ライフサイエンスコーパス: HTNV

1 HTNV causes the most severe form of HFRS (5 to 15% case-

2 HTNV Gn is structurally conserved with the Gn of a genet

3 HTNV-infected cells treated with ribavirin showed a slig

4 In contrast to NY-1V, HTNV uniquely induced a variety of chemokines and cell a

5 tive for immunoglobulin G antibodies against HTNV, whereas none of those trapped in Jeollanam Provinc

6 We found that VEGF addition to ANDV- and HTNV-infected endothelial cells results in the hyperphos

7 ted hamsters against infection with SEOV and HTNV.

8 ed trend for the peptides to inhibit SNV and HTNV to a greater extent than they inhibited PHV, a find

9 ng that supports the contention that SNV and HTNV use beta(3) integrins and PHV uses a different rece

10 novel peptides that inhibit entry by SNV and HTNV via beta(3) integrins and that can be used as lead

11 e were able to detect an interaction between HTNV N protein and importin alpha, a nuclear import mole

12 assays to define the ability of each to bind HTNV N protein.

13 ly time compared with three genes altered by HTNV or NY-1V.

14 induce most cellular chemokines directed by HTNV (3/14) or genes primarily activated by NF-kappaB.

15 imes p.i., 13 genes were commonly induced by HTNV and NY-1V that were not induced by PHV.

16 staining demonstrated that cells expressing HTNV N protein and a green fluorescent protein-p65 fusio

17 N protein showed an enhanced specificity for HTNV vRNA as compared with the S segment open reading fr

18 The K(d) values for HTNV and Sin Nombre virus N proteins were nearly identic

19 Orthohantavirus hantanense (HTNV) is a zoonotic pathogen transmitted by rodents and

20 ER-Golgi intermediate compartment (ERGIC) in HTNV-infected Vero E6 cells, not with the ER, Golgi comp

21 alteration in the level of p65 expression in HTNV N-expressing cells.

22 ssociated elevation in mutation frequency in HTNV vRNA similar to that previously reported in vitro.

23 cal for military and civilian populations in HTNV high-risk areas.

24 virin-treated mice, the amount of infectious HTNV was significantly decreased relative to that in unt

25 Interestingly, HTNV Gn crystallized at acidic pH, in a compact tetramer

26 alyses demonstrated geographic clustering of HTNV strains from clinical specimens with the HTNV strai

27 e genome, although we observed extinction of HTNV.

28 tment in the lethal, suckling mouse model of HTNV infection would act similarly.

29 s containing up to 10(3)-10(4) copies/muL of HTNV RNA.

30 es were measured for 3 days posttreatment of HTNV-infected Vero E6 cells.

31 d field mice and increased the prevalence of HTNV among them.

32 rt here that the nucleocapsid (N) protein of HTNV was able to inhibit TNF-alpha-induced activation of

33 con NGS demonstrated a high coverage rate of HTNV in Apodemus agrarius lung tissues containing up to

34 Apodemus agrarius, the primary reservoir of HTNV, assessed hantavirus seroprevalence, and conducted

35 Here, we describe the crystal structure of HTNV envelope glycoprotein Gn, an integral component of

36 terize the inhibitory effect of ribavirin on HTNV, the levels of viral RNAs, proteins, and infectious

37 d protein synthesis by PHV, but not NY-1V or HTNV, is inhibited at 2 to 4 days postinfection.

38 ed to intracellular vesicles within ANDV- or HTNV-, but not TULV-, infected endothelial cells.

39 or sphingosine-1-phosphate (S1P) to ANDV- or HTNV-infected cells blocked VE-cadherin internalization

40 (3) Fab fragment, c7E3, or specific ANDV- or HTNV-neutralizing antibodies.

41 on of rhesus monkeys with either the SEOV or HTNV M gene elicited high levels of neutralizing antibod

42 enome sequencing of Hantaan orthohantavirus (HTNV) from rodent specimens.

