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首页> 外文期刊>The Journal of Eukaryotic Microbiology >Dihydropteroate synthase (DHPS) genotyping by PCR-RFLP analysis of Pneumocystis jirovecii repeated isolates from HIV-infected patients: A preliminary study
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Dihydropteroate synthase (DHPS) genotyping by PCR-RFLP analysis of Pneumocystis jirovecii repeated isolates from HIV-infected patients: A preliminary study

机译:通过PCR-RFLP分析从HIV感染患者中反复分离出的吉氏肺孢子虫的二氢蝶呤合酶(DHPS)基因型:初步研究

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摘要

Pneumonia caused by Pneumocystis jirovecii (PcP). fomierly named Pneumocystis carinii f. sp. hominis. remains an important opportunistic infection in AIDS and other immunoconipromised patients, although widespread PcP chemoprophylaxis and highly active antiretroviral therapy (HAART) have reduced the incidence of this disease. Sulpha drugs, mainly the combination trimetoprim/ sulfamctozaxole (co-trimoxazole), are considered to be the key agents in treatment and prophylaxis of this infection. Animal studies have shown that the major target for co-trimoxazole is the enzyme dihydroptcroate synthase (DHPS) a component of the folk acid biosynthesis pathway. Point mutations, at codons 55 and 57, in the DHPS gene of P. jirovecii isolated from AIDS patients have been reported in several studies and linked to prior exposure to sulpha drugs, suggesting possible emergence of sulpha drug resistance . The aim of this study was to determine the DHPS genotype of R jirovecii isolates from repeated induced sputa by PCR-RFLP analysis, in order to assess the stability of the DHPS genotypes.
机译:吉氏肺孢子虫(PcP)引起的肺炎。俗称卡氏肺孢子虫。 sp。原始人尽管广泛的PcP化学预防和高效抗逆转录病毒疗法(HAART)降低了该疾病的发病率,但仍然是AIDS和其他免疫功能低下患者的重要机会感染。磺胺类药物,主要是曲美他滨/磺胺唑(co-trimoxazole)的组合,被认为是治疗和预防这种感染的关键药物。动物研究表明,co-trimoxazole的主要靶标是二氢ptcroate合成酶(DHPS),它是民间酸生物合成途径的组成部分。在几项研究中已经报道了从艾滋病患者中分离出的吉氏疟原虫的DHPS基因中第55和57位密码子的点突变,这些突变与先前接触过磺胺类药物有关,表明可能出现磺胺类药物耐药性。这项研究的目的是通过PCR-RFLP分析从反复诱导的痰中确定R jirovecii分离株的DHPS基因型,以评估DHPS基因型的稳定性。

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