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Review ArticleOpen Access

Abattoir and Bovine Tuberculosis as a Reemerging Foodborne Disease Volume 54- Issue 3

Fahim A Shaltout*

  • Food Control Department, Faculty of Veterinary Medicine, Benha University, Egypt

Received: December 15, 2023; Published: January 05, 2024

*Corresponding author: Fahim A Shaltout, Food Control Department, Faculty of Veterinary Medicine, Benha university, Egypt

DOI: 10.26717/BJSTR.2024.54.008545

Abstract PDF

ABSTRACT

Abattoir is the place in which the animals are slaughtered for human consumption. Abattoir plays important role in prevention of zoonotic diseases between animals and humans like Mycobacterium tuberculosis as reemerging foodborne disease and also prevent infectious diseases between animals. Mycobacterium tuberculosis is caused by a species of pathogenic bacteria in the family Mycobacteriaceae. the causative agent bacteria of Bovine tuberculosis as reemerging foodborne disease tuberculosis bacteriahas an unusual, waxy coating on its cell surface primarily due to the presence of mycolic acid. This coating makes the cells impervious to Gram staining, and as a result, the causative agent bacteria of Bovine tuberculosis as reemerging foodborne disease can appear weakly Gram-positive. Acid-fast stains such as Ziehl–Neelsen stain, or fluorescent stains such as auramine are used instead to identify the causative agent of Bovine tuberculosis as reemerging foodborne disease with a microscope. The causative agent bacteria of Bovine tuberculosis as reemerging foodborne disease is highly aerobic and requires high levels of oxygen. Primarily a pathogen of the mammalian respiratory system, it infects the lungs. The most frequently used diagnostic methods for Bovine tuberculosis as reemerging foodborne disease are the tuberculin skin examination, acid-fast stain, culture, and polymerase chain reaction.

Keywords: Abattoir; Cattle; Mycobacterium Tuberculosis; Reemerging; Foodborne Disease

Introduction

Bovine tuberculosis as reemerging foodborne disease is still one of the largely neglected foodborne zoonotic diseases in the world, particularly in developing countries [1-4]. Bovine tuberculosis as reemerging foodborne disease occurrence would be still important in many places. Thus, this zoonosis deserves further research and efforts to establish the real burden of disease in cattle, role of abattoirs as well in humans. Developing strategies of interaction between academia and health care public sectors, including medical and veterinary disciplines, would generate more accurate data [5-8]. Even more, as human tuberculosis due to Bovine tuberculosis as reemerging foodborne disease is still a public health concern internationally, in developing countries where detection is usually not depend on molecular and specific diagnostic methods, in addition to microscopy investigation for acid-fast bacilli bacteria in biological samples as well as culture, Bovine tuberculosis bacteria would be causing many of M. tuberculosis-attributed human disease, particularly in the case of outside lung forms of disease, even more in rural areas where both diseases can overlap and where human–cattle contact as consumption of raw milk and dairy products contaminated with Bovine tuberculosis bacteria would be considerable [9-11] . Control programs and human tuberculosis control programs,specially in those places, should consider the importance of Bovine tuberculosis and begin to introduce operational research into their activities as well surveillance to control and prevent disease from this bacteria [12-15].

Methods of identification and Diagnosis of Bovine Tuberculosis as a reemerging foodborne disease [16-21] Bovine Tuberculosis clinical signs are not specifically distinctive and, therefore, do not enable veterinarians to make a definitive diagnosis based on clinical signs alone. The tuberculin skin examination is the standard mean of Tuberculosis diagnosis in live cattle. It consists of injecting bovine tuberculin (a purified protein extract originated from M. bovis) intra-dermally and then measuring skin thickness at the site of injection 72 hours later to detect any subsequent swelling at the injection site. Blood-based in vitro examinations that detect bacteria, antibodies, or cell-mediated immunity are also currently available, or under development. The most common used blood-based examination is a gamma interferon release assay which detects a cell-mediated immune response to infection with M. bovis. This examination is based on the principle that bovine blood cells that have previously been exposed to M. bovis through an infection are known to produce elevated levels of gamma interferon following in vitro incubation with M. bovis antigens. The definitive diagnosis means is confirmed by bacterial culture and identification in the laboratory, a process that can take eight weeks or more. The recommended examination methods, including the procedures for manufacturing and administering bovine tuberculin. Nature of Bovine tuberculosis as reemerging foodborne disease. Bovine tuberculosis as reemerging foodborne disease is a chronic bacterial disease of cattle caused by members of the Mycobacterium tuberculosis complex primarily by Bovine tuberculosis, but also by M. caprae and to a lesser extent M. tuberculosis [22-26]. It is a major infectious disease among cattle, and also affects other domesticated cattle and certain wildlife populations, causing a general state of illness, pneumonia, weight loss, and eventual death [27-31]. The name Bovine tuberculosis as a reemerging foodborne disease comes from the nodules, called ‘tubercles’, which form in the lymph nodes and other affected tissues of affected cattle [32-35].

