reduces microbial resistance, and decreases the spread of infections caused by multidrug-resistant organisms, has become one of the important aspects of a comprehensive biosecurity and biosafety practices [7].
Kathmandu is a densely-populated metropolitan capital city of Nepal with a population of over 2 million people [19]. Any emerging, re-emerging and diseases of human health concern originating from animal production sites, such as poultry farms, can rapidly spread in a city like Kathmandu. Since disease outbreak, transmission and spread dynamics are directly linked to biosafety and biosecurity status of farms, it is vital to understand the current status of the farms located close to the city. We conducted a comprehensive risk assessment and status evaluation of biosafety, biosecurity and AMR stewardship in sixteen poultry farms located in four districts with high poultry production (Ramechhap, Nuwakot, Sindhupalchowk, and Kavre) surrounding the Kathmandu valley. In this study we aimed to better understand the implementation of biosafety and biosecurity measures in the selected poultry farms, the farmers’ knowledge, attitude, and practice towards AMR, and the dynamics of diseases detected on their farms.
Methodology
Ethical Approval
Our study followed ethical guidelines of the Department of Livestock Services (DLS) Nepal for the survey. Sampling and survey were conducted after obtaining written consent of farm owners. Biological samples were collected using proper biosecurity measures in the presence of the farm owner or caretaker. For human survey, ethical approval was obtained from Nepal Health Research Council (NHRC) (Reg. 411/2020).
Study site and data collection
Four farms (small and medium sized; poultry < 2000 per farm) in each of the four districts (Kavre, Sindhupalchowk, Ramechhap and Nuwakot) were selected for the study (Fig 1). To ensure uniformity among sampling sites within our available budget, four farms across the four districts were selected. Only commercial farms were selected as backyard poultry is more resilient to diseases [20] and they are not reared in large numbers as the commercial ones. Additionally, the sampling activities were carried out during the first year of Covid-19 pandemic (2020) and most farms were hesitant to consent to the study. Two broiler and two layer farms in each district were selected for this study (Table 1). All poultry samples were collected by trained veterinarian and veterinary technician. Ideally, 10% of total poultry would be sampled to obtain a representative data but as this was a pilot study, we utilized the practicality of Central Limit Theorem and collected samples of 30 chickens from each farm [21, 22], assuming normality of the sampling distribution and reduced variability to draw meaningful and reliable conclusions about the entire flock. Risk assessment checklist (S1 Table) and AMR stewardship questionnaire (S2 Table) were used to collect data. Risk assessment checklist assessed facility operations, personnel and standard operating procedures, water supply, cleaning and maintenance, rodent/pest control and farm record keeping.
Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study - Image 1
Fig 1. Selected poultry farms in the districts (Kavre, Sindhupalchowk, Ramechhap and Nuwakot) surrounding Kathmandu valley.
The top map shows location of the districts in Nepal and the bottom map shows their location in respect with Kathmandu District (shown just for reference, not a sampling site). The map was generated using QGIS software, Version 3.30.0 [23]. The base map of Nepal administrative shape files was obtained from Open Data Nepal
Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study - Image 2
Table 1. Types, age, and total number of chickens in each farm.
Biological sample collection
Oropharyngeal (n = 1) and cloacal (n = 1) swabs from each chicken were collected from selected farms (n = 16 farms; 30 birds per farm) and stored in viral transport media (VTM). All samples were stored in ice boxes (2−8°C) during sample collection and transported in liquid nitrogen container (-196°C) to BIOVAC’s lab in Kathmandu. The samples were then pooled (n = 10) from each farm (n = 6 pooled samples; pooled oropharyngeal swabs = 3 and pooled cloacal swabs = 3). These pooled samples were screened for eight poultry pathogens- Newcastle disease virus (NDV), Influenza A Virus (IAV), Infectious Bronchitis Virus (IBV), Infectious Bursal Disease (IBD), Mycoplasma synoviae (Ms), Mycoplasma gallisepticum (Mg), Marek’s Disease Virus-1 (MDV1) and Marek’s Disease Virus-2 (MDV2) using PCR.
