Top

Published in:

01-12-2020 | Review

Constant companion: clinical and developmental aspects of torque teno virus infections

Authors: Elena A. Lolomadze, Denis V. Rebrikov

Published in: Archives of Virology | Issue 12/2020

Abstract

Torque teno virus (TTV) is a commensal human virus observed as a circular single-negative-strand DNA molecule in various tissues and biological samples, notably in blood serum and lymphocytes. TTV has no apparent clinical significance, although it might be very useful as a prospective tool for gene delivery or as an epidemiological marker. Human populations are ubiquitously infected with TTV; the prevalence may reach 100%. The majority of babies become spontaneously infected with TTV, so that by the end of the first year of life, the prevalence reaches 'adult' values. TTV positivity in healthy early infancy and the presence of TTV in umbilical cord blood samples have been reported. The mechanism of infection and the dynamics of TTV prevalence in infants with age remain understudied. Meanwhile, the potential diagnostic and prognostic value of TTV as a marker deserves special attention and study, along with the possibility, causes and consequences of placental transmission of TTV under normal or pathological conditions.

Haynes M, Rohwer F (2010) The human virome. In: Metagenomics of the human body. Springer, New York, pp 63–77

Pride DT, Salzman J, Haynes M et al (2011) Evidence of a robust resident bacteriophage population revealed through analysis of the human salivary virome. ISME J 6:915–926. https://doi.org/10.1038/ismej.2011.169CrossRefPubMedCentral

Santiago-Rodriguez TM, Ly M, Bonilla N et al (2015) The human urine virome in association with urinary tract infections. Front Microbiol 6:1–12. https://doi.org/10.3389/fmicb.2015.00014CrossRef

Nishizawa T, Okamoto H, Konishi K, Yoshizawa H, Miyakawa Y, Mayumi M (1997) A novel DNA virus (TTV) associated with elevated transaminase levels in posttransfusion hepatitis of unknown etiology. Biochem Biophys Res Commun 241:92–97. https://doi.org/10.1006/bbrc.1997.7765CrossRef

https://talk.ictvonline.org/ictv-reports/ictv_9th_report/ssdna-viruses-2011/w/ssdna_viruses/139/anelloviridae. Accessed 8 Aug 2020

https://www.ncbi.nlm.nih.gov/genomes/GenomesGroup.cgi?taxid=687329. Accessed 8 Aug 2020]

Sarairah H, Bdour S, Gharaibeh W (2020) The molecular epidemiology and phylogeny of torque teno virus (TTV) in Jordan. Viruses 12:165. https://doi.org/10.3390/v12020165CrossRefPubMedCentral

Kaczorowska J, van der Hoek L (2020) Human anelloviruses: diverse, omnipresent and commensal members of the virome. FEMS Microbiol Rev 44:305–313. https://doi.org/10.1093/femsre/fuaa007CrossRefPubMedCentral

Payne S (2017) Viruses: from understanding to investigation. Elsevier Inc, pp 243–246

10.

Kakkola L, Tommiska J, Boele LCL, Miettinen S, Blom T, Kekarainen T et al (2007) Construction and biological activity of a full-length molecular clone of human Torque teno virus (TTV) genotype 6. FEBS J 274:4719–4730. https://doi.org/10.1111/j.1742-4658.2007.06020.xCrossRef

11.

Griffiths P (1999) Time to consider the concept of a commensal virus? Rev Med Virol 9:73–74. https://doi.org/10.1002/(sici)1099-1654(199904/06)9:2<73:aid-rmv254>3.0.co;2-5CrossRef

12.

Simmonds P, Prescott LE, Logue C, Davidson F, Thomas AE, Ludlam CA (1999) TT virus—part of the normal human flora? J Infect Dis 180:1748–1749. https://doi.org/10.1086/315105CrossRef

13.

Abe K, Inami T, Asano K, Miyoshi C, Masaki N, Hayashi S et al (1999) TT virus infection is widespread in the general populations from different geographic regions. J Clin Microbiol 37:2703–2705. https://doi.org/10.1128/JCM.37.8.2703-2705.1999CrossRefPubMedCentral

14.

AbuOdeh R, Al-Mawlawi N, Al-Qahtani AA et al (2015) Detection and genotyping of torque teno virus (TTV) in healthy blood donors and patients infected with HBV or HCV in Qatar. J Med Virol 87:1184–1191. https://doi.org/10.1002/jmv.24146CrossRef

15.

