Araştırma Makalesi
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Manda Mastitis Kökenli Streptococcus agalactiae İzolatlarının Virülens Belirleyicileri

Yıl 2024, , 196 - 204, 30.06.2024
https://doi.org/10.35229/jaes.1454258

Öz

Mastitisin bir nedeni olan streptokoklar, büyük ekonomik kayıplar nedeniyle süt endüstrisi için dünya çapında önemli bir sorundur. Streptococcus agalactiae, bulaşıcı mastitis patojeni olarak, süt sığırlarında ve mandalarda mastitisin önemli bir nedeni olmaya devam etmektedir. Bu çalışma manda sütünden izole edilen S. agalactiae suşlarının virulens belirleyicilerini belirlemek amacıyla gerçekleştirilmiştir.
Çalışma kapsamında manda mastitisinden elde edilen 24 adet S. agalactiae izolatı incelendi. İzolatların biyofilm üretimi fenotipik olarak CRA yöntemiyle araştırıldı. İzolatların 18'inin (%75) biyofilm üretimi açısından pozitif olduğu görüldü. S. agalactiae izolatlarında hylB, fnbB, scpB ve spb1 virülens genlerinin varlığı PCR ile belirlendi. İzolatların 19'unun (%79,17) scpB, 6'sının (%25) fnbB geni yönünden pozitif olduğu görüldü. İzolatların hiçbirinde hylB ve spb1 virülens genleri belirlenemedi. Kanamisin, ampisilin, enrofloksasin, eritromisin, tetrasiklin, trimetoprim-sülfametoksazol antibiyotik diskleri ile izolatların antibiyotik direnç profilleri Kirby Bauer Disk Difüzyon Yöntemi ile belirlendi ve direnç oranları sırasıyla %41,7, %45,9, %25, %12,5, %20,9 ve %33,3 olarak değerlendirildi. Tüm izolatların RAPD-PCR paternleri ERIC-2 primeri kullanılarak belirlendi ve RAPD paternlerinin dendrogramları UPGMA yöntemiyle çizildi. İzolatların %59-95 arasında benzerlik gösterdiği belirlendi.
Sonuç olarak; bu araştırma ile manda mastitisinden izole edilen S. agalactiae izolatarında çeşitli virülens genlerinin prevalansı belirlendi. Mandalardan izole edilen S. agalactiae'nin moleküler epidemiyolojisi ve değişkenliğinin belirlenmesi ve S. agalactiae ile ilgili mastitis kontrol programlarının geliştirilmesi amacıyla daha ileri çalışmalara ihtiyaç olduğu kanısına varıldı.