Nucleic acid extraction and PCR
The nucleic acid (DNA/RNA) from pooled samples were extracted using automated nucleic acid extractor (abGenix™ AITbiotech, Singapore) following manufacturer’s instructions. The pooled swab samples were stored at -20°C. PCR for detection of the eight pathogens were performed using SuperScript™ III Platinum™ One-Step qRT-PCR Kit w/ROX (Invitrogen, Catalog number 11745500). The primers for NDV, IBV, IBDV, Mg, Ms, MDV1 and MDV2 were designed using NCBI PrimerBlast® (Table 2).
Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study - Image 1
Table 2. PCR primers for each of the pathogen designed using PrimerBlast® along with the gene they encode for, primer sequence, size, and their reference sequences (GenBank accession number or citations).
For IAV, the primers IAV ISO_F and IAV ISO_R were used (Table 2) [15].
PCR condition
PCR for each pathogen test was done in a 25ul reaction containing 4 μL of extracted RNA (for NDV, IAV, IBD, IBV) and 4 μL of extracted DNA (for MG, MS, MDV1 and MDV2), 1 μL each of respective 10pm forward and reverse primers, 12.5 μL of 2X Mastermix with ROX, 0.2 μL of SuperScript™ III Platinum™ enzyme and 6.3 μL of Nuclease free water. All eight PCR were carried out with enzyme activation at 45°C for 15 minutes followed by one cycle of initial denaturation at 95°C for 5 minutes. PCR for RNA viruses consisted of 45 cycles of denaturation at 95°C for 30 seconds, annealing at 59°C for 30 seconds and extension at 72°C for 20 seconds. PCR for MS, MG, MDV1 and MDV2 consisted of 10 cycles of denaturation at 95°C for 30 seconds, annealing at 63°C for 40 seconds and extension at 72°C for 20 seconds followed by 35 cycles of denaturation at 95°C for 30 seconds, annealing at 60°C for 40 seconds and extension at 72°C for 20 seconds. The final extension for all eight PCR were carried out at 72°C for 2 minutes. All the amplified PCR products were visualized using 1.5% Agarose Gel (S1–S5 Figs).
Biosafety and biosecurity risk assessment
We created a Biosafety and Biosecurity Compliance Matrix (BBCM) score based on risk assessment checklist which included criteria such as facility operations, personnel and standard operating procedures, water supply, cleaning and maintenance, rodent/pest control and farm record keeping (S1 Table). General practices relate to infrastructure of or within the farm that aids in its biosecurity. Personnel standards and procedures include hygiene practices, use of disinfectants and precautionary measures taken to minimize pathogen contamination in farms. Water supply assessed whether the water given to poultry is adequately disinfected and clean. We also investigated preventive measures taken by farms to control rodents. Poultry rearing area and equipment cleanliness practices implemented by the farm personnel were also evaluated under cleaning and maintenance criteria. And finally, under record keeping criteria, we assessed practices of keeping records of daily activities, material usage/ consumption and any breaches detected in the farm.
For each selected criteria complied, one point was given for every activity implemented and a BBCM score was tallied for each category in every farm. A final farm BBCM score was then calculated and converted into percentage. We categorized farms that had > 90% BBCM score as high, 60–89% as medium and < 60% as low. Scores received by each farm are shown in Table 3 and visualized in Fig 2.
Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study - Image 2
Fig 2. Graphical representation of BBCM scores received by all 16 farms for various biosafety & biosecurity parameters.
Scores (percentage) received by all farms assessed in this study using BBCM score. Numbers in parenthesis in the legend refers to total number of activities assessed within each criterion.
Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study - Image 3
Table 3. Biosafety and biosecurity risk assessment results.
