Current insights into the biology and pathogenesis of Pneumocystis pneumonia
Key Points Pneumocystis pneumonia (PCP) remains the most prevalent opportunistic infection in patients with AIDS and is a significant cause of severe pneumonia in immunocompromised patients with cancer, organ transplant recipients or those receiving immunosuppressant medications. Pneumocystis is an...
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description | Key Points
Pneumocystis
pneumonia (PCP) remains the most prevalent opportunistic infection in patients with AIDS and is a significant cause of severe pneumonia in immunocompromised patients with cancer, organ transplant recipients or those receiving immunosuppressant medications.
Pneumocystis
is an intractable fungal pathogen classified phylogenetically with the Ascomycetes.
Pneumocystis
has pathways involved in cell-cycle control, signal transduction and metabolism that are analogous to the pathways in these yeast.
Pneumocystis
has a unique life cycle alternating between small trophic forms and cysts, which contain 2, 4 or 8 intracystic bodies. The airborne route of transmission is currently the favoured model for the spread of infection.
Pneumocystis
interacts with the lung epithelium and immune cells of the lower respiratory tract, resulting in inflammation, which is hazardous to the host. This is a complex interaction involving surface antigens of the organism and host surfactant proteins, adhesion molecules, macrophages, neutrophils, lymphocytes, and cytokine and chemokine responses.
Drug targets for the treatment of PCP include metabolic pathways for dihydropteroate synthase (DHPS) and dihydrofolate reductase (DHFR), DNA and protein synthesis inhibition, sterol metabolism, cytochrome
b
complex and cell-wall construction through inhibition of the GSC1 glucan synthetase.
Mutations in DHPS, DHFR, and cytochrome
b
have raised the concern of emerging resistance to the medications currently in use. The efforts of the
Pneumocystis
research community have contributed substantially to the current understanding of the complex biology of
Pneumocystis
and the intricate association with the host. Continued research is essential to continue investigating the biology of this organism in the hope of developing novel treatment strategies for PCP.
Pneumonia caused by the fungus
Pneumocystis
is the most prevalent opportunistic infection in patients with AIDS. Here, Charles Thomas and Andrew Limper review the latest knowledge on the biology and pathogenesis of this opportunistic fungal pathogen.
The fungal infection
Pneumocystis
pneumonia is the most prevalent opportunistic infection in patients with AIDS. Although the analysis of this opportunistic fungal pathogen has been hindered by the inability to isolate it in pure culture, the use of molecular techniques and genomic analysis have brought insights into its complex cell biology. Analysis of the intricate relationsh |
doi_str_mv | 10.1038/nrmicro1621 |
format | Article |
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Pneumocystis
pneumonia (PCP) remains the most prevalent opportunistic infection in patients with AIDS and is a significant cause of severe pneumonia in immunocompromised patients with cancer, organ transplant recipients or those receiving immunosuppressant medications.
Pneumocystis
is an intractable fungal pathogen classified phylogenetically with the Ascomycetes.
Pneumocystis
has pathways involved in cell-cycle control, signal transduction and metabolism that are analogous to the pathways in these yeast.
Pneumocystis
has a unique life cycle alternating between small trophic forms and cysts, which contain 2, 4 or 8 intracystic bodies. The airborne route of transmission is currently the favoured model for the spread of infection.
Pneumocystis
interacts with the lung epithelium and immune cells of the lower respiratory tract, resulting in inflammation, which is hazardous to the host. This is a complex interaction involving surface antigens of the organism and host surfactant proteins, adhesion molecules, macrophages, neutrophils, lymphocytes, and cytokine and chemokine responses.
Drug targets for the treatment of PCP include metabolic pathways for dihydropteroate synthase (DHPS) and dihydrofolate reductase (DHFR), DNA and protein synthesis inhibition, sterol metabolism, cytochrome
b
complex and cell-wall construction through inhibition of the GSC1 glucan synthetase.
