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Bacterial Zoonotic Diseases: A Public Health Nutrition Perspective and Policy Implication in Nigeria

Received: 24 June 2023    Accepted: 8 July 2023    Published: 31 August 2023
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Abstract

More than half of the infectious diseases in existence are zoonoses, hence, the necessity calls for us to exemplify these diseases with identifiable pros and cons for a better policy implementation towards improved public health. This is therefore a review of bacterial zoonoses with emphasis on those that are food-borne with the identifiable pros and cons tailored towards policy making and implementation enhancement with a conceptual framework drawn out for Nigeria. The search engines accessed are: Google search, Google scholar, PubMed and HINARI. Zoonotic diseases can be classified based on the causative pathogens which are viruses, parasites, bacteria, fungi and prions. Some of the bacterial zoonotic diseases discussed are: Anthrax, Brucellosis, Bubonic plague, Cat-scratch disease, Claymydiosis or Enzootic abortion, Food-borne diarrheal diseases, Glanders, Leprosy, etc. These diseases have associated merits and demerits. The pros as identified are: possibility of developing natural immunity against the disease in infected humans after recovery most especially in few viral zoonoses; outbreak of zoonosis may enforce proper channeling of resources for human benefits; outbreak of a zoonotic disease may also draw and command global attention to the endemic areas for aids; after an outbreak developed infrastructures, especially in the health sector, may be a trade off from an effective and prompt response to a zoonosis outbreak; there may exist a rapid concomitant technological and intellectual advancement due to the development of vaccines, drugs and other logistics to combat the disease as in the case of COVID-19. The cons are attributable to both the measureable and non measureable reduction in quality of life, loss of lives and animals which are hazardous to human, animal and environmental sustainability, hence, a defective ecosystem that work against sustainable development. Zoonotic diseases are really with accompanied merits and demerits which if properly considered and addressed may be helpful in adequate and effective policy implementation towards sustainable development.

Published in World Journal of Public Health (Volume 8, Issue 3)
DOI 10.11648/j.wjph.20230803.15
Page(s) 220-228
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Bacterial Zoonoses, Public Health Nutrition, Policy Implication

