{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,14]],"date-time":"2026-07-14T14:12:27Z","timestamp":1784038347044,"version":"3.55.0"},"reference-count":46,"publisher":"American Society for Microbiology","issue":"1","license":[{"start":{"date-parts":[[2002,1,1]],"date-time":"2002-01-01T00:00:00Z","timestamp":1009843200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Clin Microbiol"],"published-print":{"date-parts":[[2002,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            We describe here a multiplex reverse transcription-PCR (RTMNPCR) assay designed to detect and differentiate measles virus, rubella virus, and parvovirus B19. Serial dilution experiments with vaccine strains that compared cell culture isolation of measles in B95 cells and rubella in RK13 cells showed sensitivity rates of 0.004 50% tissue culture infective dose (TCID\n            <jats:sub>50<\/jats:sub>\n            ) for measles virus and 0.04 TCID\n            <jats:sub>50<\/jats:sub>\n            for rubella virus. This RTMNPCR can detect as few as 10 molecules for measles virus and rubella virus and one molecule for parvovirus B19 in dilution experiments with plasmids containing inserts of the primary reaction amplification products. Five pharyngeal exudates from measles patients and 2 of 15 cerebrospinal fluid samples from measles-related encephalitis were found to be positive for measles virus by this RTMNPCR. A total of 3 of 27 pharyngeal exudates from vaccinated children and 2 pharyngeal exudates, plus one urine sample from a case of congenital rubella syndrome, were found to be positive for rubella virus by RTMNPCR, whereas 16 of 19 sera from patients with erythema infectiosum were determined to be positive for parvovirus B19 by RTMNPCR. In view of these results, we can assess that this method is a useful tool in the diagnosis of these three viruses and could be used as an effective surveillance tool in measles eradication programs.\n          <\/jats:p>","DOI":"10.1128\/jcm.40.1.111-116.2002","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T10:03:40Z","timestamp":1027764220000},"page":"111-116","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":49,"title":["Simultaneous Detection of Measles Virus, Rubella Virus, and Parvovirus B19 by Using Multiplex PCR"],"prefix":"10.1128","volume":"40","author":[{"given":"Mari\u0301a","family":"del Mar Mosquera","sequence":"first","affiliation":[{"name":"Centro Nacional de Microbiologi\u0301a, Instituto de Salud Carlos III, Majadahonda"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fernando","family":"de Ory","sequence":"additional","affiliation":[{"name":"Centro Nacional de Microbiologi\u0301a, Instituto de Salud Carlos III, Majadahonda"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mo\u0301nica","family":"Moreno","sequence":"additional","affiliation":[{"name":"Centro de Attencion Primaria de Galapagar, Madrid, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juan E.","family":"Echevarri\u0301a","sequence":"additional","affiliation":[{"name":"Centro Nacional de Microbiologi\u0301a, Instituto de Salud Carlos III, Majadahonda"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.3201\/eid0401.980105"},{"key":"e_1_3_2_3_2","first-page":"300","year":"1994","unstructured":"Bolognia, J., and I. 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