Strongyloidiasis and Infective Dermatitis Alter Human T Lymphotropic Virus-1 Clonality
Human T-lymphotropic Virus-1 (HTLV-1) is a retrovirus that persists lifelong by driving clonal proliferation of infected T-cells. HTLV-1 causes a neuroinflammatory disease and adult T-cell leukemia/lymphoma. Strongyloidiasis, a gastrointestinal infection by the helminth Strongyloides stercoralis, and Infective Dermatitis associated with HTLV-1 (IDH), appear to be risk factors for the development of HTLV-1 related diseases. We used high-throughput sequencing to map and quantify the insertion sites of the provirus in order to monitor the clonality of the HTLV-1-infected T-cell population (i.e. the number of distinct clones and abundance of each clone). A newly developed biodiversity estimator called “DivE” was used to estimate the total number of clones in the blood. We found that the major determinant of proviral load in all subjects without leukemia/lymphoma was the total number of HTLV-1-infected clones. Nevertheless, the significantly higher proviral load in patients with strongyloidiasis or IDH was due to an increase in the mean clone abundance, not to an increase in the number of infected clones. These patients appear to be less capable of restricting clone abundance than those with HTLV-1 alone. In patients co-infected with Strongyloides there was an increased degree of oligoclonal expansion and a higher rate of turnover (i.e. appearance and disappearance) of HTLV-1-infected clones. In Strongyloides co-infected patients and those with IDH, proliferation of the most abundant HTLV-1+ T-cell clones is independent of the genomic environment of the provirus, in sharp contrast to patients with HTLV-1 infection alone. This implies that new selection forces are driving oligoclonal proliferation in Strongyloides co-infection and IDH. We conclude that strongyloidiasis and IDH increase the risk of development of HTLV-1-associated diseases by increasing the rate of infection of new clones and the abundance of existing HTLV-1+ clones.
Vyšlo v časopise:
Strongyloidiasis and Infective Dermatitis Alter Human T Lymphotropic Virus-1 Clonality. PLoS Pathog 9(4): e32767. doi:10.1371/journal.ppat.1003263
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1003263
Souhrn
Human T-lymphotropic Virus-1 (HTLV-1) is a retrovirus that persists lifelong by driving clonal proliferation of infected T-cells. HTLV-1 causes a neuroinflammatory disease and adult T-cell leukemia/lymphoma. Strongyloidiasis, a gastrointestinal infection by the helminth Strongyloides stercoralis, and Infective Dermatitis associated with HTLV-1 (IDH), appear to be risk factors for the development of HTLV-1 related diseases. We used high-throughput sequencing to map and quantify the insertion sites of the provirus in order to monitor the clonality of the HTLV-1-infected T-cell population (i.e. the number of distinct clones and abundance of each clone). A newly developed biodiversity estimator called “DivE” was used to estimate the total number of clones in the blood. We found that the major determinant of proviral load in all subjects without leukemia/lymphoma was the total number of HTLV-1-infected clones. Nevertheless, the significantly higher proviral load in patients with strongyloidiasis or IDH was due to an increase in the mean clone abundance, not to an increase in the number of infected clones. These patients appear to be less capable of restricting clone abundance than those with HTLV-1 alone. In patients co-infected with Strongyloides there was an increased degree of oligoclonal expansion and a higher rate of turnover (i.e. appearance and disappearance) of HTLV-1-infected clones. In Strongyloides co-infected patients and those with IDH, proliferation of the most abundant HTLV-1+ T-cell clones is independent of the genomic environment of the provirus, in sharp contrast to patients with HTLV-1 infection alone. This implies that new selection forces are driving oligoclonal proliferation in Strongyloides co-infection and IDH. We conclude that strongyloidiasis and IDH increase the risk of development of HTLV-1-associated diseases by increasing the rate of infection of new clones and the abundance of existing HTLV-1+ clones.
