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Bovine leukemia virus: a perspective insight into the infection and immunity | ||
| Iranian Journal of Veterinary Research | ||
| دوره 24، شماره 4 - شماره پیاپی 85، 2023، صفحه 290-300 اصل مقاله (586.63 K) | ||
| نوع مقاله: Review article | ||
| شناسه دیجیتال (DOI): 10.22099/ijvr.2023.48236.7023 | ||
| نویسندگان | ||
| Gh. Nikbakht Brujeni* 1؛ P. Houshmand2؛ P. Soufizadeh3 | ||
| 1Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran | ||
| 2Ph.D. Student in Immunology, Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran | ||
| 3Graduated from Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran | ||
| چکیده | ||
| Bovine leukemia virus (BLV) is a member of the Retroviridae family and belongs to the Deltaretrovirus genus. It has a close relationship with human T-cell leukemia virus type I. BLV is responsible for causing enzootic bovine leukosis (EBL), a contagious disease that affects the bovine lymphatic system. This virus poses challenges for the global cattle industry, as it impacts cattle populations all over the world. Despite being widespread and impactful, BLV often goes unnoticed, with many researchers unaware of its presence and the potential consequences it carries. BLV demonstrates varying levels of pathogenicity. The majority of cattle (around 70%) become seropositive asymptomatic carriers, displaying no noticeable clinical symptoms. However, a smaller proportion of infected animals experience persistent lymphocytosis, characterized by an elevated number of lymphocytes in the bloodstream. If not monitored and managed, a subset of these persistently infected cattle may advance to lymphosarcoma. This condition typically presents as tumors in different lymphoid tissues, impacting various organs and overall health and productivity. Furthermore, recent research has highlighted the potential association between the occurrence of breast and lung cancer in humans and the presence of BLV. This review will delve into the recent discoveries concerning BLV, specifically exploring its epidemiology, the economic impact it has on the global cattle industry, its implications for human medicine, and the association between different alleles of the major histocompatibility complex (MHC) and susceptibility or resistance to BLV. | ||
| کلیدواژهها | ||
| Bovine leukemia virus؛ Enzootic bovine leukosis؛ Major histocompatibility complex؛ Retroviridae | ||
| مراجع | ||
|
Aida, Y; Murakami, H; Takahashi, M and Takeshima, SN (2013). Mechanisms of pathogenesis induced by bovine leukemia virus as a model for human T-cell leukemia virus. Front. Microbiol., 4: 1-12.
Ali, AOA; Murphy, L; Stear, A; Fairlie-Clarke, K; Nikbakht Brujeni, G; Donskow-Łysoniewska, K; Groth, D; Buitkamp, J and Stear, MJ (2019). Association of MHC class II haplotypes with reduced faecal nematode egg count and IgA activity in British Texel sheep. Parasite Immunol., 41: e12626.
Alkafajy, A; Al-Karagoly, H and Nikbakht Brujeni, G (2020). Comparison of cattle BoLA-DRB3 typing by PCR-RFLP, direct sequencing, and high-resolution DNA melting curve analysis. Vet. Res. Forum., 11: 21-26.
Alkaragoly, H; Nikbakht Brujeni, G; Esmailnejad, A; Hasanzadeh, M and Tolouei, T (2018). MHC IIB genetic diversity and its association with humoral immune responses in commercial turkey. Iran. J. Vet. Med., 12: 347-356.
Baniukevic, J; Hakki Boyaci, I; Goktug Bozkurt, A; Tamer, U; Ramanavicius, A and Ramanaviciene, A (2013). Magnetic gold nanoparticles in SERS-based sandwich immunoassay for antigen detection by well oriented antibodies. Biosens. Bioelectron., 43: 281-288.
Barshevskaya, LV; Sotnikov, DV; Zherdev, AV; Khassenov, BB; Baltin, KK; Eskendirova, SZ; Mukanov, KK; Mukantayev, KK and Dzantiev, BB (2019). Triple immunochromatographic system for simultaneous serodiagnosis of bovine brucellosis, tuberculosis, and leukemia. Biosensors. 9: 1-10.
Bartlett, PC; Ruggiero, VJ; Hutchinson, HC; Droscha, CJ; Norby, B; Sporer, KRB and Taxis, TM (2020). Current developments in the epidemiology and control of enzootic bovine leukosis as caused by bovine leukemia virus. Pathogens. 9: 1-13.
