One Health surveillance of certain zoonotic bacterial pathogens in South Asia: current status, challenges, and future directions

المؤلفون

  • Irfan Ullah المؤلف
  • Zakir Ullah المؤلف
  • Aimal Ali المؤلف

DOI:

https://doi.org/10.66585/ohmi.2026.2.0030

الكلمات المفتاحية:

One Health; zoonotic bacterial pathogens; antimicrobial resistance; whole-genome sequencing; South Asia; Pakistan.

الملخص

Zoonotic bacterial pathogens impose a substantial and unevenly documented burden on public health, animal health, and food safety. South Asia is home to roughly a quarter of the world's people, and one of the densest livestock populations on earth, yet the epidemiology, antimicrobial resistance, and genomic diversity of its zoonotic bacteria remain poorly characterized. This mini-review synthesizes published evidence from 2000 to 2026 on six pathogen groups of regional priority: Brucella spp., Listeria spp., Klebsiella pneumoniae, Leptospira spp., Bacillus anthracis, and Salmonella spp., with Campylobacter spp. considered alongside Salmonella across Pakistan, India, Bangladesh, Nepal, and Sri Lanka. Evidence is distributed unevenly across these five countries. Brucellosis seroprevalence ranges from 2.0–18.75% in Pakistani livestock, 15% in Nepalese sheep, and 8.4% among Sri Lankan adults. Human leptospirosis in Sri Lanka is estimated at 300.6 per 100,000 population, with a 7.0% case fatality rate. In Bangladesh, 26 cutaneous anthrax outbreaks produced 1,210 suspected human cases between 2013 and 2016. Resistance is severe where measured: 73.5% of Klebsiella pneumoniae isolates from a referral hospital in Kathmandu, Nepal, were multidrug-resistant (MDR), and 97.1% of Campylobacter isolates from Bangladeshi chicken farms met MDR criteria. Sequencing capacity exists in the region and has been applied to typhoidal Salmonella in Bangladesh and Nepal, to Brucella melitensis and Listeria monocytogenes in India, to Leptospira in Sri Lanka, and to clinical Klebsiella collections. However, every such study is a discrete research output; no country operates whole-genome sequencing-based surveillance spanning the human, animal, food, and environmental sectors for the pathogens reviewed here. The gap is therefore one of integration and governance rather than of technology alone. A staged, costed roadmap is proposed, with priority actions, responsible institutions, and indicative timelines, drawing on models from other low- and middle-income regions where genomic surveillance has been established under comparable constraints.

السير الشخصية للمؤلفين

  • Irfan Ullah

    Department of Zoology, Shaheed Benazir Bhutto University, Sheringal, Dir Upper – 18000, Khyber Pakhtunkhwa Pakistan

  • Zakir Ullah

    Department of Zoology, Shaheed Benazir Bhutto University, Sheringal, Dir Upper – 18000, Khyber Pakhtunkhwa Pakistan

  • Aimal Ali

    Department of Zoology, Shaheed Benazir Bhutto Women University, Peshawar – 25000, Khyber Pakhtunkhwa, Pakistan

المراجع

1. Prasarnphanich OO, Berger C, Abdikadir MI, Alfonso-Dilley CS, Belot G, Boniol M, et al. Developing a Tripartite (Food and Agriculture Organization of the United Nations; World Health Organization; and World Organisation for Animal Health) tool to strengthen the workforce for effective management of zoonotic diseases. BMC Glob Public Health. 2025;3(1):75. https://doi.org/10.1186/s44263-025-00194-2

2. Zinsstag J, Schelling E, Waltner-Toews D, Tanner M. From “One Medicine” to “One Health” and systemic approaches to health and well-being. Prev Vet Med. 2011;101(3–4):148–156. https://doi.org/10.1016/j.prevetmed.2010.07.003

3. Taylor LH, Latham SM, Woolhouse ME. Risk factors for human disease emergence. Philos Trans R Soc Lond B Biol Sci. 2001;356(1411):983–989. https://doi.org/10.1098/rstb.2001.0888