Overall average BBCM score was calculated by dividing the sum of all BBCM fulfilled criteria (n) and calculating the percentage. The highest BBCM score (Sindhupalchowk Farm 4) was 67%, and the lowest BBCM score was 12% (Kavre Farm 3). The total number of activities assessed in each criterion are listed within parenthesis. Details of the activities assessed are shown in S1 Table.
Results
Biosafety and biosecurity risk assessment
Analysis of overall Biosafety and Biosecurity of all farms surveyed showed low compliance (average BBCM score = < 41%). The highest BBCM rating was scored by a farm in Sindhupalchowk (Farm 4, BBCM = 67%) and the lowest was by a farm in Kavre (Farm 3, BBCM = 12%). At district level, Sindhupalchowk had the most Biosafety and Biosecurity compliance (BBCM = 53%) whereas Ramechhap had the least (BBCM = 32%). Of all the assessed criteria, rodent control was the most neglected (BBCM = 3.1%). Only two farms (Ramechhap Farm 2 and Sindhupalchowk Farm 4) had implemented one out of four rodent control practices. General poultry farming practice was the most biosafety and biosecurity compliant criteria fulfilled by all farms (BBCM = 61.6%) (Table 3).
General practices, personnel standards and procedure, and cleaning and maintenance were the only categories implemented in all sixteen farms (Table 3, Fig 2). Only two farms (Ramechhap 2 and Sindhupalchowk 4) implemented rodent control, these were also the only farms that implement some activities of all six criteria. Water supply was implemented in all but two farms (Nuwakot 1 and Kavre 3). Similarly, record keeping was implemented in all but four farms (Kavre 3, Kavre 4, Ramechhap 1, and Ramechhap 4).
Across all 16 farms, general practices received the highest criteria average (61.6%), followed by cleaning and maintenance (50%), water supply (43.8%), record keeping (42.6%), personnel standards and procedure (42.4%), and rodent control (3.1%).
At least one of the screened pathogens was detected in all farms. Mg was the most common disease detected, in all but one farm, followed by Ms. In Nuwakot, Mg [S1 Fig–(Mg)] and IBD [S1 Fig–(IBD)] were detected. IAV [S2 Fig–(IAV)] and both bacterial diseases, Mg [S4 Fig–(Mg)] and Ms [S4 Fig–(Ms)], were detected in Ramechhap. Only Mg was detected in both Sindhupalchowk [S3 Fig–(Mg)] and Kavre [S5 Fig (Mg)].
AMR stewardship
A little over half (52%) of the surveyed farmers considered AMR as a real threat. Almost all farmers (93%) had not attended any programs or campaigns related to AMR. Very few farmers (12%) received training on AMR stewardship; these farmers received training/information on AMR from local animal health centres (21%), veterinarians (29%), vet technician (17%) or from vet suppliers (21%). Majority of the farmers (81%) did not consider implementing “withdrawal period” for antibiotics use prior to selling their meat products. Most of the famers trusted veterinarians (40%) and vet technician (14%) on receiving consultation on antibiotics use. Farmers used various antibiotics for prophylaxis (26%) and therapeutics (76%) needs (Table 4).
Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study - Image 4
Table 4. Knowledge and perception of AMR among poultry farmers.
Responses (in percentage) obtained from farmers on AMR-related questions.
The farmers were also inquired about various types and proportion of antibiotics they used (Fig 3). Tetracyclines were the most used (35%) antibiotic class, followed by polymyxins (13%), quinolones (12%), aminoglycosides (12%), macrolides (8%), and beta-lactams (8%). Sulfonamide (7%) and pleuromutilin (5%) were the least used antibiotic classes.
Antimicrobial stewardship hindered by inadequate biosecurity and biosafety practices, and inappropriate antibiotics usage in poultry farms of Nepal – A pilot study - Image 1
Fig 3. Various types of antibiotics used (in %) in the surveyed poultry farms.
Discussion
Poor biosafety and biosecurity measures on poultry farms can lead to introduction and spread of bacterial and viral diseases. Regular monitoring and testing, an important component of implementing strict biosecurity and biosafety measures, are essential for detecting and containing infections in farms. Poultry farms with compromised biosafety and biosecurity compliance often suffer from various prevalent bacterial and viral infections such as Mycoplasma, IBD and IAV- affecting overall poultry health and lowering production.