Charlton M, Adjei P, Poterucha J et al (1998) TT-virus infection in north american blood donors, patients with fulminant hepatic failure, and cryptogenic cirrhosis. Hepatology 28:839–842. https://doi.org/10.1002/hep.510280335CrossRef

16.

Irshad M, Singh S, Irshad K, Agarwal SK, Joshi YK (2008) Torque teno virus: its prevalence and isotypes in North India. World J Gastroenterol 14:6044–6051. https://doi.org/10.3748/wjg.14.6044CrossRefPubMedCentral

17.

Vasilyev EV, Trofimov DY, Tonevitsky AG, Ilinsky VV, Korostin DO, Rebrikov DV (2009) Torque teno virus (TTV) distribution in healthy Russian population. Virol J 6:134–137. https://doi.org/10.1186/1743-422X-6-134CrossRefPubMedCentral

18.

Brajão de Oliveira K (2015) Torque teno virus: a ubiquitous virus. Rev Bras Hematol Hemoter 37:357–358. https://doi.org/10.1016/j.bjhh.2015.07.009CrossRefPubMedCentral

19.

Fatholahi M, Bouzari M (2015) Torque Teno midi virus/small Anellovirus in sera of healthy, HIV/HCV and HIV infected individuals in Lorestan Province, Iran. Jundishapur J Microbiol 8:e25368. https://doi.org/10.5812/jjm.25368CrossRefPubMedCentral

20.

Ninomiya M, Takahashi M, Nishizawa T, Shimosegawa T, Okamoto H (2008) Development of PCR assays with nested primers specific for differential detection of three human anelloviruses and early acquisition of dual or triple infection during infancy. J Clin Microbiol 46:507–514. https://doi.org/10.1128/JCM.01703-07CrossRef

21.

Han TH, Chung JY (2006) Detection of small Anellovirus DNA from blood products. Korean J Blood Transfus 17:126–134

22.

Spandole S, Cimponeriu D, Berca LM, Mihaescu G (2015) Human anelloviruses: an update of molecular, epidemiological and clinical aspects. Arch Virol 160:893–908. https://doi.org/10.1007/s00705-015-2363-9CrossRef

23.

Kumata R, Ito J, Takahashi K, Suzuki T, Sato K (2020) A tissue level atlas of the healthy human virome. BMC Biol 18:55. https://doi.org/10.1186/s12915-020-00785-5CrossRefPubMedCentral

24.

Hsieh SY, Wu YH, Ho YP, Tsao KC, Yeh CT, Liaw YF (1999) High prevalence of TT virus infection in healthy children and adults and in patients with liver disease in Taiwan. Am Soc Microbiol 37:1829–1831. https://doi.org/10.1128/JCM.37.6.1829-1831.1999CrossRef

25.

Hafez MM, Shaarawy SM, Hassan AA, Salim RF, Abd El Salam FM, Ali AE (2007) Prevalence of transfusion transmitted virus (TTV) genotypes among HCC patients in Qaluobia governorate. Virol J 4:135. https://doi.org/10.1186/1743-422X-4-135CrossRefPubMedCentral

26.

Sawata T, Bando M, Nakayama M et al (2018) Clinical significance of changes in Torque teno virus DNA titer after chemotherapy in patients with primary lung cancer. Respir Investig 56:173–178. https://doi.org/10.1016/j.resinv.2017.12.004CrossRef

27.

Kosulin K, Kernbichler S, Pichler H et al (2018) Post-transplant replication of torque teno virus in granulocytes. Front Microbiol 9:2956. https://doi.org/10.3389/fmicb.2018.02956CrossRefPubMedCentral

28.

Kondili LA, Pisani G, Beneduce F et al (2001) Prevalence of TT virus in healthy children and thalassemic pediatric and young adult patients. J Pediatr Gastroenterol Nutr 33:629–632. https://doi.org/10.1097/00005176-200111000-00025CrossRef

29.

Hassuna NA, Naguib E, Abdel-Fatah M, Mousa SMO (2017) Phylogenetic analysis of torque teno virus in thalassemic children in Egypt. Intervirology 60:102–108. https://doi.org/10.1159/000480507CrossRef

30.

Hsu J, Rosenthal P, Ruel T, Kyohere M et al (2018) Etiology of non-malarial febrile illnesses in ugandan children. Pediatrics 141:463. https://doi.org/10.1542/peds.141.1_MeetingAbstract.463CrossRef

31.

