Bovine respiratory syncytial virus enhances the attachment of Trueperella pyogenes to cells
In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV and bacteria are unclear. Trueperella pyogenes (T. pyogenes) causes pneumonia in cattle and is involved in secondary infections following vi...
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Published in | Journal of Veterinary Medical Science Vol. 86; no. 10; pp. 1068 - 1075 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Japan
JAPANESE SOCIETY OF VETERINARY SCIENCE
2024
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Abstract | In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV and bacteria are unclear. Trueperella pyogenes (T. pyogenes) causes pneumonia in cattle and is involved in secondary infections following viral infections. In this study, we evaluated the effect of BRSV infection on the adhesion of T. pyogenes to BRSV-infected cells. BRSV infection significantly enhanced the adhesion of T. pyogenes to cells in a multiplicity of infection- and time-dependent manner. The BRSV-mediated change in the adhesion of T. pyogenes was widely observed in various cell types and bacterial strains. The results from the gentamicin protection assay showed that BRSV infection did not affect the intracellular invasion ability of T. pyogenes. Furthermore, adhesion assays conducted using BRSV G protein-expressing cells and anti-BRSV G antibodies revealed that the increased adhesion of T. pyogenes to cells was mediated by the G protein of BRSV. In addition, immunofluorescence assay revealed the colocalization of BRSV G protein and T. pyogenes. Thus, BRSV infection can potentially lead to bovine respiratory disease complex by promoting the adhesion of T. pyogenes to the infected cells. |
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AbstractList | In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV and bacteria are unclear. Trueperella pyogenes (T. pyogenes) causes pneumonia in cattle and is involved in secondary infections following viral infections. In this study, we evaluated the effect of BRSV infection on the adhesion of T. pyogenes to BRSV-infected cells. BRSV infection significantly enhanced the adhesion of T. pyogenes to cells in a multiplicity of infection- and time-dependent manner. The BRSV-mediated change in the adhesion of T. pyogenes was widely observed in various cell types and bacterial strains. The results from the gentamicin protection assay showed that BRSV infection did not affect the intracellular invasion ability of T. pyogenes. Furthermore, adhesion assays conducted using BRSV G protein-expressing cells and anti-BRSV G antibodies revealed that the increased adhesion of T. pyogenes to cells was mediated by the G protein of BRSV. In addition, immunofluorescence assay revealed the colocalization of BRSV G protein and T. pyogenes. Thus, BRSV infection can potentially lead to bovine respiratory disease complex by promoting the adhesion of T. pyogenes to the infected cells. In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV and bacteria are unclear. Trueperella pyogenes ( T. pyogenes ) causes pneumonia in cattle and is involved in secondary infections following viral infections. In this study, we evaluated the effect of BRSV infection on the adhesion of T. pyogenes to BRSV-infected cells. BRSV infection significantly enhanced the adhesion of T. pyogenes to cells in a multiplicity of infection- and time-dependent manner. The BRSV-mediated change in the adhesion of T. pyogenes was widely observed in various cell types and bacterial strains. The results from the gentamicin protection assay showed that BRSV infection did not affect the intracellular invasion ability of T. pyogenes . Furthermore, adhesion assays conducted using BRSV G protein-expressing cells and anti-BRSV G antibodies revealed that the increased adhesion of T. pyogenes to cells was mediated by the G protein of BRSV. In addition, immunofluorescence assay revealed the colocalization of BRSV G protein and T. pyogenes . Thus, BRSV infection can potentially lead to bovine respiratory disease complex by promoting the adhesion of T. pyogenes to the infected cells. In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV and bacteria are unclear. Trueperella pyogenes (T. pyogenes) causes pneumonia in cattle and is involved in secondary infections following viral infections. In this study, we evaluated the effect of BRSV infection on the adhesion of T. pyogenes to BRSV-infected cells. BRSV infection significantly