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Volume 14, Number 9—September 2008

Research

Circulation of 3 Lineages of a Novel Saffold Cardiovirus in Humans

Jan Felix Drexler, Luciano Kleber de Souza Luna, Andreas Stöcker, Patrícia Silva Almeida, Tereza Cristina Medrado Ribeiro, Nadine Petersen, Petra Herzog, Célia Pedroso, Hans Iko Huppertz, Hugo da Costa Ribeiro, Sigrid Baumgarte, and Christian DrostenComments to Author 
Author affiliations: Federal University of Bahia, Salvador, Brazil (J.F. Drexler, A. Stöcker, P. Silva Almeida, T.C. Medrado Ribeiro, C. Pedroso, H. da Costa Ribeiro Jr.); Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany (J.F. Drexler, L.K. de Souza Luna, N. Petersen, P. Herzog); Professor Hess Paediatric Hospital, Bremen, Germany (H.I. Huppertz); Institute of Hygiene and the Environment, Hamburg (S. Baumgarte); University of Bonn Medical Centre, Bonn, Germany (C. Drosten);

Main Article

Figure 1

Nucleic acid alignment of the hybridization sites of diagnostic reverse transcription–PCR oligonucleotides. Oligonucleotides are shown below the alignment panel. The base count in the top line is based on Saffold virus, which also serves as the comparison sequence in the alignment. Dots represent identical bases in compared sequences; deviations are spelled out. A slash (/) represents a gap in the alignment; (rc) means that the reverse complementary sequence is shown for the antisense primer.

Figure 1. Nucleic acid alignment of the hybridization sites of diagnostic reverse transcription–PCR oligonucleotides. Oligonucleotides are shown below the alignment panel. The base count in the top line is based on Saffold virus, which also serves as the comparison sequence in the alignment. Dots represent identical bases in compared sequences; deviations are spelled out. A slash (/) represents a gap in the alignment; (rc) means that the reverse complementary sequence is shown for the antisense primer.

Main Article

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