Mutations in DHPS, DHFR, and cytochrome
b
have raised the concern of emerging resistance to the medications currently in use. The efforts of the
Pneumocystis
research community have contributed substantially to the current understanding of the complex biology of
Pneumocystis
and the intricate association with the host. Continued research is essential to continue investigating the biology of this organism in the hope of developing novel treatment strategies for PCP.
Pneumonia caused by the fungus
Pneumocystis
is the most prevalent opportunistic infection in patients with AIDS. Here, Charles Thomas and Andrew Limper review the latest knowledge on the biology and pathogenesis of this opportunistic fungal pathogen.
The fungal infection
Pneumocystis
pneumonia is the most prevalent opportunistic infection in patients with AIDS. Although the analysis of this opportunistic fungal pathogen has been hindered by the inability to isolate it in pure culture, the use of molecular techniques and genomic analysis have brought insights into its complex cell biology. Analysis of the intricate relationship between
Pneumocystis
and the host lung during infection has revealed that the attachment of
Pneumocystis
to the alveolar epithelium promotes the transition of the organism from the trophic to the cyst form. It also revealed that
Pneumocystis
infection elicits the production of inflammatory mediators, culminating in lung injury and impaired gas exchange. Here we discuss these and other recent findings relating to the biology and pathogenesis of this intractable fungus.</description><identifier>ISSN: 1740-1526</identifier><identifier>EISSN: 1740-1534</identifier><identifier>DOI: 10.1038/nrmicro1621</identifier><identifier>PMID: 17363968</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Antifungal Agents - pharmacology ; Antifungal Agents - therapeutic use ; Antigens, Fungal - analysis ; Antigens, Surface - analysis ; Biology ; Biomedical and Life Sciences ; Cell Cycle ; Cysts ; Cytokines - metabolism ; Dosage and administration ; Drug Resistance, Fungal ; Drug therapy ; Fungi ; Gas exchange ; Genetic aspects ; Genome, Fungal ; Genomes ; Health aspects ; Humans ; Immune system ; Immunosuppressive agents ; Infections ; Infectious Diseases ; Laboratory animals ; Life Sciences ; Lung - microbiology ; Lung - pathology ; Medical Microbiology ; Microbiology ; Organisms ; Parasitology ; Pathogens ; Pneumocystis ; Pneumocystis - cytology ; Pneumocystis - drug effects ; Pneumocystis - pathogenicity ; Pneumocystis - physiology ; Pneumocystis carinii ; Pneumocystis carinii pneumonia ; Pneumonia ; Pneumonia, Pneumocystis - drug therapy ; Pneumonia, Pneumocystis - immunology ; Pneumonia, Pneumocystis - microbiology ; Pneumonia, Pneumocystis - pathology ; Pulmonary Alveoli - microbiology ; review-article ; Risk factors ; Signal Transduction ; Taxonomy ; Virology</subject><ispartof>Nature reviews. Microbiology, 2007-04, Vol.5 (4), p.298-308</ispartof><rights>Springer Nature Limited 2007</rights><rights>COPYRIGHT 2007 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Apr 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-7be040aa732f931b9ef421c9afc7be1df2f62a9afcc4f49a721409f505adfa893</citedby><cites>FETCH-LOGICAL-c475t-7be040aa732f931b9ef421c9afc7be1df2f62a9afcc4f49a721409f505adfa893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nrmicro1621$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nrmicro1621$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17363968$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thomas, Charles F</creatorcontrib><creatorcontrib>Limper, Andrew H</creatorcontrib><title>Current insights into the biology and pathogenesis of Pneumocystis pneumonia</title><title>Nature reviews. Microbiology</title><addtitle>Nat Rev Microbiol</addtitle><addtitle>Nat Rev Microbiol</addtitle><description>Key Points
Pneumocystis
pneumonia (PCP) remains the most prevalent opportunistic infection in patients with AIDS and is a significant cause of severe pneumonia in immunocompromised patients with cancer, organ transplant recipients or those receiving immunosuppressant medications.