Mg and Ms are bacterial diseases which spread through direct contact, respiratory secretions, or contaminated materials [25]. IBD, on the other hand, is a viral disease that can cause damage to the immune system of young chickens, often leading to mortality [26]. It is transmitted through contact with contaminated sources, such as faeces. IAV in poultry is primarily transmitted through direct contact with infected birds or through contact with contaminated surfaces, feed, or water. Wild birds, particularly waterfowl, are the natural reservoirs for the virus and are thought to be one of the major sources of avian influenza outbreaks [27, 28].
Introduction of infected birds, equipment, or materials in farms can result in the spread of diseases [29, 30]. Movement of people and animals on and off the farm can also contribute to the spread of disease [31]. Birds that are housed in crowded or unsanitary conditions are susceptible to diseases; maintaining proper biosecurity and biosafety measures in such farms are often challenging [32]. Implementation of these measures were severely lacking in the farms that we surveyed in our study. Only one farm scored medium biosafety and biosecurity compliance rating (Sindhupalchowk Farm 4, BBCM = 67%). None of the farms received a high score of > 90%, and not surprisingly, diseases were detected in all farms (Table 3). Moreover, out of all sixteen farms, only two (Ramechhap 2 and Sindhupalchowk 4) had evidence of conducting activities pertaining all six different categories of the assessment. Rest of the farms had activities/practices missing from an entire category.
Biosecurity measures, such as controlling the movement of people and animals onto the farm, implementing disinfection procedures, and providing protective clothing, can significant improve poultry production by reducing disease outbreaks and spread [33, 34]. We detected Mg and Ms in most of the farms, these bacterial infections have low mortality but associated morbidity directly affects egg and meat production [35]. Overall, the farms in Ramechhap district scored poorly in BBCM, something the district animal health authority needs to be aware of and make effort to improve.
Although majority of the farms focused on general practices, cleaning and maintenance, and personal standards and procedures, except for two farms (Ramechhap 2 and Sindhupalchowk 4) most had completely ignored rodent control (Table 3). Rodents are a major pest and a disease vector of poultry farms [36]. Rodents are also known to cause damage to farm infrastructure and feed, kill young chicks and eat eggs [37].
Poultry farms often resort to using medications to treat and salvage their flock only after disease outbreaks. We detected viral pathogens (IBD and IAV) and bacterial infections (Mg and Ms) in all but one farm (out of 16). Antibiotics was rampantly used, both as prophylaxis and therapeutics, by the farmers. Antibiotics families such as Tetracycline, Polymyxin, Quinolone, Aminoglycoside, and Macrolide were the most used by the farmers- consistent with national trend [38, 39]. More than a quarter (26%) of the farmers used antibiotics as prophylaxis as a preventive measure and 76% of farmers used them as therapeutics to treat diseases (Table 4). Detection of bacterial infections in the farms even after the use of all these antibiotics is deeply concerning.
Inappropriate (and haphazard) use of antibiotics in farms can develop AMR in bacteria, making them more difficult to treat. Such usage not only leads to altered composition and diversity of gut microbiome in poultry [40, 41] but also result in high levels of resistance to several classes of antibiotics, including widely used antibiotics such as Polymyxin, Fluoroquinolones, and Beta-Lactams [42]. Further study needs to be carried out to assess presence of AMR genes in the bacterial pathogens detected in the farms.