4. Khan MD, Khan IU, Rasool N, Shah AA, Ahmad T, Afghan SUD, et al. Epidemiology of brucellosis in humans and livestock: A systematic review and meta-analysis (2000–2025) from Pakistan. OAPH&HAR. 2025;1(1):179–193. https://doi.org/10.59644/oaphhar.1(1).258

5. Grace D, Mutua F, Ochungo P, Kruska R, Jones K, Brierley L, et al. Mapping of poverty and likely zoonoses hotspots. Nairobi: International Livestock Research Institute. 2012. https://hdl.handle.net/10568/21161

6. Islam MM, Dutta P, Bansal D, Gongal G, Farag E, Soares Magalhaes RJ, et al. Prevalence and risk factors of coxiellosis at the human–animal–environment interface in the South Asian countries: A systematic review and meta-analysis. Transbound Emerg Dis. 2025;2025:2890693. https://doi.org/10.1155/tbed/2890693

7. Ramanujam H, Ramalingam M, Refaya AK, Rajendran P, Baskar M, Palanivel N, et al. Genomic insights into Mycobacterium orygis in wild ungulates in Chennai, India. Infect Genet Evol. 2026;137:105869. https://doi.org/10.1016/j.meegid.2025.105869

8. Kemp M, Nielsen XC, Bartels MD, Hasman H, Nielsen EM. Fuldgenom-DNA-sekventering til overvågning af bakterielle infektionssygdomme [Whole genome sequencing for surveillance of bacterial infectious illnesses]. Ugeskr Laeger. 2023;185(18):V11220690.

9. Köser CU, Ellington MJ, Cartwright EJP, Gillespie SH, Brown NM, Farrington M, et al. Routine use of microbial whole genome sequencing in diagnostic and public health microbiology. PLoS Pathog. 2012;8(8):1002824. https://doi.org/10.1371/journal.ppat.1002824

10. Kwong JC, McCallum N, Sintchenko V, Howden BP. Whole genome sequencing in clinical and public health microbiology. Pathology. 2015;47(3):199–210. https://doi.org/10.1097/PAT.0000000000000235

11. Ayoub H, Kumar MS, Mehta R, Sethuraj SE, Thomas P, Dhanze H, et al. Genomic insights into Brucella melitensis in India: Stability of ST8 and the role of virulence genes in regional adaptations. Microbiol Spectr. 2025;13(6):02647-24. https://doi.org/10.1128/spectrum.02647-24

12. Chaity SC, Hosen MA, Rahman SR, Khan MAS. Genomic characterization and comparative analysis of antibiotic resistance and virulence in Bangladeshi and global Klebsiella pneumoniae ST48 strains. J Genet Eng Biotechnol. 2025;23(3):100557. https://doi.org/10.1016/j.jgeb.2025.100557

13. Dyson ZA, Ashton PM, Khanam F, Chunga Chirambo A, Shakya M, Meiring JE, et al. Pathogen diversity and antimicrobial resistance transmission of Salmonella enterica serovars Typhi and Paratyphi A in Bangladesh, Nepal, and Malawi: A genomic epidemiological study. Lancet Microbe. 2024;5(8):100841. https://doi.org/10.1016/S2666-5247(24)00047-8

14. Rahman MM, Miah M, Hossain ME, Rahim S, Sultana S, Satter SM, et al. Development of a culture-independent whole-genome sequencing of Nipah virus using the MinION Oxford Nanopore platform. Microbiol Spectr. 2025;13(6):e02492-24. https://doi.org/10.1128/spectrum.02492-24

15. Senavirathna I, Jayasundara D, Warnasekara J, Matthias MA, Vinetz JM, Agampodi S. Whole genome sequencing data of Leptospira weilii and Leptospira kirschneri isolated from human subjects of Sri Lanka. Data Brief. 2024;52:109840. https://doi.org/10.1016/j.dib.2023.109840

16. Ali Khan E, Rizwan M, Wang Y, Munir F, Hua J. Challenges and future prospects of Pakistan's animal industry: Economic potential, emerging trends, and strategic directions. Vet Sci. 2025;12(8):733. https://doi.org/10.3390/vetsci12080733