enhanced the adhesion of T. pyogenes to cells in a multiplicity of infection- and time-dependent manner. The BRSV-mediated change in the adhesion of T. pyogenes was widely observed in various cell types and bacterial strains. The results from the gentamicin protection assay showed that BRSV infection did not affect the intracellular invasion ability of T. pyogenes. Furthermore, adhesion assays conducted using BRSV G protein-expressing cells and anti-BRSV G antibodies revealed that the increased adhesion of T. pyogenes to cells was mediated by the G protein of BRSV. In addition, immunofluorescence assay revealed the colocalization of BRSV G protein and T. pyogenes. Thus, BRSV infection can potentially lead to bovine respiratory disease complex by promoting the adhesion of T. pyogenes to the infected cells.In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV and bacteria are unclear. Trueperella pyogenes (T. pyogenes) causes pneumonia in cattle and is involved in secondary infections following viral infections. In this study, we evaluated the effect of BRSV infection on the adhesion of T. pyogenes to BRSV-infected cells. BRSV infection significantly enhanced the adhesion of T. pyogenes to cells in a multiplicity of infection- and time-dependent manner. The BRSV-mediated change in the adhesion of T. pyogenes was widely observed in various cell types and bacterial strains. The results from the gentamicin protection assay showed that BRSV infection did not affect the intracellular invasion ability of T. pyogenes. Furthermore, adhesion assays conducted using BRSV G protein-expressing cells and anti-BRSV G antibodies revealed that the increased adhesion of T. pyogenes to cells was mediated by the G protein of BRSV. In addition, immunofluorescence assay revealed the colocalization of BRSV G protein and T. pyogenes. Thus, BRSV infection can potentially lead to bovine respiratory disease complex by promoting the adhesion of T. pyogenes to the infected cells. |
ArticleNumber | 24-0068 |
Author | TAKAHASHI, Fumiaki YAMAMOTO, Satomi MAEDA, Yosuke OKUMURA, Shiori KOBAYASHI, Risa TANABE, Taishi |
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Cites_doi | 10.1126/science.aad5872 10.1038/s41579-019-0149-x 10.1177/1040638720975364 10.1016/j.vetmic.2020.108748 10.3390/vaccines9040337 10.1016/j.vetmic.2019.06.010 10.1017/S1466252314000176 10.3390/v9030058 10.1371/journal.ppat.1003057 10.1128/JVI.77.7.4104-4112.2003 10.1016/j.vetmic.2018.04.031 10.2527/jas.2007-0008 10.3168/jds.2018-15501 10.3168/jds.2022-21929 10.1371/journal.ppat.1008234 10.1007/s10482-005-2316-5 10.3390/ijms20112737 10.1051/vetres:2006053 10.1093/femsle/fnv062 10.1016/j.vetimm.2005.04.004 10.1016/j.cvfa.2020.03.005 10.1099/jmm.0.47086-0 10.1186/s42523-022-00167-y 10.2527/2005.8313_supplE37x 10.1016/j.vetmic.2021.109017 10.1164/rccm.201311-2110OC 10.1016/j.vetmic.2012.07.044 |
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Keywords | co-infection bovine respiratory disease complex Trueperella pyogenes bacterial adhesion bovine respiratory syncytial virus |
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Immune mechanisms of pathogenetic synergy in concurrent bovine pulmonary infection with Haemophilus somnus and bovine respiratory syncytial virus. Vet Immunol Immunopathol 107: 119–130. 2. Avadhanula V, Wang Y, Portner A, Adderson E. 2007. Nontypeable Haemophilus influenzae and Streptococcus pneumoniae bind respiratory syncytial virus glycoprotein. J Med Microbiol 56: 1133–1137. 6. Brealey JC, Sly PD, Young PR, Chappell KJ. 2015. Viral bacterial co-infection of the respiratory tract during early childhood. FEMS Microbiol Lett 362: 362. 14. Mosier D. 2014. Review of BRD pathogenesis: the old and the new. Anim Health Res Rev 15: 166–168. 20. Smith CM, Sandrini S, Datta S, Freestone P, Shafeeq S, Radhakrishnan P, Williams G, Glenn SM, Kuipers OP, Hirst RA, Easton AJ, Andrew PW, O’Callaghan C. 2014. Respiratory syncytial virus increases the virulence of Streptococcus pneumoniae by binding to penicillin binding protein 1a. A new paradigm in respiratory infection. Am J Respir Crit Care Med 190: 196–207. 26. Timsit E, Christensen H, Bareille N, Seegers H, Bisgaard M, Assié S. 2013. Transmission dynamics of Mannheimia haemolytica in newly-received beef bulls at fattening operations. Vet Microbiol 161: 295–304. 11. Jost BH, Billington SJ. 2005. Arcanobacterium pyogenes: molecular pathogenesis of an animal opportunist. Antonie van Leeuwenhoek 88: 87–102. 