References
[1] CDC (2022). Anthrax: What is anthrax? www.cdc.gov/anthrax/basics/index/html
[2] Hamutyinei D. T., Chonzi P., Madembo C., Juru T. P., Chadambuka A., Gombe N. T., et al. (2022). Anthrax outbreak investigation in Tengwe, Mashonaland West Province, Zimbabwe, 2022. PLOS ONE; 17 (12): e0278537 doi.org/10.1371/journal.pone.0278537.
[3] Alam M. E., Kamal M. M., Rahman M., Kabir A., Islam M. S. and Hassan J. (2022). Review of anthrax: A disease of farm animals. Journal of Advanced Veterinary and Animal Research; 9 (2): 323-334.
[4] Hesse E. M., Godfrey-Cato S. and Bower W. A. (2022). Antitoxin use in the prevention and treatment of anthrax disease: A systematic review. Clinical Infectious Diseases; 75 (3): S432-S440 doi.org/10.1093/cid.ciac532.
[5] Parker C. M., Karchmer A. W., Fisher M. C., Muhammad K. M. and Yu P. A. (2022). Safety of antimicrobials for post exposure prophylaxis and treatment of anthrax: a review. Clinical Infectious Diseases; 75 (3): S417-S431 doi.org/10.1093/cid/ciac592.
[6] Majzobi M. M., Karami P., Khodavirdipour A. and Alikhani M. Y. (2022). Brucellosis in humans with the approach of Brucella species contamination in unpasteurized milk and dairy products from Hamadan, Iran. Iranian Journal of Medical Microbiology; 16 (4): 282-287.
[7] Pradhan A.. and Karanth S. (2023). Zoonoses from animal meat and milk. In: Present Knowledge in Food Safety-A risk-based approach through the food chain. Academic Press, Cambridge, U.S.A. pp 394-411.
[8] Karimitabar Z., Chegini Z., Shokoohizadeh L., Moez N. M., Arabestani M. R. and Hosseini S. M. (2023). Use of the quantum dot-labeled solid lipid nanoparticles for delivery of streptomycin and hydroxychloroquine: A new therapeutic approach for treatment of intracellular Brucella abortus infection. Biomedicine and Pharmacotherapy; 158: 114-116.
[9] Banda A., Gandiwa E., Muboko N., Mutanga C. N. and Mashapa C. (2022). Local community awareness and practices on Yersinia pestis plague disease management in Nayi and Umzingwane districts, southwestern Zimbabwe. Ecosystems and People; 18 (1): 164-173.
[10] Torrejon E., Sanches G. S., Moerbeck L., Santos L., Andre M. R., Domingos A. and Antunes S. (2022). Molecular survey of Bartonella species in stray cats and dogs, humans and questing ticks from Portugal. Pathogens; 11 (7): 749 doi.org/10.3390/pathogens11070749.
[11] Smolar A. L. O., Breitschwerdt E. B., Phillips P. H., Newman N. J. and Biousse V. (2022). Cat scratch disease: What to do with the cat? American Journal of Ophthalmology Case Reports; 28: 101702 doi.org/10.1016/j.ajoc.2022.101702.
[12] Turin L., Surini S., Wheelhouse N. and Rocchi M. S. (2022). Recent advances and public health implication for environmental exposure to Chlamydia abortus: from enzootic to zoonotic disease. Veterinary Research; 53 (37): 2022 doi.org/10.1186/s13567-022-01052-X.
[13] Godwin E. J. O., Chandrasearan V., Smah A. C. and Faith E. O. (2022). Emerging Infectious Food system related zoonotic food borne disease- A threat to global food safety and nutrition security In: Lamas A., Franco C. M. and Regal P. (eds.) Food borne Pathogens- Recent Advances in Control and Detection. IntechOpen, London, England.
[14] Pal M. and Gutama K. P. (2022). Glanders: A potential bioterrorism weapon disease. American Journal of Infectious Diseases and Microbiology; 10 (3): 98-101.
[15] CDC (2012). Glanders-Transmission www.cdc.gov/glanders/transmission/index/html
[16] Han X. Y. and Silva F.J. (2014). On the age of leprosy. PLOS Neglected Tropical Diseases; 8 (2): e2544 doi: 10.1371/journal.pntd.0002544.
[17] Sivakumar R. R. (2022). Ocular leptospirosis: lack of awareness among ophthalmologists and challenges in diagnosis. Current Opinion in Ophthalmology; 33 (6): 532-542.
[18] Karpagam K. B. and Ganesh B. (2020). Leptospirosis: a neglected tropical zoonotic infection of public health importance- An updated review. European Journal of Clinical Microbiology and Infectious Diseases; 39 (5): 835-846.
[19] Lane A. B. and Dore M. M. (2016). Leptospirosis: A clinical review of evidence based diagnosis, treatment and prevention. World Journal of Clinical Infectious Diseases; 6 (4): 61. doi: 10.5495/wjcid.v6.i4.61.
[20] Masunga. D. S., Rai A., Abbass M., Uwishema O., Wellington J, Uweis L., El-Saleh R., Arab S., Onyeaka C. V. P. and Onyeaka H. (2022). Leptospirosis outbreak in Tanzania: An alarming situation. Annals of Medicine and Surgery; 80: 104347 doi.org/10.1016/j.amsu.2022.104347.