17. Jamil T, Khan AU, Saqib M, Hussain MH, Melzer F, Rehman A, et al. Animal and human brucellosis in Pakistan. Front Public Health. 2021;9:660508. https://doi.org/10.3389/fpubh.2021.660508

18. Saleem F, Faraz A, Irtaza A, Ishaq HM, Ilyas MF, Khalid RH, et al. Policies to control zoonotic disease transmission in Pakistan. In: Khan A, Rasheed M, Abbas RZ, editors. Zoonosis. Vol. 1. Faisalabad (Pakistan): Unique Scientific Publishers. 2023. p. 348–360. https://doi.org/10.47278/book.zoon/2023.026

19. World Health Organization Regional Office for South-East Asia. Regional roadmap to advance field epidemiology capacities in the WHO South-East Asia Region 2025–2029. New Delhi: World Health Organization Regional Office for South-East Asia. 2024. https://www.who.int/publications/i/item/9789290229544

20. Yasobant S, Tadvi R, Bruchhausen W, Saxena DB. Application of the One Health Surveillance (OHS) matrix to evaluate the disease surveillance systems in Gujarat, India: A policy content analysis. J Epidemiol Glob Health. 2024;14(4):1633–1641. https://doi.org/10.1007/s44197-024-00317-2

21. Godfroid J, Al Dahouk S, Pappas G, Roth F, Matope G, Muma J, et al. A “One Health” surveillance and control of brucellosis in developing countries: Moving away from improvisation. Comp Immunol Microbiol Infect Dis. 2013;36(3):241–248. https://doi.org/10.1016/j.cimid.2012.09.001

22. Dean AS, Crump L, Greter H, Schelling E, Zinsstag J. Global burden of human brucellosis: A systematic review of disease frequency. PLoS Negl Trop Dis. 2012;6(10):1865. https://doi.org/10.1371/journal.pntd.0001865

23. Khurana SK, Sehrawat A, Tiwari R, Prasad M, Gulati B, Shabbir MZ, et al. Bovine brucellosis: A comprehensive review. Vet Q. 2021;41(1):61–88. https://doi.org/10.1080/01652176.2020.1868616

24. Franco MP, Mulder M, Gilman RH, Smits HL. Human brucellosis. Lancet Infect Dis. 2007;7(12):775–786. https://doi.org/10.1016/S

1473-3099(07)70286-4

25. Khaliq MS, Mushtaq MH, Rehman A, Awan FN, Avais M, Jamil T. Brucellosis seropositivity and risk factors in small ruminants and livestock workers: A cross-sectional study in Punjab, Pakistan. Prev Vet Med. 2026;246:106726. https://doi.org/10.1016/j.prevetmed.2025.106726

26. Ullah I, Naz S, Khattak US, Saeed M, Ul Akbar N, Rauf S. Molecular prevalence, phylogenetic analysis, and PCR-based detection of Brucella melitensis in humans and cattle in Southern Khyber Pakhtunkhwa, Pakistan. Comp Immunol Microbiol Infect Dis. 2024;115:102262. https://doi.org/10.1016/j.cimid.2024.102262

27. Aslam T, Hayat S, Alyas S, Ilyas A. Seroprevalence of brucellosis in cows and buffaloes. Int J Appl Exp Biol. 2025;4(1):1–9. https://doi.org/10.56612/ijaaeb.v1i1.112

28. Manjrekar DV, Nale TN, Bahurupi YA, Shewale AD, Kuwatada JS, Tiwari S. Epidemiology of human brucellosis in India: A systematic review. J Vector Borne Dis. 2026;63(1):106–113. https://doi.org/10.4103/jvbd.jvbd_235_24

29. Samad MA. A systematic review of pre-clinical and clinical research reports on small ruminants published during the last six decades in the then East Pakistan and in Bangladesh. J. Vet. Med. OH Res. 2019;1(2):111–183. https://doi.org/10.36111/jvmohr.2019.1(2).0010

