A possible novel Francisellagenomic species isolated from blood and urine of a patient with severe illness  R. Escudero, M. Elía, J.A. Sáez-Nieto, V.

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A possible novel Francisellagenomic species isolated from blood and urine of a patient with severe illness  R. Escudero, M. Elía, J.A. Sáez-Nieto, V. Menéndez, A. Toledo, G. Royo, M. Rodríguez-Vargas, M.J. Whipp, H. Gil, I. Jado, P. Anda  Clinical Microbiology and Infection  Volume 16, Issue 7, Pages 1026-1030 (July 2010) DOI: 10.1111/j.1469-0691.2009.03029.x Copyright © 2010 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 1 Phenotypic and genotypic characteristics of the isolate FhSp1 as compared with other members of the genus Francisella. (a) Protein profile in 12% acrylamide gels. (b) Immunoblot analysis with the patient's serum. (c) Amplification of the SSTR9 element. (d) pulsed-field gel electrophoresis analysis of PmEI-digested genomic DNA. Arrows indicate bands cited in the text. (a) Lane 1: Francisella tularensis ssp. holarctica (LVS). Lane 2: F. tularensis ssp. tularensis (B38). Lane 3: Francisella novicida F×1. Lane 4: F. novicida F×2. Lane 5: F. novicida (U112). Lane 6: isolate FhSp1. Lane 7: Francisella philomiragia (CCUG 4992). (b) Lane 1: F. philomiragia (CCUG 4992). Lane 2: F. tularensis ssp. tularensis (B38). Lane 3: F. tularensis ssp. holarctica (LVS). Lane 4: F. novicida (U112). Lane 5: isolate FhSp1. (c) Lane 1: F. tularensis ssp. holarctica (LVS). Lane 2: F. tularensis ssp. tularensis (B38). Lane 3: F. novicida (U112). Lane 4: isolate FhSp1. Lane 5: F. novicida F×1. (d) Lane 1: F. tularensis ssp. holarctica (LVS). Lane 2: F. tularensis ssp. tularensis (B38). Lane 3: F. novicida F×1. Lane 4: F. novicida F×2. Lane 5: F. novicida (U112). Lane 6: isolate FhSp1. Lane 7: F. philomiragia (CCUG 4992). Clinical Microbiology and Infection 2010 16, 1026-1030DOI: (10.1111/j.1469-0691.2009.03029.x) Copyright © 2010 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 2 Phylogenetic analyses of 16S rRNA (a) and a multilocus concatenatedsequence analysis (b). In (a), the GenBank accession numbers used are indicated, and for (b), the following sequences were used: AM261086–AM261089, AM261091, AM261093, AM261097, AM261099 and EU683021 for dnaA, AM261181 to AM261183, AM261186 to AM261188, AM261194, AM261196 and EU682965 for mutS; AM261118–AM261120, AM261123, AM261125, AM261127, AM261128, AM261133 and AM261203 for prfB; AM261165, AM261167, AM261168, AM261170, AM261177–AM261179, AM261180 and EU682989 for putA; and AM261105, AM261115–AM261117, AM261200, AM261202, AM261203, AM261206 and AM261209 for tpiA. For strains WY96-3418 and FTA, the complete genome sequence was used (CP000608 and CP000803, respectively). The percentages shown are those of the identity of FhSp1 with the rest of the strains. Clinical Microbiology and Infection 2010 16, 1026-1030DOI: (10.1111/j.1469-0691.2009.03029.x) Copyright © 2010 European Society of Clinical Infectious Diseases Terms and Conditions