dHere, we describe the first case of a Streptococcus lutetiensis isolate harboring the lnuB gene.
CASE REPORTA 70-year-old male patient had a history of fever, epigastric, and right flank pain of 1 month of evolution. One week prior to admission, residual choledochal microlithiasis without bile duct dilatation was found on echoendoscopy. The patient had had a cholecystectomy 10 years before.On the night before the emergency room consultation, the patient had postprandial epigastralgia, fever, and chills; therefore, his hospitalization was decided. During hospitalization, endoscopic retrograde cholangiopancreatography (ERCP) was performed, showing microgallstones. They were removed by the use of a Dormia basket and an extraction balloon catheter. The admission diagnosis was cholangitis due to residual lithiasis.Admission laboratory findings were as follows: white blood cell count, 4,900/mm 3 (with 86% neutrophils); hematocrit, 37%; kaolin partial thromboplastin time (KPTT), 34 s; and prothrombin time, 70%. Liver function test results were as follows: alanine aminotransferase (ALT), 716 U/liter (normal, Ͻ35 U/liter); aspartate aminotransferase (AST), 218 U/liter (normal, Ͻ35 U/liter); total bilirubin, 0.7 mg/dl (normal, Ͻ1.0 mg/dl); direct bilirubin, 0.3 (normal, Ͻ0.3 mg/dl); alkaline phosphatase, 353 U/liter (normal, Ͻ279 U/liter); and total cholesterol, 103 mg/dl (normal, 150 to 200 mg/dl).In two blood culture bottles taken on admission, after 24 h of incubation, growth of Streptococcus infantarius with Escherichia coli was obtained.Phenotypic identification was carried out by conventional biochemical tests (1). The organism was identified as Streptococcus infantarius; however, it was not possible to determine the subspecies by this methodology. In addition, we used the GP card of a Vitek 2 system (bioMérieux, Marcy-l'Etoile, France). The bionumber obtained was 141011164717711, giving an identification of S. infantarius subsp. coli/Streptococcus bovis with an excellent confidence level. Identification was also carried out by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry (MS) (Bruker Daltonik), showing a spectral score of 2.223 for Streptococcus lutetiensis (2).PCR amplification of the 16S rRNA gene was performed in order to reach definitive identification. A PCR product of the 16S rRNA gene, using the primers described by Weisburg et al. (3), was obtained with the Taq DNA polymerase based on the manufacturer's specifications (Promega). Sequencing of the 1.4-kb PCR product was performed on both DNA strands at the sequencing facility of Macrogen, Inc., Seoul, South Korea. The sequences were analyzed using BLAST V2.0 software (http://www.ncbi.nlm.nih .gov/BLAST/) and showed 99% identity with the sequences corresponding either to the 16S RNA ribosomal gene of S. infantarius subsp. infantarius (GenBank accession number EU420174) or to the 16S RNA ribosomal gene of S. lutetiensis (GenBank accession number NR_037096). In order to discriminate subspecies, we amplified the sodA ...