Porcine circovirus infection: interaction with the host and its association with disease

Main Article Content

Lucia Angelica García-Camacho
Alejandro Vargas-Ruiz

Abstract

Porcine circoviruses (PCVs) are widespread in both domestic and wild pig populations. Four PCV species have been described to date (PCV1 to PCV4), with PCV2 being the most well-documented due to its involvement in porcine circovirus disease. This infection has a complex pathology and presents in different clinical forms, causing significant economic losses for the swine industry. This paper reviews available information on PCVs, including their genotypes, possible associations between disease and the presence of PCV3 and PCV4. The difficulty of establishing this association is discussed, given the high rate of co-infection between PCVs and other pathogenic and emerging viruses.

Keywords:
PCV2, PCVAD, PMWS, Falla reproductiva, Genotipos

Article Details

Author Biography

Lucia Angelica García-Camacho, Universidad Nacional Autónoma de México. Facultad de Estudios Superiores Cuautitlán. Departamento de Ciencias Biológicas. Estado de México, México.

Profesor de carrera titular "A" tiempo completo definitiva.

Departamento de ciencias biológicas

References

Opriessnig T, Karuppannan AK, Castro AMMG, Xiao CT. Porcine circoviruses: current status, knowledge gaps and challenges. Virus Research. 2020;286:198044. doi: 10.1016/j.virusres.2020.198044.

Zhao L, Rosario K, Breitbart M, Duffy S. Eukaryotic circular Rep-encoding single-stranded DNA (CRESS DNA) viruses: ubiquitous viruses with small genomes and a diverse host range. En: M Kielian, TC Mettenleiter, MJ Roossinck, editores. Advances in Virus Research. Vol. 103. Cambridge: Academic Press; 2019. pp. 71–133. doi: 10.1016/bs.aivir.2018.10.001.

Breitbart M, Delwart E, Rosario K, Segalés J, Varsani A. ICTV virus taxonomy profile: Circoviridae. Journal of General Virology. 2017;98(8):1997–1998. doi: 10.1099/jgv.0.000871.

Juhan NM, LeRoith T, Opriessnig T, Meng XJ. The open reading frame 3 (ORF3) of porcine circovirus type 2 (PCV2) is dispensable for virus infection, but evidence of reduced pathogenicity is limited in pigs infected by an ORF3-null PCV2 mutant. Virus Research. 2010;147(1):60–66. doi: 10.1016/j.virusres.2009.10.007.

Ramamoorthy S, Meng XJ. Porcine circoviruses: a minuscule yet mammoth paradox. Animal Health Research Reviews. 2009;10(1):1–20. doi: 10.1017/s1466252308001461.

Šolaja S, Glišić D, Milićević V. Prevalence of porcine circoviruses 2 and 3 in wild boar in Serbia. Journal of Veterinary Diagnostic Investigation. 2025;37(4):674–678. doi: 10.1177/10406387251325534.

Holgado-Martín R, Risco D, Ramos A, Martínez-Pérez R, García-Jiménez WL, Hermoso-de Mendoza J, et al. Significant detection of porcine circovirus 3 and porcine circovirus 4 in wild boars from mid-western Spain without apparent sanitary consequences. Animals. 2025;15(4):523. doi: 10.3390/ani15040523.

Yang J, Kim CH, Jang G, Lee C. Molecular epidemiological surveillance and complete genome analysis of porcine circoviruses in wild boars (Sus scrofa) in Gyeongnam Province, South Korea. Journal of Veterinary Science. 2024;25(6):e79. doi: 10.4142/jvs.24252.

De Maio FA, Winter M, Abate S, Cifuentes S, Iglesias NG, Barrio DA, et al. Detection of porcine circovirus 2, porcine parvovirus 1, and Torque teno sus virus k2a in wild boars from northeastern Patagonia, Argentina. Archives of Virology. 2023;168:208. doi: 10.1007/s00705-023-05831-5.

Montenegro OL, Roncancio N, Soler-Tovar D, Cortés-Duque J, Contreras-Herrera J, Sabogal S, et al. Serologic survey for selected viral and bacterial swine pathogens in Colombian collared peccaries (Pecari tajacu) and feral pigs (Sus scrofa). Journal of Wildlife Diseases. 2018;54(4):700–707. doi: 10.7589/2017-09-236.

Tischer I, Rasch R, Tochtermann G. Characterization of papovavirus- and picornavirus-like particles in permanent pig kidney cell lines. Zentralblatt für Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Erste Abteilung Originale. Reihe A: Medizinische Mikrobiologie und Parasitolologie. 1974;226(2):153–167.