24. Sudaryatma PE, Saito A, Mekata H, Kubo M, Fahkrajang W, Okabayashi T. 2020. Bovine respiratory syncytial virus decreased Pasteurella multocida adherence by downregulating the expression of intercellular adhesion molecule-1 on the surface of upper respiratory epithelial cells. Vet Microbiol 246: 108748. 3. Battles MB, McLellan JS. 2019. Respiratory syncytial virus entry and how to block it. Nat Rev Microbiol 17: 233–245. 18. Pfeiffer JK, Virgin HW. 2016. Viral immunity. Transkingdom control of viral infection and immunity in the mammalian intestine. Science 351: aad5872–aad5872. 5. Bosch AATM, Biesbroek G, Trzcinski K, Sanders EAM, Bogaert D. 2013. Viral and bacterial interactions in the upper respiratory tract. PLoS Pathog 9: e1003057. 22. Sudaryatma PE, Mekata H, Kubo M, Subangkit M, Goto Y, Okabayashi T. 2019. Co-infection of epithelial cells established from the upper and lower bovine respiratory tract with bovine respiratory syncytial virus and bacteria. Vet Microbiol 235: 80–85. 9. Fahkrajang W, Sudaryatma PE, Mekata H, Hamabe S, Saito A, Okabayashi T. 2021. Bovine respiratory coronavirus enhances bacterial adherence by upregulating expression of cellular receptors on bovine respiratory epithelial cells. Vet Microbiol 255: 109017. 1. Almand EA, Moore MD, Jaykus LA. 2017. Virus-bacteria interactions: an emerging topic in human infection. Viruses 9: 58. 16. Okamoto S, Kawabata S, Nakagawa I, Okuno Y, Goto T, Sano K, Hamada S. 2003. Influenza A virus-infected hosts boost an invasive type of Streptococcus pyogenes infection in mice. J Virol 77: 4104–4112. 23. Sudaryatma PE, Nakamura K, Mekata H, Sekiguchi S, Kubo M, Kobayashi I, Subangkit M, Goto Y, Okabayashi T. 2018. Bovine respiratory syncytial virus infection enhances Pasteurella multocida adherence on respiratory epithelial cells. Vet Microbiol 220: 33–38. 7. Centeno-Martinez RE, Glidden N, Mohan S, Davidson JL, Fernández-Juricic E, Boerman JP, Schoonmaker J, Pillai D, Koziol J, Ault A, Verma MS, Johnson TA. 2022. Identification of bovine respiratory disease through the nasal microbiome. Anim Microbiome 4: 15. 15. Neu U, Mainou BA. 2020. Virus interactions with bacteria: Partners in the infectious dance. PLoS Pathog 16: e1008234. 19. Rzewuska M, Kwiecień E, Chrobak-Chmiel D, Kizerwetter-Świda M, Stefańska I, Gieryńska M. 2019. Pathogenicity and Virulence of Trueperella pyogenes: A Review. Int J Mol Sci 20: 2737. 21. Snowder GD, Van Vleck LD, Cundiff LV, Bennett GL, Koohmaraie M, Dikeman ME. 2007. Bovine respiratory disease in feedlot cattle: phenotypic, environmental, and genetic correlations with growth, carcass, and longissimus muscle palatability traits. J Anim Sci 85: 1885–1892. 25. Taylor JD, Fulton RW, Lehenbauer TW, Step DL, Confer AW. 2010. The epidemiology of bovine respiratory disease: What is the evidence for predisposing factors?Can Vet J 51: 1095–1102. 29. Zhou Y, Shao Z, Dai G, Li X, Xiang Y, Jiang S, Zhang Z, Ren Y, Zhu Z, Fan C, Zhang G. 2023. Pathogenic infection characteristics and risk factors for bovine respiratory disease complex based on the detection of lung pathogens in dead cattle in Northeast China. J Dairy Sci 106: 589–606. 4. Bell RL, Turkington HL, Cosby SL. 2021. The bacterial and viral agents of BRDC: immune evasion and vaccine developments. Vaccines (Basel) 9: 9. 12. Kumagai A, Kawauchi K, Andoh K, Hatama S. 2021. Sequence and unique phylogeny of G genes of bovine respiratory syncytial viruses circulating in Japan. J Vet Diagn Invest 33: 162–166. 22 23 24 25 26 27 28 29 10 11 12 13 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 21 |
References_xml | – reference: 9. Fahkrajang W, Sudaryatma PE, Mekata H, Hamabe S, Saito A, Okabayashi T. 2021. Bovine respiratory coronavirus enhances bacterial adherence by upregulating expression of cellular receptors on bovine respiratory epithelial cells. Vet Microbiol 255: 109017. – reference: 16. Okamoto S, Kawabata S, Nakagawa I, Okuno Y, Goto T, Sano K, Hamada S. 2003. Influenza A virus-infected hosts boost an invasive type of Streptococcus pyogenes infection in mice. J Virol 77: 4104–4112. – reference: 26. Timsit E, Christensen H, Bareille N, Seegers H, Bisgaard M, Assié S. 2013. Transmission dynamics of Mannheimia haemolytica in newly-received beef bulls at fattening operations. Vet Microbiol 161: 295–304. – reference: 15. Neu U, Mainou BA. 2020. Virus interactions with bacteria: Partners in the infectious dance. PLoS Pathog 16: e1008234. – reference: 20. Smith CM, Sandrini S, Datta S, Freestone P, Shafeeq S, Radhakrishnan P, Williams G, Glenn SM, Kuipers OP, Hirst