Assessment of efficacy of palm polymerase chain reaction with microscopy, rapid diagnostic test and conventional polymerase chain reaction for diagnosis of malaria

被引:2
|
作者
Mahale, Paras [1 ]
Warke, Rajas [2 ]
Ramaiya, Mira [1 ]
Balasubramanian, Deepa [2 ]
Shetty, Suvin [3 ]
Mankeshwar, Ranjit [4 ]
Chowdhary, Abhay [1 ,5 ]
机构
[1] Haffkine Inst Training Res & Testing, Dept Zoonosis, Mumbai, Maharashtra, India
[2] Himedia Labs Pvt Ltd, Dept Mol Biol, Mumbai, Maharashtra, India
[3] DR LH Hiranandani Hosp, Dept Lab Med, Mumbai, Maharashtra, India
[4] Sir JJ Grp Hosp, Grant Med Coll, Dept Communal Dis, Mumbai, Maharashtra, India
[5] DY Patil Univ, Sch Med, Dept Microbiol, Sect 7, Navi Mumbai 400705, Maharashtra, India
关键词
Conventional polymerase chain reaction; malaria; microscopy; palm polymerase chain reaction; rapid diagnostic test; PREVALENCE; PARASITES; PCR;
D O I
10.4103/ijmm.IJMM_19_169
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose: Sensitive, specific, rapid and cost-effective technique for malaria diagnosis is need of the hour. Microscopy has been the gold standard for malaria diagnosis, but its interpersonnel variability and lack of sensitivity make it subjective test. Conventional polymerase chain reaction (cPCR) has proven to be sensitive technique, but costly and time-consuming. Considering these factors, we have compared microscopy and cPCR with newly derives ultra-fast, portable PCR machine called Palm PCR. Materials and Methods: Palm PCR is arranged with three heat blocks precisely made for three stages of PCR cycles with 34 min for 1100 bp Plasmodium genus outer primer to amplify and 10 min each for Plasmodium falciparum and Plasmodium vivax inner primers of 120 bp and 205 bp, respectively. A total of 191 suspected samples were processed and evaluated using receiver operating characteristic (ROC) curve analysis. Results: The area under ROC curve analysis for Palm PCR with reference standard microscopy for P. falciparum, P. vivax and Plasmodium was 0.8969, 0.9121 and 0.9116, respectively, and with reference standard cPCR was 1.0 for all of them. ROC curve area close of suggests that Palm PCR can be as significant as cPCR in malaria diagnosis. In fact, ultra-rapid amplification with same precision makes Palm PCR better technique than cPCR. Conclusion: Palm PCR is sensitive, rapid and works on battery with simple laboratory facility requirements. Portable electrophoresis and transilluminator combined with Palm PCR could be implemented as an important diagnostic tool in resource-limited and rural areas. Similar studies with wider parameters in rural areas will help us evaluate and maybe establish Palm PCR as PCR platform of choice for such specific set-ups.
引用
收藏
页码:192 / 197
页数:6
相关论文
共 50 条
  • [1] Malaria Diagnostics: A Comparative Study of Blood Microscopy, a Rapid Diagnostic Test and Polymerase Chain Reaction in the Diagnosis of Malaria
    Runsewe-Abiodun, Iyabo T.
    Efunsile, Michael
    Ghebremedhin, Beniam
    Sotimehin, Adetoun S.
    Ajewole, Jerome
    Akinleye, James
    Koenig, Brigite
    Koenig, Wolfang
    JOURNAL OF TROPICAL PEDIATRICS, 2012, 58 (02) : 163 - 164
  • [2] Detecting Malaria Hotspots: A Comparison of Rapid Diagnostic Test, Microscopy, and Polymerase Chain Reaction
    Mogeni, Polycarp
    Williams, Thomas N.
    Omedo, Irene
    Kimani, Domtila
    Ngoi, Joyce M.
    Mwacharo, Jedida
    Morter, Richard
    Nyundo, Christopher
    Wambua, Juliana
    Nyangweso, George
    Kapulu, Melissa
    Fegan, Gregory
    Bejon, Philip
    JOURNAL OF INFECTIOUS DISEASES, 2017, 216 (09): : 1091 - 1098
  • [3] Diagnostic efficacy of microscopy, rapid diagnostic test and polymerase chain reaction for malaria using bayesian latent class analysis
    Saha, Sreemanti
    Narang, Rahul
    Deshmukh, Pradeep
    Pote, Kiran
    Anvikar, Anup
    Narang, Pratibha
    INDIAN JOURNAL OF MEDICAL MICROBIOLOGY, 2017, 35 (03) : 376 - 380
  • [4] A comparison of thick-film microscopy, rapid diagnostic test, and polymerase chain reaction for accurate diagnosis of Plasmodium falciparum malaria
    Kenji O. Mfuh
    Olivia A. Achonduh-Atijegbe
    Obase N. Bekindaka
    Livo F. Esemu
    Calixt D. Mbakop
    Krupa Gandhi
    Rose G. F. Leke
    Diane W. Taylor
    Vivek R. Nerurkar
    Malaria Journal, 18
  • [5] A comparison of thick-film microscopy, rapid diagnostic test, and polymerase chain reaction for accurate diagnosis of Plasmodium falciparum malaria
    Mfuh, Kenji O.
    Achonduh-Atijegbe, Olivia A.
    Bekindaka, Obase N.
    Esemu, Livo F.
    Mbakop, Calixt D.
    Gandhi, Krupa
    Leke, Rose G. F.
    Taylor, Diane W.
    Nerurkar, Vivek R.
    MALARIA JOURNAL, 2019, 18 (1)
  • [6] Performance of rapid diagnostic test, light microscopy, and polymerase chain reaction in pregnant women with asymptomatic malaria in Nigeria
    Adebusuyi, Sunday A.
    Olorunfemi, Adedolapo Blessing
    Fagbemi, Kaossarath Adedjoke
    Nderu, David
    Amoo, Abimbola O. J.
    Thomas, Bolaji N.
    Velavan, Thirumalaisamy P.
    Ojurongbe, Olusola
    IJID REGIONS, 2024, 12
  • [7] Rapid diagnosis of leptospirosis by polymerase chain reaction
    Ramadass, P
    Meerarani, S
    Kumar, AS
    Venkatesha, MD
    Nachimuthu, K
    INDIAN VETERINARY JOURNAL, 1997, 74 (06): : 457 - 460
  • [8] Comparison of polymerase chain reaction, microscopy, and rapid diagnostic test in malaria detection in a high burden state (Odisha) of India
    Ahmad, Amreen
    Soni, Prahalad
    Kumar, Lalit
    Singh, Mrignendra Pal
    Verma, Anil Kumar
    Sharma, Anjana
    Das, Aparup
    Bharti, Praveen Kumar
    PATHOGENS AND GLOBAL HEALTH, 2021, 115 (04) : 267 - 272
  • [9] Comparative efficacy of conventional diagnostic methods and evaluation of polymerase chain reaction for the diagnosis of bovine brucellosis
    Akhtar, Raheela
    Chaudhry, Zafar Iqbal
    Shakoori, A. R.
    Ahmad, Mansoor Ud Din
    Aslam, Asim
    VETERINARY WORLD, 2010, 3 (02) : 53 - 56
  • [10] Use of polymerase chain reaction for postmortem diagnosis of malaria
    Becker, K
    Ortmann, C
    Bajanowski, T
    Brinkmann, B
    Peters, G
    DIAGNOSTIC MOLECULAR PATHOLOGY, 1999, 8 (04) : 211 - 215