[21] Perner J., Kucera M., Frantova H., Urbanova V., Kopacek P. and Sima R. (2022). Lyme disease transmission by severely impaired ticks. Open Biology; 12 (2): doi.org/10.1098/rsob.210244.
[22] Kasimov V., Dong Y., Shao R., Brunton A., Anstey S. I., Hall C., Chalmer G., Conroy G., Booth R., Timms P. and Jelocnik M. (2022). Emerging and well characterized chlamydial infections detected in a wide range of wild Australian birds. Transboundary and Emerging Diseases; 69 (5): e3154-e3170 doi.org/10.1111/tbed.14457.
[23] Liu X., Hu H., Liu J., Chin J., Chu J. and Cheng H. (2023). Physcion, a novel anthraquinone derivative against Clamydia psittaci infection. Veterinary Microbiology; 109664 doi.org/10.1016/j.vetmic.2023.109664.
[24] Missault S., De Meyst A., Elslande J. V., Van den Abeele A. M., Steen E., Van Acker J. and Vanrompay D. (2023). Three cases of a typical pneumonia with Chlamydia psittaci: the role of laboratory vigilance in the diagnosis of psittacosis. Pathogens; 12 (1): 65 doi.org/10.3390/pathogens.120.10065.
[25] Cam H. B. (2023). Treatment of Chlamydial infections. In: Sarier M. (ed.). Chlamydia-secret enemy from past to present. IntechOpen, England doi: 10.5772/intechopen.109648.
[26] Ullah Q., Jamil T., Saqib M., Iqbal M., and Neubauer H. (2022). Q fever- A neglected zoonosis. Microorganisms; 10 (8): 1530 doi.org/10.3390/microorganisms10081530.
[27] Mathews K. O. I., Norris J. M., Phalen D., Malikides N., Savage C., Sheehy P. A. and Bosward K. L. (2023). Factors associated with Q fever vaccination in Australian wildlife rahabilitators. Vaccine; 41 (1): 201-210.
[28] Conan A., Gallagher C. A., Erskine N., Howland M., Smith-Anthony M., Marchi S., et al. (2023). Is there a higher risk of exposure to Coxiella burnetii for pre-clinical veterinary students?. One Health; 16: 100485 doi.org/10.1016/j.onehlt.2023.100485.
[29] Coessens M. and DeLaere E. (2022). Rat bite fever: a case report review. International Journal of Clinical and Laboratory Medicine; 77 (5): 883-888.
[30] Bedner K and Crago E. (2022). What a rat race: A case study of rat bite fever in an emergency department. Journal of Emergency Nursing; 48 (5): 583-585.
[31] Gong B., Li H., Feng Y., Zeng S., Zhuo Z., Luo J., Chen X. and Li X. (2022). Prevalence, serotype distribution and antimicrobial resistance of non-typhoidal Salmonella in hospitalized patients in Conghua District of Guangzhou, China. Frontiers in Cellular and Infection Microbiology; 12: 806384 doi.10.3389/fcimb.2022.806384.
[32] Dec M., Zajac M., Puchalski A., Szczepaniak K and Urban-Chmiel R. (2022). Pet reptiles in Poland as a potential source of transmission of Salmonella. Pathogens; 11 (10): 1125 doi.org/10.3390/pathogens11101125.
[33] Scoggin K., Lynch R., Gupta J., Nagarajan A., Sheffield M., Elsaadi A et al. (2022). Genetic background influences survival of infection with Salmonella enteric serovar Typhimurium in the Collaborative Cross. PLOS Genetics; 18 (4): e1010075 doi.org/10.1371/journal.pgen.1010075.
[34] Cargnel M., Filippitzi M. E., van Cauteren D., Matheus W., Botteldoorn N., Cambier L. and Welby S. (2023). Assessing evidence of a potential Salmonella transmission across the poultry food chain. Zoonoses and Public Health; 70 (1): 22-45.
[35] El-Saadony M. T., Salem H. M., El-Tahan A. M., El-Mageed T. A. A., Soliman S. M., Khafaga A. F. et al. (2022). The control of poultry salmonellosis using organic agents: an updated overview. Poultry Science; 101 (4): 101716 doi.org/10.1016/j.psj.2022.101716.
[36] Cot. B., Vieira-Pinto M. and Oliveira M. (2023). Biocide use for the control of non-typhoidal Salmonella in the food producing animal scenario: A primary food production to for perspective. In: Huang H. and Naushad S (eds.) Salmonella Past, Present and Future. IntechOpen, England.
[37] Worku W., Desta M and Menjetta T. (2022). High prevalence and antimicrobial susceptibility pattern of Salmonella species and extended-spectrum beta-lactamase producing Escherichia coli from raw cattle meat at butcher houses in Hawassa city, Sidama region state, Ethiopia. PLOS ONE; 17 (1): e0262308 doi.org/10.1371/journal.pone.0262308.
[38] Khan A. S. and Rahman S. R. (2022). Use of phages to treat antimicrobial-resistant Salmonella infections in poultry. Veterinary Science; 9 (8): 438 doi.org/10.3390/vetsci.9080438.