RA, Easton AJ, Andrew PW, O’Callaghan C. 2014. Respiratory syncytial virus increases the virulence of Streptococcus pneumoniae by binding to penicillin binding protein 1a. A new paradigm in respiratory infection. Am J Respir Crit Care Med 190: 196–207. – reference: 21. Snowder GD, Van Vleck LD, Cundiff LV, Bennett GL, Koohmaraie M, Dikeman ME. 2007. Bovine respiratory disease in feedlot cattle: phenotypic, environmental, and genetic correlations with growth, carcass, and longissimus muscle palatability traits. J Anim Sci 85: 1885–1892. – reference: 18. Pfeiffer JK, Virgin HW. 2016. Viral immunity. Transkingdom control of viral infection and immunity in the mammalian intestine. Science 351: aad5872–aad5872. – reference: 6. Brealey JC, Sly PD, Young PR, Chappell KJ. 2015. Viral bacterial co-infection of the respiratory tract during early childhood. FEMS Microbiol Lett 362: 362. – reference: 28. Zewde D, Gemeda G, Ashagrie T. 2022. Review on bovine respiratory syncytial virus characteristic, pathogenesis and control methods applied for the disease. Austin J Vet Sci Anim Husb 9: 1103. – reference: 29. Zhou Y, Shao Z, Dai G, Li X, Xiang Y, Jiang S, Zhang Z, Ren Y, Zhu Z, Fan C, Zhang G. 2023. Pathogenic infection characteristics and risk factors for bovine respiratory disease complex based on the detection of lung pathogens in dead cattle in Northeast China. J Dairy Sci 106: 589–606. – reference: 11. Jost BH, Billington SJ. 2005. Arcanobacterium pyogenes: molecular pathogenesis of an animal opportunist. Antonie van Leeuwenhoek 88: 87–102. – reference: 10. Gershwin LJ, Berghaus LJ, Arnold K, Anderson ML, Corbeil LB. 2005. Immune mechanisms of pathogenetic synergy in concurrent bovine pulmonary infection with Haemophilus somnus and bovine respiratory syncytial virus. Vet Immunol Immunopathol 107: 119–130. – reference: 14. Mosier D. 2014. Review of BRD pathogenesis: the old and the new. Anim Health Res Rev 15: 166–168. – reference: 24. Sudaryatma PE, Saito A, Mekata H, Kubo M, Fahkrajang W, Okabayashi T. 2020. Bovine respiratory syncytial virus decreased Pasteurella multocida adherence by downregulating the expression of intercellular adhesion molecule-1 on the surface of upper respiratory epithelial cells. Vet Microbiol 246: 108748. – reference: 27. Valarcher JF, Taylor G. 2007. Bovine respiratory syncytial virus infection. Vet Res 38: 153–180. – reference: 1. Almand EA, Moore MD, Jaykus LA. 2017. Virus-bacteria interactions: an emerging topic in human infection. Viruses 9: 58. – reference: 22. Sudaryatma PE, Mekata H, Kubo M, Subangkit M, Goto Y, Okabayashi T. 2019. Co-infection of epithelial cells established from the upper and lower bovine respiratory tract with bovine respiratory syncytial virus and bacteria. Vet Microbiol 235: 80–85. – reference: 5. Bosch AATM, Biesbroek G, Trzcinski K, Sanders EAM, Bogaert D. 2013. Viral and bacterial interactions in the upper respiratory tract. PLoS Pathog 9: e1003057. – reference: 2. Avadhanula V, Wang Y, Portner A, Adderson E. 2007. Nontypeable Haemophilus influenzae and Streptococcus pneumoniae bind respiratory syncytial virus glycoprotein. J Med Microbiol 56: 1133–1137. – reference: 4. Bell RL, Turkington HL, Cosby SL. 2021. The bacterial and viral agents of BRDC: immune evasion and vaccine developments. Vaccines (Basel) 9: 9. – reference: 12. Kumagai A, Kawauchi K, Andoh K, Hatama S. 2021. Sequence and unique phylogeny of G genes of bovine respiratory syncytial viruses circulating in Japan. J Vet Diagn Invest 33: 162–166. – reference: 17. Pardon B, Buczinski S. 2020. Bovine respiratory disease diagnosis: what progress has been made in infectious diagnosis?Vet Clin North Am Food Anim Pract 36: 425–444. – reference: 7. 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Snippet | In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV... In cattle, bovine respiratory syncytial virus (BRSV) is associated with secondary bacterial infections; however, the mechanisms of the interaction between BRSV... |
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SubjectTerms | bacterial adhesion Bacterial infections bovine respiratory disease complex bovine respiratory syncytial virus Cattle co-infection Gentamicin Immunofluorescence Infections Multiplicity of infection Proteins Respiratory diseases Respiratory syncytial virus Trueperella pyogenes Viral infections Virology |
Title | Bovine respiratory syncytial virus enhances the attachment of Trueperella pyogenes to cells |
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