McElvania TeKippe E, Wylie KM, Deych E, Sodergren E, Weinstock G, Storch GA (2012) Increased prevalence of anellovirus in pediatric patients with fever. PLoS ONE 7:e50937. https://doi.org/10.1371/journal.pone.0050937CrossRefPubMedCentral

32.

Maggi F, Pifferi M, Fornai C et al (2003) TT virus in the nasal secretions of children with acute respiratory diseases: relations to viremia and disease severity. J Virol 77:2418–2425. https://doi.org/10.1128/jvi.77.4.2418-2425.2003CrossRefPubMedCentral

33.

Jones MS, Kapoor A, Lukashov VV, Simmonds P, Hecht F, Delwart E (2005) New DNA viruses identified in patients with acute viral infection syndrome. J Virol 79:8230–8236CrossRefPubMedCentral

34.

Westman G, Schoofs C, Ingelsson M, Järhult JD, Muradrasoli S (2020) Torque teno virus viral load is related to age, CMV infection and HLA type but not to Alzheimer's disease. PLoS ONE 15:e0227670. https://doi.org/10.1371/journal.pone.0227670CrossRefPubMedCentral

35.

Thom K, Petrik J (2007) Progression towards AIDS leads to increased torque teno virus and torque teno minivirus titers in tissues of HIV infected individuals. J Med Virol 79:1–7. https://doi.org/10.1002/jmv.20756CrossRefPubMedCentral

36.

De Villiers E-M, Bulajic M, Nitsch C et al (2007) TTV infection in colorectal cancer tissues and normal mucosa. Int J Cancer 121:2109–2112. https://doi.org/10.1002/ijc.22931CrossRefPubMedCentral

37.

Maggi F, Pifferi M, Tempestini E, Lanini L, de Marco E, Fornai C et al (2004) Correlation between Torque tenovirus infection and serum levels of eosinophil cationic protein in children hospitalized for acute respiratory diseases. J Infect Dis 190:971–974. https://doi.org/10.1086/423143CrossRefPubMedCentral

38.

Pifferi M, Maggi F, Caramella D, de Marco E, Andreoli E, Meschi S et al (2006) High torquetenovirus loads are correlated with bronchiectasis and peripheral airflow limitation in children. Pediatr Infect Dis J 25:804–808. https://doi.org/10.1097/01.inf.0000232723.58355.f4CrossRef

39.

Albert E, Solano C, Giménez E, Focosi D, Pérez A, Macera L et al (2017) The kinetics of torque teno virus plasma DNA load shortly after engraftment predicts the risk of high-level CMV DNAemia in allogeneic hematopoietic stem cell transplant recipients. Bone Marrow Transplant 53:180–187. https://doi.org/10.1038/bmt.2017.235CrossRefPubMedCentral

40.

Abbas AA, Diamond JM, Chehoud C, Chang B, Kotzin JJ, Young JC et al (2017) The perioperative lung transplant virome: torque teno viruses are elevated in donor lungs and show divergent dynamics in primary graft dysfunction. Am J Transplant 17:1313–1324. https://doi.org/10.1111/ajt.14076CrossRef

41.

Peker BO, Daloğlu AE, Görzer I, Puchhammer-Stöckl E, Parkan ÖM, Akbaş H, Kintrup GT, Mutlu D, Küpesiz OA, Çolak D (2020) Investigation of torque teno virus (TTV) DNA as an immunological and virological marker in pediatric hematopoietic stem cell transplantation (HSCT) patients. Microb Pathog. https://doi.org/10.1016/j.micpath.2020.104397CrossRef

42.

Pradier A, Masouridi-Levrat S, Bosshard C, Dantin C, Vu DL, Zanella MC, Boely E, Tapparel C, Kaiser L, Chalandon Y, Simonetta F, Roosnek E (2020) Torque teno virus as a potential biomarker for complications and survival after allogeneic hematopoietic stem cell transplantation. Front Immunol 11:998. https://doi.org/10.3389/fimmu.2020.00998CrossRefPubMedCentral

43.

Davila S, Halstead ES, Hall MW et al (2018) A viral DNAemia and immune suppression in pediatric sepsis. Pediatr Crit Care Med 19:14–22. https://doi.org/10.1097/PCC.0000000000001376CrossRef

44.

Pifferi M, Maggi F, Andreoli E, Lanini L, Marco ED, Fornai C et al (2005) Associations between nasal torquetenovirus load and spirometric indices in children with asthma. J Infect Dis 192:1141–1148. https://doi.org/10.1086/444389CrossRef

45.