Harding JCS. The clinical expression and emergence of porcine circovirus 2. Veterinary Microbiology. 2004;98(2):131–135. doi: 10.1016/j.vetmic.2003.10.013.

Palinski R, Piñeyro P, Shang P, Yuan F, Guo R, Fang Y, et al. A novel porcine circovirus distantly related to known circoviruses is associated with porcine dermatitis and nephropathy syndrome and reproductive failure. Journal of Virology. 2017;91(1):e01879-16. doi: 10.1128/jvi.01879-16.

Phan TG, Giannitti F, Rossow S, Marthaler D, Knutson T, Li L, et al. Detection of a novel circovirus PCV3 in pigs with cardiac and multi-systemic inflammation. Virology Journal. 2016;13(1):184. doi: 10.1186/s12985-016-0642-z.

Zhang HH, Hu WQ, Li JY, Liu TN, Zhou JY, Opriessnig T, et al. Novel circovirus species identified in farmed pigs designated as porcine circovirus 4, Hunan province, China. Transboundary and Emerging Diseases. 2020;67(3):1057–1061. doi: 10.1111/tbed.13446.

Niu G, Chen S, Li X, Zhang L, Ren L. Advances in crosstalk between porcine circoviruses and host. Viruses. 2022;14(7):1419. doi: 10.3390/v14071419.

Opriessnig T, Langohr I. Current state of knowledge on porcine circovirus type 2-associated lesions. Veterinary Pathology. 2013;50(1):23–38. doi: 10.1177/0300985812450726.

Gillespie J, Opriessnig T, Meng XJ, Pelzer K, Buechner-Maxwell V. Porcine circovirus type 2 and porcine circovirus-associated disease. Journal of Veterinary Internal Medicine. 2009;23(6):1151–1163. doi: 10.1111/j.1939-1676.2009.0389.x.

Chae C. A review of porcine circovirus 2-associated syndromes and diseases. The Veterinary Journal. 2005;169(3):326–336. doi: 10.1016/j.tvjl.2004.01.012.

Wei R, Trus I, Yang B, Huang L, Nauwynck HJ. Breed differences in PCV2 uptake and disintegration in porcine monocytes. Viruses. 2018;10(10):562. doi: 10.3390/v10100562.

Lv Q, Guo K, Xu H, Wang T, Zhang Y. Identification of putative ORF5 protein of porcine circovirus type 2 and functional analysis of GFP-fused ORF5 protein. PLoS ONE. 2015;10(6):e0127859. doi: 10.1371/journal.pone.0127859.

Frant MP, Mazur-Panasiuk N, Gal-Cisoń A, Bocian Ł, Łyjak M, Szczotka-Bochniarz A. Porcine circovirus type 3 (PCV3) in Poland: prevalence in wild boar population in connection with African swine fever (ASF). Viruses. 2024;16(5):754. doi: 10.3390/v16050754.

Ha Z, Xie CZ, Li JF, Wen SB, Zhang KL, Nan FL, et al. Molecular detection and genomic characterization of porcine circovirus 3 in pigs from Northeast China. BMC Veterinary Research. 2018;14(1):321. doi: 10.1186/s12917-018-1634-6.

Mora-Díaz J, Piñeyro P, Shen H, Schwartz K, Vannucci F, Li G, et al. Isolation of PCV3 from perinatal and reproductive cases of PCV3-associated disease and in vivo characterization of PCV3 replication in CD/CD growing pigs. Viruses. 2020;12(2):219. doi: 10.3390/v12020219.

Prinz C, Stillfried M, Neubert LK, Denner J. Detection of PCV3 in German wild boars. Virology Journal. 2019;16(1):25. doi: 10.1186/s12985-019-1133-9.

Wang LQ, Li JX, Chen XM, Cao XY, Zhang HL, Zheng LL, et al. Molecular detection and genetic characteristics of porcine circovirus 3 and porcine circovirus 4 in central China. Archives of Virology. 2024;169(5):115. doi: 10.1007/s00705-024-06039-x.

Fux R, Söckler C, Link EK, Renken C, Krejci R, Sutter G, et al. Full genome characterization of porcine circovirus type 3 isolates reveals the existence of two distinct groups of virus strains. Virology Journal. 2018;15(1):25. doi: 10.1186/s12985-018-0929-3.

Wang Y, Su M, Huang Y, Ren J, Niu S, Zhao Y, et al. Development of a novel PCV2 and PCV3 vaccine using virus-like vesicles incorporating Venezuelan equine encephalomyelitis virus-containing vesicular stomatitis virus glycoprotein. Frontiers in Veterinary Science. 2024;11:1359421. doi: 10.3389/fvets.2024.1359421.