[39] Mina S. A., Hasan Z. and Chowdhury A. M. M. A. (2023). The prevalence of multi-drug resistant Salmonella typhi isolated from blood sample. Microbiology Insights doi.org/10.1177/11786361221150760.
[40] Castro-Vargas R. E., Herrera-Sanchez M. P., Rodriguez-Hernandez R. and Rondon-Barragan I. S. (2020). Antibiotic resistance in Salmonella spp. isolated from poultry: A global overview. Veterinary World; 13 (10): 2070-2084.
[41] Alshoabi S. A., Almas. A., Aldofin S. A., Hamid A. M., Alhazmi F. H., Alsharif W. M. et al. (2022). The diagnostic deceiver: Radiological pictorial review of Tuberculosis. Diagnostics; 12 (2): 306 doi.org/10.3390/diagnostics12020306.
[42] Turner R. D. (2019). Cough in pulmonary tuberculosis: existing knowledge and general insights. Pulmonary Pharmacology and Therapeutics; 55: 89-94.
[43] Azad K. A. K. and Chowdhury T. (2022). Extrapulmonary Tuberculosis (EPTB): An overview. Bangladesh Journal of Medicine; 33 (2): 130-137.
[44] Lema A. G. and Dame I. E. (2022). Bovine Tuberculosis remains a major public health concern: A review. Austin Journal of Veterinary Science and Animal Husbandry; 9 (1): 1085 www.austinpublishinggroup.com
[45] Torra E., Getachew M., Seyoum W. and Abayneh E. (2022). Public awareness, prevalence and potential determinants of bovine tuberculosis in selected districts of Gamo zone, Southern Ethiopia. Veterinary Medicine: Research and Reports; 13: 163-17.
[46] Libera K., Konieczny K., Grabska J., Szopka W., Augustyniak A. and Pomorska-Mol M. (2022). Selected livestock-associated zoonoses as a growing challenge for public health. Infectious Disease Reports; 14 (1): 63-81.
[47] Dockrell H. M., McShane H. (2022). Tuberculosis vaccines in the era of Covid-19- what is taing us so long? eBiomedicine; 79: 103993 doi.org/10.1016/j.ebiom.2022.103993.
[48] Chopra K. K., Pandey P., Malik A., Indora A. and Pandey S. (2022). Infection control and preventing the transmission of tuberculosis in high-risk centers-recovery shelter for homeless people. Indian Journal of Tuberculosis doi.org/10.1016/j.ijtb.2022.11.002.
[49] Sykes J. E. (2023). Tick-borne diseases. Veterinary Clinics: Small Animal Practice; 53 (1): 141-154.
[50] Kukla R., Kracmarova R., Ryakova L., Bavlovic J., Pellantova V., Bolehovska R. et al. (2022). Francisella tularensis caused cervical lymphadenopathy in little children after a tick bite: Two case reports and a short literature review. Ticks and Tick-borne Diseases; 13 (2): 101893 doi.org/10.1016/j.ttbdis.2021.101893.
[51] Fooladfar Z. and Moradi F. (2023). Francisella and tularemia in western Asia, Iran: a systematic review. New Microbes and New Infections; 52: 101092 doi.org/10.1016/j.nmni.2023.101092.
[52] Pal M., Shuramo M. Y. and Gutama K. P. (2022). Tularemia: A re-emerging infectious zoonotic disease of public health significance. International Journal of Clinicaland Experimental Medicine Research; 6 (1): 48-51.
[53] Sadiku I., Namani S., Berisha V. N., Bicaku A. P. and Hysen S. (2022). Tularemia in children during the last outbreak in Kosovo. The Journal of Infection in Developing Countries; 16 (8): 1364-1369.
[54] Urbancic N. B., Korva M., Avsic-Zupanic T., Battelino S. and Vozel D. (2022). Vector-borne Tularemia; A re-emerging cause of cervical lymphadenopathy. Tropical Medicine and Infectious Disease; 7 (8): 189 doi.org/10.3390/tropicalmed7080189.
[55] CDC (2018). Tularemia Transmission www.cdc.gov/tularemia/transmission/index.html
[56] Mehta H. H., Song X. and Shamoo Y. (2023). Intracellular experimental evolution of Francisella tularensis subsp holarctica Live Vaccine Strain (LVS) to anti-microbial resistance. American Chemical Society (ACS) Infectious Diseases; doi.org/10.1021/acsinfecdis.2c00483.
[57] Copur B., and Surme S. (2023). Water-borne oculoglandular tularemia: Two complicated cases and a review of the literature. Travel Medicine and Infectious Disease; 51: 102489 doi.org/10.1016/j.tmaid.2022.102489.
[58] Van Meter D. S. and Van Horn C. E. (1975). The policy implementation process: A conceptual framework. Administration and Society; 6 (4): doi.org/10.1177/009539977500600404.
Cite This Article
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    Paulina Oludoyin Adeniyi, Bassey Ekpenyong Anam. (2023). Bacterial Zoonotic Diseases: A Public Health Nutrition Perspective and Policy Implication in Nigeria. World Journal of Public Health, 8(3), 220-228. https://doi.org/10.11648/j.wjph.20230803.15

