First Korean Case of Robinsoniella peoriensis Bacteremia in a Patient with Aspiration Pneumonia.
10.3343/alm.2012.32.5.370
- Author:
Yongbum JEON
1
;
Taek Soo KIM
;
Hong Bin KIM
;
Kyoung Un PARK
;
Junghan SONG
;
Eui Chong KIM
Author Information
1. Department of Laboratory Medicine, Seoul National University Hospital, Seoul, Korea.
- Publication Type:Case Reports
- Keywords:
Robinsoniella peoriensis;
Bacteremia;
16S ribosomal RNA
- MeSH:
Aged;
Bacteremia/*microbiology;
Clostridium/classification/genetics/*isolation & purification;
Databases, Genetic;
Humans;
Male;
Phylogeny;
Pneumonia, Aspiration/*diagnosis/microbiology;
RNA, Ribosomal, 16S/chemistry/genetics;
Republic of Korea;
Sequence Analysis, DNA
- From:Annals of Laboratory Medicine
2012;32(5):370-374
- CountryRepublic of Korea
- Language:English
-
Abstract:
Robinsoniella peoriensis has recently been identified as a Gram-positive, spore-forming, anaerobic rod originally recovered from swine manure storage pits. To date, 6 cases of R. peoriensis infection have been reported, including 2 cases of bacteremia, 1 of abdominal fluid collection, and 3 of wound infection. In the present study, we report a 76-yr-old man with R. peoriensis bacteremia who developed aspiration pneumonia. Gram staining of a purified colony revealed Gram-positive, rod-shaped bacteria. Biochemical identification using API 20 A (bioMerieux, France) indicated presence of Clostridium spp. We performed both 500-bp and full-gene sequencing of 16S rRNA of the isolate. The sequence was analyzed with MicroSeq ID 16S rRNA Library v2.0 (Applied Biosystems, USA), GenBank Basic Local Alignment Search Tool (BLAST) (http://www.ncbi.nlm.nih.gov/genbank), and EzTaxon database v2.1 (http://www.eztaxon.org). The 500-bp 16S rRNA sequence of the blood culture isolate showed 99.16-99.79% similarity with R. peoriensis and the full-gene 16S rRNA sequence showed 98.87-99.50% similarity with R. peoriensis. The organism was confirmed as R. peoriensis by using all of the mentioned databases except for MicroSeq, which did not include the RNA sequence of this bacterium. This case suggests that identification of R. peoriensis might be challenging in clinical laboratories with no access to molecular methods, as certain commercial identification systems may not identify, or may misidentify, this organism. To the best of our knowledge, this is the first report of the isolation of R. peoriensis in Korea.
