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
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