Update on Dihydropteroate Synthase (DHPS) Mutations in Pneumocystis jirovecii.

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Date

2021-10-13

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de la Horra, Carmen
Friaza, Vicente
Morilla, Ruben
Delgado, Juan
Medrano, Francisco J
Miller, Robert F
de Armas, Yaxsier
Calderon, Enrique J

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MDPI AG
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Abstract

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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MeSH Terms

Humans
Pneumocystis carinii
Pneumonia, Pneumocystis
Sulfamethoxazole
Pneumocystis
Dihydropteroate Synthase
Mutation
Sulfanilamide
Disease Susceptibility

DeCS Terms

Mutación
Preparaciones farmacéuticas
Métodos
Dihidropteroato sintasa
Pneumocystis
Pneumocystis carinii
Neumonía por pneumocystis
Codón
Sulfametoxazol
Neumonía
Terapéutica

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Keywords

dihydropteroate synthase, gene mutations, pneumocystis

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