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The Genotypic False Positive Rate Determined by V3 Population Sequencing Can Predict the Burden of HIV-1 CXCR4-using Species Detected by Pyrosequencing
被引:16
|作者:
Svicher, Valentina
[1
]
Cento, Valeria
[1
]
Rozera, Gabriella
[2
]
Abbate, Isabella
[2
]
Santoro, Maria Mercedes
[1
]
Armenia, Daniele
[1
]
Fabeni, Lavinia
[2
]
Bruselles, Alessandro
[2
]
Latini, Alessandra
[3
]
Palamara, Guido
[3
]
Micheli, Valeria
[4
]
Rizzardini, Giuliano
[4
]
Gori, Caterina
[2
]
Forbici, Federica
[2
]
Ippolito, Giuseppe
[2
]
Andreoni, Massimo
[5
]
Antinori, Andrea
[2
]
Ceccherini-Silberstein, Francesca
[1
]
Capobianchi, Maria Rosaria
[2
]
Perno, Carlo Federico
[1
,2
]
机构:
[1] Univ Roma Tor Vergata, Dept Expt Med & Surg, Rome, Italy
[2] INMI L Spallanzani, Rome, Italy
[3] San Gallicano Hosp, Rome, Italy
[4] L Sacco Hosp Vialba, Milan, Italy
[5] Univ Hosp Tor Vergata, Rome, Italy
来源:
关键词:
CORECEPTOR USAGE;
TROPISM;
MARAVIROC;
LOOP;
IMPACT;
GP120;
TOOLS;
1ST;
D O I:
10.1371/journal.pone.0053603
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Objective: The false-positive rate (FPR) is a percentage-score provided by Geno2Pheno-algorithm indicating the likelihood that a V3-sequence is falsely predicted as CXCR4-using. We evaluated the correlation between FPR obtained by V3 population-sequencing and the burden of CXCR4-using variants detected by V3 ultra-deep sequencing (UDPS) and Enhanced-Sensitivity Trofile assay (ESTA). Methods: 54 HIV-1 B-subtype infected-patients (all maraviroc-naive), with viremia >10,000copies/ml, were analyzed. HIV-tropism was assessed by V3 population-sequencing, UDPS (considering variants with >0.5% prevalence), and ESTA. Results: By UDPS, CCR5-using variants were detected in 53/54 patients, irrespective of FPR values, and their intra-patient prevalence progressively increased by increasing the FPR obtained by V3 population-sequencing (rho = 0.75, p = 5.0e-8). Conversely, the intra-patient prevalence of CXCR4-using variants in the 54 patients analyzed progressively decreased by increasing the FPR (rho = -0.61; p = 9.3e-6). Indeed, no CXCR4-using variants were detected in 13/13 patients with FPR>60. They were present in 7/18 (38.8%) patients with FPR 20-60 (intra-patient prevalence range: 2.1%-18.4%), in 5/7 (71.4%) with FPR 10-20, in 4/6 (66.7%) with FPR 5-10, and in 10/10(100%) with FPR<5 (intra-patient prevalence range: 12.1%-98.1%). Conclusions: FPR by V3 population-sequencing can predict the burden of CXCR4-using variants. This information can be used to optimize the management of tropism determination in clinical practice. Due to its low cost and short turnaround time, V3 population-sequencing may represent the most feasible test for HIV-1 tropism determination. More sensitive methodologies (as UDPS) might be useful when V3 population-sequencing provides a FPR >20 (particularly in the range 20-60), allowing a more careful identification of patients harboring CXCR4-using variants.
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