Performance of Real-Time Polymerase Chain Reaction Assays for the Detection of 20 Gastrointestinal Parasites in Clinical Samples from Senegal

被引:21
|
作者
Sow, Doudou [1 ,2 ]
Parola, Philippe [2 ]
Sylla, Khadime [1 ]
Ndiaye, Magatte [1 ]
Delaunay, Pascal [3 ,4 ]
Halfon, Philippe [5 ]
Camiade, Sabine [5 ]
Dieng, Therese [1 ]
Tine, Roger C. K. [1 ]
Faye, Babacar [1 ]
Ndiaye, Jean Louis [1 ]
Dieng, Yemou [1 ]
Gaye, Oumar [1 ]
Raoult, Didier [2 ]
Bittar, Fadi [2 ]
机构
[1] UCAD, Fac Med, Serv Parasitol Mycol, Dakar 5005, Senegal
[2] Aix Marseille Univ, URMITE, UM63, CNRS 7278,IRD 198,INSERM 1095,IHU Mediterranee In, Marseille, France
[3] CHU Nice, Parasitol Mycol, Hop Archet, Nice, France
[4] Univ Montpellier, CNRS 5290, UMR IRD224, MIVEGEC, Montpellier 5, France
[5] Lab Alphabio Hop Europeen, Marseille, France
来源
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE | 2017年 / 97卷 / 01期
关键词
ETHER CONCENTRATION TECHNIQUE; ENTAMOEBA-HISTOLYTICA; DIENTAMOEBA-FRAGILIS; FECAL SAMPLES; PCR ASSAY; CRYPTOSPORIDIUM-PARVUM; QUANTITATIVE DETECTION; INTESTINAL PROTOZOA; MULTI-PARALLEL; PATHOGEN PANEL;
D O I
10.4269/ajtmh.16-0781
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Gastrointestinal parasite infections represent one of the biggest public health problems in the world. Therefore, appropriate innovative tools are needed for assessing interventions to control these infections. This study aims to compare the performance of real-time polymerase chain reaction (PCR) assays to microscopic examination for detection of intestinal parasites. A direct microscopic examination and stool concentration was performed on 98 stool samples from patients attending Senegalese hospitals. Negative microscopic control samples were also collected in Nice and Marseille (France). Species-specific primers/probes were used to detect 20commongastrointestinal protozoans and helminths. Positive frequency and the sensitivity of each real-time PCR assay were compared with conventional microscopic examination. Real-time PCR was positive in 72 of 98 samples (73.5%), whereas microscopic examination was positive in 37 (37.7%) samples (P < 0.001). The real-time PCR assays were more sensitive than microscopy, with 57.4% (31/54) versus 18.5% (10/54), respectively, in the detection of parasites in asymptomatic patients (P < 0.05). In terms of polyparasitism, there were more coinfections detected by real-time PCR assays compared with microscopic methods (25.5% versus 3.06%). In comparison to parasite prevalence on individual samples, the results showed a perfect agreement (100%) between the two techniques for seven species, whereas discrepancies were observed for the others (agreement percentage varying from 64.2% to 98.9%). Real-time PCR appeared to be superior to microscopic examination for the detection of parasites in stool samples. This assay will be useful in diagnostic laboratories and in the field for evaluating the efficacy of mass drug administration programs.
引用
收藏
页码:173 / 182
页数:10
相关论文
共 50 条
  • [31] New Developments in Quantitative Real-time Polymerase Chain Reaction Technology
    Gadkar, Vijay J.
    Filion, Martin
    CURRENT ISSUES IN MOLECULAR BIOLOGY, 2014, 16 : 1 - 5
  • [32] Development of Multiplex Real-Time Polymerase Chain Reaction for Detection of Entamoeba histolytica, Entamoeba dispar, and Entamoeba moshkovskii in Clinical Specimens
    Hamzah, Zulhainan
    Petmitr, Songsak
    Mungthin, Mathirut
    Leelayoova, Saovanee
    Chavalitshewinkoon-Petmitr, Porntip
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2010, 83 (04): : 909 - 913
  • [33] Direct Quantification and Distribution of Tetracycline-Resistant Genes in Meat Samples by Real-Time Polymerase Chain Reaction
    Guarddon, Monica
    Miranda, Jose M.
    Vazquez, Beatriz I.
    Cepeda, Alberto
    Franco, Carlos M.
    JOURNAL OF FOOD SCIENCE, 2012, 77 (07) : M372 - M376
  • [34] Use of pooled protozoal cultures of preputial scraping samples obtained from bulls for the detection of Tritrichomonas foetus by means of a real-time polymerase chain reaction assay
    Guerra, Alvaro Garcia
    Hill, Janet E.
    Campbell, John
    Waldner, Cheryl L.
    Hendrick, Steven H.
    JAVMA-JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 2014, 244 (03): : 352 - 356
  • [35] Comparison of culture versus quantitative real-time polymerase chain reaction for the detection of Taylorella equigenitalis in field samples from naturally infected horses in Canada and Germany
    Nadin-Davis, Susan
    Knowles, Margaret K.
    Burke, Teresa
    Boese, Reinhard
    Devenish, John
    CANADIAN JOURNAL OF VETERINARY RESEARCH-REVUE CANADIENNE DE RECHERCHE VETERINAIRE, 2015, 79 (03): : 161 - 169
  • [36] Identification and molecular discrimination of toxigenic and nontoxigenic diphtheria Corynebacterium strains by combined real-time polymerase chain reaction assays
    Mancini, Fabiola
    Monaco, Monica
    Pataracchia, Marco
    von Hunolstein, Christina
    Pantosti, Annalisa
    Ciervo, Alessandra
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2012, 73 (02) : 111 - 120
  • [37] Evaluation of Commercially Available Real-Time Polymerase Chain Reaction Assays for the Diagnosis of Invasive Aspergillosis in Patients with Haematological Malignancies
    Erman-Daloglu, Aylin
    Ozhak, Betil
    Salim, Ozan
    Turhan, Ozge
    Ongut, Gozde
    Gunseren, Filiz
    Colak, Dilek
    Ogunc, Dilara
    MYCOPATHOLOGIA, 2020, 185 (02) : 269 - 277
  • [38] Establishment and Modification of Ninety-seven Pneumococcal Serotyping Assays Based on Quantitative Real-time Polymerase Chain Reaction
    Jie, Che
    Han, Chen Bo
    Li, Xu
    Yuan, Gao
    Meng, Yue Meng
    Man, Chen Zi
    Jun, Zhang Mao
    Jun, Shao Zhu
    BIOMEDICAL AND ENVIRONMENTAL SCIENCES, 2023, 36 (09) : 787 - +
  • [39] Routine use of a real-time polymerase chain reaction method for detection of bloodstream infections in neutropaenic patients
    Paolucci, Michela
    Stanzani, Marta
    Melchionda, Fraia
    Tolomelli, Giulia
    Castellani, Gastone
    Landini, Maria Paola
    Varani, Stefania
    Lewis, Russell E.
    Sambri, Vittorio
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2013, 75 (02) : 130 - 134
  • [40] Real-time fluorogenic reverse transcription polymerase chain reaction assay for the specific detection of Bagaza virus
    Buitrago, Dolores
    Rocha, Ana
    Tena-Tomas, Cristina
    Vigo, Marta
    Agueero, Montserrat
    Angel Jimenez-Clavero, Miguel
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2012, 24 (05) : 959 - 963