Kaynakça

  • Abd El-Razik, K.A., Abdelrahman, K.A., Ahmed, Y.F., Gomaa, A.M. & Eldebaky, H.A. (2010). Direct identification of major pathogens of the bubaline subclinical mastitis in Egypt using PCR. J. Amer. Sci., 6(10), 652-60.
  • An der Mee-Marquet, N., Fourny, L., Arnault, L., Domelier, A.S., Salloum, M., Lartigue, M.F. & Quentin, R. (2008). Molecular characterization of humancolonizing Streptococcus agalactiae strains isolated from throat, skin, anal margin, and genital body sites. J. Clin. Microbiol., 46, 2906- 11. DOI: 10.1128/JCM.00421-08
  • Bangar, Y.C., Singh, B., Dohare, A.K. & Verma M.R. (2015). A systematic review and meta-analysis of prevalence of subclinical mastitis in dairy cows in India. Trop. Anim. Health Prod., 47, 291-297. DOI: 10.1007/s11250-014-0718-y
  • Boonyayatra, S. & Pata, P. (2016). Antimicrobial resistance of biofilm-forming Streptococcus agalactiae isolated from bovine mastitis. J. Vet. Sci. Technol., 7, 1000374. DOI: 10.4172/2157- 7579.1000374
  • Botelho, A.C.N., Ferreira, A.F.M., Fracalanzza, S.E.L., Teixeira, L.M. & Pinto, T.C.A. (2018). A perspective on the potential zoonotic role of Streptococcus agalactiae: searching for a missing link in alternative transmission routes. Front Microbiol., 9, 608. DOI: 10.3389/fmicb.2018.00608
  • Brochet, M., Couvé, E., Zouine, M., Vallaeys, T., Rusniok, C., Lamy, M.C., Buchrieser, C., Trieu-Cuot, P., Kunst, F., Poyart, C. & Glaser, P. (2006). Genomic diversity and evolution within the species Streptococcus agalactiae. Microbes Infect, 8(5), 1227-43. DOI 10.1016/j.micinf.2005.11.010
  • Carra, E., Russo, S., Micheli, A., Garbarino, C., Ricchi, M., Bergamini, F., Bassi, P., Prosperi, A., Piva, S., Cricca, M., Schiavo, R., Merialdi, G., Serraino, A. & Arrigoni, N. (2021). Evidence of common isolates of Streptococcus agalactiae in bovines and humans in Emilia Romagna Region (Northern Italy). Front Microbiol., 11, 673126. DOI: 10.3389/fmicb.2021.673126
  • Carvalho-Castro, G.A., Silva, J.R., Paiva, L.V., Custódio, D.A.C, Moreira, R.O., Mian, G.F., Prado, I.A., Chalfun-Junior, A. & Costa, G.M. (2017). Molecular epidemiology of Streptococcus agalactiae isolated from mastitis in Brazilian dairy herds. Braz. J. Microbiol., 48, 551-9. DOI: 10.1016/j.bjm.2017.02.004
  • Çiftci, A., Fındık, A., Onuk, E.E. & Savasan, S. (2009). Detection of methicillin resistance and slime factor production of Staphylococcus aureus in bovine mastitis. Braz. J. Microbiol., 40, 254-61. DOI: 10.1590/S1517-83822009000200009
  • CLSI. (Clinical and Laboratory Standards Institute). (2012). Performance Standards for Antimicrobial Susceptibility Testing: Twenty-First Informational Supplement. CLSI Document M100-S21, 31(1).
  • de Castro, M.P., Ferreira, L.M., Filho, A.N., Zafalon, L.F., Vicente, H.I. & de Souza, V. (2013). Comparison of methods for the detection of biofilm formation by Staphylococcus aureus isolated from bovine subclinical mastitis. Braz. J. Microbiol., 44(1), 119-24. DOI: 10.1590/S1517- 83822013005000031
  • Dego Kerro, O., Pacha, P.A., Gillespie, B.E. & Pighetti, G.M. (2020). Experimental Staphylococcus aureus mastitis infection model by teat dipping in bacterial culture suspension in dairy cows. Animals, 10, 751. DOI: 10.3390/ani10050751
  • Delannoy, C.M.J., Crumlish, M., Fontne, M.C., Pollock, J., Foster, G., Dagleish, M.P., Turnbull, J.F. & Zadoks, R.N. (2013). Human Streptococcus agalactiae strains in aquatic mammals and fish. BMC Microbiol., 13, 41. DOI: 10.1186/1471-2180-13-41