Cattle are considered to be the major reservoir Bovine tuberculosis as a reemerging foodborne disease, and are the main source of infection for humans. Nevertheless, the disease has been reported in many other domesticated and non-domesticated animals [36-39]. Geographical distribution of Bovine tuberculosis as reemerging foodborne disease. Bovine tuberculosis as reemerging foodborne disease is found throughout the world [40-43], but some countries have never detected tuberculosis, and many developed countries have reduced or eliminated bovine tuberculosis from their cattle population and kept the disease limited to certain areas [44-48]. However, significant zones of infection remain in wildlife. The highest prevalence of bovine tuberculosis is in Africa and parts of Asia, the disease is alsoaffects countries in Europe and the Americas [49- 56]. The most prominent Clinical signs of Bovine tuberculosis as a reemerging foodborne disease in cattle, Bovine tuberculosis as reemerging foodborne disease may be sub-acute or chronic, with a variable rate of progression [57-62]. A small number of cattle may become severely affected within a few months of infection, while others may take several years to develop symptoms. Bovine tuberculosis bacteria can also lie dormant in the host without causing symptoms for a longtimes [63-68]. The usual symptoms of Bovine tuberculosis as a reemerging foodborne disease in man include Weakness, loss of appetite and weight, fluctuating fever, dyspnoea and cough, signs of low-grade pneumonia, diarrhea, enlarged, enlargement lymph nodes [69-72].

Discussion

Mycobacterium bovis has been isolated from domestic animals as cattle, buffalo, sheep, goats, equines, camels, deer, antelopes, dogs, cats, and animals [73-76]. Bovinetuberculosis as reemerging foodborne disease is an infectious disease [77-84]. Most cases of human tuberculosis are caused by the bacterial species, Mycobacterium tuberculosis. Bovine tuberculosis as reemerging foodborne disease is a form of tuberculosis in human predominantly caused by a closely related species, Bovine tuberculosis, which belongs to the M. tuberculosis complex [85-89]. Transmissionand spread of Bovine tuberculosis as reemerging foodborne disease. The disease is contagious and can be transmitted directly by contact with infected domestic and non-domesticated animals or indirectly by oral route [90-94]. Theusual route of infection within cattle herds is by inhalation of infected aerosol, which are expelled from the lungs. Calves can be infected by ingesting colostrum or milk from infected cows [95-101]. Humans can become infected by ingesting raw milk from infected cows, or through contact with infected tissues at abattoirs or butcheries [102,103]. The course of disease is slow and takes months or years to reach the fatal stage. An infected animal can shed the bacteria within the herd before the clinical signs. Movement of subclinical infected domestic cattle is a main route of spreading the disease [104-106]. Detection of Bovine tuberculosis as reemerging foodborne disease, Bovine tuberculosis as reemerging foodborne disease clinical signs are not specifically distinctive and, therefore, do not enable veterinarians to make a definitive Detection based on clinical signs alone [107,108]. The tuberculin skin examination is the standard method for tuberculosis Detection in live domestic cattle [109-112].

Blood-based in vitro examinations that detect bacteria, antibodies, or cell-mediated immunity are also currently available, or under development [113-119]. The most widely used blood-based examination is a gamma interferon release assay which detects a cell-mediated immune response to infection with Bovine tuberculosis [1,120]. This examination is based on the principle that bovine blood cells that have previously been exposed to Bovine tuberculosis through an infection are known to produce elevated levels of gamma interferon following in vitro incubation with Bovine tuberculosis antigens [2,3]. The definitive Detection is confirmed by bacterial culture and identification in the laboratory [77,78]. The recommended detection methods of Bovine tuberculosis as reemerging foodborne disease, including the procedures for manufacturing and administering bovine tuberculin [84,85]. Public health risk of Bovine tuberculosis as reemerging foodborne disease. The most common form of tuberculosis in man is caused by M. tuberculosis bacteria [89,90]. However, it is not possible to clinically differentiate infections caused by M. tuberculosis bacteria from those caused by Bovine tuberculosis, which is estimated to account for up to 10% of human tuberculosis cases in some countries [77,93]. Detection of Bovine tuberculosis as reemerging foodborne disease may be further complicated by the tendency of Bovine tuberculosis infections to be located in tissues other than the lungs and the fact that Bovine tuberculosis bacteria is naturally resistant to one of the antimicrobials that is commonly used to treat human tuberculosis [23,24].The technical standards and recommendations that are intended to manage the human and animal health risks associated with infection of cattle with a member of the Mycobacterium tuberculosis complex, including Bovine tuberculosis [29,30].

Role of abattoir in eradication of Bovine tuberculosis as a reemerging foodborne disease. Human tuberculosis is a major cause of illness and mortality worldwide [117-119]. It is primarily caused by Bovine tuberculosis as reemerging foodborne disease and is usually transmitted through the respiratory route by close contact and inhalation of aerosols of infected persons [35,36]. Bovine tuberculosis as a reemerging foodborne disease is a less common form of human tuberculosis that is caused by a related member of the Mycobacterium tuberculosis complex (Bovine tuberculosis) [41,42]. Bovine tuberculosis as a reemerging foodborne disease is primarily transmitted indirectly, through the consumption of contaminated milk, dairy products, or meat containing infected material [114-116]. In regions where food hygiene is consistently applied, the risk to the general public has been reduced [111-113]; however Bovine tuberculosis as a reemerging foodborne disease infection remains an occupational hazard to food of animal origin eaters workers, abattoir workers, and butchers [43- 48].

