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Su, K. K.

Publications and source records attributed to Su, K. K..

2 recordsLinked to original sources

Enterobacterial repetitive intergenic consensus (ERIC)-PCR analysis as a trace for Burkholderia pseudomallei in Myanmar

Melioidosis is a potentially fatal disease caused by Burkholderia pseudomallei, which is endemic in Southeast Asia, including Myanmar. The typeability of enterobacterial repetitive intergenic consensus (ERIC)-PCR assessed for 21 B. pseudomallei, they used the results of sequence types (STs) of the multilocus sequence typing (MLST) method. Among 5 soil and 16 clinical B. pseudomallei isolates, the most significant bands were similar in position but different in minor band formation. ST 90 of two soil strains (Tontae_NMBP001 and Tontae_NMBP002) displayed the same ERIC banding pattern, while ST 56 of two clinical isolates (MMBP005 and MMBP010) from different regions exhibited a single type. The same ST found both clusters in the MLST method. The shared group STs showed four or three satellite variants in the MLST scheme. One novel studied ST (ST 1729) and regarded it as an out-group in the ERIC pattern. ERIC PCR demonstrated high discriminatory power, while MLST provided more discrimination for genetic diversity. MLST requires extensive sequencing and bioinformatics analysis, making it challenging to implement in resource-limited settings. More isolates are needed to validate these findings. Despite its limitations, ERIC PCR represents a valuable and cost-effective alternative to MLST for molecular typing of B. pseudomallei in resource-limited settings.

microbiology↗

Distribution of soil and clinical Burkholderia pseudomallei isolates in Myanmar by using MLST

Burkholderia pseudomallei can be identified as Gram-negative bacillus without spore-forming in an environment such as soil and stagnant water. Human factors and climate changes make the incidence of melioidosis higher. Soil with high moisture and clay-rich is a suitable residence for B. pseudomallei. Twenty-one isolates of B. pseudomallei were collected and performed by multilocus sequence typing. Among them, eight novel sequence types (STs) of B. pseudomallei were found, while the rest show known STs. Interestingly, ST 56 from two patients was identified as the same region, while ST 90 showed local and global distribution. Among six ST 90 B. pseudomallei, the three isolates were from soil and patients. Clinical ST 90 isolates were traced in the same region as soil ST 90 isolates. Those isolates may correlate with each other by using multilocus sequence typing (MLST) cost-effectively. However, it still needs to prove its correct relatedness. This study pointed out the reasonable assumption of Burkholderia pseudomallei for local and global distribution in Myanmar.

microbiology↗