  • Duarte, R.S., Miranda, O.P., Bellei, B.C., Brito, M.A. & Teixeira, L.M. (2004). Phenotypic and molecular characteristics of Streptococcus agalactiae isolates recovered from milk of dairy cows in Brazil. J. Clin. Microbiol., 42, 4214-22. DOI: 10.1128/JCM.42.9.4214-4222.2004
  • El-Behiry, A., Elsayed, M., Marzouk, E. & Bathich, Y. (2015). Detection of virulence genes in Staphylococcus aureus and Streptococcus agalactiae isolated from mastitis in the Middle East. Microbiol. Res. J. Int., 10, 1-9. DOI: 10.9734/BMRJ/2015/19237
  • European Centre for Disease Prevention and Control. (2018). Surveillance of antimicrobial resistance in Europe - Annual report of the European Antimicrobial Resistance Surveillance Network (EARS-Net) 2017, Stockholm, ECDC.
  • Gianneechini, R.E., Concha, C. & Franklin, A. (2002). Antimicrobial susceptibility of udder pathogens isolated from dairy herds in the west littoral region of Uruguay. Acta Vet. Scand., 43(1), 31-41. DOI: 10.1186/1751-0147-43-31
  • Han, G., Zhang, B., Luo, Z., Lu, B., Luo, Z., Zhang, J., Wang, Y., Luo, Y., Yang, Z., Shen, L., Yu, S., Cao, S. & Yao, X. (2022). Molecular typing and prevalence of antibiotic resistance and virulence genes in Streptococcus agalactiae isolated from Chinese dairy cows with clinical mastitis. PLoS One, 17(5), e0268262. DOI: 10.1371/journal.pone.0268262
  • Hernandez, L., Bottini, E., Cadona, J., Cacciato, C., Monteavaro, C., Bustamante, A. & Sanso, A.M. (2021). Multidrug resistance and molecular characterization of Streptococcus agalactiae isolates from dairy cattle with mastitis. Front Cell Infect. Microbiol., 30, 647324. DOI: 10.3389/fcimb.2021.647324
  • Jain, A. & Agarwal, A. (2009). Biofilm production, a marker of pathogenic potential of colonizing and commensal staphylococci. J. Microbiol. Method., 76(1), 88-92. DOI: 10.1016/j.mimet.2008.09.017
  • Kaczorek, E., Małaczewska, J., Wójcik, R. & Siwicki, A.K. (2017). Biofilm production and other virulence factors in Streptococcus spp. isolated from clinical cases of bovine mastitis in Poland. BMC Vet. Res., 13(1), 398. DOI: 10.1186/s12917- 017-1322-y
  • Keefe, G.P. (1997). Streptococcus agalactiae mastitis: A review. Can. Vet. J., 38, 429-37.
  • Leghari, A., Shakeel, A.L., Faiz, M.K., Khaliq, U.R.B., Sameen, Q.L., Muhammad, T.A., Iqra, B., Muhammad A.C., Jan, M.S., Hui-Xing, L. & Hong-Jie, F. (2023). Molecular epidemiology, characterization of virulence factors and antibiotic resistance profile of Streptococcus agalactiae isolated from dairy farms in China and Pakistan. J. Integrat Agricult., 22, 1514-28. DOI: 10.3390/ani14030447
  • Levy, S.B. (2002). Factors impacting on the problem of antibiotic resistance. Journal of Antimicrobial Chemotherapy, 49(1), 25-30. DOI: 10.1093/jac/49.1.25
  • Lyhs, U., Kulkas, L., Katholm, J., Waller, K.P., Saha, K. & Tomusk, R.J. (2016). Streptococcus agalactiae serotype IV in humans and Cattle, Northern Europe. Emerg Infect Di.s, 22, 2097- 103. DOI: 10.3201/eid2212.151447
  • Nam, H.M., Lim, S.K. & Kang, H.M. (2009). Antimicrobial resistance of streptococci isolated from mastitic bovine milk samples in Korea. J. Ve. Diagn. Invest., 21(5), 698-701. DOI: 10.1177/104063870902100517
  • Oliver, S.P. & Murinda, S.E. (2012). Antimicrobial resistance of mastitis pathogens. Vet Clin North Amer-Food Anim. Pract., 28, 165-85. DOI: 10.1016/j.cvfa.2012.03.005
  • Phuektes, P., Mansell, P.D. & Browning, G.F. (2001). Multiplex polymerase chain reaction assay for simultaneous detection of Staphylococcus aureus and streptococcal causes of bovine mastitis. J. Dairy Sci., 84(5), 1140-8. DOI: 10.3168/jds.S0022-0302(01)74574-2
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Virulence Determinants of Buffalo Mastitis Originated Streptococcus agalactiae Isolates

