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

• Published in: BMC microbiology Vol. 20; no. 1; p. 3
• Main Authors: Chao, Chien-Chung, Yang, Ruoting, Zhang, Zhiwen, Belinskaya, Tatyana, Chan, Chye-Teik, Miller, Stacy-Ann, Hammamieh, Rasha, Jett, Marti, Ching, Wei-Mei
• Format: Journal Article
• Language: English
• Published: England BioMed Central 06.01.2020; BMC
• Subjects: Animals; Antibiotics; Blood coagulation; cDNA microarray; Cell adhesion & migration; Cell survival; Clotting; Coagulation; Complement; Cytoplasm; Dendritic cells; Disease; Disease Models, Animal; DNA microarrays; Fatty acids; Gene expression; Gene expression profiles; Gene Expression Profiling - methods; Gene Expression Regulation; Gene Regulatory Networks; Genes; Host-Pathogen Interactions; Humans; Immune response; Immune response (cell-mediated); Immunization; Immunoglobulins; In vivo methods and tests; Infections; Mammalian cells; Metabolism; Mice; Mice, Inbred C3H; Oligonucleotide Array Sequence Analysis; Orientia - pathogenicity; Orientia tsutsugamushi infection; Pathogenesis; Pathogens; Polymerase chain reaction; Proteins; Real-Time Polymerase Chain Reaction; Replication; Scrub typhus; Scrub Typhus - genetics; Scrub Typhus - microbiology; Semi-quantitative PCR; Studies; Tryptophan; Typhus; Vaccines; India; Gene expression profiles; cDNA microarray; Scrub typhus; Semi-quantitative PCR; Orientia tsutsugamushi infection
• ISSN: 1471-2180; 1471-2180
• DOI: 10.1186/s12866-019-1684-3

Scrub 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. In 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. The 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.