Schiemann M, Puchhammer-Stöckl E, Eskandary F, Kohlbeck P, Rasoul-Rockenschaub S, Heilos A, Kozakowski N, Görzer I, Kikić Ž, Herkner H, Böhmig GA, Bond G (2017) Torque teno virus load-inverse association with antibody-mediated rejection after kidney transplantation. Transplantation 101:360–367. https://doi.org/10.1097/TP.0000000000001455CrossRefPubMedCentral

46.

Uhl P, Heilos A, Bond G, Meyer E, Böhm M, Puchhammer-Stöckl E, Arbeiter K, Müller-Sacherer T, Csaicsich D, Aufricht C, Rusai K (2020) Torque teno viral load reflects immunosuppression in paediatric kidney-transplanted patients-a pilot study. Pediatr Nephrol. https://doi.org/10.1007/s00467-020-04606-3CrossRef

47.

Beland K, Dore-Nguyen M, Gagne MJ et al (2014) Torque teno virus in children who underwent orthotopic liver transplantation: new insights about a common pathogen. J Infect Dis 209:247–254. https://doi.org/10.1093/infdis/jit423CrossRef

48.

Reshetnyak VI, Maev IV, Burmistrov AI, Chekmazov IA, Karlovich TI (2020) Torque teno virus in liver diseases: On the way towards unity of view. World J Gastroenterol 26:1691–1707. https://doi.org/10.3748/wjg.v26.i15.1691CrossRefPubMedCentral

49.

Zhang Y, Li F, Shan TL, Deng X, Delwart E, Feng XP (2016) A novel species of torque Teno mini virus (TTMV) in gingival tissue from chronic periodontitis patients. Sci Rep 6:26739. https://doi.org/10.1038/srep26739CrossRefPubMedCentral

50.

Rocchi J, Ricci V, Albani M, Lanini L, Andreoli E, Macera L, Pistello M, Ceccherini-Nelli L, Bendinelli M, Maggi F (2009) Torquetenovirus DNA drives proinflammatory cytokines production and secretion by immune cells via toll-like receptor 9. Virology 394:235–242. https://doi.org/10.1016/j.virol.2009.08.036CrossRef

51.

Kincaid RP, Burke JM, Cox JC, de Villiers EM, Sullivan CS (2013) A human torque teno virus encodes a microRNA that inhibits interferon signaling. PLoS Pathog 9(12):e1003818. https://doi.org/10.1371/journal.ppat.1003818CrossRefPubMedCentral

52.

Wohlfarth P, Leiner M, Schoergenhofer C et al (2018) Torquetenovirus dynamics and immune marker properties in patients following allogeneic hematopoietic stem cell transplantation: a prospective longitudinal study. Biol Blood Marrow Transplant 24:194–199. https://doi.org/10.1016/j.bbmt.2017.09.020CrossRef

53.

Nordén R, Magnusson J, Lundin A et al (2018) Quantification of torque teno virus and Epstein-Barr virus is of limited value for predicting the net state of immunosuppression after lung transplantation. Open Forum Infect Dis 5(4):ofy050. https://doi.org/10.1093/ofid/ofy050CrossRefPubMedCentral

54.

Mushahwar IK (2000) Recently discovered blood-borne viruses: are they hepatitis viruses or merely endosymbionts? J Med Virol 62:399–404. https://doi.org/10.1002/1096-9071(200012)62:4<399:aid-jmv1>3.0.co;2-uCrossRef

55.

Fenner's Veterinary Virology [book, 5th Edition] (2016) Chapter 13—circoviridae and anelloviridae, pp 259–268. https://www.sciencedirect.com/book/9780128009468/fenners-veterinary-virology

56.

Aramouni M, Segalés J, Sibila M, Martin-Valls GE, Nieto D, Kekarainen T (2011) Torque teno sus virus 1 and 2 viral loads in postweaning multisystemic wasting syndrome (PMWS) and porcine dermatitis and nephropathy syndrome (PDNS) affected pigs. Vet Microbiol 153:377–381. https://doi.org/10.1016/j.vetmic.2011.05.046CrossRef

57.

Aramouni M, Martínez J, Nieto D, Kekarainen T, Segalés J (2013) Exploratory study of Torque teno sus viruses in pulmonary inflammatory lesions in pigs. Vet Microbiol 162:338–344. https://doi.org/10.1016/j.vetmic.2012.09.011CrossRef

58.