Zdroje
1. ProiettiFA, Carneiro-ProiettiAB, Catalan-SoaresBC, MurphyEL (2005) Global epidemiology of HTLV-I infection and associated diseases. Oncogene 24: 6058–6068.
2. KubotaR, FujiyoshiT, IzumoS, YashikiS, MaruyamaI, et al. (1993) Fluctuation of HTLV-I proviral DNA in peripheral blood mononuclear cells of HTLV-I-associated myelopathy. J Neuroimmunol 42: 147–154.
3. NagaiM, UsukuK, MatsumotoW, KodamaD, TakenouchiN, et al. (1998) Analysis of HTLV-I proviral load in 202 HAM/TSP patients and 243 asymptomatic HTLV-I carriers: high proviral load strongly predisposes to HAM/TSP. J Neurovirol 4: 586–593.
4. EtohK, YamaguchiK, TokudomeS, WatanabeT, OkayamaA, et al. (1999) Rapid quantification of HTLV-I provirus load: detection of monoclonal proliferation of HTLV-I-infected cells among blood donors. Int J Cancer 81: 859–864.
5. NejmeddineM, BanghamCR (2010) The HTLV-1 Virological Synapse. Viruses 2: 1427–1447.
6. BanghamCR, OsameM (2005) Cellular immune response to HTLV-1. Oncogene 24: 6035–6046.
7. GilletNA, MalaniN, MelamedA, GormleyN, CarterR, et al. (2011) The host genomic environment of the provirus determines the abundance of HTLV-1-infected T-cell clones. Blood 117: 3113–3122.
8. MarcosLA, TerashimaA, DupontHL, GotuzzoE (2008) Strongyloides hyperinfection syndrome: an emerging global infectious disease. Trans R Soc Trop Med Hyg 102: 314–318.
9. RobinsonRD, LindoJF, NevaFA, GamAA, VogelP, et al. (1994) Immunoepidemiologic studies of Strongyloides stercoralis and human T lymphotropic virus type I infections in Jamaica. J Infect Dis 169: 692–696.
10. GotuzzoE, TerashimaA, AlvarezH, TelloR, InfanteR, et al. (1999) Strongyloides stercoralis hyperinfection associated with human T cell lymphotropic virus type-1 infection in Peru. Am J Trop Med Hyg 60: 146–149.
11. CouroubleG, RouetF, Hermann-StorckC, NicolasM, CandolfiE, et al. (2000) Human T-cell lymphotropic virus Type I association with Strongyloides stercoralis: a case control study among Caribbean blood donors from Guadeloupe (French West Indies). J Clin Microbiol 38: 3903–3904.
12. TerashimaA, AlvarezH, TelloR, InfanteR, FreedmanDO, et al. (2002) Treatment failure in intestinal strongyloidiasis: an indicator of HTLV-I infection. Int J Infect Dis 6: 28–30.
13. SatohM, TomaH, SatoY, TakaraM, ShiromaY, et al. (2002) Reduced efficacy of treatment of strongyloidiasis in HTLV-I carriers related to enhanced expression of IFN-gamma and TGF-beta1. Clin Exp Immunol 127: 354–359.
14. HirataT, UchimaN, KishimotoK, ZahaO, KinjoN, et al. (2006) Impairment of host immune response against strongyloides stercoralis by human T cell lymphotropic virus type 1 infection. Am J Trop Med Hyg 74: 246–249.
15. MontesM, SanchezC, VerdonckK, LakeJE, GonzalezE, et al. (2009) Regulatory T cell expansion in HTLV-1 and strongyloidiasis co-infection is associated with reduced IL-5 responses to Strongyloides stercoralis antigen. PLoS Negl Trop Dis 3: e456.
16. GabetAS, MortreuxF, TalarminA, PlumelleY, LeclercqI, et al. (2000) High circulating proviral load with oligoclonal expansion of HTLV-1 bearing T cells in HTLV-1 carriers with strongyloidiasis. Oncogene 19: 4954–4960.
