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Expression Level of the mip, pmp18D, and ompA Genes in Chlamydia abortus Isolated from Aborted Ewes
Eman Dhahir Arif1, Nahla Mohammad Saeed1, Shwan Kamal Rachid2
1Department of Microbiology, College of Veterinary Medicine, University of Sulaimani, Sulaymaniyah, Iraq.
Abstract:
In this manuscript, we report the proteins macrophage infectivity potentiator (mip, CAB080), major outer membrane protein (momp, CAB048), and polymorphic outer membrane protein (pmp18D, CAB776) that are expressed in different times of pregnancy in mice infected with Chlamydia abortus. Enzootic abortion of ewes (EAE) by C. abortus, an obligate intracellular pathogen, is a critical zoonotic disease-causing significant economic loss to livestock farming globally. This study was carried out for the detection and characterization of macrophage infectivity potentiator (mip, CAB080), major outer membrane protein (momp, CAB048), and polymorphic outer membrane protein (pmp18D, CAB776) using RT-qPCR. These proteins are believed to be expressed as virulence factors in C. abortus isolated from aborted ewes. BALB/c mice (pregnant and nonpregnant) were used as an animal model to be injected intraperitoneally with C. abortus culture in Vero cells since the endometrial lymphoid tissues of these animals resembles that of ewes. Also, the short duration of pregnancy in mice makes them a suitable animal model for obstetric studies. Tissue samples were taken from the mice after 10, 15, and 20 days of pregnancy to compare the expression of the genes mip, pmp18D, and ompA. Transcription level was quantified using RT-qPCR, the GAPDH transcription quantification, as a normalization signal. Abortion occurred in pregnant mice, and apparent differences between the transcriptional levels of the mip, pmp18D, and ompA genes in the samples taken during different time intervals of pregnancy were not observed (p > 0.05). The result indicated that the three bacterial genes, mip, pmp18D, and ompA, play a role as virulence factors in abortion and are differentially expressed in pregnant and nonpregnant animals. Inactivation of the genes is suggested to confirm the hypothesis.
Insights
Chlamydia abortus infection causes abortion in mice. The study investigated virulence factors macrophage infectivity potentiator (mip) and polymorphic outer membrane protein (pmp18D) gene expression during pregnancy. Their differential expression suggests a role in abortion.
Area of Science:
- Veterinary Microbiology
- Infectious Diseases
- Bacterial Pathogenesis
Background:
- Enzootic abortion of ewes (EAE) caused by *Chlamydia abortus* is a significant zoonotic disease in livestock.
- Virulence factors of *C. abortus*, such as macrophage infectivity potentiator (mip) and polymorphic outer membrane protein (pmp18D), are crucial for pathogenesis.
- Understanding the expression of these factors during pregnancy is vital for controlling EAE.
Purpose of the Study:
- To detect and characterize the expression of *mip*, *momp*, and *pmp18D* genes in *C. abortus* during different stages of pregnancy in a mouse model.
- To investigate the role of these genes as virulence factors in *C. abortus*-induced abortion.
- To compare gene expression in pregnant versus nonpregnant animals.
Main Methods:
- BALB/c mice (pregnant and nonpregnant) were infected with *C. abortus*.
- Tissue samples were collected at 10, 15, and 20 days post-infection.
- Quantitative reverse transcription PCR (RT-qPCR) was used to measure the transcription levels of *mip*, *pmp18D*, and *ompA* genes, with GAPDH as a reference.
Main Results:
- Abortion occurred in pregnant mice infected with *C. abortus*.
- No significant differences in the transcriptional levels of *mip*, *pmp18D*, and *ompA* were observed across different pregnancy time points (p > 0.05).
- The study indicated differential expression of *mip*, *pmp18D*, and *ompA* between pregnant and nonpregnant animals.
Conclusions:
- The bacterial genes *mip*, *pmp18D*, and *ompA* play a role as virulence factors in *C. abortus*-induced abortion.
- These genes are differentially expressed in pregnant and nonpregnant animals, suggesting a role in the disease's progression.
- Further studies involving gene inactivation are recommended to confirm their specific roles.
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