Agaton-Flores L. Estandarización e implementación de una técnica de PCR convencional para la amplificación de la región genética VP1 parcial del circovirus porcino 3 (PCV3) a partir de sangre de cerdas reproductoras de granjas de baja densidad del Estado de México, Hidalgo y Querétaro [tesis de licenciatura]. Cuautitlán, Estado de México: Universidad Nacional Autónoma de México; 2025.

Sidler X, Sydler T, Mateos JM, Klausmann S, Brugnera E. Porcine circovirus type 2 pathogenicity alters host’s central tolerance for propagation. Pathogens. 2020;9(10):839. doi: 10.3390/pathogens9100839.

Afghah Z, Webb B, Meng XJ, Ramamoorthy S. Ten years of PCV2 vaccines and vaccination: is eradication a possibility? Veterinary Microbiology. 2017;206:21–28. doi: 10.1016/j.vetmic.2016.10.002.

Carman S, Cai HY, DeLay J, Youssef SA, McEwen BJ, Gagnon CA, et al. The emergence of a new strain of porcine circovirus-2 in Ontario and Quebec swine and its association with severe porcine circovirus-associated disease 2004–2006. Canadian Journal of Veterinary Research. 2008;72(3):259–268.

Dupont K, Nielsen EO, Bækbo P, Larsen LE. Genomic analysis of PCV2 isolates from Danish archives and a current PMWS case-control study supports a shift in genotypes with time. Veterinary Microbiology. 2008;128(1–2):56–64. doi: 10.1016/j.vetmic.2007.09.016.

Olvera A, Cortey M, Segalés J. Molecular evolution of porcine circovirus type 2 genomes: phylogeny and clonality. Virology. 2007;357(2):175–185. doi: 10.1016/j.virol.2006.07.047.

Ellis J, Clark E, Haines D, West K, Krakowka S, Kennedy S, et al. Porcine circovirus 2 and concurrent infections in the field. Veterinary Microbiology. 2004;98(2):159–163. doi: 10.1016/j.vetmic.2003.10.008.

Allan GM, McNeilly F, McMenamy M, McNair I, Krakowka SG, Timmusk S, et al. Temporal distribution of porcine circovirus 2 genogroups recovered from postweaning multisystemic wasting syndrome-affected and non-affected farms in Ireland and Northern Ireland. Journal of Veterinary Diagnostic Investigation. 2007;19(6):668–673. doi: 10.1177/104063870701900608.

Gagnon CA, Tremblay D, Tijssen P, Venne MH, Houde A, Mehdy Elahi S. The emergence of porcine circovirus 2b genotype (PCV-2b) in swine in Canada. The Canadian Veterinary Journal. 2007;48(8):811–819.

Seo HW, Park C, Kang I, Choi K, Jeong J, Park SJ, et al. Genetic and antigenic characterization of a newly emerging porcine circovirus type 2b mutant first isolated in cases of vaccine failure in Korea. Archives of Virology. 2014;159(11):3107–3111. doi: 10.1007/s00705-014-2164-6.

Opriessnig T, Xiao CT, Gerber PF, Halbur PG. Emergence of a novel mutant PCV2b variant associated with clinical PCVAD in two vaccinated pig farms in the U.S. concurrently infected with PPV2. Veterinary Microbiology. 2013;163(1–2):177–183. doi: 10.1016/j.vetmic.2012.12.019.

Xiao CT, Harmon KM, Halbur PG, Opriessnig T. PCV2d-2 is the predominant type of PCV2 DNA in pig samples collected in the U.S. during 2014–2016. Veterinary Microbiology. 2016;197:72–77. doi: 10.1016/j.vetmic.2016.11.009.

Sibila M, Rocco C, Franzo G, Huerta E, Domingo M, Núñez JI, et al. Genotyping of porcine circovirus 2 (PCV-2) in vaccinated pigs suffering from PCV-2-systemic disease between 2009 and 2020 in Spain. Pathogens. 2021;10(8):1016. doi: 10.3390/pathogens10081016.

Bedolla López F, Trujillo Ortega ME, Mendoza Elvira S, Quintero Ramírez V, Alonso Morales R, Ramírez-Mendoza H, et al. Identification and genotyping of porcine circovirus type II (PCV2) in Mexico. Virus Disease. 2018;29(3):385–389. doi: 10.1007/s13337-018-0460-6.