17. PagliucaA, LaytonDM, AllenS, MuftiGJ (1988) Hyperinfection with strongyloides after treatment for adult T cell leukaemia-lymphoma in an African immigrant. BMJ 297: 1456–1457.
18. MasseyAC, WeinsteinDL, PetriWA, WilliamsME, HessCE (1990) ATLL complicated by strongyloidiasis and isosporiasis: case report. Va Med Q 117: 311–316.
19. PhelpsKR (1993) Strongyloides hyperinfection in patients coinfected with HTLV-I and S. stercoralis. Am J Med 94: 447–449.
20. PhelpsKR, GinsbergSS, CunninghamAW, TschachlerE, DosikH (1991) Case report: adult T-cell leukemia/lymphoma associated with recurrent strongyloides hyperinfection. Am J Med Sci 302: 224–228.
21. PlumelleY, GoninC, EdouardA, BucherBJ, ThomasL, et al. (1997) Effect of Strongyloides stercoralis infection and eosinophilia on age at onset and prognosis of adult T-cell leukemia. Am J Clin Pathol 107: 81–87.
22. PlumelleY, PascalineN, NguyenD, PanelattiG, JouannelleA, et al. (1993) Adult T-cell leukemia-lymphoma: a clinico-pathologic study of twenty-six patients from Martinique. Hematol Pathol 7: 251–262.
23. AgapeP, CopinMC, CavroisM, PanelattiG, PlumelleY, et al. (1999) Implication of HTLV-I infection, strongyloidiasis, and P53 overexpression in the development, response to treatment, and evolution of non-Hodgkin's lymphomas in an endemic area (Martinique, French West Indies). J Acquir Immune Defic Syndr Hum Retrovirol 20: 394–402.
24. PagliucaA (1999) Strongyloides hyperinfection in adult T-cell leukaemia/lymphoma. Br J Haematol 105: 1.
25. LeeR, SchwartzRA (2011) Human T-lymphotrophic virus type 1-associated infective dermatitis: a comprehensive review. J Am Acad Dermatol 64: 152–160.
26. PrimoJ, SiqueiraI, NascimentoMC, OliveiraMF, FarreL, et al. (2009) High HTLV-1 proviral load, a marker for HTLV-1 associated myelopathy/tropical spastic paraparesis, is also detected in patients with infective dermatitis associated with HTLV-1. Braz J Med Biol Res 42: 761–764.
27. de Oliveira MdeF, BittencourtAL, BritesC, SoaresG, HermesC, et al. (2004) HTLV-I associated myelopathy/tropical spastic paraparesis in a 7-year-old boy associated with infective dermatitis. J Neurol Sci 222: 35–38.
28. NascimentoMC, PrimoJ, BittencourtA, SiqueiraI, de Fatima OliveiraM, et al. (2009) Infective dermatitis has similar immunological features to human T lymphotropic virus-type 1-associated myelopathy/tropical spastic paraparesis. Clin Exp Immunol 156: 455–462.
29. de Oliveira MdeF, VieiraMG, PrimoJ, SiqueiraIC, CarvalhoEM, et al. (2010) Flower cells in patients with infective dermatitis associated with HTLV-1. J Clin Virol 48: 288–290.
30. SatohM, TomaH, SugaharaK, EtohK, ShiromaY, et al. (2002) Involvement of IL-2/IL-2R system activation by parasite antigen in polyclonal expansion of CD4(+)25(+) HTLV-1-infected T-cells in human carriers of both HTLV-1 and S. stercoralis. Oncogene 21: 2466–2475.
31. GessainA, CassarO (2012) Epidemiological Aspects and World Distribution of HTLV-1 Infection. Front Microbiol 3: 388.
32. VineAM, WitkoverAD, LloydAL, JefferyKJ, SiddiquiA, et al. (2002) Polygenic control of human T lymphotropic virus type I (HTLV-I) provirus load and the risk of HTLV-I-associated myelopathy/tropical spastic paraparesis. J Infect Dis 186: 932–939.
