Evidence map›Paper›PMID 20377877›Full record

ArticleBMC microbiology2010

Microarray studies on effects of Pneumocystis carinii infection on global gene expression in alveolar macrophages.

Bi-Hua Cheng, Yunlong Liu, Xiaoling Xuei, Chung-Ping Liao, Debao Lu, Mark E Lasbury, Pamela J Durant, Chao-Hung Lee

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Role of the pioneer transcription factor GATA2 in health and disease.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Bi-Hua ChengDepartment of Obstetrics and Gynecology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Yunlong Liu
Xiaoling Xuei
Chung-Ping Liao
Debao Lu
Mark E Lasbury
Pamela J Durant
Chao-Hung Lee
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineKaohsiung Chang Gung Memorial Hospital · TWTEDA International Cardiovascular Hospital · CN

Funding

Aveolar Macrophage Apoptosis and PneumocystisR01AI062259 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI LEE, CHAO-HUNG · 2006 to 2009
$1.5M
MOLECULAR PATHOLOGY OF PNEUMOCYSTIS PNEUMONIAR01HL065170 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI LEE, CHAO-HUNG · 2001 to 2004
$1.0M
NHLBI NIH HHS R01 HL65170NIAID NIH HHS R01 AI062259
6 · The paper itself

Abstract

backgroundPneumocystis pneumonia is a common opportunistic disease in AIDS patients. The alveolar macrophage is an important effector cell in the clearance of Pneumocystis organisms by phagocytosis. However, both the number and phagocytic activity of alveolar macrophages are decreased in Pneumocystis infected hosts. To understand how Pneumocystis inactivates alveolar macrophages, Affymetrix GeneChip RG-U34A DNA microarrays were used to study the difference in global gene expression in alveolar macrophages from uninfected and Pneumocystis carinii-infected Sprague-Dawley rats.

resultsAnalyses of genes that were affected by Pneumocystis infection showed that many functions in the cells were affected. Antigen presentation, cell-mediated immune response, humoral immune response, and inflammatory response were most severely affected, followed by cellular movement, immune cell trafficking, immunological disease, cell-to-cell signaling and interaction, cell death, organ injury and abnormality, cell signaling, infectious disease, small molecular biochemistry, antimicrobial response, and free radical scavenging. Since rats must be immunosuppressed in order to develop Pneumocystis infection, alveolar macrophages from four rats of the same sex and age that were treated with dexamethasone for the entire eight weeks of the study period were also examined. With a filter of false-discovery rate less than 0.1 and fold change greater than 1.5, 200 genes were found to be up-regulated, and 144 genes were down-regulated by dexamethasone treatment. During Pneumocystis pneumonia, 115 genes were found to be up- and 137 were down-regulated with the same filtering criteria. The top ten genes up-regulated by Pneumocystis infection were Cxcl10, Spp1, S100A9, Rsad2, S100A8, Nos2, RT1-Bb, Lcn2, RT1-Db1, and Srgn with fold changes ranging between 12.33 and 5.34; and the top ten down-regulated ones were Lgals1, Psat1, Tbc1d23, Gsta1, Car5b, Xrcc5, Pdlim1, Alcam, Cidea, and Pkib with fold changes ranging between -4.24 and -2.25.

conclusionsIn order to survive in the host, Pneumocystis organisms change the expression profile of alveolar macrophages. Results of this study revealed that Pneumocystis infection affects many cellular functions leading to reduced number and activity of alveolar macrophages during Pneumocystis pneumonia.

Indexed as

Gene Expression RegulationAnimalsCell DeathDexamethasoneDisease Models, AnimalFemaleGene Expression ProfilingImmunityInflammationMacrophages, AlveolarOligonucleotide Array Sequence AnalysisPhagocytosisPneumocystis cariniiPneumocystis InfectionsPrincipal Component AnalysisRatsDexamethasone

Identifiers

PMID20377877
PMCPMC2858032
OpenAlexW2119119521

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.