Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Nat Med ; 23(9): 1080-1085, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28759053

ABSTRACT

Much attention has been focused on the role of the bacterial microbiome in human health, but the virome is understudied. Although previously investigated in individuals with inflammatory bowel diseases or solid-organ transplants, virome dynamics in allogeneic hematopoietic stem cell transplantation (HSCT) and enteric graft-versus-host disease (GVHD) remain unexplored. Here we characterize the longitudinal gut virome in 44 recipients of HSCT using metagenomics. A viral 'bloom' was identified, and significant increases were demonstrated in the overall proportion of vertebrate viral sequences following transplantation (P = 0.02). Increases in both the rates of detection (P < 0.0001) and number of sequences (P = 0.047) of persistent DNA viruses (anelloviruses, herpesviruses, papillomaviruses and polyomaviruses) over time were observed in individuals with enteric GVHD relative to those without, a finding accompanied by a reduced phage richness (P = 0.01). Picobirnaviruses were detected in 18 individuals (40.9%), more frequently before or within a week after transplant than at later time points (P = 0.008). In a time-dependent Cox proportional-hazards model, picobirnaviruses were predictive of the occurrence of severe enteric GVHD (hazard ratio, 2.66; 95% confidence interval (CI) = 1.46-4.86; P = 0.001), and correlated with higher fecal levels of two GVHD severity markers, calprotectin and α1-antitrypsin. These results reveal a progressive expansion of vertebrate viral infections over time following HSCT, and they suggest an unexpected association of picobirnaviruses with early post-transplant GVHD.


Subject(s)
DNA, Viral/analysis , Gastrointestinal Microbiome/immunology , Graft vs Host Disease/immunology , Hematopoietic Stem Cell Transplantation , Intestinal Diseases/immunology , Intestines/virology , Adolescent , Adult , Aged , Anelloviridae/genetics , Anelloviridae/immunology , Feces/chemistry , Female , Gastrointestinal Microbiome/genetics , Herpesviridae/genetics , Herpesviridae/immunology , Humans , Leukocyte L1 Antigen Complex/metabolism , Male , Metagenomics , Middle Aged , Papillomaviridae/genetics , Papillomaviridae/immunology , Picobirnavirus/genetics , Picobirnavirus/immunology , Polyomaviridae/genetics , Polyomaviridae/immunology , Proportional Hazards Models , Risk Factors , Severity of Illness Index , Transplantation, Homologous , Young Adult , alpha 1-Antitrypsin/metabolism
2.
J Gen Virol ; 95(Pt 10): 2233-2239, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24584476

ABSTRACT

The full-length genome sequence of a porcine picobirnavirus (PBV) detected in Italy in 2004 was determined. The smaller (S) genome segment was 1730 nt, coding for a putative RNA-dependent RNA polymerase. Two distinct subpopulations of larger (L) genome segment (LA and LB) were identified in the sample, with the sizes ranging from 2351 to 2666 nt. The ORF1, coding for a protein of unknown function, contained a variable number of repetitions of the ExxRxNxxxE motif. The capsid protein-coding ORF2 spanned nt 810-2447 in the LB variants and started at nt 734 in the LA variants. However, a termination codon was present only in one of all the LA segment variants. Three-dimensional modelling of the porcine PBV capsids suggested structural differences in the protruding domain, tentatively involved as antigens in the humoral immune response. Altogether, these findings suggest the simultaneous presence of two different PBV strains sharing the same S segment but displaying genetically diverse L segments. In addition, the sample probably contained a mixture of PBVs with aberrant RNA replication products. Altered structure in the L segments could be tolerated and retained in the presence of functionally integer-cognate genes and represents a mechanism of virus diversification.


Subject(s)
Antigenic Variation , Genetic Variation , Genome, Viral , Picobirnavirus/genetics , Picobirnavirus/immunology , RNA Virus Infections/veterinary , Animals , Antigens, Viral/genetics , Antigens, Viral/immunology , Cluster Analysis , Italy , Models, Molecular , Molecular Sequence Data , Phylogeny , Picobirnavirus/classification , Picobirnavirus/isolation & purification , Protein Conformation , RNA Virus Infections/virology , RNA, Viral/genetics , Sequence Analysis, DNA , Swine , Viral Proteins/chemistry , Viral Proteins/genetics
3.
Res Vet Sci ; 59(3): 222-5, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8588095

ABSTRACT

Picobirnaviruses are a novel group of viruses recently found in the faeces of several species of vertebrates. Examination by polyacrylamide gel electrophoresis of rabbit faecal samples collected in one animal facility revealed the viruses in 23 (11 per cent) of 211 samples. Further analysis by electron microscopy and caesium chloride isopycnic centrifugation confirmed the presence of picobirnaviruses in the samples. The oral inoculation of three newly weaned rabbits with purified viruses resulted in the excretion of a virus with an electropherotype similar to the inoculum, by two of the three inoculated animals. Maximal viral shedding was detected 13 days after inoculation. No sign of diarrhoea was observed either in the inoculated animals or in the virus excreting animals surveyed. No antibody activity could be detected in the paired serum samples taken from the inoculated animals.


Subject(s)
Feces/virology , Picobirnavirus/isolation & purification , RNA, Double-Stranded/analysis , RNA, Viral/analysis , Rabbits/virology , Virus Diseases/veterinary , Animals , Antibodies, Viral/analysis , Antibodies, Viral/immunology , Electrophoresis, Polyacrylamide Gel/veterinary , Female , Microscopy, Immunoelectron/veterinary , Picobirnavirus/genetics , Picobirnavirus/immunology , RNA, Double-Stranded/genetics , RNA, Viral/genetics , Virus Diseases/diagnosis , Virus Diseases/genetics
SELECTION OF CITATIONS
SEARCH DETAIL
...