Update on Dihydropteroate Synthase (DHPS) Mutations in Pneumocystis jirovecii

被引:14
作者
de la Horra, Carmen [1 ]
Friaza, Vicente [1 ,2 ]
Morilla, Ruben [1 ,3 ]
Delgado, Juan [1 ]
Medrano, Francisco J. [1 ,2 ,4 ]
Miller, Robert F. [5 ,6 ]
de Armas, Yaxsier [7 ,8 ]
Calderon, Enrique J. [1 ,2 ,4 ]
机构
[1] Univ Seville, Inst Biomed Sevilla, Hosp Univ Virgen Rocio, CSIC, Seville 41013, Spain
[2] Ctr Invest Biomed Red Epidemiol & Salud Publ CIBE, Madrid 28029, Spain
[3] Univ Seville, Dept Enfermeria, Seville 41009, Spain
[4] Univ Seville, Dept Med, Seville 41009, Spain
[5] UCL, Inst Global Hlth, London WC1E 6JB, England
[6] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, London WC1E 7HT, England
[7] Inst Trop Med Pedro Kouri, Hosp Ctr, Dept Clin Microbiol Diagnost, Havana 11400, Cuba
[8] Inst Trop Med Pedro Kouri, Hosp Ctr, Pathol Dept, Havana 11400, Cuba
关键词
pneumocystis; dihydropteroate synthase; gene mutations; HIV-INFECTED PATIENTS; COMBINED ANTIRETROVIRAL THERAPY; REDUCTASE GENE-MUTATIONS; PCR-RFLP ANALYSIS; REAL-TIME PCR; SULFAMETHOXAZOLE RESISTANCE; IMMUNOCOMPROMISED PATIENTS; SULFONE PROPHYLAXIS; INTERHUMAN TRANSMISSION; MOLECULAR EVIDENCE;
D O I
10.3390/jof7100856
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A Pneumocystis jirovecii is one of the most important microorganisms that cause pneumonia in immunosupressed individuals. The guideline for treatment and prophylaxis of Pneumocystis pneumonia (PcP) is the use of a combination of sulfa drug-containing trimethroprim and sulfamethoxazole. In the absence of a reliable method to culture Pneumocystis, molecular techniques have been developed to detect mutations in the dihydropteroate synthase gene, the target of sulfa drugs, where mutations are related to sulfa resistance in other microorganisms. The presence of dihydropteroate synthase (DHPS) mutations has been described at codon 55 and 57 and found almost around the world. In the current work, we analyzed the most common methods to identify these mutations, their geographical distribution around the world, and their clinical implications. In addition, we describe new emerging DHPS mutations. Other aspects, such as the possibility of transmitting Pneumocystis mutated organisms between susceptible patients is also described, as well as a brief summary of approaches to study these mutations in a heterologous expression system
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页数:15
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