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Kurakado, S.

Publications and source records attributed to Kurakado, S..

2 recordsLinked to original sources

Determination of effective meropenem and gentamicin doses in a silkworm infection model using a clinical Klebsiella aerogenes isolate

Klebsiella aerogenes, a member of the Enterobacteriaceae, is a causative agent of healthcare-associated infections, and outbreaks caused by drug-resistant K. aerogenes have been reported worldwide. The range of antimicrobial agents available for treating infections caused by carbapenem-resistant K. aerogenes is limited. While in vivo animal experiments using clinical K. aerogenes isolates to evaluate antimicrobial therapy could facilitate selection of the most effective treatment, conducting infection experiments involving large numbers of mammals such as mice is challenging due to ethical concerns related to animal welfare. Silkworms are invertebrates increasingly used as experimental models for infectious disease research to evaluate antimicrobial efficacy. In this study, we aimed to establish a silkworm infection model using a clinical K. aerogenes isolate to evaluate its utility for determining effective antimicrobial doses. K. aerogenes strains were isolated from a patient at a Japanese hospital, and a silkworm infection model was established using the clinical isolate. The non-metallo-beta-lactamase-producing strain K. aerogenes TUM25562, isolated from a patient with a complicated urinary tract infection, was susceptible to meropenem (MEPM) and gentamicin (GM) in vitro. During treatment, additional isolates with increased resistance to MEPM and subsequently to both MEPM and GM emerged. K. aerogenes TUM25562 caused dose-dependent mortality in silkworms. Treatment with clinically equivalent weight-based doses of MEPM or GM did not cure the infected silkworms. The median effective (ED50) doses of MEPM and GM were therefore investigated using the silkworm infection model. Administration of higher doses corresponding to four times the ED50 significantly prolonged the survival of infected silkworms. These results suggest that a silkworm infection model using clinical K. aerogenes isolates may provide a practical approach for evaluating antimicrobial efficacy and determining effective antimicrobial doses.

microbiology↗

Role of Atg1 in morphologic changes of the pathogenic fungus Trichosporon asahii

Trichosporon asahii is a dimorphic fungus that causes severe invasive fungal infections, particularly in patients with neutropenia. Depending on nutrient availability, T. asahii exists in yeast, hyphae, or arthroconidia forms. Autophagy, a cellular degradation pathway that removes old or damaged organelles, is essential for the survival of many eukaryotic organisms under nutrient-limited conditions. Atg1 is a key regulator of the early phases of autophagy, especially under nitrogen starvation. The role of Atg1 in regulating morphology, stress resistance, or virulence in T. asahii, however, remains poorly understood. Here, we generated three atg1 gene-deficient T. asahii mutants and investigated their phenotypic characteristics to reveal the role of Atg1 in T. asahii. The atg1 gene-deficient mutants exhibited no growth defects under high-temperature or various chemical stress conditions, including antifungal drugs. The mutants exhibited an increased proportion of hyphal cells when cultured in Sabouraud dextrose broth (SB), a medium commonly used for fungi. On the other hand, no morphologic differences were observed between the parent strain and the atg1 gene-deficient mutants under a nitrogen-limited condition. The virulence of these atg1 gene-deficient mutants was maintained in a silkworm infection model. Furthermore, all three generated atg1 gene-deficient mutants exhibited consistent phenotypes. Our findings suggest that while Atg1 does not play a major role in stress tolerance or virulence in T. asahii, it plays a role in regulating its dimorphic morphologic changes.

microbiology↗