30. Gompo TR, Shah R, Tiwari I, Gurung YB. Sero-epidemiology and associated risk factors of brucellosis among sheep and goat population in the south western Nepal: A comparative study. BMC Vet Res. 2021;17(1):132. https://doi.org/10.1186/s12917-021-02835-8

31. Karunanayake L, Karunanayake P, Rathnayaka CS, Senarath U, Ranbanda JM, Kothalawala M. Seroprevalence and associated risk factors of human Brucella infection in selected provinces in Sri Lanka. Ceylon Med J. 2019;64(1):25–29. https://doi.org/10.4038/cmj.v64i1.8824

32. de Oliveira MM, Pereira CR, de Oliveira IRC, Godfroid J, Lage AP, Dorneles EMS. Efficacy of Brucella abortus S19 and RB51 vaccine strains: A systematic review and meta-analysis. Transbound Emerg Dis. 2022;69(4):32–51. https://doi.org/10.1111/tbed.14259

33. Akar K, Brangsch H, Jamil T, Öz GY, Baklan EA, Eroğlu B, et al. Genomic analysis of Brucella isolates from animals and humans, Türkiye, 2010 to 2020. Euro Surveill. 2024;29(38):2400105. https://doi.org/10.2807/1560-7917.ES.2024.29.38.2400105

34. Wareth G, El-Diasty M, Melzer F, Schmoock G, Moustafa SA, El-Beskawy M, et al. MLVA-16 genotyping of Brucella abortus and Brucella melitensis isolates from different animal species in Egypt: Geographical relatedness and the Mediterranean lineage. Pathogens. 2020;9(6):498. https://doi.org/10.3390/pathogens9060498

35. Vázquez-Boland JA, Kuhn M, Berche P, Chakraborty T, Domínguez-Bernal G, Goebel W, et al. Listeria pathogenesis and molecular virulence determinants. Clin Microbiol Rev. 2001;14(3):584–640. https://doi.org/10.1128/CMR.14.3.584-640.2001

36. Swaminathan B, Gerner-Smidt P. The epidemiology of human listeriosis. Microbes Infect. 2007;9(10):1236–1243. https://doi.org

/10.1016/j.micinf.2007.05.011

37. Bagatella S, Tavares-Gomes L, Oevermann A. Listeria monocytogenes at the interface between ruminants and humans: A comparative pathology and pathogenesis review. Vet Pathol. 2022;59(2):186–210. https://doi.org/10.1177/03009858211052659

38. Pirzada AR, Rather MA, Shoukat S, Shah SA, Shafi M, Qureshi S. Molecular epidemiology, virulence gene profile and antibiogram of Listeria monocytogenes from foods of animal origin and ovines in Kashmir, India. Cogent Food Agric. 2025;11(1):2563188. https://doi.org/10.1080/23311932.2025.2563188

39. Rivu S, Rahman SMM, Ahmed S. Environmental surveillance of Listeria spp. in cattle farms in Bangladesh: Prevalence, distribution, and hemolytic diversity. Bangla. J. Microbiol. 2025;41(1):1–11. https://doi.org/10.3329/bjm.v41i1.84477

40. Chandio TH, Soomro AH, Bhutto MB, Dewani P, Shah G. Occurrence of Listeria monocytogenes in bovine milk in Hyderabad, Pakistan. Ann Microbiol. 2007;57(3):341–344. https://doi.org/10.1007/BF03175070

41. Barbuddhe SB, Rawool DB, Doijad SP, Vergis J, Malik SS, Chakraborty T. Ecology of Listeria monocytogenes and Listeria species in India: The occurrence, resistance to biocides, genomic landscape and biocontrol. Environ Microbiol. 2022;24(6):2759–2780. https://doi.org/10.1111/1462-2920.15819

42. D'Ambrosio G, Schirone M, Paparella A. Listeria monocytogenes in ready-to-eat foods: Risk perspectives across different regulatory systems. Foods. 2026;15(3):470. https://doi.org/10.3390/foods15030470

43. Albert V, Ramamurthy T, Das S, Dolma KG, Majumdar T, Baruah PJ, et al. Comprehending the risk of foodborne and waterborne disease outbreaks: Current situation and control measures with special reference to the Indian scenario. Heliyon. 2024;10(16):36344. https://doi.org/10.1016/j.heliyon.2024.e36344