Bovine tuberculosis as a reemerging foodborne disease is depend up on a One Health approach recognizing the interdependence of human and animal health sectors for addressing the main health and economic effects of this disease [51-54,105-110]. Effective action from government agencies, donors, academia, non-governmental units and private stakeholders through different methods as political, financial and investigation methods [56-60]. Defining the priorities for control Bovine tuberculosis as a reemerging foodborne disease in man and bovine tuberculosis in cattle [66-68]. By Improving the scientific evidence base, Reduce transmission between cattle and humans, Supporting the cooperation between sectors, Prevention and control of Bovine tuberculosis as reemerging foodborne disease [100-103]. The National control and eradication system based on examination and slaughter of infected cattle at abattoir under hygienic precautions is successfully used to control and eradicate Bovine tuberculosis as a reemerging foodborne disease [74,75]. This method remains inapplicable in some heavily infected countries because it could necessitate slaughtering large numbers of cattle, and this may not be suitable, due to human resources are limited [16-18]. So, most of countries apply varying forms of examination and segregation in early state, and then switch to examine-and-slaughter methods in the final stage [78-80].

Several disease eradication system have been very successful in control or eradicate the Bovine tuberculosis as reemerging foodborne disease in cattle, by employing a multi-faceted approach that includes, post mortem meat inspection at abattoir, for detection of infected cattle and herds for Bovine tuberculosis as reemerging foodborne disease , intensive surveillance including on-farm visits, systematic individual examination of cattle, removal of infected and in-contact cattle, adequate local legislation, effective movement controls, individual animal identification, and effective traceability [16-19]. Detecting infected cattle in abattoirs prevents unsafe meat from entering the food chain and allows Veterinary Services to trace-back to the herd of origin of the infected animal which can then be examined and eliminated if needed [5-9]. Pasteurisation or heat treatment of cow's milk to a temperature sufficient to kill the bacteria has proven effective for preventing the spread of disease to humans [24-27]. Antimicrobial treatment of infected cattle is rarely attempted because of the doses and duration of treatment that would be required, high cost of medications, and interference with the primary goal of eliminating the disease, and potential risk of developing resistance [28-34].

Conclusion

Vaccination is practiced in human medicine, but it is, so far, not used as a preventive [121,122] measure in cattle, due to the lack of availability of safe and effective method of vaccination, and potential interference with bovine tuberculosis surveillance and examinations, due to false reactions in vaccinated cattle. Researchers and studies are actively investigating potential new or improved bovine tuberculosis kinds of vaccines and alternate routes of vaccine delivery for use in cattle and wildlife reservoirs, as well as new examinations to reliably differentiate vaccinated cattle from infected cattle.

