A new Real-Time-RT-PCR for quantitation of human endogenous retroviruses type K (HERV-K) RNA load in plasma samples: Increased HERV-K RNA titers in HIV-1 patients with HAART non-suppressive regimens

2006 ◽  
Vol 136 (1-2) ◽  
pp. 51-57 ◽  
Author(s):  
Rafael Contreras-Galindo ◽  
Marta González ◽  
Sharilyn Almodovar-Camacho ◽  
Sandra González-Ramírez ◽  
Eric Lorenzo ◽  
...  
2006 ◽  
Vol 20 (3-4) ◽  
pp. 223-229 ◽  
Author(s):  
Davide Gibellini ◽  
Federica Gardini ◽  
Francesca Vitone ◽  
Pasqua Schiavone ◽  
Giuliano Furlini ◽  
...  

Retrovirology ◽  
2006 ◽  
Vol 3 (S1) ◽  
Author(s):  
Rafael Contreras-Galindo ◽  
Angie Contreras-Galindo ◽  
Eric Lorenzo ◽  
Yasuhiro Yamamura

2007 ◽  
Vol 23 (1) ◽  
pp. 116-122 ◽  
Author(s):  
Rafael Contreras-Galindo ◽  
Pablo López ◽  
Rosa Vélez ◽  
Yasuhiro Yamamura

2009 ◽  
Vol 58 (9) ◽  
pp. 1168-1172 ◽  
Author(s):  
J.-N. Telles ◽  
K. Le Roux ◽  
P. Grivard ◽  
G. Vernet ◽  
A. Michault

The Chikungunya virus (CHIKV) is a member of the genus Alphavirus that is transmitted to humans by Aedes mosquitoes. In 2005 and 2006, the Indian Ocean island of La Réunion was hit with an unprecedented CHIKV fever outbreak that infected 300 000 people. In the present study, we describe the evaluation of real-time nucleic acid sequence-based amplification (RT-NASBA) for the detection of CHIKV in clinical samples. A co-extracted and co-amplified chimerical CHIKV RNA sequence was used as an internal control to eliminate false-negative results. The detection threshold of the assay was determined from quantified CHIKV-positive plasma, and estimated to be 200 copies per NASBA reaction. The specificity of the assay was determined using blast analyses and non-cross-reactivity using an O'nyong-nyong virus culture and 250 CHIKV RT-PCR-negative plasma samples. A 100 % specificity was found and no invalid result was obtained, showing the good quality of the nucleic acid extraction. The assay was then evaluated using 252 CHIKV-positive RT-PCR plasma samples. The samples were all tested positive, including those with low viral load. This evaluation showed that the RT-NASBA is a rapid (5 h from sample nucleic acid extraction to detection), sensitive, specific and reliable method for the routine diagnosis of CHIKV in clinical samples.


2006 ◽  
Vol 12 (6) ◽  
pp. 698-703 ◽  
Author(s):  
S Sotgiu ◽  
G Arru ◽  
G Mameli ◽  
C Serra ◽  
M Pugliatti ◽  
...  

The human endogenous retroviruses (HERV)-W family contains an extracellular particle detected in multiple sclerosis (MS) patients and designated as MS-associated retrovirus (MSRV). Through nested RT-PCR assays specific for pol MSRV gene, we preliminary reported that its presence in the cerebrospinal fluid (CSF) of early MS patients could be indicative of a poor prognosis upon a three-year follow-up. In the present clinical study, we enlarged our blind observation up to six years. At study entry, 10 MS patients were MSRV- and eight were MSRV+ in the CSF, both groups having a similar mean age and Expanded Disability Status Scale (EDSS) score. After six year follow-up, the mean EDSS significantly differed between the MSRV- and MSRV+ cohorts (4.3 versus 2.2; P = 0.004), as did the annual relapse rate (0.5 in the MSRV- versus 0.3 in the MSRV+; P = 0.01). Finally, two MSRV- patients entered the progressive phase, whilst none of the MSRV+ group entered this phase, and 9/10 MSRV- versus 2/8 MSRV+ patients were treated with immunomodulatory or immunosuppressive drugs (P = 0.009). In conclusion, we found that the presence of MSRV virions in the CSF at the onset of MS is associated, not only with disability accumulation, but also with a higher rate of clinical re-exacerbations. With the known potential pathogenic effects of MSRV given in the literature, further investigations on MSRV are warranted.


2007 ◽  
Vol 144 (1-2) ◽  
pp. 109-114 ◽  
Author(s):  
Chin-Yih Ou ◽  
Hua Yang ◽  
Steven Balinandi ◽  
Souleymane Sawadogo ◽  
Vedapuri Shanmugam ◽  
...  

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