Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG Pathways

Nosocomial (hospital-acquired) infections remain a serious challenge for health systems. The reason for this lies not only in the local imperfection of medical practices and protocols. The frequency of infection with antibiotic-resistant strains of bacteria is growing every year, both in developed a...

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Main Authors: Mikhail V. Slizen, Oxana V. Galzitskaya
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/21/7839
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author Mikhail V. Slizen
Oxana V. Galzitskaya
author_facet Mikhail V. Slizen
Oxana V. Galzitskaya
author_sort Mikhail V. Slizen
collection DOAJ
description Nosocomial (hospital-acquired) infections remain a serious challenge for health systems. The reason for this lies not only in the local imperfection of medical practices and protocols. The frequency of infection with antibiotic-resistant strains of bacteria is growing every year, both in developed and developing countries. In this work, a pangenome and comparative analysis of 201 genomes of <i>Staphylococcus aureus</i>, <i>Enterobacter</i> spp., <i>Pseudomonas aeruginosa</i>, and <i>Mycoplasma</i> spp. was performed on the basis of high-level functional annotations—KEGG pathways and KEGG modules. The first three organisms are serious nosocomial pathogens, often exhibiting multidrug resistance. Analysis of KEGG modules revealed methicillin resistance in 25% of <i>S. aureus</i> strains and resistance to carbapenems in 21% of <i>Enterobacter</i> spp. strains. <i>P. aeruginosa</i> has a wide range of unique efflux systems. One hundred percent of the analyzed strains have at least two drug resistance systems, and 75% of the strains have seven. Each of the organisms has a characteristic set of metabolic features, whose impact on drug resistance can be considered in future studies. Comparing the genomes of nosocomial pathogens with each other and with <i>Mycoplasma</i> genomes can expand our understanding of the versatility of certain metabolic features and mechanisms of drug resistance.
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spelling doaj.art-f4677a4d64e14d39815d3ef8df3a7d6e2023-11-20T18:10:46ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-10-012121783910.3390/ijms21217839Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG PathwaysMikhail V. Slizen0Oxana V. Galzitskaya1Institute of Protein Research, Russian Academy of Sciences, 142290 Pushchino, Moscow Region, RussiaInstitute of Protein Research, Russian Academy of Sciences, 142290 Pushchino, Moscow Region, RussiaNosocomial (hospital-acquired) infections remain a serious challenge for health systems. The reason for this lies not only in the local imperfection of medical practices and protocols. The frequency of infection with antibiotic-resistant strains of bacteria is growing every year, both in developed and developing countries. In this work, a pangenome and comparative analysis of 201 genomes of <i>Staphylococcus aureus</i>, <i>Enterobacter</i> spp., <i>Pseudomonas aeruginosa</i>, and <i>Mycoplasma</i> spp. was performed on the basis of high-level functional annotations—KEGG pathways and KEGG modules. The first three organisms are serious nosocomial pathogens, often exhibiting multidrug resistance. Analysis of KEGG modules revealed methicillin resistance in 25% of <i>S. aureus</i> strains and resistance to carbapenems in 21% of <i>Enterobacter</i> spp. strains. <i>P. aeruginosa</i> has a wide range of unique efflux systems. One hundred percent of the analyzed strains have at least two drug resistance systems, and 75% of the strains have seven. Each of the organisms has a characteristic set of metabolic features, whose impact on drug resistance can be considered in future studies. Comparing the genomes of nosocomial pathogens with each other and with <i>Mycoplasma</i> genomes can expand our understanding of the versatility of certain metabolic features and mechanisms of drug resistance.https://www.mdpi.com/1422-0067/21/21/7839KEGG modulesKEGG pathwaysdrug resistance<i>Staphylococcus aureus</i><i>Enterobacter</i> spp.<i>Pseudomonas aeruginosa</i>
spellingShingle Mikhail V. Slizen
Oxana V. Galzitskaya
Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG Pathways
International Journal of Molecular Sciences
KEGG modules
KEGG pathways
drug resistance
<i>Staphylococcus aureus</i>
<i>Enterobacter</i> spp.
<i>Pseudomonas aeruginosa</i>
title Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG Pathways
title_full Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG Pathways
title_fullStr Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG Pathways
title_full_unstemmed Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG Pathways
title_short Comparative Analysis of Proteomes of a Number of Nosocomial Pathogens by KEGG Modules and KEGG Pathways
title_sort comparative analysis of proteomes of a number of nosocomial pathogens by kegg modules and kegg pathways
topic KEGG modules
KEGG pathways
drug resistance
<i>Staphylococcus aureus</i>
<i>Enterobacter</i> spp.
<i>Pseudomonas aeruginosa</i>
url https://www.mdpi.com/1422-0067/21/21/7839
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