Evidence map›Paper›PMID 31906849›Full record

ArticleBMC microbiology2020

Temporal analysis of mRNA expression profiles in Orientia infected C3HeB/FeJ mouse.

Chien-Chung Chao, Ruoting Yang, Zhiwen Zhang, Tatyana Belinskaya, Chye-Teik Chan, Stacy-Ann Miller, Rasha Hammamieh, Marti Jett, Wei-Mei Ching

Abstract read
In one paragraph

Article in BMC microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. 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

9 authors.

Chien-Chung ChaoViral and Rickettsial Diseases Department, Infectious Diseases Directorate, Naval Medical Research Center, 503 Robert Grant Ave, RM3N71, Silver Spring, MD, 20910, USA. chien-chung.chao.civ@mail.mil.ORCID 0000-0003-3567-3419
Ruoting YangIntegrative Systems Biology, US Army Medical Research and Material Command, USACEHR, Ft Detrick, Ft Federick, MD, USA.
Zhiwen ZhangUniformed Services University of the Health Sciences, Bethesda, MD, USA.
Tatyana BelinskayaUniformed Services University of the Health Sciences, Bethesda, MD, USA.
Chye-Teik ChanUniformed Services University of the Health Sciences, Bethesda, MD, USA.
Stacy-Ann MillerIntegrative Systems Biology, US Army Medical Research and Material Command, USACEHR, Ft Detrick, Ft Federick, MD, USA.
Rasha HammamiehIntegrative Systems Biology, US Army Medical Research and Material Command, USACEHR, Ft Detrick, Ft Federick, MD, USA.
Marti JettIntegrative Systems Biology, US Army Medical Research and Material Command, USACEHR, Ft Detrick, Ft Federick, MD, USA.
Wei-Mei ChingViral and Rickettsial Diseases Department, Infectious Diseases Directorate, Naval Medical Research Center, 503 Robert Grant Ave, RM3N71, Silver Spring, MD, 20910, USA.

Funding

Naval Medical Research Center 6000.RAD1.J.A0311
6 · The paper itself

Abstract

backgroundScrub typhus causes up to 35% mortality if left untreated. One billion people living in the endemic regions are at risk. In spite of its heavy disease burden in some of the most populated areas in the world, there is no vaccine available. Although the disease can be effectively treated by proper antibiotics, timely and accurate diagnosis remains a challenge. Orientia tsutsugamushi infects a variety of mammalian cells in vitro and replicates in the cytoplasm of the infected cells. Microarray analysis has been used extensively to study host-pathogen interactions in in vitro models to understand pathogenesis. However there is a lack of in vivo studies.

resultsIn this study, C3HeB/FeJ (C3H) mice were infected by O. tsutsugamushi via the intraperitoneal route and monitored gene expression at 10 different time points post infection. We observed two distinct types of expression profiles in the genes that we analyzed. There are two valleys (4-18 h and 2-4 days) with low number of differentially expressed genes (DEG) with three peaks with high number of DEG at 2 h, 1-day and 7-day post infection. Further analysis revealed that pathways like complement and coagulation cascade, and blood clotting cascade pathways showed significant global changes throughout entire time course. Real time quantitative Polymerase Chain Reaction (RT-qPCR) confirmed the change of expression for genes involved in complement and coagulation cascade. These results suggested dynamic regulation of the complement and coagulation cascades throughout most of the time post infection while some other specific pathways, such as fatty acid metabolism and tryptophan metabolism, are turned on or off at certain times post infection.

conclusionsThe findings highlight the complex interconnection among all different biological pathways. It is conceivable that specific pathways such as cell growth control and cell development in the host are affected by Orientia in the initial phase of infection for Orientia to grow intracellularly. Once Orientia is replicating successfully inside the host as infection progresses, the infection could activate pathways involved in cellular immune responses to defend for host cell survival and try to eliminate the pathogen.

Indexed as

Gene Regulatory NetworksAnimalsDisease Models, AnimalGene Expression ProfilingGene Expression RegulationHost-Pathogen InteractionsHumansMiceMice, Inbred C3HOligonucleotide Array Sequence AnalysisOrientiaReal-Time Polymerase Chain ReactionScrub TyphuscDNA microarrayGene expression profilesOrientia tsutsugamushi infectionScrub typhusSemi-quantitative PCR

Identifiers

PMID31906849
PMCPMC6945539

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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.