References

  1. Abdel Moein KA, Hamed O, Fouad H (2016) Molecular detection of Mycobacterium tuberculosis in cattle and buffaloes: A cause for public health concern. Trop Anim Health Prod 48: 1541-1545.
  2. Shaltout FA, Riad EM, AbouElhassan, Asmaa A (2017) Prevalence of Mycobacterium Tuberculosis in Imported cattle Offals and Its lymph Nodes. Veterinary Medical Journal Giza (VMJG) 63(2): 115-122.
  3. (2023) Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (12th ).,.
  4. Shaltout FA, Riad EM, Asmaa AbouElhassan (2017) Prevalence of Mycobacterium Spp. In Cattle Meat and Offal's Slaughtered in And Out Abattoir. Egyptian Veterinary medical Association 77(2): 407-420.
  5. (2017) (WHO) Roadmap for zoonotic tuberculosis © World Health Organization, (FAO) Food and Agriculture Organization of the United Nations (OIE) World Organisation for Animal Health.
  6. Abd Elaziz O, Fatin S, Hassanin, Fahim A Shaltout (2021) Prevalence of Some Foodborne Parasitic Affection in Slaughtered Animals in Loacal Egyptian Abottoir. Journal of Nutrition Food Science and Technology 2(3): 1-5.
  7. Smith TA (1898) A comparative study of bovine tubercle bacilli and of human bacilli from sputum. J Exp Med 3(4-5): 451-511.
  8. Abd Elaziz O, Fatin S Hassanin, Fahim A Shaltout, Othman A Mohamed (2021) Prevalence of some zoonotic parasitic affections in sheep carcasses in a local abattoir in Cairo, Egypt. Advances in Nutrition & Food Science 6(2): 25-31.
  9. Borham M, Oreiby A, El Gedawy A, Hegazy Y, Al Gaabary M (2021) Tuberculin test errors and its effect on detection of bovine tuberculosis. J Hell Vet Med 72: 3263-3270.
  10. Al Shorman AAM, Shaltout FA, hilat N (1999) Detection of certain hormone residues in meat marketed in Jordan. Jordan University of Science and Technology, 1st International Conference on Sheep and goat Diseases and Productivity.
  11. Alvarez AH, EstradaChávez C, Flores Valdez MA (2009) Molecular findings and approaches spotlighting Mycobacterium bovis persistence in cattle. Vet Res 40(3): 22.
  12. Edris AM, Shaltout FA, Salem GH, El Toukhy EI (2011) Plasmid profile analysis of Salmonellae isolated from some meat products. Benha veterinary medical journal.
  13. Krajewska Wędzina M, Didkowska A, Sridhara AA, Elahi R, JohnathanLee A, et al. (2020) Transboundary tuberculosis: Importation of alpacas infected with Mycobacterium bovis from the United Kingdom to Poland and potential for serodiagnostic assays in detecting tuberculin skin test false-negative animals. Transbound Emerg Dis 67(3): 1306-1314.
  14. Hassanien FS, Shaltout FA, Fahmey MZ, Elsukkary HF (2020) Bacteriological quality guides in local and imported beef and their relation to public health. Benha Veterinary Medical Journal 39: 125-129.
  15. Egbe NF, Muwonge A, Ndip L, Kelly RF, Sander M, et al. (2017) Molecular epidemiology of Mycobacterium bovis in Cameroon. Sci Rep 7: 4652.
  16. Hassanin FS, Shaltout FA, Lamada HM, Abd Allah EM (2011) THE EFFECT OF PRESERVATIVE (NISIN) ON THE SURVIVAL OF LISTERIA MONOCYTOGENES. BENHA VETERINARY MEDICAL JOURNAL SPECIAL ISSUE, pp. 141-145.
  17. Ameni G, Tadesse K, Hailu E, Deresse Y, Medhin G, et al. (2014) Transmission of Mycobacterium tuberculosis between farmers and cattle in central Ethiopia. PLoS ONE 8: e76891.
  18. Khattab E, Fahim Shaltout, Islam Sabik (2021) Hepatitis A virus related to foods. BENHA VETERINARY MEDICAL JOURNAL 40(1): 174-179.
  19. Abdellrazeq GS, Elnaggar MM, Osman HS, Davis WC, Singh M (2016) Prevalence of Bovine Tuberculosis in Egyptian Cattle and the Standardization of the Interferon-gamma Assay as an Ancillary Test. Transbound Emerg Dis 63: 497-507.
  20. Saif M, Saad SM, Hassanin FS, Shaltout FA, Marionette Zaghloul (2019) Molecular detection of enterotoxigenic Staphylococcus aureus in ready-to-eat beef products. Benha Veterinary Medical Journal 37(1): 7-11.
  21. Charles OT, James HS, Michael JG (2006) Mycobacterium bovis Infection in Animals and Humans (2nd)., Emerg Infect Dis 12(8): 1306.
  22. Shaltout FA, Mona N, Hussein, Nada Kh Elsayed (2023) Histological Detection of Unauthorized Herbal and Animal Contents in Some Meat Products. Journal of Advanced Veterinary Research 13(2): 157-160.
  23. Klepp LI, Eirin ME, Garbaccio S, Soria M, Bigi F, et al. (2019) Identification of bovine tuberculosis biomarkers to detect tuberculin skin test and IFNγ release assay false negative cattle. Res Vet Sci 122: 7-14.
  24. Shaltout FA, Abdelazez Ahmed Helmy Barr, Mohamed Elsayed Abdelaziz (2022) Pathogenic Microorganisms in Meat Products. Biomedical Journal of Scientific & Technical Research 41(4): 32836-32843.
