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Rita Sousa,3
Ana L. García-Pérez,4
Manuela Rodríguez-Vargas,1
Bruno Lobo,1 and
Pedro Anda1*
Laboratorio de Espiroquetas y Patógenos Especiales, Servicio de Bacteriología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain,1 Unidad de Alertas y Emergencias, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain,2 Centro de Estudos de Vectores e Doenças Infecciosas (CEVDI), Instituto Nacional de Saude, Lisboa, Portugal,3 Instituto Vasco de Investigación y Desarrollo Agrario (NEIKER), Derio, Vizcaya, Spain4
Received 15 June 2006/ Returned for modification 25 July 2006/ Accepted 22 September 2006
We present a PCR method targeting the 23S-5S internal transcribed spacer coupled with reverse line blotting that allows Rickettsia species detection and identification in a single step. The method is highly sensitive and specific in identifying Rickettsia species from both patient and environmental samples. The generic approach used allowed us to identify new pathogens.
Published ahead of print on 11 October 2006.
Present address: Servicio de Parasitología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
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