Bartlett, PC; Sordillo, LM; Byrem, TM; Norby, B; Grooms, DL; Swenson, CL; Zalucha, J and Erskine, RJ (2014). Options for the control of bovine leukemia virus in dairy cattle. JAVMA. 244: 914-922.
Bazargani, TT; Tooloei, M; Nikbakht Brujeni, G; Garagozlo, MJ; Bokaei, S; Khormali, M and Barjaste, N (2010). The first survey on the status of the bovine immunudeficiency virus infection and associated clinical, pathological, haematological and flowcytometric findings in holestein cattle in Iran. J. Vet. Res., 65: 1-12.
Behl, JD; Verma, NK; Tyagi, N; Mishra, P; Behl, R and Joshi, BK (2012). The major histocompatibility complex in bovines: a review. ISRN Vet. Sci., 2012: 1-12.
Buehring, GC and Sans, HM (2020). Breast cancer gone viral? Review of possible role of bovine leukemia virus in breast cancer, and related opportunities for cancer prevention. IJERPH. 17: 1-10.
Buehring, GC; Shen, HM; Jensen, HM; Yeon Choi, K; Sun, D and Nuovo, G (2014). Bovine leukemia virus DNA in human breast tissue. Emerg. Infect. Dis., 20: 772-782.
Calafat, J and Ressang, AA (1977). Morphogenesis of bovine leukemia virus. Virology. 80: 42-53.
Canova, R; Weber, MN; Budaszewski, RF; da Silva, MS; Schwingel, D; Canal, CW and Kreutz, LC (2021). Bovine leukemia viral DNA found on human breast tissue is genetically related to the cattle virus. One Health. 13: 1-10.
Delarmelina, E; Buzelin, MA; de Souza, BS; Souto, FM; Bicalho, JM; Falcão Câmara, RJ; Resende, CF; Bueno, BL; Victor, RM; Florentino Galinari, GC; Nunes, CB; Leite, RC; Costa, ÉA and dos Reis, JKP (2020). High positivity values for bovine leukemia virus in human breast cancer cases from Minas Gerais, Brazil. PLoS ONE. 15: e0239745.
Esmailnejad, A and Nikbakht Brujeni, G (2016). Study of MHC polymorphism and its linkage to IGF1 gene in Khorasan indigenous chicken. J. Vet. Res., 71: 481-489.
Gillet, N; Florins, A; Boxus, M; Burteau, C; Nigro, A; Vandermeers, F; Balon, H; Bouzar, AB; Defoiche, J; Burny, A; Reichert, M; Kettmann, R and Willems, L (2007). Mechanisms of leukemogenesis induced by bovine leukemia virus: Prospects for novel anti-retroviral therapies in human. Retrovirology. 4: 1-10.
Gross, JJ (2023). Dairy cow physiology and production limits. Anim. Front., 13: 44-50.
Heinecke, N; Tórtora, J; Martínez, HA; González-Fernández, VD and Ramírez, H (2017). Detection and genotyping of bovine leukemia virus in Mexican cattle. Arch. Virol., 162: 3191-3196.
Hernandez, D; Montes, D and Alvarez, LA (2018). Association of BoLA-DRB3.2 alleles with enzootic bovine leukosis: profiles BLV infection, persistent lymphocytosis and antibody production in Harton del Valle Cattle. Indian J. Sci. Technol., 11: 1-14.
Hiraoka, M; Takashima, S; Wakihara, Y; Kamatari, YO; Shimizu, K; Okada, A and Inoshima, Y (2022). Identification of potential mRNA biomarkers in milk small extracellular vesicles of enzootic bovine leukosis cattle. Viruses. 14: 1-10.
Hopkins, SG and DiGiacomo, RF (1997). Natural transmission of bovine leukemia virus in dairy and beef cattle. Vet. Clin. North Am. Food Anim., 13: 107-128.
Juliarena, MA; Barrios, CN; Ceriani, MC and Esteban, EN (2016). Hot topic: Bovine leukemia virus (BLV)-infected cows with low proviral load are not a source of infection for BLV-free cattle. J. Dairy Sci., 99: 4586-4589.
Juliarena, MA; Barrios, CN; Lützelschwab, CM; Esteban, EN and Gutiérrez, SE (2017). Bovine leukemia virus: Current perspectives. Virus Adapt. Treat., 9: 13-26.