  25. Helmy NM, Abdel Moghney ARF, Atia MA (2015) Evaluation of Different PCR-Based Techniques in Diagnosis of Bovine Tuberculosis in Infected Cattle Lymph Nodes. Am J Microbiol Biotechnol 2: 75-81.
  26. Shaltout FA, EM Eldiasty, MA AsmaaHassan (2020) HYGIENIC QUALITY OF READY TO EAT COOKED MEAT IN RESTAURANTS AT Cairo. Journal of Global Biosciences 8(12): 6627-6641.
  27. Domingo M, Vidal E, Marco A (2014) Pathology of bovine tuberculosis. Res Vet Sci 97: S20-S29.
  28. Shaltout FA (2019) Food Hygiene and Control. Food Science and Nutrition Technology 4(5): 1-2.
  29. Orłowska B, KrajewskaWędzina M, Augustynowicz Kopeć E, Kozińska M, Brzezińska S, et al. (2020) Epidemiological characterization of Mycobacterium caprae strains isolated from wildlife in the Bieszczady Mountains, on the border of Southeast Poland. BMC Vet Res 16: 362.
  30. Gaafar R, Hassanin FS, Shaltout FA, Marionette Zaghloul (2019) Hygienic profile of some ready to eat meat product sandwiches sold in Benha city, Qalubiya Governorate, Egypt. Benha Veterinary Medical Journal 37(2): 16-21.
  31. Radostits OM, Gay CC, Blood DC, Hinchliff KW (2007) Veterinary Medicine. A Textbook of the Diseases of Cattle, Sheep, Goats and Horses. (8th)., Ballier Tindals; London, UK, pp. 830-838.
  32. Saad SM, Shaltout FA, Nahla A Abou Elroos, Saber B Elnahas (2019) Antimicrobial Effect of Some Essential Oils on Some Pathogenic Bacteria in Minced Meat. J Food Sci Nutr Res 2(1): 012-020.
  33. Osman MM, Shanahan JK, Chu F, Takaki KK, Pinckert ML, et al. (2022) The C terminus of the mycobacterium ESX-1 secretion system substrate ESAT-6 is required for phagosomal membrane damage and virulence. Proc Natl Acad Sci USA 119: e2122161119.
  34. Saad SM, Shaltout FA, Nahla A Abou Elroos, Saber B Elnahas (2019) Incidence of Staphylococci and E. coli in Meat and Some Meat Products. EC Nutrition 14(6).
  35. Miller MA, Kerr TJ, de Waal CR, Goosen WJ, Streicher EM, et al. (2021) Mycobacterium bovis Infection in Free-Ranging African Elephants. Emerg Infect Dis 27: 990-992.
  36. Saad SM, Hassanin FS, Shaltout FA, Marionette Z Nassif, Marwa Z Seif (2019) Prevalence of Methicillin-Resistant Staphylococcus Aureus in Some Ready-to-Eat Meat Products. American Journal of Biomedical Science & Research 4(6): 460-464.
  37. Fielding HR, McKinley TJ, Delahay RJ, Silk MJ, McDonald RA (2021) Characterization of potential superspreader farms for bovine tuberculosis: A review. Vet Med Sci 7: 310-321.
  38. Shaltout FA, EM ELdiasty, MS M Mohamed (2018) Effects of chitosan on quality attributes fresh meat slices stored at 40C. BENHA VETERINARY MEDICAL JOURNAL 35(2): 157-168.
  39. Byrne AW, Graham J, Brown C, Donaghy, Guelbenzu Gonzalo M, et al. (2018) Modelling the variation in skin-test tuberculin reactions, post-mortem lesion counts and case pathology in tuberculosis-exposed cattle: Effects of animal characteristics, histories and co-infection. Transbound. Emerg Dis 65: 844-858.
  40. Shaltout FA, Mohamed AH ElShater, Wafaa Mohamed Abd ElAziz (2015) Bacteriological assessment of Street Vended Meat Products sandwiches in kalyobia Governorate. BENHA VETERINARY MEDICAL JOURNAL 28(2): 58‐66.
  41. Elsayed MSAE, Amer A (2019) The rapid detection and differentiation of Mycobacterium tuberculosis complex members from cattle and water buffaloes in the delta area of Egypt, using a combination of real-time and conventional PCR. Mol Biol Rep 46: 3909-3919.
  42. Shaltout FA, Mohamed A El shatter, Heba M Fahim (2019) Studies on Antibiotic Residues in Beef and Effect of Cooking and Freezing on Antibiotic Residues Beef Samples. Scholarly Journal of Food and Nutritionm 2(1): 1-4.
  43. Dejene SW, Heitkönig IM, Prins HH, Lemma FA, Mekonnen DA, et al. (2016) Risk factors for bovine tuberculosis (bTB) in cattle in Ethiopia. PLoS ONE 11: e0159083.
  44. Shaltout FA, Ahmed AA Maarouf, Mahmoud ES Elkhouly (2017) Bacteriological Evaluation of Frozen Sausage. Nutrition and Food Toxicology 1(5): 174-185.
  45. Belinda ST, Erin LG (2018) Rebhun’s Diseases of Dairy Cattle. (3rd)., Elsevier; Amsterdam, The Netherlands: Miscellaneous Infectious Diseases, pp. 745-746.
  46. Shaltout FA, AM Ali, SM Rashad (2016) Bacterial Contamination of Fast Foods. Benha Journal of Applied Sciences (BJAS) 1(2): 45-51.
  47. Bezos J, Casal C, Romero B, Schroeder B, Hardegger R, et al. (2014) Current ante-mortem techniques for diagnosis of bovine tuberculosis. Res Vet Sci 97: S44-S52.