43 , the assembly of Sin Nombre virus N protein-HTNV vRNA complexes was inhibited by the presence of Mg(

44 Collectively, our data suggest that HTNV N protein can sequester NF-kappaB in the cytoplasm,

45 The HTNV genomic RNA (vRNA) copy number and infectious virus

46 ein was examined for its ability to bind the HTNV S segment vRNA with filter binding and gel electrop

47 specific recognition of the HTNV vRNA by the HTNV N protein resides in the noncoding regions of the H

48 95-217 retained 94% of the vRNA bound by the HTNV N protein, while peptides 175-186 and 205-217 bound

49 aluation of a DNA vaccine that expresses the HTNV M gene products, G1 and G2.

50 However, the HTNV N protein showed an enhanced specificity for HTNV v

51 We analyzed the coverage of the HTNV genome based on the viral RNA copy number, which is

52 ization compatible with recombination of the HTNV S segment.

53 a model in which specific recognition of the HTNV vRNA by the HTNV N protein resides in the noncoding

54 tein resides in the noncoding regions of the HTNV vRNA.

55 cells transfected with cDNA representing the HTNV N gene, were confirmed using HTNV-infected cells.

56 Structural overlay analysis reveals that the HTNV Gn fold is highly similar to the Gn of Puumala viru

57 DNA vaccination of hamsters with the HTNV M gene conferred sterile protection against infecti

58 TNV strains from clinical specimens with the HTNV strains circulating in rodents, suggesting the most

59 e studies mapped a minimal region within the HTNV N protein (amino acids 175 to 217) that bound vRNA.

60 d a positive selection for codons within the HTNV N protein gene in the ribavirin-treated vRNA popula

61 Surprisingly, in ribavirin-treated, HTNV-infected mice, vRNA levels were similar to those in

62 RNA increased to that observed for untreated HTNV-infected cells on day 2, whereas mRNA levels were m

63 contrast, the vRNA population in untreated, HTNV-infected mice showed a lower level of diversity, re

64 In untreated, HTNV-infected mice, the vRNA copy number increased for 1

65 enting the HTNV N gene, were confirmed using HTNV-infected cells.

66 Hantaviruses such as Hantaan virus (HTNV) and Andes virus cause two human diseases, hemorrha

67 tivity and GTP repression for Hantaan virus (HTNV) and evidence for RBV's ability to promote error-pr

68 ogenic Andes virus (ANDV) and Hantaan virus (HTNV) and nonpathogenic Tula virus (TULV) hantaviruses.

69 virus (ANDV) and HFRS causing Hantaan virus (HTNV) are inhibited by alpha(v)beta(3) integrin antibodi

70 her whole genome sequences of Hantaan virus (HTNV) from HFRS patients and rodent hosts in endemic are

71 ), for the interaction of the Hantaan virus (HTNV) N protein and its genomic S segment (vRNA) was mea

72 acids 175 to 217) within the Hantaan virus (HTNV) N protein that interacts with a high affinity with

73 define the domain within the Hantaan virus (HTNV) N protein that mediates these interactions, 14 N-

74 ted from the S segment of the Hantaan virus (HTNV) vRNA.

75 eir abilities to inhibit SNV, Hantaan virus (HTNV), and Prospect Hill virus (PHV) infection.

76 ogenic NY-1 virus (NY-1V) and Hantaan virus (HTNV), nonpathogenic Prospect Hill virus (PHV) elicits e

77 Four hantaviruses-Hantaan virus (HTNV), Seoul virus (SEOV), Dobrava virus (DOBV) and Puum

78 n ectodomain from the Asiatic Hantaan virus (HTNV), the most prevalent pathogenic hantavirus.

79 ey were found to be caused by Hantaan virus (HTNV), the most prevalent pathogenic hantavirus.

80 e that Andes virus (ANDV)- or Hantaan virus (HTNV)-infected endothelial cells specifically direct the

81 n acts as a lethal mutagen in Hantaan virus (HTNV)-infected Vero E6 cells, resulting in an increased

82 ototype Old World hantavirus, Hantaan virus (HTNV).

83 a critical reservoir host of Hantaan virus (HTNV).

84 the production of infectious Hantaan virus (HTNV); however, its mechanism of action is unknown.

85 [New York-1 virus (NY-1V) and Hantaan virus (HTNV)] bind immobilized beta3 polypeptides containing th

86 York-1 virus (NY-1V)], HFRS [Hantaan virus (HTNV)], or by a hantavirus not associated with human dis

87 ed sterile protection against infection with HTNV, SEOV, and DOBV.