Y-chromosome identification in circulating cell-free fetal DNA using surface plasmon resonance

被引:16
作者
Breveglieri, Giulia [1 ,2 ]
Bassi, Elisabetta [1 ]
Carlassara, Silvia [1 ]
Cosenza, Lucia Carmela [1 ,2 ]
Pellegatti, Patrizia [3 ]
Guerra, Giovanni [3 ]
Finotti, Alessia [1 ]
Gambari, Roberto [1 ,2 ]
Borgatti, Monica [1 ]
机构
[1] Univ Ferrara, Biochem & Mol Biol Sect, Dept Life Sci & Biotechnol, I-44100 Ferrara, Italy
[2] Univ Ferrara, Biotechnol Ctr, I-44100 Ferrara, Italy
[3] Univ Hosp S Anna, Lab Anal, Operat Unit, Ferrara, Italy
关键词
REAL-TIME DETECTION; STAPHYLOCOCCAL-ENTEROTOXIN-B; FIBROSIS W1282X MUTATION; PEPTIDE NUCLEIC-ACIDS; MATERNAL PLASMA; BIOSENSOR TECHNOLOGY; SEX DETERMINATION; PRENATAL-DIAGNOSIS; PREGNANT-WOMEN; KINETICS;
D O I
10.1002/pd.4788
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ObjectiveSince the discovery of cell-free fetal DNA (cffDNA) in maternal plasma, diagnostic non-invasive prenatal methods have been developed or optimized for fetal sex determination and identification of genetic diseases. As far as fetal sex determination, this might be important for therapeutic intervention on sex-associated pathologies such as Duchenne muscular dystrophy, hemophilia and congenital adrenal hyperplasia. Surface plasmon resonance (SPR)-based biosensors might be useful for these studies, because they allow to monitor the molecular interactions in real-time providing qualitative and quantitative information, through kinetics, affinity and concentration analyses. MethodsThe Biacore(TM) X100 has been applied to identify Y-chromosome sequence in cffDNA obtained from plasma samples of 26 pregnant women at different gestational ages. We have performed SPR-based analysis of SRY PCR products using SRY-specific probes immobilized on the sensor chip. ResultsWe have demonstrated that there is a statistically significant difference between samples collected by pregnancies carrying male or female fetuses. Moreover, cffDNA obtained at early gestational ages and not detectable by conventional quantitative real-time PCR can be discriminated with high accuracy and reliability using SPR-based biosensors. ConclusionsThese data, in addition to their direct applicability in more extensive diagnostic trials, should be considered as the basis of future developments. (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:353 / 361
页数:9
相关论文
共 54 条
[1]   Kinetics of fetal cellular and cell-free DNA in the maternal circulation during and after pregnancy: implications for noninvasive prenatal diagnosis [J].
Ariga, H ;
Ohto, H ;
Busch, MP ;
Imamura, S ;
Watson, R ;
Reed, W ;
Lee, TH .
TRANSFUSION, 2001, 41 (12) :1524-1530
[2]   Non-invasive diagnosis of fetal sex; utilisation of free fetal DNA in maternal plasma and ultrasound [J].
Avent, Neil D. ;
Chitty, Lyn S. .
PRENATAL DIAGNOSIS, 2006, 26 (07) :598-603
[3]  
Avent Neil D., 2008, V444, P185, DOI 10.1007/978-1-59745-066-9_14
[4]   Biosensor technology and surface plasmon resonance for real-time detection of HIV-1 genomic sequences amplified by polymerase chain reaction [J].
Bianchi, N ;
Rutigliano, C ;
Tomassetti, M ;
Feriotto, G ;
Zorzato, F ;
Gambari, R .
CLINICAL AND DIAGNOSTIC VIROLOGY, 1997, 8 (03) :199-208
[5]   Accurate and robust quantification of circulating fetal and total DNA in maternal plasma from 5 to 41 weeks of gestation [J].
Birch, L ;
English, CA ;
O'Donoghue, K ;
Barigye, O ;
Fisk, NM ;
Keer, JT .
CLINICAL CHEMISTRY, 2005, 51 (02) :312-320
[6]   Cell-free fetal DNA in maternal blood: kinetics, source and structure [J].
Bischoff, FZ ;
Lewis, DE ;
Simpson, JL .
HUMAN REPRODUCTION UPDATE, 2005, 11 (01) :59-67
[7]   New Method Based on Capillary Electrophoresis with Laser-Induced Fluorescence Detection (CE-LIF) to Monitor Interaction between Nanoparticles and the Amyloid-β Peptide [J].
Brambilla, Davide ;
Verpillot, Romain ;
Taverna, Myriam ;
De Kimpe, Line ;
Le Droumaguet, Benjamin ;
Nicolas, Julien ;
Canovi, Mara ;
Gobbi, Marco ;
Mantegazza, Francesco ;
Salmona, Mario ;
Nicolas, Valerie ;
Scheper, Wiep ;
Couvreur, Patrick ;
Andrieux, Karine .
ANALYTICAL CHEMISTRY, 2010, 82 (24) :10083-10089
[8]   FETAL LOSS RATE AFTER CHORIONIC VILLUS SAMPLING AND SUBSEQUENT AMNIOCENTESIS [J].
BRANDENBURG, H ;
JAHODA, MGJ ;
PIJPERS, L ;
REUSS, A ;
KLEYER, WJ ;
WLADIMIROFF, JW .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 35 (02) :178-180
[9]   Size distributions of maternal and fetal DNA in maternal plasma [J].
Chan, KCA ;
Zhang, J ;
Hui, ABY ;
Wong, N ;
Lau, TK ;
Leung, TN ;
Lo, KW ;
Huang, DWS ;
Lo, YMD .
CLINICAL CHEMISTRY, 2004, 50 (01) :88-92
[10]   Non-invasive first trimester determination of fetal gender: a new approach for prenatal diagnosis of haemophilia [J].
Chi, C ;
Hyett, JA ;
Finning, KM ;
Lee, CA ;
Kadir, RA .
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2006, 113 (02) :239-242