  48. Shaltout FA, Zakaria IM, Jehan Eltanani, Asmaa Elmelegy (2015) Microbiological status of meat and chicken received to Universitystudent hostel. BENHA VETERINARY MEDICAL JOURNAL 29(2): 187‐192.
  49. Abbate JM, Arfuso F, Iaria C, Arestia G, Lanteri G (2020) Prevalence of bovine tuberculosis in slaughtered cattle in Sicily, Southern Italy. Animals 10: 1473.
  50. Saad SM, Shaltout FA (1998) Mycological Evaluation of camel carcasses at Kalyobia Abattoirs. Vet Med J Giza 46(3): 223-229.
  51. Krajewska M, Załuski M, Zabost A, Orłowska B, Augustynowicz Kopeć E, et al. (2015) Tuberculosis in antelopes in a zoo in Poland–Problem of Public Health. Pol J Microbiol 4: 405-407.
  52. Saad SM, Shaltout FA, Nahla A Abou Elroos, Saber B Elnahas (2019) Antimicrobial Effect of Some Essential Oils on Some Pathogenic Bacteria in Minced Meat. J Food Sci Nutr Res 2(1): 012-020.
  53. Constable PD, Hinchcliff KW, Done SH, Grünberg (2016) Veterinary Medicine-e-Book: A Textbook of the Diseases of Cattle, Horses, Sheep, Pigs and Goats. (11th).,.
  54. Shaltout FA, Riad EM, TES Ahmed, AbouElhassan A (2017) Studying the Effect of Gamma Irradiation on Bovine Offal's Infected with Mycobacterium tuberculosis Bovine Type. Journal of Food Biotechnology Research 1(6): 1-5.
  55. Romha G, Gebru G, Asefa A, Mamo G (2018) Epidemiology of Mycobacterium bovis and Mycobacterium tuberculosis in animals: Transmission dynamics and control challenges of zoonotic tuberculosis in Ethiopia. Prev Vet Med 158: 1-17.
  56. Shaltout FA, Ahmed AA Maarouf, Mahmoud ES Elkhouly (2017) Bacteriological Evaluation of Frozen Sausage. Nutrition and Food Toxicology 1(5): 174-185.
  57. Howell AK, McCann CM, Wickstead F, Williams DJ (2019) Co-infection of cattle with Fasciola hepatica or F gigantica and Mycobacterium bovis: A systematic review. PLoS ONE 14: e0226300.
  58. Shaltout A Faheim, Mohamed A Hassan, S Hassanin (2004) THERMAL INACTIVATION OF ENTEROHAEMORRHAGIC ESCHERICHIA COLI O157:H7 AND ITS SENSTIVITY TO NISIN AND LACTIC ACID CULTURES. 1rst Ann Confr FVM Moshtohor.
  59. Shaltout FA, Mohammed Farouk, Hosam AA, Ibrahim, Mostafa EM Afifi (2017) Incidence of Coliform and Staphylococcus aureus in ready to eat fast foods. BENHA VETERINARY MEDICAL JOURNAL 32(1): 13-17.
  60. Le Roex N, Koets AP, Van Helden PD, Hoal EG (2013) Gene polymorphisms in African buffalo associated with susceptibility to bovine tuberculosis infection. PLoS ONE 8: e64494.
  61. Shaltout FA (1992) Studies on Mycotoxins in Meat and Meat by Products. M.V.Sc Thesis Faculty of Veterinary Medicine, Moshtohor, Zagazig University Benha branch.
  62. Vordermeier HM, Jones GJ, Buddle BM, Hewinson RG, Villarreal Ramos B (2016) Bovine tuberculosis in cattle: Vaccines, DIVA tests, and host biomarker discovery. Annu Rev Anim Biosci 4: 87-109.
  63. Shaltout FA (1996) Mycological and Mycotoxicological profile Of Some Meat products. Ph.D. Thesis, Faculty of Veterinary Medicine, Moshtohor, Zagazig University Benha branch.
  64. Shaltout FA (1998) Proteolytic Psychrotrophes in Some Meat products. Alex Vet Med J 14(2): 97-107.
  65. Shaltout FA (1999) Anaerobic Bacteria in Vacuum Packed Meat Products. Benha Vet Med J 10(1): 1-10.
  66. Hlokwe TM, Said H, Gcebe N (2017) Mycobacterium tuberculosis infection in cattle from the Eastern Cape Province of South Africa. BMC Vet Res 13: 299.
  67. Shaltout FA (2000) Protozoal Foodborne Pathogens in some Meat Products. Assiut Vet Med J 42(84): 54-59.
  68. Didkowska A, Orłowska B, Krajewska Wędzina M, Krzysiak M, Bruczyńska M, et al. (2022) Intra-palpebral tuberculin skin test and interferon gamma release assay in diagnosing tuberculosis due to Mycobacterium caprae in European Bison (Bison bonasus) Pathogens 11(2): 260.
  69. Shaltout FA (2001) Quality evaluation of sheep carcasses slaughtered at Kalyobia abattoirs. Assiut Veterinary Medical Journal 46(91): 150-159.
  70. Jaouad B (1993) Mycobacterium bovis Infection in Cattle in Morocco: Preparation and Evaluation of Chemical Extracts for Use in Detection of Immune Responses.
  71. Shaltout FA (2003) Yersinia Enterocolitica in some meat products and fish marketed at Benha city. The Third international conference Mansoura.
  72. Kuria JK (2019) Bacterial Cattle Diseases. IntechOpen; London, UK: Diseases Caused by Bacteria in Cattle: Tuberculosis.
  73. Shaltout FA, Abdel Aziz AM (2004) ESCHERICHIA COLI STRAINS IN SLAUGHTERED ANIMALS AND THEIR PUBLIC HEALTH IMPORTENCE. JEgypt Vet Med Association 64(2): 7-21.
  74. Mittal M, Chakravarti S, Sharma V, Sanjeeth BS, Churamani CP, et al. (2014) Evidence of presence of Mycobacterium tuberculosis in bovine tissue samples by multiplex PCR: Possible relevance to reverse zoonosis. Transbound Emerg Dis 61: 97-104.