33. JefferyKJ, UsukuK, HallSE, MatsumotoW, TaylorGP, et al. (1999) HLA alleles determine human T-lymphotropic virus-I (HTLV-I) proviral load and the risk of HTLV-I-associated myelopathy. Proc Natl Acad Sci U S A 96: 3848–3853.
34. BanghamCR (2009) CTL quality and the control of human retroviral infections. Eur J Immunol 39: 1700–1712.
35. GabetAS, KazanjiM, CouppieP, ClityE, PouliquenJF, et al. (2003) Adult T-cell leukaemia/lymphoma-like human T-cell leukaemia virus-1 replication in infective dermatitis. Br J Haematol 123: 406–412.
36. SwaimsAY, KhaniF, ZhangY, RobertsAI, DevadasS, et al. (2010) Immune activation induces immortalization of HTLV-1 LTR-Tax transgenic CD4+ T cells. Blood 116: 2994–3003.
37. RatnerL, GrantC, ZimmermanB, FritzJ, WeilG, et al. (2007) Effect of treatment of Strongyloides infection on HTLV-1 expression in a patient with adult T-cell leukemia. Am J Hematol 82: 929–931.
38. QuZ, XiaoG (2011) Human T-cell lymphotropic virus: a model of NF-kappaB-associated tumorigenesis. Viruses 3: 714–749.
39. BallardDW, BohnleinE, LowenthalJW, WanoY, FranzaBR, et al. (1988) HTLV-I tax induces cellular proteins that activate the kappa B element in the IL-2 receptor alpha gene. Science 241: 1652–1655.
40. AsquithB, ZhangY, MosleyAJ, de LaraCM, WallaceDL, et al. (2007) In vivo T lymphocyte dynamics in humans and the impact of human T-lymphotropic virus 1 infection. Proc Natl Acad Sci U S A 104: 8035–8040.
41. ToulzaF, HeapsA, TanakaY, TaylorGP, BanghamCR (2008) High frequency of CD4+FoxP3+ cells in HTLV-1 infection: inverse correlation with HTLV-1-specific CTL response. Blood 111: 5047–5053.
42. TatenoM, KondoN, ItohT, ChubachiT, TogashiT, et al. (1984) Rat lymphoid cell lines with human T cell leukemia virus production. I. Biological and serological characterization. J Exp Med 159: 1105–1116.
43. BerryCC, GilletNA, MelamedA, GormleyN, BanghamCR, et al. (2012) Estimating abundances of retroviral insertion sites from DNA fragment length data. Bioinformatics 28: 755–762.
44. CookLB, RowanAG, MelamedA, TaylorGP, BanghamCR (2012) HTLV-1-infected T cells contain a single integrated provirus in natural infection. Blood 120: 3488–90.
45. TamiyaS, MatsuokaM, EtohK, WatanabeT, KamihiraS, et al. (1996) Two types of defective human T-lymphotropic virus type I provirus in adult T-cell leukemia. Blood 88: 3065–3073.
46. OhshimaK, OhgamiA, MatsuokaM, EtohK, UtsunomiyaA, et al. (1998) Random integration of HTLV-1 provirus: increasing chromosomal instability. Cancer Lett 132: 203–212.
47. GiniC (1914) Sulla misura della concentrazione e della variabilita dei caratteri: Transactions of the Real Istituto Veneto di Scienze. Ferrari
Štítky
Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
PLOS Pathogens
2013 Číslo 4
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Koronavirus hýbe světem: Víte jak se chránit a jak postupovat v případě podezření?
Najčítanejšie v tomto čísle
- Strongyloidiasis and Infective Dermatitis Alter Human T Lymphotropic Virus-1 Clonality
- A Disconnect between the Neurospirochetoses in Humans and Rodent Models of Disease
- Parasites FeS Up: Iron-Sulfur Cluster Biogenesis in Eukaryotic Pathogens
- Regulatory T Cells Negatively Affect IL-2 Production of Effector T Cells through CD39/Adenosine Pathway in HIV Infection