Okamoto H, Nishizawa T, Kato N, Ukita M, Ikeda H, Iizuka H, Mayumi M (1998) Molecular cloning and characterization of a novel DNA virus (TTV) associated with posttransfusion hepatitis of unknown etiology. Hepatol Res 10:1–16. https://doi.org/10.1016/S1386-6346(97)00123-XCrossRef

59.

Hsiao KL, Wang LY, Lin CL, Liu HF (2016) New phylogenetic groups of torque teno virus identified in Eastern Taiwan Indigenes. PLoS ONE 11(2):e0149901. https://doi.org/10.1371/journal.pone.0149901CrossRefPubMedCentral

60.

Jelcic I, Hotz-Wagenblatt A, Hunziker A, Zur Hausen H, de Villiers EM (2004) Isolation of multiple TT virus genotypes from spleen biopsy tissue from a Hodgkin's disease patient: genome reorganization and diversity in the hypervariable region. J Virol 78:7498–7507. https://doi.org/10.1128/JVI.78.14.7498-7507.2004CrossRefPubMedCentral

61.

Wei Y, Chen M, Yang X, Zhang L, Rao L, Yuan F, Wang Y, Gong J, Li L (2015) Molecular characterization of human torque teno virus. Biomed Rep 3:821–826. https://doi.org/10.3892/br.2015.508CrossRefPubMedCentral

62.

Spandole S, Cimponeriu D, Toma M, Radu I, Ion DA (2013) Rapid detection of human torque teno viruses using high-resolution melting analysis. Balkan J Med Genet 16:55–62. https://doi.org/10.2478/bjmg-2013-0018CrossRefPubMedCentral

63.

Kulifaj D, Tilloy V, Scaon E, Guerin E, Essig M, Pichon N, Hantz S, De Bernardi A, Joannes M, Barranger C, Alain S (2020) Viral metagenomics analysis of kidney donors and recipients: torque teno virus genotyping and prevalence. J Med Virol. https://doi.org/10.1002/jmv.26298CrossRef

64.

Tanaka T, Kuroda K, Kobayashi M, Sato K (2001) Detection and typing of TT virus DNA genotype by the PCR-RFLP method. Mol Cell Probes 15:195–200. https://doi.org/10.1006/mcpr.2001.0358CrossRef

65.

Mankotia DS, Irshad M (2014) Cloning and expression of N22 region of torque teno virus (TTV) genome and use of peptide in developing immunoassay for TTV antibodies. Virol J 11:96. https://doi.org/10.1186/1743-422X-11-96CrossRefPubMedCentral

66.

Mankotia DS, Irshad M (2017) Development of an immunoassay for detection of torque teno virus (TTV) antibodies using the N22 expression product from TTV genotype 2. Intervirology 60:207–216. https://doi.org/10.1159/000487481CrossRef

67.

Toyoda H, Naruse M, Yokozaki S, Morita K, Nakano I, Itakura A, Okamura M, Fukuda Y, Hayakawa T (1999) Prevalence of infection with TT virus (TTV), a novel DNA virus, in healthy Japanese subjects, newborn infants, cord blood and breast milk. J Infect 38(3):198–199. https://doi.org/10.1016/s0163-4453(99)90254-2CrossRef

68.

El-Esnawy NA, Bacheer HH, Ezzat E, Mostafa A, Ashour E et al (2007) TT virus in infants sera and mother breast milks. JGEB 5:19–26

69.

Inami T, Konomi N, Arakawa Y, Abe K (2000) High prevalence of TT virus DNA in human saliva and semen. J Clin Microbiol 38(6):2407–2408CrossRefPubMedCentral

70.

Fornai C, Maggi F, Vatteroni ML, Pistello M, Bendinelli M (2001) High prevalence of TT virus (TTV) and TTV-like minivirus in cervical swabs. J Clin Microbiol 39(5):2022–2024. https://doi.org/10.1128/JCM.39.5.2022-2024.2001CrossRefPubMedCentral

71.

Matsubara H, Michitaka K, Horiike N, Yano M, Akbar SM, Torisu M, Onji M (2000) Existence of TT virus DNA in extracellular body fluids from normal healthy Japanese subjects. Intervirology 43(1):16–19. https://doi.org/10.1159/000025018CrossRef

72.

Pinho-Nascimento CA, Leite JP, Niel C, Diniz-Mendes L (2011) Torque teno virus in fecal samples of patients with gastroenteritis: prevalence, genogroups distribution, and viral load. J Med Virol 83(6):1107–1111. https://doi.org/10.1002/jmv.22024CrossRef

73.

