2018
DOI: 10.1002/jcla.22644
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The changes of antifungal susceptibilities caused by the phenotypic switching of Candida species in 229 patients with vulvovaginal candidiasis

Abstract: In the study, C. albicans was the commonest pathogenic species in patients with VVC, in which the phenotypic switching was easy to occur. The susceptible rates of C. albicans to all antifungal drugs were higher than that of non-albicans Candida species. The susceptible rate to fluconazole was all influenced by the phenotypic switching in C. albicans and non-albicans Candida species.

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Cited by 11 publications
(9 citation statements)
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References 26 publications
(32 reference statements)
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“…To avoid this, a new short cross-linked palindromic/CRISPR repeat associated with Cas9 has been used for gene deletions (Min et al, 2019). Tang et al (2019) demonstrated that the majority of C. albicans strains are capable of undergoing the phenomenon of phenotypic switch, which is associated with the manifestation of phenotypic changes at high frequency and a consequence of the action of numerous environmental factors. This phenomenon induces an epigenetic change in colonial morphology.…”
Section: Morphogenesismentioning
confidence: 99%
“…To avoid this, a new short cross-linked palindromic/CRISPR repeat associated with Cas9 has been used for gene deletions (Min et al, 2019). Tang et al (2019) demonstrated that the majority of C. albicans strains are capable of undergoing the phenomenon of phenotypic switch, which is associated with the manifestation of phenotypic changes at high frequency and a consequence of the action of numerous environmental factors. This phenomenon induces an epigenetic change in colonial morphology.…”
Section: Morphogenesismentioning
confidence: 99%
“…Основною перевагою сполук на основі вищезазначеного гетероциклу є те, що вони виявляють низькі показники гострої токсичності одночасно з широким спектром фармакологічної дії. На сьогодні вже створено велику кількість лікарських субстанцій, які містять структурний фрагмент 1,2,4-триазолу, а саме флуконазол [7], вориконазол [8], анастрозол [9], ітраконазол [10], летрозол [11]. Враховуючи вищезазначене пошук та створення нових молекул на основі 1,2,4-триазолу є актуальним завданням сучасної синтетичної та фармацевтичної хімії.…”
Section: запорожский государственный медицинский университет украинаunclassified
“…Thus, there is the question of the creation of new antimicrobial medicines. 1,2,4-Triazole derivatives have already proven themselves [1][2][3][4][5][6][7][8] as compounds with low toxicity and high antimicrobial, antifungal, antiviral, hepatoprotective activity [9][10][11][12][13][14].…”
Section: Issn 2306-8094mentioning
confidence: 99%