Clonal Diversity of Candida auris, Candida blankii, and Kodamaea ohmeri Isolated from Septicemia and Otomycosis in Bangladesh as Determined by Multilocus Sequence Typing

Author:

Sathi Fardousi Akter1ORCID,Aung Meiji Soe2ORCID,Paul Shyamal Kumar3,Nasreen Syeda Anjuman1,Haque Nazia1,Roy Sangjukta1,Ahmed Salma4,Alam Mohammad Monirul5,Khan Shahed6,Rabbany Mohammad Arif7,Biswas Joy Prokas8,Kobayashi Nobumichi2ORCID

Affiliation:

1. Department of Microbiology, Mymensingh Medical College, Mymensingh 2200, Bangladesh

2. Department of Hygiene, School of Medicine, Sapporo Medical University, Sapporo 060-8556, Japan

3. Netrokona Medical College, Netrokona 2400, Bangladesh

4. Mugda Medical College, Dhaka 1214, Bangladesh

5. Department of ENT, Mymensingh Medical College Hospital, Mymensingh 2200, Bangladesh

6. Department of Oral Microbiology, Mymensingh Medical College Hospital, Mymensingh 2200, Bangladesh

7. Department of Neonatology, Mymensingh Medical College Hospital, Mymensingh 2200, Bangladesh

8. Department of Pathology, Netrokona Medical College, Netrokona 2400, Bangladesh

Abstract

Candida auris, Candida blankii, and Kodamaea ohmeri have been regarded as emerging fungal pathogens that can cause infections with high mortality. For genotyping of C. auris, a multilocus sequence typing (MLST) scheme based on four locus sequences has been reported, while there is no typing scheme for C. blankii and K. ohmeri. In the present study, the existing MLST scheme of C. auris was modified by adding more locus types deduced from sequence data available in the GenBank database. Furthermore, MLST schemes of C. blankii and K. ohmeri were developed using the four cognate loci (ITS, RPB1, RPB2, D1/D2) and similar sequence regions to those of C. auris. These MLST schemes were applied to identify the ST (sequence type) of clinical isolates of C. auris (n = 7), C. blankii (n = 9), and K. ohmeri (n = 6), derived from septicemia or otomycosis in Bangladesh in 2021. All the C. auris isolates were classified into a single ST (ST5) and clade I, having a Y132F substitution in ERG11p, which is associated with azole resistance. Similarly, all the C. blankii isolates belonged to a single type (ST1). In contrast, six K. ohmeri isolates were assigned to five types (ST1-ST5), suggesting its higher genetic diversity. These findings revealed the availability of MLST schemes for these three fungal species for understanding their clonal diversity among clinical isolates.

Publisher

MDPI AG

Subject

Plant Science,Ecology, Evolution, Behavior and Systematics,Microbiology (medical)

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