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    ACS Style

    Paulina Oludoyin Adeniyi; Bassey Ekpenyong Anam. Bacterial Zoonotic Diseases: A Public Health Nutrition Perspective and Policy Implication in Nigeria. World J. Public Health 2023, 8(3), 220-228. doi: 10.11648/j.wjph.20230803.15

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    AMA Style

    Paulina Oludoyin Adeniyi, Bassey Ekpenyong Anam. Bacterial Zoonotic Diseases: A Public Health Nutrition Perspective and Policy Implication in Nigeria. World J Public Health. 2023;8(3):220-228. doi: 10.11648/j.wjph.20230803.15

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  • @article{10.11648/j.wjph.20230803.15,
      author = {Paulina Oludoyin Adeniyi and Bassey Ekpenyong Anam},
      title = {Bacterial Zoonotic Diseases: A Public Health Nutrition Perspective and Policy Implication in Nigeria},
      journal = {World Journal of Public Health},
      volume = {8},
      number = {3},
      pages = {220-228},
      doi = {10.11648/j.wjph.20230803.15},
      url = {https://doi.org/10.11648/j.wjph.20230803.15},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.wjph.20230803.15},
      abstract = {More than half of the infectious diseases in existence are zoonoses, hence, the necessity calls for us to exemplify these diseases with identifiable pros and cons for a better policy implementation towards improved public health. This is therefore a review of bacterial zoonoses with emphasis on those that are food-borne with the identifiable pros and cons tailored towards policy making and implementation enhancement with a conceptual framework drawn out for Nigeria. The search engines accessed are: Google search, Google scholar, PubMed and HINARI. Zoonotic diseases can be classified based on the causative pathogens which are viruses, parasites, bacteria, fungi and prions. Some of the bacterial zoonotic diseases discussed are: Anthrax, Brucellosis, Bubonic plague, Cat-scratch disease, Claymydiosis or Enzootic abortion, Food-borne diarrheal diseases, Glanders, Leprosy, etc. These diseases have associated merits and demerits. The pros as identified are: possibility of developing natural immunity against the disease in infected humans after recovery most especially in few viral zoonoses; outbreak of zoonosis may enforce proper channeling of resources for human benefits; outbreak of a zoonotic disease may also draw and command global attention to the endemic areas for aids; after an outbreak developed infrastructures, especially in the health sector, may be a trade off from an effective and prompt response to a zoonosis outbreak; there may exist a rapid concomitant technological and intellectual advancement due to the development of vaccines, drugs and other logistics to combat the disease as in the case of COVID-19. The cons are attributable to both the measureable and non measureable reduction in quality of life, loss of lives and animals which are hazardous to human, animal and environmental sustainability, hence, a defective ecosystem that work against sustainable development. Zoonotic diseases are really with accompanied merits and demerits which if properly considered and addressed may be helpful in adequate and effective policy implementation towards sustainable development.},
     year = {2023}
    }
    

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  • TY  - JOUR
    T1  - Bacterial Zoonotic Diseases: A Public Health Nutrition Perspective and Policy Implication in Nigeria
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    AB  - More than half of the infectious diseases in existence are zoonoses, hence, the necessity calls for us to exemplify these diseases with identifiable pros and cons for a better policy implementation towards improved public health. This is therefore a review of bacterial zoonoses with emphasis on those that are food-borne with the identifiable pros and cons tailored towards policy making and implementation enhancement with a conceptual framework drawn out for Nigeria. The search engines accessed are: Google search, Google scholar, PubMed and HINARI. Zoonotic diseases can be classified based on the causative pathogens which are viruses, parasites, bacteria, fungi and prions. Some of the bacterial zoonotic diseases discussed are: Anthrax, Brucellosis, Bubonic plague, Cat-scratch disease, Claymydiosis or Enzootic abortion, Food-borne diarrheal diseases, Glanders, Leprosy, etc. These diseases have associated merits and demerits. The pros as identified are: possibility of developing natural immunity against the disease in infected humans after recovery most especially in few viral zoonoses; outbreak of zoonosis may enforce proper channeling of resources for human benefits; outbreak of a zoonotic disease may also draw and command global attention to the endemic areas for aids; after an outbreak developed infrastructures, especially in the health sector, may be a trade off from an effective and prompt response to a zoonosis outbreak; there may exist a rapid concomitant technological and intellectual advancement due to the development of vaccines, drugs and other logistics to combat the disease as in the case of COVID-19. The cons are attributable to both the measureable and non measureable reduction in quality of life, loss of lives and animals which are hazardous to human, animal and environmental sustainability, hence, a defective ecosystem that work against sustainable development. Zoonotic diseases are really with accompanied merits and demerits which if properly considered and addressed may be helpful in adequate and effective policy implementation towards sustainable development.
    VL  - 8
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Author Information
  • Wageningen Center for Development Innovation, Wageningen University and Research, Wageningen, Netherlands

  • Institute of Public Policy and Administration, University of Calabar, Calabar, Nigeria

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