Prevalence and Genetic Diversity of Torque Teno Sus Viruses 1 and 2 in Pigs in Chiang Mai and Lamphun, Thailand
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Abstract
Torque teno sus viruses 1 and 2 (TTSuV1 and 2) belong to the family Anelloviridae, which is known to commonly infect pigs; however, their pathogenesis is unclear. Studies of TTSuV1 and TTSuV2 in pigs worldwide, especially with regard to their prevalence and genetic diversity, have been conducted; however, the prevalence and genetic diversity of both viruses have not been studied in Chiang Mai and Lamphun, Thailand. Therefore, this study aimed to investigate both viruses in terms of their prevalence and genetic diversity using polymerase chain reaction with specific primers in the tonsils of 100 apparently clinically healthy pigs that are being raised in this region. Overall, the prevalence rates of TTSuV1, TTSuV2, and both in combination, in the pigs were 62% (62/100), 68% (68/100), and 50% (50/100), respectively. Phylogenetic analysis of 5' untranslated regions of 19 nucleotide sequences of both viruses was conducted. Both viruses were separated into 2 groups. The first group displayed a lack of geographic clustering because the nucleotide sequences in these groups showed extreme differences (TTSuV1 minimum nucleotide sequence identity was recorded at 87% and TTSuV1 minimum nucleotide sequence identity was recorded at 85%). The second group revealed the identical nucleotide sequences as no differences were observed in terms of the nucleotide sequences among the specimens. Our data indicate that the nucleotide sequences of TTSuV1s and s that were detected in Chiang Mai and Lamphun, Thailand, likely were adapted from their genome.
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References
Bigarre, L., V. Beven, C. de Boisseson, B. Grasland, N. Rose, P. Biagini, and A. Jestin. 2005. Pig anelloviruses are highly prevalent in swine herds in France. J. Gen. Virol. 86(Pt 3): 631-635.
Cortey, M., E. Pileri, J. Segales, and T. Kekarainen. 2012. Globalizations and global trade influence molecular viral population genetics of Torque Teno Sus Viruses 1 and 2 in pigs. Vet. Microbiol. 156(1-2): 81–87.
Gimenez-Lirola, L. G., P. F. Gerber, R. R. Rowland, P. G. Halbur, Y. W. Huang, X. J. Meng, and T. Opriessnig. 2014. Development and validation of a 4-plex antibody assay for simultaneous detection of IgG antibodies against Torque teno sus virus 1 (TTSuV1), TTSuV2, and porcine reproductive and respiratory syndrome virus types 1 and 2. Res. Vet. Sci. 96(3): 543–550.
Hino, S., and H. Miyata. 2007. Torque teno virus (TTV): current status. Rev. Med. Virol. 17(1): 45–57.
Kamahora, T., S. Hino, and H. Miyata. 2000. Three spliced mRNAs of TT virus transcribed from a plasmid containing the entire genome in COS1 cells. J. Virol. 74(21): 9980–9986.
Karuppannan, A. K., and T. Opriessnig. 2018. Possible risks posed by single-stranded DNA viruses of pigs associated with xenotransplantation. Xenotransplantation. 25: e12453.
Kekarainen, T., S. Lopez-Soria, and J. Segales. 2007. Detection of swine Torque teno virus genogroups 1 and 2 in boar sera and semen. Theriogenology. 68(7): 966–971.
Kekarainen, T., M. Sibila, and J. Segales. 2006. Prevalence of swine Torque teno virus in post-weaning multisystemic wasting syndrome (PMWS)-affected and non-PMWS-affected pigs in Spain. J. Gen. Virol. 8(Pt4): 833–837.
Kumar, S., G. Stecher, M. Li, C. Knyaz, and K. Tamura. 2018. MEGA X: Molecular evolutionary genetics analysis across computing platforms. Mol. Biol. Evol. 35(6): 1547–1549.
Lee, S. S., S. Sunyoung, H. Jung, J. Shin, and Y. S. Lyoo. 2010. Quantitative detection of porcine Torque teno virus in Porcine circovirus-2-negative and Porcine circovirus-associated disease-affected pigs. J. Vet. Diagn. Invest. 22(2): 261–264.