The World Health Organization (WHO) has developed a classification system for antibiotics called Access, Watch, and Reserve (AWaRe) to guide the appropriate use of antibiotics and combat antimicrobial resistance. The Access group contains antibiotics that should be widely available and affordable, including first-line treatments for common infections. The Watch group contains antibiotics that should be used with caution and reserved for specific indications to prevent the development of resistance. The Reserve group contains last-resort antibiotics, which should be used sparingly and only when all other options have been exhausted [43]. Apart from tetracycline, the other two antibiotics that are classified as ‘Access’ by the WHO are used by farmers sparingly (Pleuromutilin– 7% and Penicillin– 5%). Antibiotics under ‘Watch’, such as Quinolone (12%), Aminoglycoside (12%) and Macrolide (9%) are widely used by poultry farmers. Alarmingly, Polymyxin (19%) which is listed as a ‘Reserve’ by the WHO is the second most abundantly used antibiotics (Fig 3).
A complete disregard to AMR stewardship combined with lack of knowledge among poultry farmers can have devastating impact on propagation of AMR. Widespread use of strong antibiotics and indifference to implementing withdrawal period not only aggravates the AMR situation in Nepal but also pose serious food-safety risks. Withdrawal period is a withhold time prior to market distribution of poultry products after antibiotic usage in production; this is to ensure antibiotics have been degraded sufficiently and rendered inactive [44]. A survey conducted in Kathmandu of more than 200 farmers revealed only few poultry farmers knew about withdrawal periods [7] or were aware of the importance of adhering to withdrawal periods after antibiotic use to prevent the development of AMR [16, 17]. All of these indicate the need of strict monitoring and control of antibiotic use by concerned government agencies.
Farmers in this study mentioned consulting either veterinarians or veterinary technicians regarding antibiotics usage (Table 4), however, either they did not fully comprehend the gravity of the looming AMR threat, or they disregarded the information they received. Majority of the farmers (88%) claimed to have received trusted information on AMR from various experts, but almost half of the farmers were unclear about AMR and majority (80%) of them were not willing to observe withdrawal period for their products.
In order to enhance biosecurity and reduce the risk of disease outbreaks in the poultry industry, it is necessary to raise awareness among poultry farmers about the usage of antibiotics along with significance of biosecurity measures [17, 45]. This can be done through extensive practical training amongst network of poultry farmers. Proper biosecurity measures, such as the frequent disinfection of farm premises and equipment and the provision of protective clothing and footwear for workers can greatly help in prevention and containment of farm borne diseases. Additionally, reducing the use of antibiotics in poultry production and promoting alternative methods of disease prevention, such as immunization, use of probiotics and immune modulators can play a crucial role in improving poultry health and reducing disease risks.
Strengths and limitations
Overall, this pilot study provides a snapshot of critical issues in the poultry industry in Nepal pertaining to poor biosafety, biosecurity, and antibiotic usage that have direct implications for public health, food safety, and AMR concerns. Incorporations of multiple pathogens also provides an insight into disease transmission dynamics in small to medium-sized farms in Nepal. However, there are few limitations of the study. The study’s sample size of sampling 30 chickens per farm may limit the generalizability of the findings to the broader poultry industry in different geographical regions. Likewise, the pathogens screened from the farms were based on Biovac’s experience with commercial diagnostics analyzing samples from poultry farms around the country. The pathogens could have been selected based on diseases prevalent in the sampling region. We recommend conducting a larger study with a more comprehensive sample size and in additional locations to ensure generalizability of the findings. Assessment of economic impact of the diseases would also provide insights into farmers’ usage of stronger or un-prescribed medications. Additionally, bacteria like E. coli, Salmonella, Campylobacter, Enterococcus spp., should be included in future studies as they would serve as better indicators of antibiotics usage and AMR issues in poultry farms and laboratory analyses should go a step beyond PCR to sequence the pathogens to provide a deeper understanding of the potential spread of AMR bacteria.
     