Ouyang T, Niu G, Liu X, Zhang X, Zhang Y, Ren L. Recent progress on porcine circovirus type 3. Infection, Genetics and Evolution. 2019;73:227–233. doi: 10.1016/j.meegid.2019.05.009.

Chung HC, Nguyen VG, Park YH, Park BK. Genotyping of PCV3 based on reassembled viral gene sequences. Veterinary Medicine and Science. 2021;7(2):474–482. doi: 10.1002/vms3.374.

Li G, He W, Zhu H, Bi Y, Wang R, Xing G, et al. Origin, genetic diversity, and evolutionary dynamics of novel porcine circovirus 3. Advanced Science. 2018;5(9):1800275. doi: 10.1002/advs.201800275.

Saraiva GL, Vidigal PMP, Assao VS, Fajardo MLM, Loreto ANS, Fietto JLR, et al. Retrospective detection and genetic characterization of porcine circovirus 3 (PCV3) strains identified between 2006 and 2007 in Brazil. Viruses. 2019;11(3):201. doi: 10.3390/v11030201.

Franzo G, Delwart E, Fux R, Hause B, Su S, Zhou JY, et al. Genotyping porcine circovirus 3 (PCV-3) nowadays: does it make sense? Viruses. 2020;12(3):265. doi: 10.3390/v12030265.

Reséndiz-Sandoval M, Vázquez-García VA, Contreras-Vega K, Melgoza-González EA, Mata-Haro V, Gimenez-Lirola L, et al. A retrospective analysis of porcine circovirus type 3 in samples collected from 2008 to 2021 in Mexico. Viruses. 2023;15(11):12225. doi: 10.3390/v15112225.

Visuthsak W, Woonwong Y, Thanantong N, Poolperm P, Boonsoongnern A, Ratanavanichrojn N, et al. PCV3 in Thailand: molecular epidemiology and relationship with PCV2. Transboundary and Emerging Diseases. 2021;68(6):2980–2989. doi: 10.1111/tbed.14294.

Nauwynck HJ, Sanchez R, Meerts P, Lefebvre DJ, Saha D, Huang L, et al. Cell tropism and entry of porcine circovirus 2. Virus Research. 2012;164(1–2):43–45. doi: 10.1016/j.virusres.2011.11.003.

Misinzo G, Delputte PL, Meerts P, Lefebvre DJ, Nauwynck HJ. Porcine circovirus 2 uses heparan sulfate and chondroitin sulfate B glycosaminoglycans as receptors for its attachment to host cells. Journal of Virology. 2006;80(7):3487–3494. doi: 10.1128/jvi.80.7.3487-3494.2006.

Ouyang Y, Nauwynck HJ. PCV2 uptake by porcine monocytes is strain-dependent and is associated with amino acid characteristics on the capsid surface. Microbiology Spectrum. 2023;11(2):e0380522. doi: 10.1128/spectrum.03805-22.

Wei R, Xie J, Theuns S, Nauwynck HJ. Changes on the viral capsid surface during the evolution of porcine circovirus type 2 (PCV2) from 2009 till 2018 may lead to a better receptor binding. Virus Evolution. 2019;5(2):vez026. doi: 10.1093/ve/vez026.

Kekarainen T, McCullough K, Fort M, Fossum C, Segalés J, Allan GM. Immune responses and vaccine-induced immunity against porcine circovirus type 2. Veterinary Immunology and Immunopathology. 2010;136(3–4):185–193. doi: 10.1016/j.vetimm.2010.03.025.

Grierson SS, King DP, Tucker AW, Donadeu M, Mellencamp MA, Haverson K, et al. Ontogeny of systemic cellular immunity in the neonatal pig: correlation with the development of post-weaning multisystemic wasting syndrome. Veterinary Immunology and Immunopathology. 2007;119(3–4):254–268. doi: 10.1016/j.vetimm.2007.06.004.

Wei C, Lin Z, Dai A, Chen H, Ma Y, Li N, et al. Emergence of a novel recombinant porcine circovirus type 2 in China: PCV2c and PCV2d recombinant. Transboundary and Emerging Diseases. 2019;66(6):2496–2506. doi: 10.1111/tbed.13307.

Fort M, Sibila M, Nofrarías M, Pérez-Martín E, Olvera A, Mateu E, et al. Porcine circovirus type 2 (PCV2) Cap and Rep proteins are involved in the development of cell-mediated immunity upon PCV2 infection. Veterinary Immunology and Immunopathology. 2010;137(3–4):226–234. doi: 10.1016/j.vetimm.2010.05.013.