Pneumocystis
is an intractable fungal pathogen classified phylogenetically with the Ascomycetes.
Pneumocystis
has pathways involved in cell-cycle control, signal transduction and metabolism that are analogous to the pathways in these yeast.
Pneumocystis
has a unique life cycle alternating between small trophic forms and cysts, which contain 2, 4 or 8 intracystic bodies. The airborne route of transmission is currently the favoured model for the spread of infection.
Pneumocystis
interacts with the lung epithelium and immune cells of the lower respiratory tract, resulting in inflammation, which is hazardous to the host. This is a complex interaction involving surface antigens of the organism and host surfactant proteins, adhesion molecules, macrophages, neutrophils, lymphocytes, and cytokine and chemokine responses.
Drug targets for the treatment of PCP include metabolic pathways for dihydropteroate synthase (DHPS) and dihydrofolate reductase (DHFR), DNA and protein synthesis inhibition, sterol metabolism, cytochrome
b
complex and cell-wall construction through inhibition of the GSC1 glucan synthetase.
Mutations in DHPS, DHFR, and cytochrome
b
have raised the concern of emerging resistance to the medications currently in use. The efforts of the
Pneumocystis
research community have contributed substantially to the current understanding of the complex biology of
Pneumocystis
and the intricate association with the host. Continued research is essential to continue investigating the biology of this organism in the hope of developing novel treatment strategies for PCP.
Pneumonia caused by the fungus
Pneumocystis
is the most prevalent opportunistic infection in patients with AIDS. Here, Charles Thomas and Andrew Limper review the latest knowledge on the biology and pathogenesis of this opportunistic fungal pathogen.
The fungal infection
Pneumocystis
pneumonia is the most prevalent opportunistic infection in patients with AIDS. Although the analysis of this opportunistic fungal pathogen has been hindered by the inability to isolate it in pure culture, the use of molecular techniques and genomic analysis have brought insights into its complex cell biology. Analysis of the intricate relationship between
Pneumocystis
and the host lung during infection has revealed that the attachment of
Pneumocystis
to the alveolar epithelium promotes the transition of the organism from the trophic to the cyst form. It also revealed that
Pneumocystis
infection elicits the production of inflammatory mediators, culminating in lung injury and impaired gas exchange. Here we discuss these and other recent findings relating to the biology and pathogenesis of this intractable fungus.</description><subject>Animals</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antifungal Agents - therapeutic use</subject><subject>Antigens, Fungal - analysis</subject><subject>Antigens, Surface - analysis</subject><subject>Biology</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Cycle</subject><subject>Cysts</subject><subject>Cytokines - metabolism</subject><subject>Dosage and administration</subject><subject>Drug Resistance, Fungal</subject><subject>Drug therapy</subject><subject>Fungi</subject><subject>Gas exchange</subject><subject>Genetic aspects</subject><subject>Genome, Fungal</subject><subject>Genomes</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunosuppressive agents</subject><subject>Infections</subject><subject>Infectious Diseases</subject><subject>Laboratory animals</subject><subject>Life Sciences</subject><subject>Lung - microbiology</subject><subject>Lung - pathology</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>Organisms</subject><subject>Parasitology</subject><subject>Pathogens</subject><subject>Pneumocystis</subject><subject>Pneumocystis - cytology</subject><subject>Pneumocystis - drug effects</subject><subject>Pneumocystis - pathogenicity</subject><subject>Pneumocystis - physiology</subject><subject>Pneumocystis carinii</subject><subject>Pneumocystis carinii pneumonia</subject><subject>Pneumonia</subject><subject>Pneumonia, Pneumocystis - drug