This article was originally published in PLoS ONE 19(3): e0296911. https://doi.org/ 10.1371/journal.pone.0296911. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.

1. FAO. Poultry Sector nepal. 2014.

2.Sharma B. Poultry Production, Management and Bio-Security Measures. J Agric Environ. 2010;11: 120–125.

3. Osti R, Bhattarai D, Zhou D. Climatic Variation: Effects on Stress Levels, Feed Intake, and Bodyweight of Broilers. Brazilian J Poult Sci. 2017;19: 489–496.

4. Gompo TR, Pokhrel U, Shah BR, Bhatta DD. Epidemiology of Important Poultry Diseases in Nepal. Nepal Vet J. 2019;36: 8–14.

5. CBS. Nepal—Nepal Commercial Poultry Survey 2014–2015. 2015 [cited 26 Mar 2023]. Available: https://microdata.cbs.gov.np/index.php/catalog/72

6. Nelson AJ, Manandhar S, Ruzante JM, Gywali A, Dhakal B, Dulal S, et al. Antimicrobial drug resistant non-typhoidal Salmonella enterica in commercial poultry value chain in Chitwan, Nepal. One Heal Outlook. 2020;2. pmid:33829137

7. Dhakal S, Gompo TR, Dhakal S. Assessment of Farmer’s Knowledge of Antimicrobial Resistance, Their Practice of Antimicrobial Usage and Biosecurity Status of Poultry Farms in Kathmandu Valley and Chitwan District, Nepal. Int J Appl Sci Biotechnol. 2022;10: 50–59

8. Maduka C V., Igbokwe IO, Atsanda NN. Appraisal of Chicken Production with Associated Biosecurity Practices in Commercial Poultry Farms Located in Jos, Nigeria. Scientifica (Cairo). 2016;2016. pmid:27200208

9. Karki S, Lupiani B, Budke CM, Karki N, Rushton J, Ivanek R. Cost-benefit analysis of avian influenza control in Nepal. Rev Sci Tech. 2015; 813–827. pmid:27044153

10. Conan A, Goutard FL, Sorn S, Vong S. Biosecurity measures for backyard poultry in developing countries: A systematic review. BMC Vet Res. 2012;8: 1–10.

11. Veterinary Standards and Drugs Admnistration Office (VSDAO). Biosecurity Manual for Commercial Poultry Production. 2013.

12. Paudel M, Acharya B, Adhikari M. Social determinants that lead to poor knowledge about, and inappropriate precautionary practices towards, avian influenza among butchers in Kathmandu, Nepal. Infect Dis Poverty. 2013;2: 1–10.

13. Okiki PA, Edafiadhe WE, Ogbimi AO. Use of poultry manure in vegetable cultivation and influenza pandemic. Adv Appl Sci Res. 2010;1: 1–7.

14. Lambrou AS, Luitel H, Bhattarai RK, Basnet HB, Heaney CD. Informing influenza pandemic preparedness using commercial poultry farmer knowledge, attitudes, and practices (KAP) surrounding biosecurity and self-reported avian influenza outbreaks in Nepal. One Heal. 2020;11: 100189. pmid:33392379

15. Napit R, Poudel A, Pradhan SM, Manandhar P, Ghaju S, Sharma AN, et al. Newcastle disease burden in Nepal and efficacy of Tablet I2 vaccine in commercial and backyard poultry production. PLoS One. 2022;18.