Yıl 2024, , 196 - 204, 30.06.2024
https://doi.org/10.35229/jaes.1454258

Öz

Streptococci as a cause of mastitis have become the major concern to the dairy industry worldwide due to huge economic losses. Streptococcus agalactiae is a major contagious mastitis pathogen and continues to be a major cause of mastitis in dairy cattle and buffaloes. The aim of the study was to investigate the virulence determinants of S. agalactiae strains isolated from buffalo milk.
Within the scope of the study, 24 S. agalactiae isolates from buffalo mastitis were examined. Biofilm production of isolates was investigated phenotypically by CRA method. It was observed that 18 (75%) isolates were positive for biofilm production. The presence of hylB, fnbB, scpB and spb1 virulence genes in S. agalactiae isolates were investigated by PCR. It was determined that 19 (79.17%) of the isolates were positive for scpB and 6 (25%) for fnbB virulence genes. None of the isolates were found to contain hylB and spb1 virulence genes. The antibiotic resistance profiles of the isolates among kanamycin, ampicillin, enrofloxacin, erythromycin, tetracycline, trimethoprim-sulfamethoxazole antibiotic discs were determined by Kirby Bauer Disc Diffusion Method. Resistance were evaluated as % 41.7, % 45.9, % 25, % 12.5, % 20.9, and % 33.3, respectively. RAPD-PCR patterns of all isolates were determined using the ERIC-2 primer. The dendrograms of the RAPD patterns were plotted with the UPGMA method. It was determined that the isolates showed similarity between 59-95%.
In conclusion, the research confirms the prevalence of various virulence genes in S. agalactiae isolated from buffalo mastitis. Further studies are therefore necessary to determine the molecular epidemiology and variability of S. agalactiae isolated from buffaloes, with the aim of improving mastitis control programs with regard to S. agalactiae.