therapy</subject><subject>Pneumonia, Pneumocystis - immunology</subject><subject>Pneumonia, Pneumocystis - microbiology</subject><subject>Pneumonia, Pneumocystis - pathology</subject><subject>Pulmonary Alveoli - microbiology</subject><subject>review-article</subject><subject>Risk factors</subject><subject>Signal Transduction</subject><subject>Taxonomy</subject><subject>Virology</subject><issn>1740-1526</issn><issn>1740-1534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkUtr3DAUhUVJaB7tqvviJpBNMqleluzlMOQFA-2iXQuNfeVRsKWpJC_m31dTD0kaAkEL3aP73YMuB6EvBF8TzKrvLgy2CZ4ISj6gYyI5npGS8YOnmoojdBLjI8a0LCX9iI6IZILVojpGy8UYArhUWBdtt04xF8kXaQ3Fyvred9tCu7bY6LT2HTiINhbeFD8djINvtjFlvfknnNWf0KHRfYTP-_sU_b69-bW4ny1_3D0s5stZw2WZZnIFmGOtJaOmZmRVg-GUNLU2TW6R1lAjqN7Jhhtea0kJx7Upcalbo6uanaKLyXcT_J8RYlKDjQ30vXbgx6gkppIzgd8FKRasFHQHnr0CH_0YXF5CUcoFz44kQ-cT1OkelHXGp6CbnaOak6qqSyYJz9T1G1Q-LeScvANj8_t_A5fTQA4xxgBGbYIddNgqgtUuYfUi4Ux_3f90XA3QPrP7SDNwNQExt1wH4XmVt_2-TbjTaQzw5PeS-Qs2zb0g</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Thomas, Charles F</creator><creator>Limper, Andrew H</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070401</creationdate><title>Current insights into the biology and pathogenesis of Pneumocystis pneumonia</title><author>Thomas, Charles F ; Limper, Andrew H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-7be040aa732f931b9ef421c9afc7be1df2f62a9afcc4f49a721409f505adfa893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Antifungal Agents - pharmacology</topic><topic>Antifungal Agents - therapeutic use</topic><topic>Antigens, Fungal - analysis</topic><topic>Antigens, Surface - analysis</topic><topic>Biology</topic><topic>Biomedical and Life Sciences</topic><topic>Cell Cycle</topic><topic>Cysts</topic><topic>Cytokines - metabolism</topic><topic>Dosage and administration</topic><topic>Drug Resistance, Fungal</topic><topic>Drug therapy</topic><topic>Fungi</topic><topic>Gas exchange</topic><topic>Genetic aspects</topic><topic>Genome, Fungal</topic><topic>Genomes</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Immune system</topic><topic>Immunosuppressive agents</topic><topic>Infections</topic><topic>Infectious Diseases</topic><topic>Laboratory animals</topic><topic>Life Sciences</topic><topic>Lung - microbiology</topic><topic>Lung - pathology</topic><topic>Medical Microbiology</topic><topic>Microbiology</topic><topic>Organisms</topic><topic>Parasitology</topic><topic>Pathogens</topic><topic>Pneumocystis</topic><topic>Pneumocystis - cytology</topic><topic>Pneumocystis - drug effects</topic><topic>Pneumocystis - pathogenicity</topic><topic>Pneumocystis - physiology</topic><topic>Pneumocystis carinii</topic><topic>Pneumocystis carinii pneumonia</topic><topic>Pneumonia</topic><topic>Pneumonia, Pneumocystis - drug therapy</topic><topic>Pneumonia, Pneumocystis - immunology</topic><topic>Pneumonia, Pneumocystis - microbiology</topic><topic>Pneumonia, Pneumocystis - pathology</topic><topic>Pulmonary Alveoli - microbiology</topic><topic>review-article</topic><topic>Risk factors</topic><topic>Signal Transduction</topic><topic>Taxonomy</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomas, Charles F</creatorcontrib><creatorcontrib>Limper, Andrew H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature reviews. Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomas, Charles F</au><au>Limper, Andrew H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current insights into the biology and pathogenesis of Pneumocystis pneumonia</atitle><jtitle>Nature reviews. Microbiology</jtitle><stitle>Nat Rev Microbiol</stitle><addtitle>Nat Rev Microbiol</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>5</volume><issue>4</issue><spage>298</spage><epage>308</epage><pages>298-308</pages><issn>1740-1526</issn><eissn>1740-1534</eissn><abstract>Key Points
Pneumocystis
pneumonia (PCP) remains the most prevalent opportunistic infection in patients with AIDS and is a significant cause of severe pneumonia in immunocompromised patients with cancer, organ transplant recipients or those receiving immunosuppressant medications.