Segalés J, Domingo M. Postweaning multisystemic wasting syndrome (PMWS) in pigs: a review. Veterinary Quarterly. 2002;24(3):125–180. doi: 10.1080/01652176.2002.9695133.

Resendes A, Segalés J, Balasch M, Calsamiglia M, Sibila M, Ellerbrok H, et al. Lack of an effect of a commercial vaccine adjuvant on the development of postweaning multisystemic wasting syndrome (PMWS) in porcine circovirus type 2 (PCV2) experimentally infected conventional pigs. Veterinary Research. 2004;35(1):83–90. doi: 10.1051/vetres:2003039.

Ma Z, Liu M, Liu Z, Meng F, Wang H, Cao L, et al. Epidemiological investigation of porcine circovirus type 2 and its coinfection rate in Shandong province in China from 2015 to 2018. BMC Veterinary Research. 2021;17(1):17. doi: 10.1186/s12917-020-02718-4.

Opriessnig T, Fenaux M, Yu S, Evans RB, Cavanaugh D, Gallup JM, et al. Effect of porcine parvovirus vaccination on the development of PMWS in segregated early weaned pigs coinfected with type 2 porcine circovirus and porcine parvovirus. Veterinary Microbiology. 2004;98(3–4):209–220. doi: 10.1016/j.vetmic.2003.11.006.

Jiang H, Wang D, Wang J, Zhu S, She R, Ren X, et al. Induction of porcine dermatitis and nephropathy syndrome in piglets by infection with porcine circovirus type 3. Journal of Virology. 2019;93(4). doi: 10.1128/jvi.02045-18.

Wang D, Mai J, Yang Y, Xiao CT, Wang N. Current knowledge on epidemiology and evolution of novel porcine circovirus 4. Veterinary Research. 2022;53(1):38. doi: 10.1186/s13567-022-01053-w.

Opriessnig T, Ramamoorthy S, Madson DM, Patterson AR, Pal N, Carman S, et al. Differences in virulence among porcine circovirus type 2 isolates are unrelated to cluster type 2a or 2b and prior infection provides heterologous protection. Journal of General Virology. 2008;89(10):2482–2491. doi: 10.1099/vir.0.2008/001081-0.

Park JS, Ha Y, Kwon B, Cho KD, Lee BH, Chae C. Detection of porcine circovirus 2 in mammary and other tissues from experimentally infected sows. Journal of Comparative Pathology. 2009;140(2–3):208–211. doi: 10.1016/j.jcpa.2008.11.004.

Shibata I, Okuda Y, Kitajima K, Asai T. Shedding of porcine circovirus into colostrum of sows. Journal of Veterinary Medicine, Series B, Infectious Diseases and Veterinary Public Health. 2006;53(6):278–280. doi: 10.1111/j.1439-0450.2006.00953.x.

Dupont K, Hjulsager CK, Kristensen CS, Baekbo P, Larsen LE. Transmission of different variants of PCV2 and viral dynamics in a research facility with pigs mingled from PMWS-affected herds and non-affected herds. Veterinary Microbiology. 2009;139(3–4):219–226. doi: 10.1016/j.vetmic.2009.06.001.

Calsamiglia M, Fraile L, Espinal A, Cuxart A, Seminati C, Martín M, et al. Sow porcine circovirus type 2 (PCV2) status effect on litter mortality in postweaning multisystemic wasting syndrome (PMWS). Research in Veterinary Science. 2007;82(3):299–304. doi: 10.1016/j.rvsc.2006.08.007.

Rose N, Blanchard P, Cariolet R, Grasland B, Amenna N, Oger A, et al. Vaccination of porcine circovirus type 2 (PCV2)-infected sows against porcine parvovirus (PPV) and erysipelas: effect on post-weaning multisystemic wasting syndrome (PMWS) and on PCV2 genome load in the offspring. Journal of Comparative Pathology. 2007;136(2–3):133–144. doi: 10.1016/j.jcpa.2007.01.006.

Mateusen B, Sanchez RE, Van Soom A, Meerts P, Maes DGD, Nauwynck HJ. Susceptibility of pig embryos to porcine circovirus type 2 infection. Theriogenology. 2004;61(1):91–101. doi: 10.1016/S0093-691X(03)00187-0.

Pensaert MB, Sanchez RE, Ladekjær-Mikkelsen AS, Allan GM, Nauwynck HJ. Viremia and effect of fetal infection with porcine viruses with special reference to porcine circovirus 2 infection. Veterinary Microbiology. 2004;98(2):175–183. doi: 10.1016/j.vetmic.2003.10.011.

