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Lim, Y. K.

Publications and source records attributed to Lim, Y. K..

2 recordsLinked to original sources

Phytoplankton recruitment of specific microbial assemblages and phylosymbiotic patterns

Phytoplankton and bacteria represent two major pillars of the carbon cycle in marine ecosystems. While their interactions are known to be tightly linked, the specific mechanisms underlying these interactions remain largely unexplored. Evidence of host-specific microbial assemblages could serve as a foundation for studies of detailed host-microbe interactions, yet such research remains limited in phytoplankton. Here, we not only investigate the microbial assemblages of six phytoplankton species, including multiple strains of dinoflagellates and diatoms, but also samples of phytoplankton blooms from the field. Our results reveal the presence of host-specific microbial assemblages in phytoplankton, with members of the core microbial lineages (MCGs) playing pivotal roles in shaping host-specific microbial assemblages and contributing to network structures. Deterministic processes, particularly host genotypes, were the dominant factors shaping microbial assemblages, overriding environmental influences. Consequently, microbial composition reflected the evolutionary relationships of the host species, demonstrating phylosymbiotic patterns. These findings suggest that studying MCGs will be a crucial foundation for investigating specific phytoplankton-microbe interactions and highlight the ecological and evolutionary importance of host-microbial specificity in phytoplankton.

ecology↗

Comparison of New and Old BacT/Alert Aerobic Bottles for Detection of Candida spp.

PurposeA new version of aerobic blood culture media has been developed for the BacT/Alert (bioMerieux) blood culture system. We evaluated the TTD and yeast cell counts in positive blood cultures for each Candida spp. according to changes in media. MethodsIsolates from defibrinated horse blood were inoculated into three types of bottles: the old version of FA Plus (Old FA Plus), New FA Plus, and FN Plus. All bottles were incubated in the BacT/Alert Virtuo blood culture system. The TTD was monitored for each bottle, and yeast cell counts were performed immediately after testing positive, determined via the plate count method. Clinical retrospective data of the candidemia samples before and after aerobic bottle change also were analyzed. ResultsThe mean TTD was 51.2 hours in the Old FA Plus bottles versus 19.5 hours in the New FA Plus bottles (P < 0.001) for Candida glabrata, and standard and clinical strains showed similar results. C. albicans (27.6 to 25.1 hours) and C. guilliermondii (28.8 to 27.3 hours) had shorter TTDs. However, C. auris (25.6 to 28.1 hours) had a longer TTD in the New FA Plus bottle. The retrospective clinical analysis showed a significant decrease in TTD (45.0 to 19.4 hours) for C. glabrata, which is consistent with our simulated study. ConclusionThis study shows that the TTD of C. glabrata was markedly reduced in the New FA Plus bottle due to the optimized growth performance. The reduction of TTD enables faster detection and therapeutic approach for C. glabrata infections.

microbiology↗