  75. Shaltout FA, Amin R, Marionet Z Nassif, Shimaa (2014) Detection of aflatoxins in some meat products. Benha veterinary medical journal 27(2): 368-374.
  76. Pollock JM, Neill SD (2002) Mycobacterium bovis infection and tuberculosis in cattle. Vet J 163: 115-127.
  77. Shaltout FA (2012) Improvement of microbiological status of oriental sausage. Journal of Egyptian Veterinary Medical Association 72(2): 157-167.
  78. Kassa GM, Abebe F, Worku Y, Legesse M, Medhin G, et al. (2012) Tuberculosis in goats and sheep in Afar Pastoral Region of Ethiopia and isolation of Mycobacterium tuberculosis from goat. Vet Med Int 2012: 869146.
  79. Shaltout FA, Edris AM (1999) Contamination of shawerma with pathogenic yeasts. Assiut Veterinary Medical Journal 40(64): 34-39.
  80. Pascual Linaza AV, Gordon AW, Stringer LA, Menzies FD (2017) Efficiency of slaughterhouse surveillance for the detection of bovine tuberculosis in cattle in Northern Ireland. Epidemiol Infect 145: 995-1005.
  81. Shaltout FA, Salem R, Eldiasty E, Diab, Fatema (2016) Mycological evaluation of some ready to eat meat products with special reference to molecular chacterization. Veterinary Medical Journal Giza 62(3): 9-14.
  82. Broughan JM, Judge J, Ely E, Delahay RJ, Wilson G, et al. (2016) A review of risk factors for bovine tuberculosis infection in cattle in the UK and Ireland. Epidemiol Infect 144: 2899-2926.
  83. Shaltout FA, Elshater M, Wafaa, Abdelaziz (2015) Bacteriological assessment of street vended meat products sandwiches in Kalyobia Governorat. Benha Vet Med J 28(2): 58-66.
  84. Cvetkovikj I, Mrenoshki S, Krstevski K, Djadjovski I, Angjelovski B, et al. (2017) Bovine tuberculosis in the Republic of Macedonia: Postmortem, microbiological and molecular study in slaughtered reactor cattle. Maced Vet Rev 40: 43-52.
  85. Shaltout FA, Ibrahim HM (1997) Quality evaluation of luncheon and Alexandrian sausage. Benha Vet Med J 10(1): 1-10.
  86. Ameni G, Vordermeier M, Firdessa R, Aseffa A, Hewinson G, et al. (2011) Mycobacterium tuberculosis infection in grazing cattle in central Ethiopia. Vet J 188: 359-361.
  87. Shaltout FA, Amani M, Salem AH, Mahmoud KA (2013) Bacterial aspect of cooked meat and offal at street vendor level. Benha veterinary medical journal 24(1): 320-328.
  88. Oreiby AF, Hegazy YM, Al Gaabary MH, Osman SA, Marzok MA (2015) Studies on clinical identification, elisa, bacteriological isolation, PCR and x-ray radiography for diagnosis of ovine caseous lymphadenitis. J Anim Vet Adv 14: 250-253.
  89. Shaltout FA, Salem RM (2000) Moulds, aflatoxin B1 and Ochratoxin A in Frozen Livers and meat products. Vet Med JGiza 48(3): 341-346.
  90. Murai K, Tizzani P, Awada L, Mur L, Mapitse NJ, et al. (2019) Panorama 2019-1: Bovine tuberculosis: Global distribution and implementation status of prevention and control measures according to WAHIS data. OIE Bulletin de 1(1): 3.
  91. Shaltout FA, Salem RM, El diasty, Eman, Fatema, et al. (2016) Mycological evaluation of some ready to eat meat products with special reference to molecular characterization. Veterinary Medical Journal Giza 62(3): 9-14.
  92. Brahma D, Narang D, Chandra M, Filia G, Singh A, et al. (2019) Diagnosis of Bovine Tuberculosis by Comparative Intradermal Tuberculin Test, Interferon Gamma Assay and esxB (CFP-10) PCR in Blood and Lymph Node Aspirates. Open J Vet Med 9: 55-65.
  93. Shaltout FA, Reham A Amin, Marionette Z Nassif, Shimaa A Abd Elwahab (2014) Detection of aflatoxins in some meat products. BENHA VETERINARY MEDICAL JOURNAL 27(2): 368‐374.
  94. Didkowska A, Orłowska B, Krajewska Wędzina M, Augustynowicz Kopeć E, Brzezińska S, et al. (2021) Microbiological and molecular monitoring for bovine tuberculosis in the Polish population of European bison (Bison bonasus). Ann Agric Environ Med 28: 575-578.
  95. Shaltout FA, Hanan M Lamada, Ehsan AM, Edris (2020) Bacteriological examination of some ready to eat meat and chicken meals. Biomed J Sci & Tech Res 27(1): 20461-20465.
  96. Koch R (1882) Die aetiologie der tuberkulose. Berl Klin Wochenschr 19: 221-230.
  97. Edris AM, Hassan MA, Shaltout FA, Elhosseiny S (2012) Detection of E. coli and Salmonella organisms in cattle and camel meat. BENHA VETERINARY MEDICAL JOURNAL 24(2): 198-204.
  98. Ibrahim S, Danbirni S, Abubakar UB, Usman A, Saidu AS, et al. (2018) Estimates of Mycobacterial Infections Based on Abattoir Surveillance in Two North-Eastern States of Nigeria. Acta Sci Microbiol 1: 60-65.
