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. 2011 Dec 15:8:545.
doi: 10.1186/1743-422X-8-545.

Histopathological investigation in porcine infected with torque teno sus virus type 2 by inoculation

Affiliations

Histopathological investigation in porcine infected with torque teno sus virus type 2 by inoculation

Miao Mei et al. Virol J. .

Abstract

Background: Porcine torque teno sus virus (TTSuV) is a small icosahedral and non-enveloped virus which contains a single-stranded (ssDNA), circular and negative DNA genome and infects mainly vertebrates and is currently classified into the 'floating' genus Anellovirus of Circoviridae with two species. Viral DNA of both porcine TTSuV species has a high prevalence in both healthy and diseased pigs worldwide and multiple infections of TTSuV with distinct genotypes or subtypes of the same species has been documented in the United States, Europe and Asia. However, there exists no information about histopathological lesions caused by infection with porcine TTSuV2.

Methods: Porcine liver tissue homogenate with 1 ml of 6.91 × 107 genomic copies viral loads of porcine TTSuV2 that had positive result for torque teno sus virus type 2 and negative result for torque teno sus virus type 1 and porcine pseudorabies virus type 2 were used to inoculate specific pathogen-free piglets by intramuscular route and humanely killed at 3,7,10,14,17,21 and 24 days post inoculation (dpi), the control pigs were injected intramuscularly with 1 ml of sterile DMEM and humanely killed the end of the study for histopathological examination routinely processed, respectively.

Results: All porcine TTSuV2 inoculated piglets were clinic asymptomatic but developed myocardial fibroklasts and endocardium, interstitial pneumonia, membranous glomerular nephropathy, and modest inflammatory cells infiltration in portal areas in the liver, foci of hemorrhage in some pancreas islet, a tiny amount red blood cells in venule of muscularis mucosae and outer longitudinal muscle, rarely red blood cells in the microvasculation and infiltration of inflammatory cells (lymphocytes and eosinophils) of tonsil and hilar lymph nodes, infiltration of inflammatory lymphocytes and necrosis or degeneration and focal gliosis of lymphocytes in the paracortical zone after inoculation with porcine TTSuV2-containing tissue homogenate.

Conclusions: Analysis of these presentations revealed that porcine TTSuV2 was readily transmitted to TTSuV-negative swine and that infection was associated with characteristic pathologic changes in specific pathogen-free piglets inoculated with porcine TTSuV2. Those results indicated no markedly histopathological changes happened in those parenchymatous organs, especially the digestive system and immune system when the specific pathogen-free pigs were infected with porcine TTSuV2, hence, to some extent, it was not remarkable pathological agent for domestic pigs at least. So, porcine TTSuV2 could be an unrecognized pathogenic viral infectious etiology of swine. This study indicated a directly related description of lesions responsible for TTSuV2 infection in swine.

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Figures

Figure 1
Figure 1
Photomicrograph of heart from two of the pigs. There is hyperemia in artery and subtle congestion among myocardial fibroklasts at 17 dpi. (HE. ×400), and large number of red blood cells distribute in endocardium, but cells of endocardium were not found changes and lesions from a specific pathogen-free pig euthanized at 14 dpi. with the liver homogenate of porcine TTSuV2 (HE. ×200). Those histopathological lesions were marked with arrowheads.
Figure 2
Figure 2
The lung lesions contained of a mild interstitial pneumonia. The lung lesions contained of a mild interstitial pneumonia characterized by a slight thickening of the alveolar septa by mononuclear cells and congestion, and bronchial epithelial cells happened defluvium and inflammation infiltration in pulmonary alveolus(c, 10 dpi. HE. ×100; d,24 dpi HE. ×200).
Figure 3
Figure 3
Sections of porcine kidney. Sections of porcine kidney showed slight congestion in the renal tube at 7 dpi. (e, HE. ×100), the degeneration and necrosis in renal capsular epithelial cells and the ventral cells defluvium of renal capsule in capsular space at 17 dpi (f. HE. ×400).
Figure 4
Figure 4
Histopathological observation of the digestive system. Histopathological observation of the digestive system including live, pancreas and duodenum: (g) showed that there existed a tiny amount of red blood cells in the interlobular veins and sinusoid and a bit of inflammatory cells infiltration in portal areas from a specific pathogen- free piglets killed at 10 dpi. (HE. ×200), but no various pathological lesions were observed at other parts of the liver at 10 dpi. (h. HE. ×200); (i) and (j) manifested subtle congestion among pancreas islets and foci of hemorrhage in some pancreas islet, a little of infiltration was inferred as pancreatic juice or electrolyte inner interlobular duct at 21 dpi. (HE. ×200); however, non-specific histopathological lesions of the duodenum except a tiny amount red blood cells in venule of muscularis mucosae and outer longitudinal muscle was observed and could be pictured as normal histological graph (k, at 3 dpi. HE. ×200; l, at 24 dpi, HE. x200).
Figure 5
Figure 5
Photomicrograph of the main immune system. Photomicrograph of the main immune system involving in spleen, tonsil, hilar lymph nodes, mesenteric lymph nodes and inguinal lymph nodes collected from experimental groups weaned piglets euthanized at different days post inoculation porcine TTSuV2. With the development of infection, the sections of tonsil, spleen, hilar lymph nodes and mesenteric lymph nodes showed the normal architecture with no special lesions through the study but only rarely red blood cells in the microvasculation and infiltration of inflammatory cells (lymphocytes and eosinophils) of tonsiland hilar lymph nodes marked by black arrowheads (m, o, p, s. HE. ×100; n, t. HE. ×200; r. HE. ×400). In addition, inguinal lymph nodes' architecture was normal, but congestion, infiltration of inflammatory lymphocytes and necrosis or degeneration and focal gliosis of lymphocytes in the paracortical zone were observed at 24 dpi. (u. HE. ×100; v. HE. ×200). The red four-point star, five-point star and rhomboid represent the normal architecture of those immune organs.

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References

    1. Nishizawa T, Okamoto H, Konishi K, Yoshizawa H, Miyakawa Y, Mayumi M. A Novel DNA Virus (TTV) Associated with Elevated Transaminase Levels in Posttransfusion Hepatitis of Unknown Etiology. Biochem Biophys Res Commun. 1997;241:92–97. doi: 10.1006/bbrc.1997.7765. - DOI - PubMed
    1. Mushahwar IK, Erker JC, Muerhoff AS, Leary TP, Simons JN, Birkenmeyer LG, Chalmers ML, Pilot-Matias TJ, Dexai SM. Molecular and biophysical characterization of TT virus: evidence for a new virus family infecting humans. Proc Natl Acad Sci USA. 1999;96:3177–3182. doi: 10.1073/pnas.96.6.3177. - DOI - PMC - PubMed
    1. Martinez L, Kekarainen T, Sibila M, Ruiz-Fons F, Vidal D, Gortazar C, Segales J. Torque teno virus (TTV) is highly prevalent in the European wild boar (Sus scrofa) Vet Microbiol. 2006;118:223–229. doi: 10.1016/j.vetmic.2006.07.022. - DOI - PubMed
    1. Kekarainen T, Segalés J. Torque teno virus infection in the pig and its potential role as a model of human infection. The Veterinary J. 2009;180:163–168. doi: 10.1016/j.tvjl.2007.12.005. - DOI - PubMed
    1. Leary TP, Erker JC, Chalmers ML, Desai SM, Mushahwar IK. Improved detection systems for TT virus reveal high prevalence in humans, non-human primates and farm animals. J Gen Virol. 1999;80:2115. - PubMed

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