alexa Advances In Molecular Analysis In HTLV Infection
ISSN 2155-6113

Journal of AIDS & Clinical Research
Open Access

Like us on:
OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations

700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Share This Page

Additional Info

Loading
Loading Please wait..
 

2nd International Conference on HIV/AIDS, STDs, & STIs
October 27-29, 2014 Embassy Suites Las Vegas, USA

Carolina Rosadas de Oliveira
ScientificTracks Abstracts: J AIDS Clin Res
DOI: 10.4172/2155-6113.S1.006
Abstract
HTLV is a sexually transmitted retrovirus endemic in several countries/continents. The great majority of infected individuals remain asymptomatic. However, 1-5% of infected individuals may develop clinical presentation such as HAM/TSP and LLTA.The laboratory diagnosis of this infection is based on immunoassays. These techniques have several disadvantages, as indeterminate results. In such cases, molecular biology techniques are an alternative. Beyond qualitative results, real-time PCR can quantify proviral load, which may help to assess disease progression. Furthermore, molecular analysis also permits evaluation of the genetic diversity of circulating HTLV. Until today, there are no studies regarding HTLV-1 strains in Rio de Janeiro, Brazil. The present study aim to present a TaqMan real-time PCR assay for HTLV-1 proviral load detection in PBMCs and determine the genetic diversity of HTLV-1 strains isolated from asymptomatic (n=7) and HAM/TSP (n=14) individuals (RJ, Brazil). PBMCg DNA from 27 seropositive and 23 seronegative samples were analyzed. All of the positive samples amplified the target gene. All negative samples amplified only the control gene. The assay presented 100% specificity and sensibility. The intra- and inter-assay variability was 2.4% and 2.2%. The qPCR efficiency, slope and correlation coefficients were acceptable. The limit of detection was 1 copy/rxn. This assay can reliably quantify HTLV-1 proviral load. For genetic diversity analysis LTR region were amplified by nested PCR. The product were purified and directly sequenced. Twenty patients samples belong to Cosmopolitan subtype Transcontinental (A) subgroup. One HTLV-1 from an asymptomatic individual was classified in the Japanese subgroup (B) of Cosmopolitan subtype.
Biography
Carolina Rosadas de Oliveira has completed her MSc from Instituto Oswaldo Cruz and is a PhD student from Universidade Federal do Rio de Janeiro. She is the professor of Virology and Molecular Biology at Universidade Est?cio de S?, and has been serving as an editorial board member of repute.
image PDF   |   image HTML
 
Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
adwords