  99. Hassanin FS, Shaltout FA, Mostafa EM (2013) Parasitic affections in edible offal. Benha Vet MedJ 25(2): 34-39.
  100. Markey B, Leonard F, Archambault M, Cullinane A, Maguire D (2013) Clinical Veterinary Microbiology e- Book. (2nd)., Elsevier.
  101. Ebeed Saleh, Fahim Shaltout, Essam Abd Elaal (2021) Effect of some organic acids on microbial quality of dressed cattle carcasses in Damietta abattoirs, Egypt. Damanhour Journal of Veterinary Sciences 5(2): 17-20.
  102. McCallan L, McNair J, Skuce R, Branch BA (2014) A Review of the Potential Role of Cattle Slurry in the Spread of Bovine Tuberculosis. Agri-food and Biosciences Institute.
  103. Hassanin FS, Hassan MA, Shaltout FA, ElraisAminaM (2014) CLOSTRIDIUM PERFRINGENS IN VACUUM PACKAGED MEAT PRODUCTS. BENHA VETERINARY MEDICAL JOURNAL 26(1): 49-53.
  104. Taylor SJ, Ahonen LJ, de Leij FA, Dale JW (2003) Infection of Acanthamoeba castellanii with Mycobacterium bovis and bovis BCG and survival of M. bovis within the amoebae. Appl Environ Microbiol 69: 4316-4319.
  105. Hassan MA, Shaltout FA (2004) Comparative Study on Storage Stability of Beef, Chicken meat, and Fish at Chilling Temperature. Alex J Vet Science 20(21): 21-30.
  106. In: Mukundan H, Chambers M, Waters R, Larsen MH (Eds.)., (2015) Tuberculosis, Leprosy and Mycobacterial Diseases of Man and Animals. The Many Hosts of Mycobacteria. Immunopathogenesis of Mycobacterium bovis Infection of Cattle, pp. 136.
  107. Edris AM, Shaltout FA, Abd Allah AM (2005) Incidence of Bacillus cereus in some meat products and the effect of cooking on its survival. Zag Vet J 33(2): 118-124.
  108. Liebana E, Johnson L, Gough J, Durr P, Jahans K, et al. (2008) Pathology of naturally occurring bovine tuberculosis in England and Wales Vet J 176(3): 354-360.
  109. Saad SM, Shaltout FA, Nahla A Abou Elroos, Saber B Elnahas (2019) Incidence of Staphylococci and coli in Meat and Some Meat Products. EC Nutrition 14.6.
  110. Waters WR (2015) Large Animal Internal Medicine-e-Book. Elsevier; Amsterdam, The Netherlands: Bovine Tuberculosis, pp. 633-636.
  111. Hazaa W, Shaltout FA, Mohamed El Shater (2019) Identification of Some Biological Hazards in Some Meat Products. Benha Veterinary Medical Journal 37(2): 27-31.
  112. Stear M (2005) OIE Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (Mammals, Birds and Bees) (5th)., Volumes 1 and 2. World Organization for Animal Health 2004. ISBN 92 9044 622 6. €140. Parasitology 130(06): 727-727.
  113. Elnaggar MM, Abdellrazeq GS, Elsisy A, Mahmoud AH, Shyboub A, et al. (2017) Evaluation of antigen specific interleukin-1β as a biomarker to detect cattle infected with Mycobacterium bovis. Tuberculosis 105: 53-59.
  114. De la RuaDomenech R, Goodchild AT, Vordermeier HM, Hewinson RG, Christiansen KH, et al. (2006) Ante mortem diagnosis of tuberculosis in cattle: A review of the tuberculin tests, γ-interferon assay and other ancillary diagnostic techniques. Res Vet Sci 81: 190-210.
  115. PicassoRisso C, Grau A, Bakker D, Nacar J, Mínguez O, et al. (2019) Association between results of diagnostic tests for bovine tuberculosis and Johne’s disease in cattle. Vet Rec 185(22): 693.
  116. Saif M, Saad SM, Hassanin FS, Shaltout FA, Marionette Zaghlou (2019) Prevalence of methicillin-resistant Staphylococcus aureus in some ready-to-eat meat products. Benha Veterinary Medical Journal 37(1): 12-15.
  117. Parlane NA, Chen S, Jones GJ, Vordermeier HM, Wedlock DN, et al. (2016) Display of antigens on polyester inclusions lowers the antigen concentration required for a bovine tuberculosis skin test. Clin Vaccine Immunol 23: 19-26.
  118. Gaafar R, Hassanin FS, Saad saad, Shaltout FA, Marionette Zaghloul (2019) Molecular detection of enterotoxigenic Staphylococcus aureus in some ready to eat meat-based sandwiches. Benha Veterinary Medical Journal 37(2): 22-26.
  119. Picasso Risso C, Alvarez J, VanderWaal K, Kinsley A, Gil A, et al. (2021) Modelling the effect of test-and-slaughter strategies to control bovine tuberculosis in endemic high prevalence herds. Transbound Emerg Dis 68: 1205-1215.
  120. Shaltout FA, ElToukhy EI, Abd ElHai MM (2019) Molecular Diagnosis of Salmonellae in Frozen Meat and Some Meat Products. Nutrition and Food Technology Open Acces 5(1): 1-6.
  121. ElSawalhy A (2012) Veterinary Infectious Diseases in Domestic Animals. (3rd)., Vetbook; Cairo Egypt, pp. 305-308.
  122. Edris AM, Shaltout FA, Salem GH, ElToukhy EI (2011) Incidence and isolation of Salmonellae from some meat products. Benha Veterinary Medical Journal (I): 194-200.