Pneumocystis
is an intractable fungal pathogen classified phylogenetically with the Ascomycetes.
Pneumocystis
has pathways involved in cell-cycle control, signal transduction and metabolism that are analogous to the pathways in these yeast.
Pneumocystis
has a unique life cycle alternating between small trophic forms and cysts, which contain 2, 4 or 8 intracystic bodies. The airborne route of transmission is currently the favoured model for the spread of infection.
Pneumocystis
interacts with the lung epithelium and immune cells of the lower respiratory tract, resulting in inflammation, which is hazardous to the host. This is a complex interaction involving surface antigens of the organism and host surfactant proteins, adhesion molecules, macrophages, neutrophils, lymphocytes, and cytokine and chemokine responses.
Drug targets for the treatment of PCP include metabolic pathways for dihydropteroate synthase (DHPS) and dihydrofolate reductase (DHFR), DNA and protein synthesis inhibition, sterol metabolism, cytochrome
b
complex and cell-wall construction through inhibition of the GSC1 glucan synthetase.
Mutations in DHPS, DHFR, and cytochrome
b
have raised the concern of emerging resistance to the medications currently in use. The efforts of the
Pneumocystis
research community have contributed substantially to the current understanding of the complex biology of
Pneumocystis
and the intricate association with the host. Continued research is essential to continue investigating the biology of this organism in the hope of developing novel treatment strategies for PCP.
Pneumonia caused by the fungus
Pneumocystis
is the most prevalent opportunistic infection in patients with AIDS. Here, Charles Thomas and Andrew Limper review the latest knowledge on the biology and pathogenesis of this opportunistic fungal pathogen.
The fungal infection
Pneumocystis
pneumonia is the most prevalent opportunistic infection in patients with AIDS. Although the analysis of this opportunistic fungal pathogen has been hindered by the inability to isolate it in pure culture, the use of molecular techniques and genomic analysis have brought insights into its complex cell biology. Analysis of the intricate relationship between
Pneumocystis
and the host lung during infection has revealed that the attachment of
Pneumocystis
to the alveolar epithelium promotes the transition of the organism from the trophic to the cyst form. It also revealed that
Pneumocystis
infection elicits the production of inflammatory mediators, culminating in lung injury and impaired gas exchange. Here we discuss these and other recent findings relating to the biology and pathogenesis of this intractable fungus.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>17363968</pmid><doi>10.1038/nrmicro1621</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Antifungal Agents - pharmacology Antifungal Agents - therapeutic use Antigens, Fungal - analysis Antigens, Surface - analysis Biology Biomedical and Life Sciences Cell Cycle Cysts Cytokines - metabolism Dosage and administration Drug Resistance, Fungal Drug therapy Fungi Gas exchange Genetic aspects Genome, Fungal Genomes Health aspects Humans Immune system Immunosuppressive agents Infections Infectious Diseases Laboratory animals Life Sciences Lung - microbiology Lung - pathology Medical Microbiology Microbiology Organisms Parasitology Pathogens Pneumocystis Pneumocystis - cytology Pneumocystis - drug effects Pneumocystis - pathogenicity Pneumocystis - physiology Pneumocystis carinii Pneumocystis carinii pneumonia Pneumonia Pneumonia, Pneumocystis - drug therapy Pneumonia, Pneumocystis - immunology Pneumonia, Pneumocystis - microbiology Pneumonia, Pneumocystis - pathology Pulmonary Alveoli - microbiology review-article Risk factors Signal Transduction Taxonomy Virology |
title | Current insights into the biology and pathogenesis of Pneumocystis pneumonia |
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