Itoh M, Shimomura H, Fujioka S et al (2001) High prevalence of TT virus in human bile juice samples: importance of secretion through bile into feces. Dig Dis Sci 46(3):457–462. https://doi.org/10.1023/a:1005618308943CrossRef

74.

Gallian P, Biagini P, Zhong S et al (2000) TT virus: a study of molecular epidemiology and transmission of genotypes 1, 2 and 3. J Clin Virol 17(1):43–49. https://doi.org/10.1016/s1386-6532(00)00066-4CrossRef

75.

Deng X, Terunuma H, Handema R et al (2000) Higher prevalence and viral load of TT virus in saliva than in the corresponding serum: another possible transmission route and replication site of TT virus. J Med Virol 62(4):531–537CrossRef

76.

Zhong S, Yeo W, Tang M, Liu C, Lin XR, Ho WM, Hui P, Johnson PJ (2002) Frequent detection of the replicative form of TT virus DNA in peripheral blood mononuclear cells and bone marrow cells in cancer patients. J Med Virol 66(3):428–434. https://doi.org/10.1002/jmv.2163CrossRef

77.

Mueller B, Maerz A, Doberstein K, Finsterbusch T, Mankertz A (2008) Gene expression of the human Torque Teno Virus isolate P/1C1. Virology 381(1):36–45. https://doi.org/10.1016/j.virol.2008.08.017CrossRef

78.

Okamoto H, Nishizawa T, Takahashi M, Asabe S, Tsuda F, Yoshikawa A (2001) Heterogeneous distribution of TT virus of distinct genotypes in multiple tissues from infected humans. Virology 288(2):358–368CrossRef

79.

Silasi M, Cardenas I, Racicot K, Kwon JY, Aldo P, Mor G (2015) Viral infections during pregnancy. Am J Reprod Immunol 73(3):199–213. https://doi.org/10.1111/aji.12355CrossRefPubMedCentral

80.

Stagno S, Pass RF, Dworsky ME, Alford CA (1982) Maternal cytomegalovirus infection and perinatal transmission. Clin Obstet Gynecol 25:563–576CrossRef

81.

James SH, Kimberlin DW (2015) Neonatal herpes simplex virus infection. Infect Dis Clin N Am 29(3):391–400. https://doi.org/10.1016/j.idc.2015.05.001CrossRef

82.

Luoto R, Jartti T, Ruuskanen O, Waris M (2016) Review of the clinical significance of respiratory virus infections in newborn infants. Acta Paediatr 105:1132–1139. https://doi.org/10.1111/apa.13519CrossRefPubMedCentral

83.

Pinninti SG, Kimberlin DW (2018) Neonatal herpes simplex virus infections. Semin Perinatol 42(3):168–175. https://doi.org/10.1053/j.semperi.2018.02.004CrossRef

84.

Carneiro-Proietti ABF, Amaranto-Damasio MS, Leal-Horiguchi CF et al (2014) Mother-to-child transmission of human T-cell lymphotropic viruses-1/2: what we know, and what are the gaps in understanding and preventing this route of infection. J Pediatric Infect Dis Soc 3(1):24–29. https://doi.org/10.1093/jpids/piu070CrossRef

85.

Smith EM, Parker MA, Rubenstein LM, Haugen TH, Hamsikova E, Turek LP (2010) Evidence for vertical transmission of HPV from mothers to infants. Infect Dis Obstet Gynecol 2010:326369. https://doi.org/10.1155/2010/326369CrossRefPubMedCentral

86.

Indolfi G, Moriondo M, Galli L, Azzari C, Poggi GM et al (2007) Mother-to-infant transmission of multiple blood-borne viral infections from multi-infected mothers. J Med Virol 79(6):743–747. https://doi.org/10.1002/jmv.20885CrossRef

87.

Pozzuto T, Mueller B, Meehan B, Ringler SS, McIntosh KA, Ellis JA, Mankertz A, Krakowka S (2009) In utero transmission of porcine torque teno viruses. Vet Microbiol 137:375–379. https://doi.org/10.1016/j.vetmic.2009.02.001CrossRef

88.

Martínez-Guinó L, Kekarainen T, Segalés J (2009) Evidence of torque teno virus (TTV) vertical transmission in swine. Theriogenology 71:1390–1395. https://doi.org/10.1016/j.theriogenology.2009.01.010CrossRef

89.

