A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5

Torque teno virus (TTV) is a circular, single-stranded DNA virus that chronically infects healthy individuals of all ages worldwide. TTV has an extreme genetic heterogeneity which is reflected in its current classification into five main phylogenetic groups (1-5). Using specific PCR assays, it has b...

Full description

Bibliographic Details
Main Authors: S. Devalle, C. Niel
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2005-06-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2005000600006
_version_ 1829500365112868864
author S. Devalle
C. Niel
author_facet S. Devalle
C. Niel
author_sort S. Devalle
collection DOAJ
description Torque teno virus (TTV) is a circular, single-stranded DNA virus that chronically infects healthy individuals of all ages worldwide. TTV has an extreme genetic heterogeneity which is reflected in its current classification into five main phylogenetic groups (1-5). Using specific PCR assays, it has been shown that many individuals are co-infected with TTV isolates belonging to different phylogenetic groups. Here, a multiplex PCR assay was developed, using five recombinant plasmids. Each plasmid carried an insert of different size issued from a TTV isolate belonging to a different group. The assay was able to simultaneously amplify DNAs of TTV isolates belonging to all five phylogenetic groups. Multiplex PCR was then tested satisfactorily on DNAs extracted from 55 serum samples (47 health care workers and 8 AIDS patients). All individuals but nine were infected with at least one TTV isolate. Co-infection with multiple isolates was found in 29/47 (62%) health care workers and in 8/8 (100%) AIDS patients. A number of discrepancies were observed when results obtained with three thermostable DNA polymerases were compared. For example, four TTV phylogenetic groups were detected in a particular serum sample by using one of the three DNA polymerases, whereas the other two enzymes were able to detect only three TTV groups. However, none of the three enzymes used could be broadly considered to be more efficient than the others. Despite its limitations, the assay described here constitutes a suitable tool to visualize the degree of co-infection of a given population, avoiding time-consuming experiments.
first_indexed 2024-12-16T08:54:46Z
format Article
id doaj.art-a87b1a6445a2415092efb3686ac9fd18
institution Directory Open Access Journal
issn 0100-879X
1414-431X
language English
last_indexed 2024-12-16T08:54:46Z
publishDate 2005-06-01
publisher Associação Brasileira de Divulgação Científica
record_format Article
series Brazilian Journal of Medical and Biological Research
spelling doaj.art-a87b1a6445a2415092efb3686ac9fd182022-12-21T22:37:19ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X2005-06-0138685386010.1590/S0100-879X2005000600006A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5S. DevalleC. NielTorque teno virus (TTV) is a circular, single-stranded DNA virus that chronically infects healthy individuals of all ages worldwide. TTV has an extreme genetic heterogeneity which is reflected in its current classification into five main phylogenetic groups (1-5). Using specific PCR assays, it has been shown that many individuals are co-infected with TTV isolates belonging to different phylogenetic groups. Here, a multiplex PCR assay was developed, using five recombinant plasmids. Each plasmid carried an insert of different size issued from a TTV isolate belonging to a different group. The assay was able to simultaneously amplify DNAs of TTV isolates belonging to all five phylogenetic groups. Multiplex PCR was then tested satisfactorily on DNAs extracted from 55 serum samples (47 health care workers and 8 AIDS patients). All individuals but nine were infected with at least one TTV isolate. Co-infection with multiple isolates was found in 29/47 (62%) health care workers and in 8/8 (100%) AIDS patients. A number of discrepancies were observed when results obtained with three thermostable DNA polymerases were compared. For example, four TTV phylogenetic groups were detected in a particular serum sample by using one of the three DNA polymerases, whereas the other two enzymes were able to detect only three TTV groups. However, none of the three enzymes used could be broadly considered to be more efficient than the others. Despite its limitations, the assay described here constitutes a suitable tool to visualize the degree of co-infection of a given population, avoiding time-consuming experiments.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2005000600006BrazilCo-infectionsMultiplexPCRTorque teno virus
spellingShingle S. Devalle
C. Niel
A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5
Brazilian Journal of Medical and Biological Research
Brazil
Co-infections
Multiplex
PCR
Torque teno virus
title A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5
title_full A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5
title_fullStr A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5
title_full_unstemmed A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5
title_short A multiplex PCR assay able to simultaneously detect Torque teno virus isolates from phylogenetic groups 1 to 5
title_sort multiplex pcr assay able to simultaneously detect torque teno virus isolates from phylogenetic groups 1 to 5
topic Brazil
Co-infections
Multiplex
PCR
Torque teno virus
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2005000600006
work_keys_str_mv AT sdevalle amultiplexpcrassayabletosimultaneouslydetecttorquetenovirusisolatesfromphylogeneticgroups1to5
AT cniel amultiplexpcrassayabletosimultaneouslydetecttorquetenovirusisolatesfromphylogeneticgroups1to5
AT sdevalle multiplexpcrassayabletosimultaneouslydetecttorquetenovirusisolatesfromphylogeneticgroups1to5
AT cniel multiplexpcrassayabletosimultaneouslydetecttorquetenovirusisolatesfromphylogeneticgroups1to5