Sanchez RE, Meerts P, Nauwynck HJ, Pensaert MB. Change of porcine circovirus 2 target cells in pigs during development from fetal to early postnatal life. Veterinary Microbiology. 2003;95(1–2):15–25. doi: 10.1016/S0378-1135(03)00120-2.

Sanchez RE, Nauwynck HJ, McNeilly F, Allan GM, Pensaert MB. Porcine circovirus 2 infection in swine foetuses inoculated at different stages of gestation. Veterinary Microbiology. 2001;83(2):169–176. doi: 10.1016/S0378-1135(01)00425-4.

Yuan AW, Pang P, Gong QL, Deng ZB. Germocyte lesions caused by porcine circovirus type 2b in Kunming mice. Polish Journal of Veterinary Sciences. 2017;20(1):25–29. doi: 10.1515/pjvs-2017-0004.

Schmoll F, Lang C, Steinrigl AS, Schulze K, Kauffold J. Prevalence of PCV2 in Austrian and German boars and semen used for artificial insemination. Theriogenology. 2008;69(7):814–821. doi: 10.1016/j.theriogenology.2007.12.009.

Madson DM, Patterson AR, Ramamoorthy S, Pal N, Meng XJ, Opriessnig T. Reproductive failure experimentally induced in sows via artificial insemination with semen spiked with porcine circovirus type 2. Veterinary Pathology. 2009;46(4):707–716. doi: 10.1354/vp.08-VP-0234-O-FL.

Ostanello F, Caprioli A, di Francesco A, Battilani M, Sala G, Sarli G, et al. Experimental infection of 3-week-old conventional colostrum-fed pigs with porcine circovirus type 2 and porcine parvovirus. Veterinary Microbiology. 2005;108(3–4):179–186. doi: 10.1016/j.vetmic.2005.04.010.

Meerts P, Misinzo G, Lefebvre D, Nielsen J, Bøtner A, Kristensen CS, et al. Correlation between the presence of neutralizing antibodies against porcine circovirus 2 (PCV2) and protection against replication of the virus and development of PCV2-associated disease. BMC Veterinary Research. 2006;2:6. doi: 10.1186/1746-6148-2-6.

Fort M, Olvera A, Sibila M, Segalés J, Mateu E. Detection of neutralizing antibodies in postweaning multisystemic wasting syndrome (PMWS)-affected and non-PMWS affected pigs. Veterinary Microbiology. 2007;125(3–4):244–255. doi: 10.1016/j.vetmic.2007.06.004.

Carasova P, Celer V, Takacova K, Trundova M, Molinkova D, Lobova D, et al. The levels of PCV2 specific antibodies and viremia in pigs. Research in Veterinary Science. 2007;83(2):274–278. doi: 10.1016/j.rvsc.2006.11.013.

Liu S, Li Q, Qiao J, Wang J, Cui D, Gu K, et al. Endothelial IL-8 induced by porcine circovirus type 2 affects dendritic cell maturation and antigen-presenting function. Virology Journal. 2019;16(1):154. doi: 10.1186/s12985-019-1256-z.

Fort M, Fernandes LT, Nofrarias M, Díaz I, Sibila M, Pujols J, et al. Development of cell-mediated immunity to porcine circovirus type 2 (PCV2) in caesarean-derived, colostrum-deprived piglets. Veterinary Immunology and Immunopathology. 2009;129(1–2):101–107. doi: 10.1016/j.vetimm.2008.12.024.

Du Q, Wu X, Wang T, Yang X, Wang Z, Niu Y, et al. Porcine circovirus type 2 suppresses IL-12p40 induction via Capsid/gC1qR-mediated microRNAs and signalings (sic.). Journal of Immunology. 2018;201(2):533–547. doi: 10.4049/jimmunol.1800250.

Kekarainen T, Montoya M, Dominguez J, Mateu E, Segalés J. Porcine circovirus type 2 (PCV2) viral components immunomodulate recall antigen responses. Veterinary Immunology and Immunopathology. 2008;124(1–2):41–49. doi: 10.1016/j.vetimm.2008.01.031.

Vincent IE, Balmelli C, Meehan B, Allan G, Summerfield A, McCullough KC. Silencing of natural interferon producing cell activation by porcine circovirus type 2 DNA. Immunology. 2007;120(1):47–56. doi: 10.1111/j.1365-2567.2006.02476.x.

Kekarainen T, Segalés J. Porcine circovirus 2 immunology and viral evolution. Porcine Health Management. 2015;1:17. doi: 10.1186/s40813-015-0012-z.

Trujano M, Iglesias G, Segalés J, Palacios JM. PCV-2 from emaciated pigs in Mexico. Veterinary Record. 2001;148(25):792.