44. Wareth G, Neubauer H. The striking incidence of animal listeriosis in Germany (2014–2024) indicates a persistent but neglected risk for One Health. Vet Res. 2025;56(1):53. https://doi.org/10.1186/s13567-025-01481-4

45. Kozytska T, Neubauer H, Wareth G. Listeria ivanovii—An underestimated pathogen in veterinary medicine. Front Vet Sci. 2026;13:1844936. https://doi.org/10.3389/fvets.2026.1844936

46. Martin RM, Bachman MA. Colonization, infection, and the accessory genome of Klebsiella pneumoniae. Front Cell Infect Microbiol. 2018;8:4. https://doi.org/10.3389/fcimb.2018.00004

47. Santajit S, Indrawattana N. Mechanisms of antimicrobial resistance in ESKAPE pathogens. Biomed Res Int. 2016;2016:2475067. https://doi.org/10.1155/2016/2475067

48. Siu LK, Yeh KM, Lin JC, Fung CP, Chang FY. Klebsiella pneumoniae liver abscess: A new invasive syndrome. Lancet Infect Dis. 2012;12(11):881–887. https://doi.org/10.1016/S1473-3099(12)70205-0

49. Castro J, Oliveira R, Fernandes L, Carvalho I, Oliveira H, Brinks E, et al. Molecular characterization and virulence profile of Klebsiella pneumoniae and Klebsiella oxytoca isolated from ill cats and dogs in Portugal. Vet Microbiol. 2024;292:110056. https://doi.org/10.1016

/j.vetmic.2024.110056

50. Payros D, Auvray F, Foucras G, Oswald E. Is Klebsiella pneumoniae-associated bovine mastitis an emerging public health issue? A One Health perspective. ASM Anim Microbiol. 2026;1(2):00023-25. https://doi.org/10.1128/asmam.00023-25

51. Ilyas R, Asghar S, Zehra M, Usmani Y, Khan RMA, Mirani ZA, et al. Molecular assessment of carbapenem-resistant and ESBL Klebsiella pneumoniae clinical isolates to decipher the correlation of antimicrobial resistance with virulence traits. Infect Genet Evol. 2025;133:105785. https://doi.org/10.1016/j.meegid.2025.105785

52. Mehmood MS, Saddique MN, Iqbal MU. Prevalence and antimicrobial resistance of Klebsiella pneumonia in Pakistan, 2015–2025: A systematic review and meta-analysis [Preprint]. SSRN. 2025. https://doi.org/10.2139/ssrn.5868054

53. Desai D, Sharma T, Gandham N, Khopkar-Kale P, Bharti N, Kasibhatla SM, et al. Genomic characterization of multidrug-resistant Klebsiella pneumoniae clinical isolates from India. Sci Rep. 2026;16(1):25547. https://doi.org/10.1038/s41598-026-54711-w

54. Hinthong W, Phelan J, Hussain A, Mazumder R, Azra, Haq IU, et al. Genomic insights into Klebsiella pneumoniae: Virulence, resistance, and transmission in South and Southeast Asia. Int J Med Microbiol. 2025;320:151666. https://doi.org/10.1016/j.ijmm.2025.151666

55. Neupane B, Devkota MD, Pokhrel BM, Rimal S, Banjara MR. Phenotypic characteristics and carbapenemase genes in Klebsiella pneumoniae from patients at Upendra Devkota Memorial National Institute of Neurological and Allied Sciences, Kathmandu, Nepal. BMC Infect Dis. 2025;25(1):1119. https://doi.org/10.1186/s12879-025-11530-0

56. Sanam, Haq IU, Kamal M, Khan S, Khattak I, Khan NU, et al. Prevalence and antimicrobial resistance of Klebsiella pneumoniae isolated from subclinical mastitis in selected pure dairy cattle breeds in Pakistan. Curr Microbiol. 2025;82(12):548. https://doi.org/10.1007/s00284-025-04550-1

