Evaluation of Diagnostic Markers for Measles Virus Infection in the Context of an Outbreak in Spain

Author:

Mosquera María M.1,de Ory Fernando1,Gallardo Virtudes2,Cuenca Loreto3,Morales Mercedes4,Sánchez-Yedra Waldo4,Cabezas Teresa5,Hernández Juan M.6,Echevarría Juan E.1

Affiliation:

1. Servicio de Microbiología Diagnóstica, Centro Nacional de Microbiología, Instituto de Salud Carlos III, 28220 Majadahonda, Madrid

2. Dirección General de Salud Pública, Consejería de Salud, Junta de Andalucía, 41020 Sevilla

3. Delegación de Salud de Almería, Consejería de Salud, Junta de Andalucía, Almería

4. Hospital Torrecárdenas, 4009 Almería

5. Hospital de Poniente, 4700 El Ejido (Almería)

6. Hospital La Inmaculada, 4600 Almería, Spain

Abstract

ABSTRACT A measles outbreak occurred from January to July 2003 in Spain, despite the fact that the Plan of Eradication of Measles and its surveillance program had been set up in 2001. Different diagnostic markers for measles virus infection were compared for 246 patients in tests of serum, urine, and pharyngeal exudate specimens. Measles virus immunoglobulin M (IgM) and IgG and rubella virus and parvovirus IgM levels in serum were assayed. Multiplex PCR was done on urine, serum, and pharyngeal exudates, and isolation of measles virus in the B95a cell line from urine was attempted. At least one positive marker for measles virus was obtained from 165 patients (67.1%; total number of patients, 246). A total of 136 cases (82.4% of the patients showing positive markers) were diagnosed by PCR and/or isolation and IgM detection methods. The results for 27 patients (16.4%) were positive only by direct methods. The results for two patients (1.2%) were positive only by IgM detection. In the case of the first group (136 cases), the time elapsed from appearance of the rash was significantly longer than in the case of the group which was only positive by PCR. Besides, 8 out of 27 PCR-positive IgM-negative cases showed specific IgG results, suggesting either secondary vaccine failure or reinfection. Numbers resulting from PCR performed with pharyngeal exudates proved to be significantly higher than those obtained with other specimens. Phylogenetic analysis showed the presence of genotype B3. The results strongly back the World Health Organization recommendation that detection of IgM should be supplemented by PCR and isolation for the diagnosis of measles virus infection.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference18 articles.

1. Amela, C., I. Pachon, and F. de Ory. 2003. Evaluation of the measles, mumps and rubella immunisation programme in Spain by using a sero-epidemiological survey. Eur. J. Epidemiol.18:71-79.

2. Avellon, A., P. Perez, J. C. Aguilar, R. Lejarazu, and J. E. Echevarria. 2001. Rapid and sensitive diagnosis of human adenovirus infections by a generic polymerase chain reaction. J. Virol. Methods92:113-120.

3. Carlson, J., H. Artsob, M. Douville-Fradet, P. Duclos, M. Fearon, S. Ratnam, G. Tipples, P. Varughese, B. Ward, J. Sciberras, and the Working Group on Measles Elimination. 1998. Measles surveillance: guidelines for laboratory support. Can. Commun. Dis. Rep.24:33-44.

4. Casas, I., A. Tenorio, J. M. Echevarria, P. E. Klapper, and G. M. Cleator. 1997. Detection of enteroviral RNA and specific DNA of herpesviruses by multiplex genome amplification. J. Virol. Methods66:39-50.

5. Castillo, O., G. Rey, D. Pastor, J. Quintero, L. Suarez, E. Eguis, E. Eslait, M. Donado, X. Carreno, N. Ortiz, P. Hernandez, B. Sanabria, S. Penaloza, E. Pretelt, M. Cutha, N. Perez, M. Cabas, H. Oliveros, H. Pertuz, and L. Bruzon. 2002. [Measles outbreaks in Colombia, February-March 2002]. Biomedica22:219. (In Spanish.)

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