García-Camacho L, Enríquez-Ramírez K, Araiza-Nava D, Rangel-Rodríguez I, Quintero-Ramírez V, García-Reyna P. Porcine circovirus 2-associated syndromes in Mexican farms as detected by in situ hybridization. Veterinary Pathology. 2006;43(5):15.

Enriquez K. Relationship of histopathology and PCV2 detection in fetal and neonatal myocardium from cases of reproductive failure in sows. En: Proceedings of the 21st International Pig Veterinary Society Congress; 2010. p. 467.

Enríquez Ramírez K. Evaluación de la participación del circovirus porcino tipo 2 (PCV-2) en la falla reproductiva [tesis de maestría]. Cuautitlán, Estado de México: Universidad Nacional Autónoma de México; 2009.

García-Camacho L, Enríquez-Ramírez K, Rangel-Rodríguez I, Quintero-Ramírez V, Romero-Sánchez Y, García-Reyna P. Histological patterns for PCV2-associated enteritis and the co-infection with Lawsonia intracellularis. Veterinary Pathology. 2007;44(5).

Jensen TK, Vigre H, Svensmark B, Bille-Hansen V. Distinction between Porcine Circovirus type 2 enteritis and porcine proliferative enteropathy caused by Lawsonia intracellularis. Journal of Comparative Pathology. 2006;135(4):176–182. doi: 10.1016/j.jcpa.2006.08.006.

Garcia-Camacho LA, Vargas-Ruiz A, Marin-Flamand E, Ramírez-Álvarez H, Brown C. A retrospective study of DNA prevalence of porcine parvoviruses in Mexico and its relationship with porcine circovirus-associated disease. Microbiology and Immunology. 2020;64(5):366–376. doi: 10.1111/1348-0421.12782.

Servicio de Información Agroalimentaria y Pesquera (SIAP). SIACON: Sistema de Información Agroalimentaria de Consulta [Internet]. Gobierno de México; 2025 ago 12. https://www.gob.mx/siap/documentos/siacon-ng-161430

Vargas-Ruiz A, Acevedo-Díaz K, Delgado-Joya A, González-Díaz F, Araiza-Hernández D, Marín-Flamand E, et al. Detection of Parvoviridae and Circoviridae family species from (sic.)blood of gilts in central Mexico backyard farms. Agro Productividad. 2025;18(3):37–44. doi: 10.32854/agrop.v17i3.3282.

Galindo-Barboza AJ, Rivera-Benítez JF, de la Luz-Armendáriz J, Sánchez-Betancourt JI, Hernández J, Sauceda-Cerecer SG, et al. Molecular positivity of Porcine circovirus type 2 associated with production practices on farms in Jalisco, Mexico. Viruses. 2024;16(10):1633. doi: 10.3390/v16101633.

Shen H, Wang C, Madson DM, Opriessnig T. High prevalence of porcine circovirus viremia in newborn piglets in five clinically normal swine breeding herds in North America. Preventive Veterinary Medicine. 2010;97(3-4):228–236. doi: 10.1016/j.prevetmed.2010.09.020.

Harmon KM, Gauger PC, Zhang J, Piñeyro PE, Dunn DD, Chriswell AJ. Whole-genome sequences of novel Porcine circovirus type 2 viruses detected in swine from Mexico and the United States. Genome Announcements. 2015;3(6):e01315-15. doi: 10.1128/genomeA.01315-15.

Rivera-Benítez JF, de la Luz-Armendáriz J, Gómez-Núñez L, Diosdado Vargas F, Socci Escatell G, Ramírez-Medina E, et al. Salud porcina: historia, retos y perspectivas. Revista Mexicana de Ciencias Pecuarias. 2021;12(Suppl 3):149–185. doi: 10.22319/rmcp.v12s3.5879.

Orozco V, Hernández J, Vargas A, González F, García L, Flores A. Caso clínico reproductivo de coinfección PCV3-PCV2-PPV1 en una granja del Bajío mexicano. En: Memorias LVI Congreso Nacional AMVEC; Querétaro: AMVEC; 2024. https://www.amvec.com/blog/amvec-1/memorias-amvec-14

Orozco V, Hernández J, Quintero V, Torres A, Flores A, Piñeyro PE. Caso clínico reproductivo diagnosticado como PCV3 en una granja del Bajío mexicano. En: Memorias LV Congreso Nacional AMVEC; Querétaro: AMVEC; 2023. https://www.amvec.com/blog/amvec-1/memorias-amvec-14

De la Luz AJ, Rivera BJF, Gómez NL. Phylogenetic analysis of porcine circovirus type 3 infecting a swine production system in Mexico City. En: Proceedings of the 10th European Symposium of Porcine Health Management; 2018. https://www.ecphm.org/european-symposium-porcine-health-management

Vlasakova M, Leskova V, Sliz I, Jackova A, Vilcek S. The presence of six potentially pathogenic viruses in pigs suffering from post-weaning multisystemic wasting syndrome. BMC Veterinary Research. 2014;10(1):221. doi: 10.1186/s12917-014-0221-8.