Lee, Y., C. M. Lin, C. R. Jeng, H. W. Chang, C. C. Chang, and V. F. Pang. 2015. The pathogenic role of torque teno sus virus 1 and 2 and their correlations with various viral pathogens and host immunocytes in wasting pigs. Vet. Microbiol. 180(3-4):186–195.
Martelli, F., A. Caprioli, I. Di Bartolo, V. Cibin, G. Pezzotti, F. M. Ruggeri, and F. Ostanello. 2006. Detection of swine torque teno virus in Italian pig herds. J. Vet. Med. B. Infect. Dis. Vet. Public. Health. 53(5): 234–238.
McKeown, N. E., M. Fenaux, P. G. Halbur, and X. J. Meng. 2004. Molecular characterization of porcine TT virus, an orphan virus, in pigs from six different countries. Vet. Microbiol. 104(1-2): 113–117.
Meng, X. J., 2012. Emerging and re-emerging swine viruses. Transbound. Emerg. Dis. 59(Suppl1): 85–102.
Nieto, D., T. Kekarainen, M. Aramouni, and J. Segales. 2013. Torque teno sus virus 1 and 2 distribution in tissues of porcine circovirus type 2-systemic disease affected and age-matched healthy pigs. Vet. Microbiol. 163(3-4): 364–367.
Ninomiya, M., T. Nishizawa, M. Takahashi, F. R. Lorenzo, T. Shimosegawa, and H. Okamoto. 2007. Identification and genomic characterization of a novel human torque teno virus of 3.2 kb. J. Gen. Virol. 88(Pt4): 1939–1944.
Novosel, D., V. Cubric-Curik, A. Jungic, and Z. Lipej. 2012. Presence of Torque teno sus virus in porcine circovirus type 2-associated disease in Croatia. Vet. Rec. 171(21): 529.
Okamoto, H., 2009. History of discoveries and pathogenicity of TT viruses. Curr Top Microbiol. Immunol. 331: 1–20.
Ramos, N., S. Mirazo, G. Botto, T. F. Teixeira, S. P. Cibulski, G. Castro, K. Cabrera, P. M. Roehe, and J. Arbiza. 2018. High frequency and extensive genetic heterogeneity of TTSuV1 and TTSuVk2a in PCV2- infected and non-infected domestic pigs and wild boars from Uruguay. Vet. Microbiol. 224: 78–87.
Saekhow, P., and H. Ikeda. 2015. Prevalence and genomic characterization of porcine parvoviruses detected in Chiangmai area of Thailand in 2011. Microbiol. Immunol. 59(2): 82–88.
Spandole, S., D. Cimponeriu, L. M. Berca, and G. Mihaescu. 2015. Human anelloviruses: an update of molecular, epidemiological and clinical aspects. Arch. Virol. 160(4): 893–908.
Taira, O., H. Ogawa, A. Nagao, K. Tuchiya, T. Nunoya, and S. Ueda. 2009. Prevalence of swine Torque teno virus genogroups 1 and 2 in Japanese swine with suspected post-weaning multisystemic wasting syndrome and porcine respiratory disease complex. Vet. Microbiol. 139(3-4): 347–350.
Tscherne, D. M., and A. Garcia-Sastre. 2011. Virulence determinants of pandemic influenza viruses. J. Clin. Invest. 121(1): 6–13.
Xiao, C. T., L. Gimenez-Lirola, Y. W. Huang, X. J. Meng, P. G. Halbur, and T. Opriessnig. 2012. The prevalence of Torque teno sus virus (TTSuV) is common and increases with the age of growing pigs in the United States. J. Virol. Methods. 183(1):40–44.
Zhai, S. L., J. X. Long, W. K. Wei, Q. L. Chen, M. L. Luo, D. H. Lv, D. C. Wu, F. Gao, S. S. Yuan, G. Z. Tong, and Z. Z. Wei. 2013. High prevalence of torque teno sus virus in China and genetic diversity of the 5' non-coding region. Arch. Virol. 158(7): 1567–1573.
Zheng, S., J. Shi, X. Wu, Z. Peng, C. Xin, L. Zhang, Y. Liu, M. Gao, S. Xu, H. Han, J. Yu, W. Sun, X. Cong, J. Li, and J. Wang. 2018. Presence of Torque teno sus virus 1 and 2 in porcine circovirus 3-positive pigs. Transbound. Emerg. Dis. 65(2): 327–330.