Martínez-Guinó L, Kekarainen T, Maldonado J, Aramouni M, Llorens A, Segalés J (2010) Torque teno sus virus (TTV) detection in aborted and slaughterhouse collected foetuses. Theriogenology 74:277–281. https://doi.org/10.1016/j.theriogenology.2010.02.011]CrossRef

90.

Matsubara H, Michitaka K, Horiike N, Kihana T, Yano M, Mori T, Onji M (2001) Existence of TT virus DNA and TTV-like mini virus DNA in infant cord blood: mother-to-neonatal transmission. Hepatol Res 21(3):280–287. https://doi.org/10.1016/s1386-6346(01)00115-2CrossRef

91.

Saback FL, Gomes SA, de Paula VS, da Silva RR, Lewis-Ximenez LL, Niel C (1999) Age-specific prevalence and transmission of TT virus. J Med Virol 59(3):318–322CrossRef

92.

Xin X, Xiaoguang Z, Ninghu Z, Youtong L, Liumei X, Boping Z (2004) Mother-to-infant vertical transmission of the transfusion-transmitted virus in South China. J Perinat Med 32(5):404–406. https://doi.org/10.1515/JPM.2004.136CrossRef

93.

Morrica A, Maggi F, Vatteroni ML et al (2000) TT virus: evidence for transplacental transmission. J Infect Dis 181:803–804. https://doi.org/10.1086/315296CrossRef

94.

Tyschik EA, Sherbakova SM, Ibragimov RR, Rebrikov DV (2017) Transplacental transmission of torque teno virus. Virol J 14(1):92–94. https://doi.org/10.1186/s12985-017-0762-0CrossRefPubMedCentral

95.

Ohto H, Ujiie N, Takeuchi C et al (2002) TT virus infection during childhood. Transfusion 42:892–898. https://doi.org/10.1046/j.1537-2995.2002.00150.xCrossRef

96.

Fang F, Zhong W, Wang H (2001) Study on infection of transfusion transmitted virus in serum, breast milk of pregnant women and umbilical venous blood from their newborns [Article in Chinese]. Zhonghua Fu Chan Ke Za Zhi 36:330–332

97.

Kazi A, Miyata H, Kurokawa K, Khan MA, Kamahora T, Katamine S, Hino S (2000) High frequency of postnatal transmission of TT virus in infancy. Arch Virol 145:535–540. https://doi.org/10.1007/s007050050044CrossRef

98.

Gerner P, Oettinger R, Gerner W, Falbrede J, Wirth S (2000) Mother-to-infant transmission of TT virus: prevalence, extent, and mechanism of vertical transmission. Pediatr Infect Dis J 19(11):1074–1077. https://doi.org/10.1097/00006454-200011000-00009CrossRef

99.

Iso K, Suzuki Y, Takayama M (2001) Mother-to-infant transmission of TT virus in Japan. Int J Gynaecol Obstet 75:11–19. https://doi.org/10.1016/s0020-7292(01)00450-7CrossRef

100.

Chan PK, Tam WH, Yeo W, Cheung JL, Zhong S, Cheng AF (2001) High carriage rate of TT virus in the cervices of pregnant women. Clin Infect Dis 32:1376–1377. https://doi.org/10.1086/319983CrossRef

101.

Bagaglio S, Sitia G, Prati D et al (2002) Mother-to-child transmission of TT virus: sequence analysis of the non-coding region of TT virus in infected mother-infant pairs. Arch Virol 147(4):803–812. https://doi.org/10.1007/s007050200027CrossRef

102.

Sloan P, Rodriguez C, Bedell BA, Murray J, Dagle J, Ryckman K, Holtz L (2020) Alphatorquevirus is the most prevalent virus identified in blood from a matched maternal-infant preterm cohort. J Matern Fetal Neonatal Med. https://doi.org/10.1080/14767058.2020.1763298CrossRef

103.

Bzhalava D, Ekström J, Lysholm F, Hultin E, Faust H, Persson B, Lehtinen M, de Villiers EM, Dillner J (2012) Phylogenetically diverse TT virus viremia among pregnant women. Virology 432:427–434. https://doi.org/10.1016/j.virol.2012.06.022CrossRef

104.

Tyschik EA, Rasskazova AS, Degtyareva AV, Rebrikov DV, Sukhikh GT (2018) Torque teno virus dynamics during the first year of life. Virol J 15(1):96–99. https://doi.org/10.1186/s12985-018-1007-6CrossRefPubMedCentral

105.