Khan, Z; Abubakar, M; Arshed, MJ; Aslam, R; Sattar, S; Shah, NA; Javed, S; Tariq, A; Bostan, N and Manzoor, S (2022). Molecular investigation of possible relationships concerning bovine leukemia virus and breast cancer. Sci. Rep., 12: 1-10.
Klestova, ZS; Yuschenko, AY; Dremukh Julia, YY; Blotska, OF; Yevgen Venger, EF; Dorozinsky, GV; Kravchenko, SO; Ushenin, YV; Kachur, NV and Maslov, VP (2019). Diagnostics of cattle leucosis by using a biosensor based on surface plasmon resonance phenomenon. SPQEO. 22: 111-118.
Kucerova, L; Altanerova, V; Altaner, C and Boris-Lawrie, K (1999). Bovine leukemia virus structural gene vectors are immunogenic and lack pathogenicity in a rabbit model. J. Virol., 73: 8160-8166.
Ladronka, RM; Ainsworth, S; Wilkins, MJ; Norby, B; Byrem, TM and Bartlett, PC (2018). Prevalence of bovine leukemia virus antibodies in US dairy cattle. Vet. Med. Int., 2018: 1-6.
Lewin, HA; Russell, GC and Glass, EJ (1999). Comparative organization and function of the major histocompatibility complex of domesticated cattle. Immunol. Rev., 167: 145-158.
Lo, CW and Aida, Y (2022). Association of BoLA-DRB3 with bovine leukemia virus. MHC. 29: 158-167.
Lo, CW; Borjigin, L; Saito, S; Fukunaga, K; Saitou, E; Okazaki, K; Mizutani, T; Wada, S; Takeshima, SN and Aida, Y (2020). BoLA-DRB3 polymorphism is associated with differential susceptibility to bovine leukemia virus-induced lymphoma and proviral load. Viruses. 12: 1-5.
Lo, CW; Takeshima, SN; Okada, K; Saitou, E; Fujita, T; Matsumoto, Y; Wada, S; Inoko, H and Aida, Y (2021). Association of bovine leukemia virus-induced lymphoma with bola-drb3 polymorphisms at dna, amino acid, and binding pocket property levels. Pathogens. 10: 1-15.
Lotfollahzadeh, S; Nikbakht Brujeni, G; Atyabi, N and Mohammadi, V (2014). Evaluation of presence of MHC class II susceptible and resistant alleles to oncovirus in seropositive and seronegative Holstein-Frisian dairy cattle in Iran. Austin J. Clin. Med., 1: id1017.
Ma, BY; Gong, QL; Sheng, CY; Liu, Y; Ge, GY; Li, DL; Diao, NC; Shi, K; Li, JM; Sun, ZB; Zong, Y; Leng, X and Du, R (2021). Prevalence of bovine leukemia in 1983-2019 in China: A systematic review and meta-analysis. Microb. Pathog., 150: 1-6.
Maezawa, M; Sakaguchi, K; Tagaino, Y; Fujii, Y; Akagami, M; Kawakami, J; Watanabe, KI; Kobayashi, Y; Ogawa, H and Inokuma, H (2022). Enzootic bovine leukosis in a 21-month-old Japanese Black cow with high susceptibility. J. Vet. Diagn. Invest., 34: 733-737.
Mirsky, ML; Olmstead, C; Da, Y and Lewin, HA (1998). Reduced bovine leukaemia virus proviral load in genetically resistant cattle. Anim. Genet., 29: 245-252.
Mohammadi, V; Atyabi, N; Nikbakht Brujeni, G; Lotfollahzadeh, S and Mostafavi, E (2011). Seroprevalence of bovine leukemia virus in some dairy farms in Iran. Glob. Vet., 7: 305-309.
Nakada, S; Fujimoto, Y; Kohara, J; Adachi, Y and Makita, K (2022). Estimation of economic loss by carcass weight reduction of Japanese dairy cows due to infection with bovine leukemia virus. Prev. Vet. Med., 198: 1-8.
Nakada, S; Fujimoto, Y; Kohara, J and Makita, K (2023). Economic losses associated with mastitis due to bovine leukemia virus infection. J. Dairy Sci., 106: 576-588.