Kaynakça

  • Abd El-Razik, K.A., Abdelrahman, K.A., Ahmed, Y.F., Gomaa, A.M. & Eldebaky, H.A. (2010). Direct identification of major pathogens of the bubaline subclinical mastitis in Egypt using PCR. J. Amer. Sci., 6(10), 652-60.
  • An der Mee-Marquet, N., Fourny, L., Arnault, L., Domelier, A.S., Salloum, M., Lartigue, M.F. & Quentin, R. (2008). Molecular characterization of humancolonizing Streptococcus agalactiae strains isolated from throat, skin, anal margin, and genital body sites. J. Clin. Microbiol., 46, 2906- 11. DOI: 10.1128/JCM.00421-08
  • Bangar, Y.C., Singh, B., Dohare, A.K. & Verma M.R. (2015). A systematic review and meta-analysis of prevalence of subclinical mastitis in dairy cows in India. Trop. Anim. Health Prod., 47, 291-297. DOI: 10.1007/s11250-014-0718-y
  • Boonyayatra, S. & Pata, P. (2016). Antimicrobial resistance of biofilm-forming Streptococcus agalactiae isolated from bovine mastitis. J. Vet. Sci. Technol., 7, 1000374. DOI: 10.4172/2157- 7579.1000374
  • Botelho, A.C.N., Ferreira, A.F.M., Fracalanzza, S.E.L., Teixeira, L.M. & Pinto, T.C.A. (2018). A perspective on the potential zoonotic role of Streptococcus agalactiae: searching for a missing link in alternative transmission routes. Front Microbiol., 9, 608. DOI: 10.3389/fmicb.2018.00608
  • Brochet, M., Couvé, E., Zouine, M., Vallaeys, T., Rusniok, C., Lamy, M.C., Buchrieser, C., Trieu-Cuot, P., Kunst, F., Poyart, C. & Glaser, P. (2006). Genomic diversity and evolution within the species Streptococcus agalactiae. Microbes Infect, 8(5), 1227-43. DOI 10.1016/j.micinf.2005.11.010
  • Carra, E., Russo, S., Micheli, A., Garbarino, C., Ricchi, M., Bergamini, F., Bassi, P., Prosperi, A., Piva, S., Cricca, M., Schiavo, R., Merialdi, G., Serraino, A. & Arrigoni, N. (2021). Evidence of common isolates of Streptococcus agalactiae in bovines and humans in Emilia Romagna Region (Northern Italy). Front Microbiol., 11, 673126. DOI: 10.3389/fmicb.2021.673126
  • Carvalho-Castro, G.A., Silva, J.R., Paiva, L.V., Custódio, D.A.C, Moreira, R.O., Mian, G.F., Prado, I.A., Chalfun-Junior, A. & Costa, G.M. (2017). Molecular epidemiology of Streptococcus agalactiae isolated from mastitis in Brazilian dairy herds. Braz. J. Microbiol., 48, 551-9. DOI: 10.1016/j.bjm.2017.02.004
  • Çiftci, A., Fındık, A., Onuk, E.E. & Savasan, S. (2009). Detection of methicillin resistance and slime factor production of Staphylococcus aureus in bovine mastitis. Braz. J. Microbiol., 40, 254-61. DOI: 10.1590/S1517-83822009000200009
  • CLSI. (Clinical and Laboratory Standards Institute). (2012). Performance Standards for Antimicrobial Susceptibility Testing: Twenty-First Informational Supplement. CLSI Document M100-S21, 31(1).
  • de Castro, M.P., Ferreira, L.M., Filho, A.N., Zafalon, L.F., Vicente, H.I. & de Souza, V. (2013). Comparison of methods for the detection of biofilm formation by Staphylococcus aureus isolated from bovine subclinical mastitis. Braz. J. Microbiol., 44(1), 119-24. DOI: 10.1590/S1517- 83822013005000031
  • Dego Kerro, O., Pacha, P.A., Gillespie, B.E. & Pighetti, G.M. (2020). Experimental Staphylococcus aureus mastitis infection model by teat dipping in bacterial culture suspension in dairy cows. Animals, 10, 751. DOI: 10.3390/ani10050751
  • Delannoy, C.M.J., Crumlish, M., Fontne, M.C., Pollock, J., Foster, G., Dagleish, M.P., Turnbull, J.F. & Zadoks, R.N. (2013). Human Streptococcus agalactiae strains in aquatic mammals and fish. BMC Microbiol., 13, 41. DOI: 10.1186/1471-2180-13-41
  • Duarte, R.S., Miranda, O.P., Bellei, B.C., Brito, M.A. & Teixeira, L.M. (2004). Phenotypic and molecular characteristics of Streptococcus agalactiae isolates recovered from milk of dairy cows in Brazil. J. Clin. Microbiol., 42, 4214-22. DOI: 10.1128/JCM.42.9.4214-4222.2004
  • El-Behiry, A., Elsayed, M., Marzouk, E. & Bathich, Y. (2015). Detection of virulence genes in Staphylococcus aureus and Streptococcus agalactiae isolated from mastitis in the Middle East. Microbiol. Res. J. Int., 10, 1-9. DOI: 10.9734/BMRJ/2015/19237
  • European Centre for Disease Prevention and Control. (2018). Surveillance of antimicrobial resistance in Europe - Annual report of the European Antimicrobial Resistance Surveillance Network (EARS-Net) 2017, Stockholm, ECDC.