57. Wareth G, Brangsch H, Nguyen NH, Nguyen TNM, Pletz MW, Neubauer H, et al. WGS analysis of hypervirulent and MDR Klebsiella pneumoniae from Vietnam reveales an inverse relationship between resistome and virulome. Ger. J. Microbiol. 2024;4(1):15–24. https://doi.org/10.51585/gjm.2024.1.0030

58. Levett PN. Leptospirosis. Clin Microbiol Rev. 2001;14(2):296–326. https://doi.org/10.1128/CMR.14.2.296-326.2001

59. Vijayachari P, Sugunan AP, Shriram AN. Leptospirosis: An emerging global public health problem. J Biosci. 2008;33(4):557–569. https://doi.org/10.1007/s12038-008-0074-z

60. Warnasekara J, Koralegedara I, Agampodi S. Estimating the burden of leptospirosis in Sri Lanka: A systematic review. BMC Infect Dis. 2019;19(1):119. https://doi.org/10.1186/s12879-018-3655-y

61. Hugh-Jones M, Blackburn J. The ecology of Bacillus anthracis. Mol Aspects Med. 2009;30(6):356–367. https://doi.org/10.1016/j.mam

.2009.08.003

62. Inglesby TV, O'Toole T, Henderson DA, Bartlett JG, Ascher MS, Eitzen E, et al. Anthrax as a biological weapon, 2002: Updated recommendations for management. JAMA. 2002;287(17):2236–2252. https://doi.org/10.1001/jama.287.17.2236

63. Chowdhury S, Islam MS, Haider N, Hossain MB, Alam MA, Sharif MAR, et al. Risk factors associated with cutaneous anthrax outbreaks in humans in Bangladesh. Front Public Health. 2024;12:1442937. https://doi.org/10.3389/fpubh.2024.1442937

64. Roonie A, Majumder S, Kingston JJ, Parida M. Molecular characterization of B. anthracis isolates from the anthrax outbreak among cattle in Karnataka, India. BMC Microbiol. 2020;20(1):232. https://doi.org/10.1186/s12866-020-01917-1

65. Majowicz SE, Musto J, Scallan E, Angulo FJ, Kirk M, O'Brien SJ, et al. The global burden of nontyphoidal Salmonella gastroenteritis. Clin Infect Dis. 2010;50(6):882–889. https://doi.org/10.1086/650733

66. Shil S, Haldar S, Arora SS, Pan D, Koley H, Chowdhury J, et al. Antimicrobial resistance in Salmonella from Indian poultry: Trends, challenges, and One Health perspectives. J Pure Appl Microbiol. 2026;20(1):1–32. https://doi.org/10.22207/JPAM.20.1.31

67. Harun AB, Khatri B, Karim MR. Phenotypic and genotypic patterns of antimicrobial resistance in livestock and poultry in South Asia: A systematic review and meta-analysis. Food Control. 2024;164:110575. https://doi.org/10.1016/j.foodcont.2024.110575

68. Humphrey T, O'Brien S, Madsen M. Campylobacters as zoonotic pathogens: A food production perspective. Int J Food Microbiol. 2007;117(3):237–257. https://doi.org/10.1016/j.ijfoodmicro.2007.01.006

69. Van TTH, Nguyen HNK, Smooker PM, Coloe PJ. The antibiotic resistance characteristics of non-typhoidal Salmonella enterica isolated from food-producing animals, retail meat and humans in South East Asia. Int J Food Microbiol. 2012;154(3):98–106. https://doi.org/10.1016/j.ijfoodmicro.2011.12.032

70. Leclercq R, Cantón R, Brown DFJ, Giske CG, Heisig P, MacGowan AP, et al. EUCAST expert rules in antimicrobial susceptibility testing. Clin Microbiol Infect. 2013;19(2):141–160. https://doi.org/10.1111/j.1469-0691.2011.03703.x

71. Hasan M, Talukder S, Mandal AK, Tasmim ST, Parvin S, Ali Y, et al. Antimicrobial resistance profiles of Campylobacter spp. recovered from chicken farms in two districts of Bangladesh. Foodborne Pathog Dis. 2025;22(2):118–130. https://doi.org/10.1089/fpd.2023.0079