16. Koju P, Shrestha R, Shrestha A, Tamrakar S, Rai A, Shrestha P, et al. Antimicrobial Resistance in E. coli Isolated from Chicken Cecum Samples and Factors Contributing to Antimicrobial Resistance in Nepal. Trop Med Infect Dis 2022, Vol 7, Page 249. 2022;7: 249. pmid:36136660

17. Koirala A, Bhandari P, Shewade HD, Tao W, Thapa B, Terry R, et al. Antibiotic use in broiler poultry farms in kathmandu valley of nepal: Which antibiotics and why? Trop Med Infect Dis. 2021;6: 1211. pmid:33916475

18. Subedi M, Luitel H, Devkota B, Bhattarai RK, Phuyal S, Panthi P, et al. Antibiotic resistance pattern and virulence genes content in avian pathogenic Escherichia coli (APEC) from broiler chickens in Chitwan, Nepal. BMC Vet Res. 2018;14: 1–6.

19. The Kathmandu Post. Nepal’s population is 29,192,480. 2022. Available: https://tkpo.st/3IDg6cD

20. Kumar M, Dahiya SP, Ratwan P. Backyard poultry farming in India: A tool for nutritional security and women empowerment. Biol Rhythm Res. 2021;52: 1476–1491.

21. Islam MR (Mohammad). Sample Size and Its Role in Central Limit Theorem (CLT). Int J Phys Math. 2018;1: 37–47.

22. Kwak SG, Kim JH. Central limit theorem: the cornerstone of modern statistics. Korean J Anesthesiol. 2017;70: 144–156. pmid:28367284

23. QGIS. 2023 [cited 28 Mar 2023]. Available: https://www.qgis.org/en/site/

24. Sprygin A V., Andreychuk DB, Kolotilov AN, Volkov MS, Runina IA, Mudrak NS, et al. Development of a duplex real-time TaqMan PCR assay with an internal control for the detection of Mycoplasma gallisepticum and Mycoplasma synoviae in clinical samples from commercial and backyard poultry. 2010;39: 99–109. pmid:20390544

25. Ferguson-Noel N, Armour NK, Noormohammadi AH, El-Gazzar M, Bradbury JM. Mycoplasmosis. Dis Poult. 2019; 907–965.

26. Saif Y, Barnes HJ, Glisson JR, Fadly AM, McDougald LR, Swayne DE. Diseases of poultry. Dis poultry. 2003

27. Blagodatski A, Trutneva K, Glazova O, Mityaeva O, Shevkova L, Kegeles E, et al. Avian Influenza in Wild Birds and Poultry: Dissemination Pathways, Monitoring Methods, and Virus Ecology. Pathog 2021, Vol 10, Page 630. 2021;10: 630. pmid:34065291

28. Hill NJ, Bishop MA, Trovão NS, Ineson KM, Schaefer AL, Puryear WB, et al. Ecological divergence of wild birds drives avian influenza spillover and global spread. PLOS Pathog. 2022;18: e1010062. pmid:35588106

29. Tanquilut NC, Espaldon MVO, Eslava DF, Ancog RC, Medina CDR, Paraso MGV, et al. Quantitative assessment of biosecurity in broiler farms using Biocheck.UGent in Central Luzon, Philippines. Poult Sci. 2020;99: 3047–3059. pmid:32475441

30. Ayim-Akonor M, Krumkamp R, May J, Mertens E. Understanding attitude, practices and knowledge of zoonotic infectious disease risks among poultry farmers in Ghana. Vet Med Sci. 2020;6: 631–638. pmid:32243723

31. Melo AM, Stevens DA, Tell LA, Veríssimo C, Sabino R, Xavier MO. Aspergillosis, Avian Species and the One Health Perspective: The Possible Importance of Birds in Azole Resistance. Microorg 2020, Vol 8, Page 2037. 2020;8: 2037. pmid:33352774

32. An HSI Report: Human Health Implications of Intensive Poultry Production and Avian Influenza.

33. Collins JD, Wall PG. Food safety and animal production systems: controlling zoonoses at farm level. Rev Sci Tech. 2004;23: 685–700. pmid:15702728

34. Davies R, Wales A. Antimicrobial Resistance on Farms: A Review Including Biosecurity and the Potential Role of Disinfectants in Resistance Selection. Compr Rev Food Sci Food Saf. 2019;18: 753–774. pmid:33336931

35. Bagal UR. Pathology and Molecular Diagnosis of Mycoplasma gallisepticum and Mycoplasma synoviae Infections in Broiler Chickens from Western Maharashtra, India. J Anim Res. 2019.