Lim ES, Zhou Y, Zhao G, Bauer IK, Droit L (2015) Early life dynamics of the human gut virome and bacterial microbiome in infants. Nat Med 21(10):1228–1234. https://doi.org/10.1038/nm.3950CrossRefPubMedCentral

106.

Yu JC, Khodadadi H, Malik A, Davidson B, Salles ÉDSL, Bhatia J, Hale VL, Baban B (2018) Innate immunity of neonates and infants. Front Immunol 9:1759. https://doi.org/10.3389/fimmu.2018.01759CrossRefPubMedCentral

107.

Yokozaki S, Fukuda Y, Nakano I, Katano Y (1999) TT virus: a mother to child transmitted rather than blood borne virus. Blood 93(10):3569–3570

108.

Komatsu H, Inui A, Sogo T, Kuroda K, Tanaka T, Fujisawa T (2004) TTV infection in children born to mothers infected with TTV but not with HBV, HCV, or HIV. J Med Virol 74(3):499–506. https://doi.org/10.1002/jmv.20204CrossRef

109.

Sugiyama K, Goto K, Ando T, Mizutani F, Terabe K, Yokoyama T (2001) Highly diverse TTV population in infants and their mothers. Virus Res 73:183–188. https://doi.org/10.1016/s0168-1702(00)00242-2CrossRef

110.

Abdalla NM, Galal A, Fatouh AA, Eid K, Salama EEE, Gomma HE (2006) Transfusion transmitted virus (TTV) infection in polytransfused egyptian thalassemic children. J Med Sci 6(5):833–837. https://doi.org/10.3923/jms.2006.833.837CrossRef

111.

Peng YH, Nishizawa T, Takahashi M, Ishikawa T, Yoshikawa A, Okamoto H (2002) Analysis of the entire genomes of thirteen TT virus variants classifiable into the fourth and fifth genetic groups, isolated from viremic infants. Arch Virol 147(1):21–41. https://doi.org/10.1007/s705-002-8301-7CrossRef

112.

Lin HH, Kao JH, Lee PI, Chen DS (2002) Early acquisition of TT virus in infants: possible minor role of maternal transmission. J Med Virol 66(2):285–290. https://doi.org/10.1002/jmv.2143CrossRef

Title: Constant companion: clinical and developmental aspects of torque teno virus infections
Authors: Elena A. Lolomadze
Denis V. Rebrikov
Publication date: 01-12-2020
Publisher: Springer Vienna
Published in: Archives of Virology / Issue 12/2020
Print ISSN: 0304-8608
Electronic ISSN: 1432-8798
DOI: https://doi.org/10.1007/s00705-020-04841-x

ACC 2024 Congress Coverage

Heart Failure Video

At a glance: The ONWARDS insulin icodec trials

Springer Medicine

Constant companion: clinical and developmental aspects of torque teno virus infections

Abstract

ACC 2024 Congress Coverage

Year in Review: Heart failure and cardiomyopathies

Semaglutide benefits people with type 2 diabetes and obesity-related heart failure

Incentivised to exercise

New intervention for STEMI-related cardiogenic shock

» View more highlights on the ACC 2024 congress hub page

At a glance: The ONWARDS insulin icodec trials

Springer Medicine

Abstract

Please log in to get access to this content

Other articles of this Issue 12/2020

A novel foveavirus identified in wild grapevine (Vitis vinifera subsp. sylvestris)

Identification and characterization of a novel orbivirus, Yonaguni orbivirus, isolated from cattle on the westernmost island of Japan

Characterization of horizontal transmission of blueberry latent spherical virus by pollen

Multiple genotypes of enterovirus G carrying a papain-like cysteine protease (PL-CP) sequence circulating on two pig farms in Japan: first identification of enterovirus G10 carrying a PL-CP sequence

A decrease in hepatitis C virus RNA to undetectable levels in chronic hepatitis C patients after PegIFNα + RVB or sofosbuvir + NS5A inhibitor treatment is associated with decreased insulin resistance and persistent oxidative stress

Identification and genome sequencing of RNA viruses in the eucalyptus snout beetle Gonipterus spp. (Coleoptera: Curculionidae)

ACC 2024 Congress Coverage

Year in Review: Heart failure and cardiomyopathies

Semaglutide benefits people with type 2 diabetes and obesity-related heart failure

Incentivised to exercise

New intervention for STEMI-related cardiogenic shock

» View more highlights on the ACC 2024 congress hub page