Nikbakht Brujeni, G (2009). Immunofluorescent protein detection in Western blotting. Iran. J. Vet. Med., 3: 107-111.
Nikbakht Brujeni, G (2022). Novel insights into infection and immunity. Iran. J. Vet. Med., 16: 99-100.
Nikbakht Brujeni, G; Emam, M and Barjesteh, N (2008). Detection of tumor antigens in bovine viral lymphosarcoma by immunoprecipitation method. J. Vet. Res., 63: 141-146.
Nikbakht Brujeni, G; Emam, SM and Rezaei, H (2011). Detection of bovine leukemia virus infection by nested-PCR analysis. Vet. Res. Bio. Prod., 24: 1-8.
Nikbakht Brujeni, G and Esmailnejad, A (2015). Chicken major histocompatibility complex polymorphism and its association with production traits. Immunogenetics. 67: 247-252.
Nikbakht Brujeni, G; Ghorbanpour, R and Esmailnejad, A (2016). Association of BoLA-DRB3.2 alleles with BLV infection profiles (persistent lymphocytosis/ lymphosarcoma) and lymphocyte subsets in Iranian Holstein cattle. Biochem. Genet., 54: 194-207.
Nikbakht Brujeni, G; Hemmatzadeh, F; Emam, SM and Ghaffari, M (2007). Detecting the P24 antigen in lymph nodes of BLV infected cattle. J. Vet. Res., 62: 285-289.
Nikbakht Brujeni, G; Hematzadeh, F and Mahbubi, B (2006). Study on tumor antigens of BLV infected lymph nodes in comparison with FLK-BLV cell culture. J. Vet. Res., 61: 51-55.
Nikbakht Brujeni, G; Houshmand, P; Esmailnejad, A and Abasabadi, F (2022). Major histocompatibility complex as marker assisted selection for breeding immunocompetent animal. Iran. J. Vet. Med., 16: 211-227.
Nikbakht Brujeni, G; Poorbazargani, TT; Nadin-Davis, S; Tolooie, M and Barjesteh, N (2010a). Bovine immunodeficiency virus and bovine leukemia virus and their mixed infection in Iranian holstein cattle. J. Infect. Dev. Ctries., 4: 576-579.
Nikbakht Brujeni, G; Rabbani, M; Emam, M and Rezatogfighi, E (2010b). Serological and genomic detection of bovine leukemia virus in human and cattle samples. Int. J. Vet. Sci. Res., 4: 253-258.
Nikbakht Brujeni, G; Tabatabaei, S; Lotfollahzadeh, S; Nayeri Fasaei, B; Bahonar, A and Khormali, M (2015). Seroprevalence of bovine viral diarrhoea virus, bovine herpesvirus 1 and bovine leukaemia virus in Iranian cattle and associations among studied agents. J. Appl. Anim. Res., 43: 22-25.
Norby, B; Bartlett, PC; Byrem, TM and Erskine, RJ (2016). Effect of infection with bovine leukemia virus on milk production in Michigan dairy cows. J. Dairy Sci., 99: 2043-2052.
Olaya-Galán, NN; Corredor-Figueroa, AP; Velandia-Álvarez, S; Vargas-Bermudez, DS; Fonseca-Ahumada, N; Nuñez, K; Jaime, J and Gutiérrez, MF (2022). Evidence of bovine leukemia virus circulating in sheep and buffaloes in Colombia: insights into multispecies infection. Arch. Virol., 167: 807-817.
Otta, SL; Johnson, R and Wells, SJ (2003). Association between bovine-leukosis virus seroprevalence and herd-level productivity on US dairy farms. Prev. Vet. Med., 61: 249-262.
Panei, CJ; Suzuki, K; Echeverría, MG; Serena, MS; Metz, GE and González, ET (2009). Association of BoLA-DRB3.2 alleles with resistance and susceptibility to persistent lymphocytosis in BLV infected cattle in Argentina. Int. J. Dairy Sci., 4: 123-128.
Polat, M; Moe, HH; Shimogiri, T; Moe, KK; Takeshima, SN and Aida, Y (2017a). The molecular epidemiological study of bovine leukemia virus infection in Myanmar cattle. Arch. Virol., 162: 425-437.
Polat, M; Ohno, A; Takeshima, SN; Kim, J; Kikuya, M; Matsumoto, Y; Mingala, CN; Onuma, M and Aida, Y (2015). Detection and molecular characterization of bovine leukemia virus in Philippine cattle. Arch. Virol., 160: 285-296.
