Interleukin-22 Polymorphisms in Plasmodium falciparum-Infected Malaria Patients. (19th February 2020)
- Record Type:
- Journal Article
- Title:
- Interleukin-22 Polymorphisms in Plasmodium falciparum-Infected Malaria Patients. (19th February 2020)
- Main Title:
- Interleukin-22 Polymorphisms in Plasmodium falciparum-Infected Malaria Patients
- Authors:
- Aljarba, Nada H.
Al-Anazi, Mashael R.
Shafeai, Mohammed I.
Rudiny, Fuad H.
Bin Dajem, Saad M.
Alothaid, Hani
Darraj, Majid
Alkahtani, Saad
Alghamdi, Jahad
Al-Ahdal, Mohammed N.
Al-Qahtani, Ahmed A. - Other Names:
- Migliorini Paola Academic Editor.
- Abstract:
- Abstract : Background and Objectives . Malaria infection, caused by Plasmodium falciparum, is the most lethal and frequently culminates in severe clinical complications. Interleukin-22 (IL-22) has been implicated in several diseases including malaria. The objective of this study was to investigate the role of IL-22 gene polymorphisms in P . falciparum infection. Material and Methods . Ten single-nucleotide polymorphisms (SNPs), rs976748, rs1179246, rs2046068, rs1182844, rs2227508, rs2227513, rs2227478, rs2227481, rs2227491, and rs2227483, of IL-22 gene were genotyped through PCR-based assays of 250 P . falciparum -infected patients and 200 healthy controls. In addition, a luciferase reporter assay was done to assess the role of the rs2227513 SNP in IL - 22 gene promoter activity. Results . We found that the rs2227481 TT genotype (odds ratio 0.254, confidence interval = 0.097-0.663, P = 0.002 ) and the T allele is associated with protection against P . falciparum malaria as well as the rs2227483 AT genotype (odds ratio 0.375, confidence interval = 0.187-0.754, P = 0.004 ). The haplotype A-T-T of rs1179246, rs1182844, and rs976748 was statistically more frequent in the control group (frequency 41%, P = 0.034 ) as well as the haplotype A-G of rs2046068 and rs2227491 (frequency 49.4%, P = 0.041 ). The variant rs2227513 G allele had a statistically higher activity (P < 0.0001 ) with the luciferase reporter assay. Conclusion . The study suggests that IL-22 polymorphisms inAbstract : Background and Objectives . Malaria infection, caused by Plasmodium falciparum, is the most lethal and frequently culminates in severe clinical complications. Interleukin-22 (IL-22) has been implicated in several diseases including malaria. The objective of this study was to investigate the role of IL-22 gene polymorphisms in P . falciparum infection. Material and Methods . Ten single-nucleotide polymorphisms (SNPs), rs976748, rs1179246, rs2046068, rs1182844, rs2227508, rs2227513, rs2227478, rs2227481, rs2227491, and rs2227483, of IL-22 gene were genotyped through PCR-based assays of 250 P . falciparum -infected patients and 200 healthy controls. In addition, a luciferase reporter assay was done to assess the role of the rs2227513 SNP in IL - 22 gene promoter activity. Results . We found that the rs2227481 TT genotype (odds ratio 0.254, confidence interval = 0.097-0.663, P = 0.002 ) and the T allele is associated with protection against P . falciparum malaria as well as the rs2227483 AT genotype (odds ratio 0.375, confidence interval = 0.187-0.754, P = 0.004 ). The haplotype A-T-T of rs1179246, rs1182844, and rs976748 was statistically more frequent in the control group (frequency 41%, P = 0.034 ) as well as the haplotype A-G of rs2046068 and rs2227491 (frequency 49.4%, P = 0.041 ). The variant rs2227513 G allele had a statistically higher activity (P < 0.0001 ) with the luciferase reporter assay. Conclusion . The study suggests that IL-22 polymorphisms in rs2227481 and rs2227483 could contribute to protection against P . falciparum malaria. Also, the G allele of rs2227513, located in the promoter region of IL - 22 gene, could be essential for higher expression levels of IL-22 cytokine. … (more)
- Is Part Of:
- Mediators of inflammation. Volume 2020(2020)
- Journal:
- Mediators of inflammation
- Issue:
- Volume 2020(2020)
- Issue Display:
- Volume 2020, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 2020
- Issue:
- 2020
- Issue Sort Value:
- 2020-2020-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-02-19
- Subjects:
- Inflammation -- Mediators -- Periodicals
Biological response modifiers -- Periodicals
Inflammation (Pathologie) -- Médiateurs
Immunomodulateurs
Biological response modifiers
Inflammation -- Mediators
Immunology
Autacoids
Immunologic Factors
Cell Adhesion Molecules
Cell Communication
Cytokines
Inflammation
Periodicals
Electronic journals
616.0473 - Journal URLs:
- https://www.hindawi.com/journals/mi/ ↗
- DOI:
- 10.1155/2020/5193723 ↗
- Languages:
- English
- ISSNs:
- 0962-9351
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 12940.xml