Development of Low Cost Two-Step Reverse Transcription-Quantitative Polymerase Chain Reaction Assays for Rotavirus Detection in Foul Surface Water Drains

被引:5
|
作者
Chung, J. W. [1 ]
Foppen, J. W. [2 ]
Lens, P. N. L. [1 ]
机构
[1] UNESCO IHE Inst Water Educ, Dept Environm Engn & Water Technol, NL-2601 DA Delft, Netherlands
[2] UNESCO IHE Inst Water Educ, Dept Water Sci & Engn, NL-2601 DA Delft, Netherlands
关键词
Rotavirus; RT-qPCR; Surface water; Slums; Kampala; Uganda; TIME RT-PCR; CHILDREN; DISEASE;
D O I
10.1007/s12560-013-9111-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Commercial kits to determine RNA concentrations are expensive, and sometimes too expensive for laboratories working with tight budgets, especially those in developing countries. We developed, tested, and evaluated two home-made two-step reverse transcription-quantitative polymerase chain reaction assays aimed to detect rotavirus in surface water samples. A commercial one-step master kit was used for comparison. Our results indicated that the efficiency of the home-made assays was comparable to the commercial kit. Furthermore, the lowest detection limit of all assays corresponded to 10(-0.2) TCID50 (50 % tissue Culture Infective Dose) per ml. The home-made assays were able to detect rotavirus concentrations in complex surface waters in a slum area in Kampala (Uganda) and their performance was comparable to the commercial kit. The total costs of the two home-made assays was 11 times less than the selected commercial kit. Although preparing home-made assays is more time consuming, the assays can be useful for cases in which consumable costs are more important than personnel costs.
引用
收藏
页码:126 / 133
页数:8
相关论文
共 48 条
  • [21] Detection of Viral Hemorrhagic Septicemia Virus by Quantitative Reverse Transcription Polymerase Chain Reaction from Two Fish Species at Two Sites in Lake Superior
    Cornwell, Emily R.
    Eckerlin, Geofrey E.
    Getchell, Rodman G.
    Groocock, Geoffrey H.
    Thompson, Tarin M.
    Batts, William N.
    Casey, Rufina N.
    Kurath, Gael
    Winton, James R.
    Bowser, Paul R.
    Bain, Mark B.
    Casey, James W.
    JOURNAL OF AQUATIC ANIMAL HEALTH, 2011, 23 (04) : 207 - 217
  • [22] Optimization of one-step real-time reverse transcription-polymerase chain reaction assays for norovirus detection and molecular epidemiology of noroviruses in Thailand
    Neesanant, Pimmnapar
    Sirinarumitr, Theerapol
    Chantakru, Siriruk
    Boonyaprakob, Ukadaj
    Chuwongkomon, Kaittawee
    Bodhidatta, Ladaporn
    Sethabutr, Orntipa
    Abente, Eugenio J.
    Supawat, Krongkaew
    Mason, Carl J.
    JOURNAL OF VIROLOGICAL METHODS, 2013, 194 (1-2) : 317 - 325
  • [23] Rapid detection and quantification of Ebola Zaire virus by one-step real-time quantitative reverse transcription-polymerase chain reaction
    Ro, Young-Tae
    Ticer, Anysha
    Carrion, Ricardo, Jr.
    Patterson, Jean L.
    MICROBIOLOGY AND IMMUNOLOGY, 2017, 61 (3-4) : 130 - 137
  • [24] A SIMPLE DEVICE FOR THE CONCENTRATION AND DETECTION OF ENTEROVIRUS, HEPATITIS-E VIRUS AND ROTAVIRUS FROM WATER SAMPLES BY REVERSE TRANSCRIPTION-POLYMERASE CHAIN-REACTION
    JOTHIKUMAR, N
    KHANNA, P
    PAULMURUGAN, R
    KAMATCHIAMMAL, S
    PADMANABHAN, P
    JOURNAL OF VIROLOGICAL METHODS, 1995, 55 (03) : 401 - 415
  • [25] Development of a reverse transcription quantitative polymerase chain reaction-based assay for broad coverage detection of African and Asian Zika virus lineages
    Yang Yang
    Gary Wong
    Baoguo Ye
    Shihua Li
    Shanqin Li
    Haixia Zheng
    Qiang Wang
    Mifang Liang
    George F Gao
    Lei Liu
    Yingxia Liu
    Yuhai Bi
    Virologica Sinica, 2017, (03) : 199 - 206
  • [26] Development of a reverse transcription quantitative polymerase chain reaction-based assay for broad coverage detection of African and Asian Zika virus lineages
    Yang Yang
    Gary Wong
    Baoguo Ye
    Shihua Li
    Shanqin Li
    Haixia Zheng
    Qiang Wang
    Mifang Liang
    George F Gao
    Lei Liu
    Yingxia Liu
    Yuhai Bi
    Virologica Sinica, 2017, 32 (03) : 199 - 206
  • [27] Development of a TaqMan minor groove binding probe-based quantitative reverse transcription polymerase chain reaction for the detection and quantification of Zika virus
    Chin, K. L.
    Teoh, B. T.
    Sam, S. S.
    Loong, S. K.
    Tan, K. K.
    Azizan, N. S.
    Lim, Y. K.
    Khor, C. S.
    Nor'e, S. S.
    Abd-Jamil, J.
    AbuBakar, S.
    TROPICAL BIOMEDICINE, 2022, 39 (04) : 518 - 523
  • [28] Development of a reverse transcription quantitative polymerase chain reaction-based assay for broad coverage detection of African and Asian Zika virus lineages
    Yang, Yang
    Wong, Gary
    Ye, Baoguo
    Li, Shihua
    Li, Shanqin
    Zheng, Haixia
    Wang, Qiang
    Liang, Mifang
    Gao, George F.
    Liu, Lei
    Liu, Yingxia
    Bi, Yuhai
    VIROLOGICA SINICA, 2017, 32 (03) : 199 - 206
  • [29] Single-step multiplex conventional and real-time reverse transcription polymerase chain reaction assays for simultaneous detection and subtype differentiation of Influenza A virus in swine
    Nagarajan, Malliga M.
    Simard, Genevieve
    Longtin, Diane
    Simard, Carole
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2010, 22 (03) : 402 - 408
  • [30] One-step triplex TaqMan quantitative reverse transcription polymerase chain reaction for the detection of feline coronavirus, feline panleukopenia virus, and feline leukemia virus
    He, Mengyi
    Feng, Shuping
    Shi, Kaichuang
    Shi, Yandi
    Long, Feng
    Yin, Yanwen
    Li, Zongqiang
    VETERINARY WORLD, 2024, 17 (05) : 946 - 955