McMenamy MJ, McKillen J, McNair I, Duffy C, Blomström AL, Charreyre C, et al. Detection of a porcine boca-like virus in combination with porcine circovirus type 2 genotypes and Torque teno sus virus in pigs from postweaning multisystemic wasting syndrome (PMWS)-affected and non-PMWS-affected farms in archival samples from Great Britain. Veterinary Microbiology. 2013;164(3–4):293–298. doi: 10.1016/j.vetmic.2013.03.009.

Teixeira TF, Dezen D, Cibulski SP, Varela APM, Sheffer CM, Holz CL, et al. Torque teno sus virus (TTSuV) in tissues of pigs and its relation with the occurrence of postweaning multisystemic wasting syndrome. Virus Genes. 2013;47(2):276–281. doi: 10.1007/s11262-013-0940-0.

Nieto D, Aramouni M, Grau-Roma L, Segalés J, Kekarainen T. Dynamics of Torque teno sus virus 1 (TTSuV1) and 2 (TTSuV2) DNA loads in serum of healthy and postweaning multisystemic wasting syndrome (PMWS)-affected pigs. Veterinary Microbiology. 2011;152(3–4):284–290. doi: 10.1016/j.vetmic.2011.05.020.

Pérez LJ, Arce HD de, Frias MT, Perera CL, Ganges L, Núñez JI. Molecular detection of Torque teno sus virus in lymphoid tissues in concomitant infections with other porcine viral pathogens. Research in Veterinary Science. 2011;91(3):154–157. doi: 10.1016/j.rvsc.2011.02.012.

Blomström AL, Belák S, Fossum C, Fuxler L, Wallgren P, Berg M. Studies of porcine circovirus type 2, porcine boca-like virus and Torque teno virus indicate the presence of multiple viral infections in postweaning multisystemic wasting syndrome pigs. Virus Research. 2010;152(1-2):59–64. doi: 10.1016/j.virusres.2010.06.004.

Krakowka S, Hartunian C, Hamberg A, Shoup D, Rings M, Zhang Y, et al. Evaluation of induction of porcine dermatitis and nephropathy syndrome in gnotobiotic pigs with negative results for porcine circovirus type 2. American Journal of Veterinary Research. 2008;69(12):1615–1622. doi: 10.2460/ajvr.69.12.1615.

Vargas-Ruiz A, Ramírez-Álvarez H, Sánchez-Betancourt JI, Quintero-Ramírez V, Rangel-Rodríguez IC, Vázquez-Pérez JA, et al. Retrospective study of the relationship of Torque teno sus virus 1a and 1b with porcine circovirus-associated disease. Canadian Journal of Veterinary Research. 2017;81(3):178–185. PMCID: PMC5508382.

Saekhow P, Kishizuka S, Sano N, Mitsui H, Akasaki H, Mawatari T, et al. Coincidental detection of genomes of porcine parvoviruses and porcine circovirus type 2 infecting pigs in Japan. The Journal of Veterinary Medical Science. 2016;77(12):1581–1586. doi: 10.1292/jvms.15-0167.

Sun J, Huang L, Wei Y, Wang Y, Chen D, Du W, et al. Prevalence of emerging porcine parvoviruses and their co-infections with porcine circovirus type 2 in China. Archives of Virology. 2015;160(5):1339–1344. doi: 10.1007/s00705-015-2373-7.

Opriessnig T, Xiao CT, Gerber PF, Halbur PG. Identification of recently described porcine parvoviruses in archived North American samples from 1996 and association with porcine circovirus-associated disease. Veterinary Microbiology. 2014;173(1–2):9–16. doi: 10.1016/j.vetmic.2014.06.024.

Darwich L, Segalés J, Resendes A, Balasch M, Plana-Durán J, Mateu E. Transient correlation between viremia levels and IL-10 expression in pigs subclinically infected with porcine circovirus type 2 (PCV2). Research in Veterinary Science. 2008;84(2):194–198. doi: 10.1016/j.rvsc.2007.04.005.