72. Laxminarayan R, Duse A, Wattal C, Zaidi AK, Wertheim HF, Sumpradit N, et al. Antibiotic resistance—the need for global solutions. Lancet Infect Dis. 2013;13(12):1057–1098. https://doi.org/10.1016/S1473-3099(13)70318-9

73. Review on Antimicrobial Resistance. Tackling drug-resistant infections globally: Final report and recommendations. London: Review on Antimicrobial Resistance. 2016. https://amr-review.org/sites/default/files/160525_Final%20paper_with%20cover.pdf

74. Arshed MJ, Umair M, Talib U, Tahir MF, Abubakar M, Bahadur SUK, et al. Status of antimicrobial resistance in food animals in Pakistan (2016–2020): A systematic review and meta-analysis. J Adv Vet Anim Res. 2025;12(2):668–679. https://doi.org/10.5455/javar.2025.l930

75. Zeb S, Yasmin H, Malik IR, Farah MA, Arya VM, Hassan MN. Antimicrobial resistant Brucella spp. prevail in raw milk and animal feces of different livestock farms. BMC Microbiol. 2025;25(1):231. https://doi.org/10.1186/s12866-025-03930-8

76. Nayakvadi S, Prakash K, Revanasiddappa ST, Gowda R, Ramamurthy AS, Shome R, et al. Antimicrobial resistance and virulence profiles of MRSA and MRCoNS across the livestock–human–environment nexus in Karnataka. Microb Pathog. 2026;211:108259. https://doi.org/10.1016/j.micpath.2025.108259

77. Van Boeckel TP, Brower C, Gilbert M, Grenfell BT, Levin SA, Robinson TP, et al. Global trends in antimicrobial use in food animals. Proc Natl Acad Sci U S A. 2015;112(18):5649–5654. https://doi.org/10.1073/pnas.1503141112

78. Cuong NV, Padungtod P, Thwaites G, Carrique-Mas JJ. Antimicrobial usage in animal production: A review of the literature with a focus on low- and middle-income countries. Antibiotics. 2018;7(3):75. https://doi.org/10.3390/antibiotics7030075

79. Woolhouse M, Ward M, Van Bunnik B, Farrar J. Antimicrobial resistance in humans, livestock and the wider environment. Philos Trans R Soc Lond B Biol Sci. 2015;370(1670):20140083. https://doi.org/10.1098/rstb.2014.0083

80. Deka D, Malakar D, Kumari A, Islam J, Dutta R. Emerging viral zoonoses: Challenges in surveillance, prevention, and global response. Thai J Vet Med. 2025;55(Suppl 2):S13–S29.

81. Nguyen TT, Mai TN, Dang-Xuan S, Nguyen-Viet H, Unger F, Lee HS. Emerging zoonotic diseases in Southeast Asia in the period 2011–2022: A systematic literature review. Vet Q. 2024;44(1):1–15. https://doi.org/10.1080/01652176.2023.2300965

82. Fèvre EM, Bronsvoort BMdC, Hamilton KA, Cleaveland S. Animal movements and the spread of infectious diseases. Trends Microbiol. 2006;14(3):125–131. https://doi.org/10.1016/j.tim.2006.01.004

83. Didelot X, Bowden R, Wilson DJ, Peto TE, Crook DW. Transforming clinical microbiology with bacterial genome sequencing. Nat Rev Genet. 2012;13(9):601–612. https://doi.org/10.1038/nrg3226

84. Chattaway MA, Dallman TJ, Gentle A, Wright MJ, Long SE, Ashton PM, et al. Whole genome sequencing for public health surveillance of Shiga toxin-producing Escherichia coli other than serogroup O157. Front Microbiol. 2016;7:258. https://doi.org/10.3389/fmicb.2016.00258

85. Zaidi AKM, Awasthi S, deSilva HJ. Burden of infectious diseases in South Asia. BMJ. 2004;328(7443):811–815. https://doi.org/10.113