Polat, M; Takeshima, SN and Aida, Y (2017b). Epidemiology and genetic diversity of bovine leukemia virus. Virol. J., 14: 1-9.
Porta, NG; Alvarez, I; Suarez Archilla, G; Ruiz, V; Abdala, A and Trono, K (2019). Experimental infection of sheep with Bovine leukemia virus (BLV): Minimum dose of BLV-FLK cells and cell-free BLV and neutralization activity of natural antibodies. Rev. Argent. Microbiol., 51: 316-323.
Roberts, DH; Lucas, MH and Swallow, C (1989). Comparison of the agar gel immunodiffusion test and ELISA in the detection of bovine leukosis virus antibody in cattle persistently infected with bovine virus diarrhoea virus. Vet. Immunol. Immunopathol., 22: 275-281.
Robinson, LA; Jaing, CJ; Pierce Campbell, C; Magliocco, A; Xiong, Y; Magliocco, G; Thissen, JB and Antonia, S (2016). Molecular evidence of viral DNA in non-small cell lung cancer and non-neoplastic lung. Br. J. Cancer. 115: 497-504.
Rodríguez, SM; Florins, A; Gillet, N; de Brogniez, A; Sánchez-Alcaraz, MT; Boxus, M; Boulanger, F; Gutiérrez, G; Trono, K; Alvarez, I; Vagnoni, L and Willems, L (2011). Preventive and therapeutic strategies for bovine leukemia virus: Lessons for HTLV. Viruses. 3: 1210-1248.
Ruban, Y; Shpyrka, N; Pareniuk, O; Galat, M; Taran, MS; Ishchenko, L; Malienko, V; Spyrydonov, V; Samofalova, D; Nesterova, N and Shavanova, K (2017). BLV leucosis biosensor based on ZnO nanorods photoluminescence. 2017 IEEE 37th International Conference on Electronics and Nanotechnology, ELNANO 2017 - Proceedings. PP: 333-337.
Segerstrom, SC (2007). Stress, energy, and immunity: An ecological view. Curr. Dir. Psychol. Sci., 16: 326-330.
Şevik, M; Avcı, O and İnce, ÖB (2015). An 8-year longitudinal sero-epidemiological study of bovine leukaemia virus (BLV) infection in dairy cattle in Turkey and analysis of risk factors associated with BLV seropositivity. Trop. Anim. Health Prod., 47: 715-720.
Stear, A; Ali, AOA; Nikbakht Brujeni, G; Buitkamp, J; Donskow-Łysoniewska, K; Fairlie-Clarke, K; Groth, D; Isa, NMM and Stear, MJ (2019). Identification of the amino acids in the Major Histocompatibility Complex class II region of Scottish Blackface sheep that are associated with resistance to nematode infection. Int. J. Parasitol., 49: 797-804. Stear, MJ; Nikbakht Brujeni, G; Matthews, L and Jonsson, NN (2012). Breeding for disease resistance in livestock and fish. In CAB Reviews: Perspect. Agric. Vet. Sci. Nutr. Nat. Resour., 7: 1-10.
Tajima, S; Ikawa, Y and Aida, Y (1998). Complete bovine leukemia virus (BLV) provirus is conserved in BLV-infected cattle throughout the course of B-cell lymphosarcoma development. J. Virol., 72: 7569-7576.
Tooloei, M; Bazargani, TT; Nikbakht Brujeni, G; Khaki, Z; Bokaei, S and Ashrafei, I (2009). An abattoir surveyon prevalence of enzootic bovine leukosis virus infection and associated clinical, haematologicaland flowcytometric findings in holestein cattle in Tehran. J. Vet. Res., 64: 147-156.
Willems, L; Kerkhofs, P; Dequiedt, F; Portetelle, D; Mammerickx, M; Burny, A and Kettmann, R (1994). Attenuation of bovine leukemia virus by deletion of R3 and G4 open reading frames. Proc. Natl. Acad. Sci. U.S.A., 91: 11532-11536.
Zyrianova, IM and Kovalchuk, SN (2020). Bovine leukemia virus tax gene/Tax protein polymorphism and its relation to Enzootic Bovine Leukosis. Virulence. 11: 80-87. | ||
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