Elizabethkingia bruuniana Infections in Humans, Taiwan, 2005–2017

Using 16S rRNA and rpoB gene sequencing, we identified 6 patients infected with Elizabethkingia bruuniana treated at E-Da Hospital (Kaohsiung, Taiwan) during 2005–2017. We describe patient characteristics and the molecular characteristics of the E. bruuniana isolates, including their MICs. Larger-scale studies are needed for more robust characterization of this pathogen.

T he Elizabethkingia genus comprises gram-negative, aerobic, nonmotile, nonspore-forming, nonfermenting rod-shaped bacteria (1). This genus previously comprised E. meningoseptica, E. miricola, and E. anophelis. In August 2017, Nicholson et al. proposed adding 3 new species, namely E. bruuniana, E. ursingii, and E. occulta, to this genus (1). However, little information exists about these species. In this study, we report the clinical characteristics and demographics of a group of patients with E. bruuniana infection in Taiwan and the molecular features of their E. bruuniana isolates.
We conducted this study at E-Da Hospital, a 1,000bed university-affiliated medical center in Kaohsiung, Taiwan; this study was approved by the institutional review board of the hospital (no. EMRP-106-105). We searched the hospital database to identify microbial cultures performed during January 2005-December 2017 that yielded Elizabethkingia. The isolates were initially identified by staff in the clinical microbiology laboratory using API/ID32 phenotyping kits or VITEK MS (both from bioMérieux, https://www.biomerieux.com). We reidentified these species as Elizabethkingia using both 16S rRNA and rpoB gene sequencing. The primers and methods we used for amplification and sequencing of the 16S rRNA and rpoB genes were described previously (1,2). We compared the assembled 16S rRNA gene sequences with the nucleotide sequences of Elizabethkingia-type strains present in GenBank. We considered isolates with >99.5% similarity in the 16S rRNA gene sequence members of the same species, as recommended in a previous study (3). We constructed a phylogenetic tree using the rpoB genes of the isolates exhibiting >99.5% 16S rRNA gene sequence identity with the E. bruuniana type strain G0146 T . We calculated the average nucleotide identity using OrthoANI (4) and computed in silico DNA-DNA hybridization (DDH) using the Genome-to-Genome Distance Calculator (5), using the average nucleotide identity value of >95% and the DDH value of >70% separately as criteria for species delineation (4,5). We sequenced the quinolone resistance-determining regions of DNA gyrase (gyrA and gyrB) and topoisomerase IV (parC and parE) to look for mutations associated with resistance (Appendix Table, https://wwwnc.cdc.gov/EID/article/25/7/18-0768-App1.pdf).
These 6 isolates were collected from 6 (4 male and 2 female) patients (Table) with a mean age of 71.7 (SD +11) years. The sources of isolation included bronchoalveolar lavage fluid (n = 2), blood (n = 2), urine (n = 1), and the tip of the central venous catheter (n = 1). All infections were healthcare associated. Two patients had septic shock, and all patients had >1 concurrent medical condition, such as hypertension, diabetes mellitus, or a malignancy. Antimicrobial therapy included piperacillin/tazobactam, trimethoprim/sulfamethoxazole, levofloxacin, or tigecycline, either singly or in combination. None of the patients died of E. bruuniana infection.
To investigate the association between target gene mutations and fluoroquinolone resistance, we examined the mutations present in quinolone resistance-determining regions in these 6 isolates. We did not find nonsynonymous substitutions in the quinolone resistance-determining regions of gyrA, gyrB, parC, and parE, which suggests that mutations in these genes are not the cause of fluoroquinolone resistance.
In summary, our study demonstrates the clinical manifestations of E. bruuniana infection and the molecular characteristics of the pathogen. Because cases in our study were limited in number, further large-scale studies are necessary to investigate the antimicrobial susceptibility patterns of E. bruuniana and elucidate the clinical characteristics and treatment of E. bruuniana infection.