  • Gianneechini, R.E., Concha, C. & Franklin, A. (2002). Antimicrobial susceptibility of udder pathogens isolated from dairy herds in the west littoral region of Uruguay. Acta Vet. Scand., 43(1), 31-41. DOI: 10.1186/1751-0147-43-31
  • Han, G., Zhang, B., Luo, Z., Lu, B., Luo, Z., Zhang, J., Wang, Y., Luo, Y., Yang, Z., Shen, L., Yu, S., Cao, S. & Yao, X. (2022). Molecular typing and prevalence of antibiotic resistance and virulence genes in Streptococcus agalactiae isolated from Chinese dairy cows with clinical mastitis. PLoS One, 17(5), e0268262. DOI: 10.1371/journal.pone.0268262
  • Hernandez, L., Bottini, E., Cadona, J., Cacciato, C., Monteavaro, C., Bustamante, A. & Sanso, A.M. (2021). Multidrug resistance and molecular characterization of Streptococcus agalactiae isolates from dairy cattle with mastitis. Front Cell Infect. Microbiol., 30, 647324. DOI: 10.3389/fcimb.2021.647324
  • Jain, A. & Agarwal, A. (2009). Biofilm production, a marker of pathogenic potential of colonizing and commensal staphylococci. J. Microbiol. Method., 76(1), 88-92. DOI: 10.1016/j.mimet.2008.09.017
  • Kaczorek, E., Małaczewska, J., Wójcik, R. & Siwicki, A.K. (2017). Biofilm production and other virulence factors in Streptococcus spp. isolated from clinical cases of bovine mastitis in Poland. BMC Vet. Res., 13(1), 398. DOI: 10.1186/s12917- 017-1322-y
  • Keefe, G.P. (1997). Streptococcus agalactiae mastitis: A review. Can. Vet. J., 38, 429-37.
  • Leghari, A., Shakeel, A.L., Faiz, M.K., Khaliq, U.R.B., Sameen, Q.L., Muhammad, T.A., Iqra, B., Muhammad A.C., Jan, M.S., Hui-Xing, L. & Hong-Jie, F. (2023). Molecular epidemiology, characterization of virulence factors and antibiotic resistance profile of Streptococcus agalactiae isolated from dairy farms in China and Pakistan. J. Integrat Agricult., 22, 1514-28. DOI: 10.3390/ani14030447
  • Levy, S.B. (2002). Factors impacting on the problem of antibiotic resistance. Journal of Antimicrobial Chemotherapy, 49(1), 25-30. DOI: 10.1093/jac/49.1.25
  • Lyhs, U., Kulkas, L., Katholm, J., Waller, K.P., Saha, K. & Tomusk, R.J. (2016). Streptococcus agalactiae serotype IV in humans and Cattle, Northern Europe. Emerg Infect Di.s, 22, 2097- 103. DOI: 10.3201/eid2212.151447
  • Nam, H.M., Lim, S.K. & Kang, H.M. (2009). Antimicrobial resistance of streptococci isolated from mastitic bovine milk samples in Korea. J. Ve. Diagn. Invest., 21(5), 698-701. DOI: 10.1177/104063870902100517
  • Oliver, S.P. & Murinda, S.E. (2012). Antimicrobial resistance of mastitis pathogens. Vet Clin North Amer-Food Anim. Pract., 28, 165-85. DOI: 10.1016/j.cvfa.2012.03.005
  • Phuektes, P., Mansell, P.D. & Browning, G.F. (2001). Multiplex polymerase chain reaction assay for simultaneous detection of Staphylococcus aureus and streptococcal causes of bovine mastitis. J. Dairy Sci., 84(5), 1140-8. DOI: 10.3168/jds.S0022-0302(01)74574-2
  • Preez, J.H. (2000). Bovine mastitis therapy and why it fails. J. South Afr. Vet. Assoc., 71, 201-8. DOI: 10.4102/jsava.v71i3.714
  • Rajagopal, L. (2009). Understanding the regulation of group B Streptococcal virulence factors. Fut. Microbiol., 4, 201-21. DOI: 10.2217/17460913.4.2.201
  • Richards, V.P., Velsko, I.M., Alam, T., Zadoks, R.N., Manning, S.D., Pavinski, B.P.D., Hasler, H.B., Crestani, C., Springer, G., Probert, B., Town, C.D. & Stanhope, M.J. (2019). Population gene introgression and high genome plasticity for the zoonotic pathogen Streptococcus agalactiae. Mol. Biol. Evol., 36, 2572-90. DOI: 10.1093/molbev/msz169
  • Richardson, E.J., Bacigalupe, R., Harrison, E.M., Weinert, L.A., Lycett, S., Vrieling, M., Robb, K., Hoskisson, P.A., Holden, M.T.G., Feil, E.J., Paterson, G.K., Tong, S.Y.C., Shittu, A., van Wamel, W., Aanensen, D.M., Parkhill, J., Peacock, S.J., Corander, J., Holmes, M. & Fitzgerald, J.R. (2018). Gene exchange drives the ecological success of a multi-host bacterial pathogen. Nat. Ecol. Evol., 2, 1468-1478. DOI: 10.1038/s41559-018-0617-0
  • Rosini, R. & Margarit, I. (2015) Biofilm formation by Streptococcus agalactiae: influence of environmental conditions and implicated virulence factors. Front Cell Infect. Microbiol., 4, 6. DOI: 10.3389/fcimb.2015.00006