6/bmj.328.7443.811

86. Inzaule SC, Tessema SK, Kebede Y, Ouma AEO, Nkengasong JN. Genomic-informed pathogen surveillance in Africa: Opportunities and challenges. Lancet Infect Dis. 2021;21(9):281–289. https://doi.org/10.1016/S1473-3099(20)30939-7

87. Halbedel S, Wamp S, Lachmann R, Holzer A, Pietzka A, Ruppitsch W, et al. High-density genomic surveillance and risk profiling of clinical Listeria monocytogenes subtypes in Germany. Genome Med. 2024;16(1):115. https://doi.org/10.1186/s13073-024-01389-2

88. Soliman EA, Saad A, Abd El Tawab AA, Elhofy FI, Rizk AM, Elkhayat M, et al. Exploring AMR and virulence in Klebsiella pneumoniae isolated from humans and pet animals: A complement of phenotype by WGS-derived profiles in a One Health study in Egypt. One Health. 2024;19:100904. https://doi.org/10.1016/j.onehlt.2024.100904

89. Davedow T, Carleton H, Kubota K, Palm D, Schroeder M, Gerner-Smidt P, et al. PulseNet International survey on the implementation of whole genome sequencing in low and middle-income countries for foodborne disease surveillance. Foodborne Pathog Dis. 2022;19(5):332–340. https://doi.org/10.1089/fpd.2021.0110

90. Brito AF, Semenova E, Dudas G, Hassler GW, Kalinich CC, Kraemer MUG, et al. Global disparities in SARS-CoV-2 genomic surveillance. Nat Commun. 2022;13(1):7003. https://doi.org/10.1038/s41467-022-33713-y

91. Thompson L, Cayol C, Awada L, Muset S, Shetty D, Wang J, et al. Role of the World Organisation for Animal Health in global wildlife disease surveillance. Front Vet Sci. 2024;11:1269530. https://doi.org/10.3389/fvets.2024.1269530

92. Kelly TR, Karesh WB, Johnson CK, Gilardi KVK, Anthony SJ, Goldstein T, et al. One Health proof of concept: Bringing a transdisciplinary approach to surveillance for zoonotic viruses at the human–wild animal interface. Prev Vet Med. 2017;137(Pt B):112–118. https://doi.org/10.1016/j.prevetmed.2016.11.023

93. Huq MS, Acharya SC, Gautam M, Silwal SR, Sapkota S, Poudyal S, et al. Cancer research in South Asian Association for Regional Cooperation (SAARC) countries. Lancet Oncol. 2024;25(12):675–684. https://doi.org/10.1016/S1470-2045(24)00518-7

94. Perez-Sepulveda BM, Heavens D, Pulford CV, Predeus AV, Low R, Webster H, et al. An accessible, efficient and global approach for the large-scale sequencing of bacterial genomes. Genome Biol. 2021;22(1):349. https://doi.org/10.1186/s13059-021-02536-3

95. Qiu Y, Ferreira JP, Ullah RW, Flanagan P, Zaheer MU, Tahir MF, et al. Assessment of the implementation of Pakistan's national action plan on antimicrobial resistance in the agriculture and food sectors. Antibiotics. 2024;13(3):206. https://doi.org/10.3390/antibiotics13030206

96. Queenan K, Häsler B, Rushton J. A One Health approach to antimicrobial resistance surveillance: Is there a business case for it? Int J Antimicrob Agents. 2016;48(4):422–427. https://doi.org/10.1016/j.ijantimicag.2016.06.014

97. World Health Organization. Global genomic surveillance strategy for pathogens with pandemic and epidemic potential, 2022–2032. Geneva: World Health Organization. 2022. https://www.who.int/publications/i/item/9789240046979

منشور

2026-09-02

إصدار

القسم

Review Article

كيفية الاقتباس

Ullah, I., Ullah, Z., & Ali, A. (2026). One Health surveillance of certain zoonotic bacterial pathogens in South Asia: current status, challenges, and future directions. One Health Microbiology & Infection, 2(1), 211-227. https://doi.org/10.66585/ohmi.2026.2.0030

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