2015, Number 1
<< Back Next >>
VacciMonitor 2015; 24 (1)
Obtaining of a rapid diagnostic test for Cholera, based on latex particles coupled with a monoclonal antibody against Vibrio cholerae O1 lipopolysaccharide
Cuello-Pérez M, Otero-Alfaro O, Reyes-López F, Camacho-Casanova F, Duranti G, Morales-Leslie MM, Mora-Guerra RZ, Fernández-Castillo S, González-Aznar E, Piermatte C, Cardoso-González DT, García-Imías LG
Language: Spanish
References: 19
Page: 10-20
PDF size: 250.45 Kb.
ABSTRACT
Cholera is an acute contagious intestinal disease caused by ingestion of food or water contaminated
with O1 and O139 serotypes of the bacterium
Vibrio cholerae. Cholera is characterized by abundant
secretory diarrhea leading to dehydration. Death occurs within hours without treatment, so early
diagnosis is very important, especially at the beginning of the disease, because it is difficult to
differentiate from other acute diarrheal diseases. The diagnostic golden test is the stool culture;
however, it does not guarantee a rapid detection of the disease. Rapid tests have been recently
developed; they are based on test strips and agglutination with latex particles, which are very
effective, but difficult to acquire for their high prices. The objective of this research was to obtain a
quick assay based on latex particles coupled with a monoclonal antibody (mAb) against
V. cholerae O1 lipopolysaccharide obtained in Finlay Institute. Latex particles of 0.8 µm were used in a 10%
suspension, and they were coupled to the mAb (0.25 mg/ml) for 2 hours at 37°C. The sensitivity,
specificity and performance were evaluated in 84 stool samples from patients with presumptive
diagnosis of cholera. The diagnostic test obtained showed no cross-reactivity against no-O1 strains
and other enteropathogens. Latex diagnostic test showed values of sensitivity, specificity and
efficacy of 97.87; 97.29 and 97.6% respectively, very similar to the commercial diagnostic test CTKBiotech.
The latex reagent obtained can be used in the rapid diagnosis of the disease.
REFERENCES
Faruque SM, Albert MJ, Mekalanos JJ. Epidemiology, genetics, and ecology of toxigenic Vibrio cholerae. Microbiol Mol Biol Rev 1998;62:1301-14.
Ali M, López AL, You YA, Kim YE, Sah B, Maskery B, et al. The global burden of cholera. Bull World Health Organ 2012;90(3):209-18.
World Health Organization (WHO). Cholera, 2012, Monthly report on dracunculiasis cases, January-May 2013. Weekly Epidemiological Record 2013;88(31):321-36.
Global Health Observatory (GHO). Cholera. Geneva: WHO; 2013. Disponible en: http://www.who.int/gho/ epidemic_diseases/cholera/
Organización Panamericana de la Salud (OPS). Actualización Epidemiológica del cólera 20 de marzo 2014. Washington, DC: OPS; 2014. Disponible en: http://www.paho.org/hq/ index.php?option=com_docman&task=doc_view&gid=24600 &Itemid=
Global Health Observatory (GHO). Number of reported cholera cases. Geneva: WHO; 2013. Disponible en: http://www.who.int/gho/epidemic_diseases/cholera
Instituto Nacional de Enfermedades Infecciosas ANLIS “CARLOS G. MALBRAN”. III Curso Avanzado de Diagnóstico de Vibrio Cholerae y Salmonella. Buenos Aires: OMS; 2010.
Waldor MK, Mekalanos JJ. Lysogenic conversion by a filamentous phage encoding cholera toxin. Science 1996;272(5270):1910-4.
Farmer JJ, Kelly T. Enterobacteriaceae. In: Balows A, Hausler NJ, Herrmann KL, Isenberg HD, Shadomy HJ, eds. Manual of clinical microbiology. Washington, DC: ASM Press; 1991.p.360-83.
Holmgren J. Actions of cholera toxin and the prevention and treatment of cholera. Nature 1981;292(5822):413-7.
Centro para el Control y Prevención de las Enfermedades. Centro Nacional para las Enfermedades Infecciosas. Métodos de laboratorio para el diagnóstico de Vibrio cholerae. Atlanta: CDC; 1994.
Bolaños HM, Acuña MT, Serrano AM, Obando X, Mairena H, Cháves L, et al. Desempeño de los sistemas Cholera-SMART® y Pathogen-Detection-Kit® en el diagnóstico rápido del cólera. Rev Panam Salud Pública 2004;16(4):233-41.
Kelly MT, Hickman-Brenner FW, Farmer JJ. Vibrio. In: Balows A, Hausler NJ, Herrmann KL, Isenberg HD, Shadomy HJ, eds. Manual of clinical microbiology. Washington, DC: ASM Press; 1991.p.384-95.
Sinha A, SenGupta S, Ghosh S, Basu S, Sur D, Kanungo S, et al. Evaluation of a rapid dipstick test for identifying cholera cases during the outbreak Indian. J Med Res 2012;135(4):523- 8.
Choo YY, Geik YA, Ang LC, Elina HT, Su YL, Falero G, et al. Dry-Reagent Gold Nanoparticle-Based Lateral Flow Biosensor for the Simultaneous Detection of Vibrio cholerae Serogroups O1 and O139. Journal of Microbiological Methods 2011;86(3):277-82.
Nato F, Boutonnier A, Rajerison M, Grosjean P, Dartevelle S, Guénolé A, et al. One-step immunochromatographic dipstick tests for rapid detection of Vibrio cholera O1 and O139 in stool samples. Clin Diagn Lab Immunol 2003;10(3):476-8.
Reyes F, Amín N, Otero O, Aguilar A, Cuello M, Valdés Y, et al. Four monoclonal antibodies against capsular polysaccharides of Neisseria meningitidis serogroups A, C, Y and W135: its application in identity tests. Biologicals 2013;41(4):275-8.
Falero G, Rodríguez BL, Rodríguez I, Campos J, Ledon T, Valle E, et al. Production and characterization of monoclonal antibodies to E1 Tor toxin co-regulated pilus of Vibrio cholerae Hybrid. Hybridomics 2003;22(5):315-20.
Ochoa RF. Técnicas inmunoenzimáticas en el desarrollo clínico de vacunas. La Habana: Finlay Ediciones; 2013.p.25- 41