36. Meerburg BG, Bonde M, Brom FWA, Endepols S, Jensen AN, Leirs H, et al. Towards sustainable management of rodents in organic animal husbandry. [cited 11 Apr 2023].

37. Rodents in poultry housing: A multi-faceted plan of attack | Stockfarm. [cited 11 Apr 2023]. Available: https://journals.co.za/doi/abs/10.10520/ejc-vp_stock_v11_n5_a25

38. Prajapati M, Ranjit E, Shrestha R, Shrestha SP, Adhikari SK, Khanal DR. Status of Antibiotic Residues in Poultry Meat of Nepal. Nepal Vet J. 2018;35: 55–62.

39. Rijal KR, Banjara MR, Dhungel B, Kafle S, Gautam K, Ghimire B, et al. Use of antimicrobials and antimicrobial resistance in Nepal: a nationwide survey. Sci Reports 2021 111. 2021;11: 1–14. pmid:34078956

40. Yadav S, Jha R. Strategies to modulate the intestinal microbiota and their effects on nutrient utilization, performance, and health of poultry. J Anim Sci Biotechnol. 2019;10: 1–11.

41. Schokker D, Jansman AJM, Veninga G, de Bruin N, Vastenhouw SA, de Bree FM, et al. Perturbation of microbiota in one-day old broiler chickens with antibiotic for 24 hours negatively affects intestinal immune development. BMC Genomics. 2017;18: 1–14.

42. Dandachi I, Chabou S, Daoud Z, Rolain JM. Prevalence and emergence of extended-spectrum cephalosporin-, carbapenem- and colistin-resistant gram negative bacteria of animal origin in the Mediterranean basin. Front Microbiol. 2018;9: 2299. pmid:30323797

43. WHO. 2021 ‎AWaRe classification‎. [cited 27 Mar 2023]. Available: https://www.who.int/publications/i/item/2021-aware-classification

44. Ahmed S, Hasan A, Khatun R, Howlader AJ, Islam N, Alam K, et al. Validation of the Declared Withdrawal Periods of Antibiotics Evaluation of Disinfectants towards Pathogens View project Razia Khatun Validation of the Declared Withdrawal Periods of Antibiotics. Univers J Public Heal. 2018;6: 14–22.

45. Dhakal S, Gompo TR. Farmer’s Knowledge on Anti-Microbial Resistance, Their Practise Of Antimicrobials Usage and Biosecurity Status of Poultry Farms in Kathmandu Valley and Chitwan District. Malaysian Anim Husb J. 2021;1: 26–32.

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Related Questions

With increased commercial poultry production, maintaining biosecurity and biosafety measures in farms have been challenging [6]. Lack of government initiatives (and efforts), both in developing and developed countries alike, to raise awareness and implement regulations on biosecurity and biosafety have also grossly undermined proper safe farming practices [10].

IBD, on the other hand, is a viral disease that can cause damage to the immune system of young chickens, often leading to mortality [26]. IAV in poultry is primarily transmitted through direct contact with infected birds or through contact with contaminated surfaces, feed, or water. Wild birds, particularly waterfowl, are the natural reservoirs for the virus and are thought to be one of the major sources of avian influenza outbreaks [27, 28].

In order to enhance biosecurity and reduce the risk of disease outbreaks in the poultry industry, it is necessary to raise awareness among poultry farmers about the usage of antibiotics along with the significance of biosecurity measures [17, 45]. This can be done through extensive practical training amongst a network of poultry farmers.
Authors:
Kavya Dhital
Dibesh karmacharya
University of Queensland
University of Queensland
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Dr Humphrey Mbugua
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