  • Shome, B.R., Bhuvana, M., Mitra, S.D., Krithiga, N., Shome, R., Velu, D., Banerjee, A., Barbuddhe, S.B., Prabhudas, K. & Rahman, H. (2012). Molecular characterization of Streptococcus agalactiae and Streptococcus uberis isolates from bovine milk. Trop. Anim. Health Prod., 44(8), 1981-92. DOI: 10.1007/s11250-012-0167-4
  • Sukhnanand, S., Dogan, B., Ayodele, M.O., Zadoks, R.N., Craver, M.P., Dumas, N.B., Schukken, Y.H., Boor, K.J. & Wiedmann, M. (2005). Molecular subtyping and characterization of bovine and human Streptococcus agalactiae isolates. J. Clin. Microbiol., 43(3), 1177-86. DOI: 10.1128/JCM.43.3.1177-1186.2005
  • Sullivan, C. B., Diggle, M. A. & Clarke, S.C. (2005). Review-Multilocus sequence typing-Data analysis in clinical microbiology and public health. Mol. Biotechnol., 29, 245-254. DOI: 10.1385/MB:29:3:245
  • Tamba, M., Rocca, R., Prosperi, A., Pupillo, G., Bassi, P., Galletti, G., Martini, E., Santi, A., Casadei, G. & Arrigoni, N. (2022). Evaluation of control program against Streptococcus agalactiae infection in dairy herds during 2019-2021 in Emilia-Romagna Region, Northern Italy. Front Vet. Sci., 23, 904527. DOI: 10.3389/fvets.2022.904527
  • Tenhagen, B.A., Köster, G., Wallmann, J. & Heuwieser, W. (2006). Prevalence of mastitis pathogens and their resistance against antimicrobial agents in dairy cows in Brandenburg, Germany. J. Dairy Sci., 89, 2542- 2551. DOI: 10.3168/jds.S0022-0302(06)72330-X
  • Tomazi, T., de Souza, F.A.F., Heinemann, M.B. & Santos, M.V. (2018) Molecular characterization and antimicrobial susceptibility pattern of Streptococcus agalactiae isolated from clinical mastitis in dairy cattle. PLoS ONE, 13(6), e0199561. DOI: 10.1371/journal.pone.0199561
  • Tuzcu, N., Hadimli, H.H. & Padron, B. (2023). Determination of virulence genes and antibiotic resistance profiles of Streptococcus agalactiae isolated from buffalo milk. Turk. J. Vet. Anim. Sci., 47, 7. DOI: 10.55730/1300-0128.4304
  • Uffe, B., Sørensen, S., Ilka, C., Klaas, J.B. & Farre, M. (2019). The distribution of clones of Streptococcus agalactiae (group B streptococci) among herdspersons and dairy cows demonstrates lack of host specificity for some lineages. Vet. Microbiol., 235, 71-9. DOI: 10.1016/j.vetmic.2019.06.008
  • Verma, S., Kumari, M., Pathak, A., Yadav, V., Johri, A.K. & Yadav, P. (2023). Antibiotic resistance, biofilm formation, and virulence genes of Streptococcus agalactiae serotypes of Indian origin. BMC Microbiol., 23(1), 176. DOI: 10.1186/s12866-023-02877-y
  • Versalovic, J. & Lupski, J.R. (2002). Molecular detection and genotyping of pathogens: more accurate and rapid answers. Trends Microbiol., 10, 15-21. DOI: 10.1016/s0966-842x(02)02438-1 Zadoks, R.N., Middleton, J.R., McDougall, S., Katholm, J. & Schukken, Y.H. (2011).
  • Molecular epidemiology of mastitis pathogens of dairy cattle and comparative relevance to humans. J. Mammary Gland Biol. Neoplasia, 16, 357-372. https://doi.org/10.1007/s10911-011-9236-y
  • Zadoks, R.N. & Fitzpatrick, J.L. (2009). Changing trends in mastitis. Irish. Vet. J., 62(4), 59-70. DOI: 10.1186/2046-0481-62-S4-S59
  • Zastempowska, E., Twarużek, M., Grajewski, J. & Lassa, H. (2022). Virulence factor genes and cytotoxicity of Streptococcus agalactiae isolated from bovine mastitis in Poland. Microbiol. Spectr., 10(3), e0222421. DOI: 10.1128/spectrum.02224-21.
Toplam 46 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Veteriner Mikrobiyolojisi
Bölüm Makaleler
Yazarlar

Şeyda Yaman 0000-0002-8872-6070

Murat Karahan 0000-0002-7024-1649

Alper Çiftci 0000-0001-8370-8677

Arzu Findik 0000-0002-9123-6160

Erken Görünüm Tarihi 14 Haziran 2024
Yayımlanma Tarihi 30 Haziran 2024
Gönderilme Tarihi 18 Mart 2024
Kabul Tarihi 22 Nisan 2024
Yayımlandığı Sayı Yıl 2024

Kaynak Göster

APA Yaman, Ş., Karahan, M., Çiftci, A., Findik, A. (2024). Virulence Determinants of Buffalo Mastitis Originated Streptococcus agalactiae Isolates. Journal of Anatolian Environmental and Animal Sciences, 9(2), 196-204. https://doi.org/10.35229/jaes.1454258


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