Development of a low-cost copro-LAMP assay for simultaneous copro-detection of Toxocara canis and Toxocara cati

被引:10
作者
Avila, Hector Gabriel [1 ,2 ]
Risso, Marikena Guadalupe [3 ]
Ruybal, Paula [3 ]
Repetto, Silvia Analia [3 ]
Butti, Marcos Javier [4 ]
Trangoni, Marcos David [5 ]
Loffler, Sylvia Grune [6 ]
Perez, Veronica Mirtha [7 ]
Periago, Maria Victoria [2 ,8 ]
机构
[1] Univ Catolica Cuyo, Fac Ciencias Vet, Fac Ciencias Quim & Tecnol, Lab Prov Zoonosis San Juan, San Juan, Argentina
[2] Consejo Nacl Invest Cient & Tecn, CABA, Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Fac Med, Inst Invest Microbiol & Parasitol Med, IMPAM,UBA,CONICET,CABA, Buenos Aires, DF, Argentina
[4] Univ Nacl La Plata, Fac Ciencias Vet, Catedra Parasitol Comparada, Lab Parasitosis Humanas & Zoonosis Parasitarias, Buenos Aires, DF, Argentina
[5] Inst Agrobiotecnol & Biol Mol IB IABIMO, Lab Brucella Campylobacter & Microbiota Rumen, Inst Biotecnol, UEDD INTA,CONICET,CICVyA,CNIA,INTA Castelar, Hurlingham, Buenos Aires, Argentina
[6] Inst Nacl Tecnol Agr Castelar, Inst Patobiol, Ctr Invest Ciencias Vet & Agron, Lab Leptospirosis, Buenos Aires, DF, Argentina
[7] Minist Salud Publ San Juan, Direcc Epidemiol, Secc Rabia & Zoonosis, San Juan, Argentina
[8] Fdn Mundo Sano, Buenos Aires, DF, Argentina
关键词
Copro-diagnosis; Loop-Mediated Isothermal Amplification; Low-cost; Toxocara canis; Toxocara cati; Toxocariasis; MEDIATED ISOTHERMAL AMPLIFICATION; PERFORMANCE EVALUATION; RAPID DETECTION; PCR; CRYPTOSPORIDIUM; IDENTIFICATION; PARASITES; DOGS; DIAGNOSIS; CHILDREN;
D O I
10.1017/S0031182021000342
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Toxocariasis is a zoonotic disease caused mainly by Toxocara canis and Toxocara cati and diagnosis in dogs and cats is an important tool for its control. For this reason, a new coprological loop-mediated isothermal amplification (LAMP) assay was developed for the simultaneous detection of these species. The primer set was designed on a region of the mitochondrial cox-1 gene. Amplification conditions were evaluated using a temperature gradient (52 degrees C to 68 degrees C), different incubation times (15-120 min), and different concentrations of malachite green dye (0.004-0.4% w/v). The analytical sensitivity was evaluated with serial dilutions of genomic DNA from T. canis and T. cati adult worms, and with serial dilutions of DNA extracted from feces using a low-cost in-house method. The specificity was evaluated using genomic DNA from Canis lupus familiaris, Felis catus, Escherichia coli, Toxascaris leonina, Ancylostoma caninum, Echinococcus granulosus sensu stricto and Taenia hydatigena. The LAMP assay applied to environmental fecal samples from an endemic area showed an analytical sensitivity of 10-100 fg of genomic DNA and 10-(5) serial dilutions of DNA extracted from feces using the low-cost in-house method; with a specificity of 100%. Additionally, the total development of the assay was carried out in a basic laboratory and per-reaction reagent cost decreased by similar to 80%. This new, low-cost tool can help identify the most common agents of toxocariasis in endemic areas in order to manage prevention strategies without having to rely on a laboratory with sophisticated equipment.
引用
收藏
页码:819 / 826
页数:8
相关论文
共 69 条
  • [1] Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method
    Abdullah, J.
    Saffie, N.
    Sjasri, F. A. R.
    Husin, A.
    Abdul-Rahman, Z.
    Ismail, A.
    Aziah, I.
    Mohamed, M.
    [J]. BRAZILIAN JOURNAL OF MICROBIOLOGY, 2014, 45 (04) : 1385 - 1391
  • [2] Toxocariasis: seroprevalence in abandoned-institutionalized children and infants
    Archelli, Susana
    Santillan, Graciela I.
    Fonrouge, Reinaldo
    Cespedes, Graciela
    Burgos, Lola
    Radman, Nilda
    [J]. REVISTA ARGENTINA DE MICROBIOLOGIA, 2014, 46 (01): : 3 - 6
  • [3] Archelli S, 2008, ACTA BIOQUIM CLIN L, V42, P379
  • [4] Avila HG, 2019, ECHINOCOCCUS GRANULO
  • [5] Pathogenic Bacteria Detection Using RNA-Based Loop-Mediated Isothermal-Amplification-Assisted Nucleic Acid Amplification via Droplet Microfluidics
    Azizi, Morteza
    Zaferani, Meisam
    Cheong, Soon Hon
    Abbaspourrad, Alireza
    [J]. ACS SENSORS, 2019, 4 (04): : 841 - 848
  • [6] Development and Diagnostic Evaluation of Loop-Mediated Isothermal Amplification Using a New Gene Target for Rapid Detection of Helicobacter pylori
    Bakhtiari, Somaye
    Alvandi, Amirhooshang
    Pajavand, Hamid
    Navabi, Jafar
    Najafi, Farid
    Abiri, Ramin
    [J]. JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 2016, 9 (05)
  • [7] Analytical sensitivity and specificity of a loop-mediated isothermal amplification (LAMP) kit prototype for detection of Trypanosoma cruzi DNA in human blood samples
    Besuschio, Susana A.
    Llano Murcia, Monica
    Benatar, Alejandro F.
    Monnerat, Severine
    Cruz, Israel
    Picado, Albert
    de los Angeles Curto, Maria
    Kubota, Yutaka
    Wehrendt, Diana P.
    Pavia, Paula
    Mori, Yasuyoshi
    Puerta, Concepcion
    Ndung'u, Joseph M.
    Schijman, Alejandro G.
    [J]. PLOS NEGLECTED TROPICAL DISEASES, 2017, 11 (07):
  • [8] Evaluation of four novel isothermal amplification assays towards simple and rapid genotyping of chloroquine resistant Plasmodium falciparum
    Chahar, Madhvi
    Anvikar, Anup
    Dixit, Rajnikant
    Valecha, Neena
    [J]. EXPERIMENTAL PARASITOLOGY, 2018, 190 : 1 - 9
  • [9] Multisite Performance Evaluation of an Enzyme-Linked Immunosorbent Assay for Detection of Giardia, Cryptosporidium, and Entamoeba histolytica Antigens in Human Stool
    Christy, Nathaniel C. V.
    Hencke, Janice D.
    Escueta-De Cadiz, Aleyla
    Nazib, Forida
    von Thien, Heidrun
    Yagita, Kenji
    Ligaba, Segni
    Haque, Rashidul
    Nozaki, Tomoyoshi
    Tannich, Egbert
    Herbein, Joel F.
    Petri, William A., Jr.
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (05) : 1762 - 1763
  • [10] Ciarmela M L, 2016, Curr Health Sci J, V42, P5, DOI 10.12865/CHSJ.42.01.01