Effects of TNF-α and IL-10-819 T>C single nucleotide polymorphisms on urogenital schistosomiasis in preschool children in Zimbabwe.

Schistosoma haematobium cytokines polymorphisms protective immunity susceptibility

Journal

African journal of laboratory medicine
ISSN: 2225-2002
Titre abrégé: Afr J Lab Med
Pays: South Africa
ID NLM: 101603205

Informations de publication

Date de publication:
2021
Historique:
received: 22 11 2019
accepted: 28 01 2021
entrez: 19 5 2021
pubmed: 20 5 2021
medline: 20 5 2021
Statut: epublish

Résumé

Knowledge gaps exist between host genetic factors and susceptibility to schistosomiasis. This study determined cytokine levels and single nucleotide polymorphisms of tumour necrosis factor (TNF)-α (rs1800629) and interleukin (IL)-10 (rs1800871) and their possible impact on susceptibility to schistosomiasis in preschool-age children in the Madziva area of Shamva district, Mashonaland Central province, Zimbabwe. Urogenital schistosomiasis was diagnosed using the urine filtration method, while a sandwich enzyme-linked immunosorbent assay was used for cytokine level determination. The survey was done in August 2015 and reinfection levels post treatment were assessed at 3, 6 and 12 months. Amplification refractory mutation system polymerase chain reaction with visualisation on 2% agarose gel electrophoresis was used for genotyping. Schistosomiasis prevalence was found to be 10.5% (59/563). Reinfections were detected in only six children at 3 months and only one was reinfected at 12 months. There were no significant differences in TNF-α-308 G/A allele or genotype frequencies between the Higher TNF-α levels and lower IL-10 levels are potentially protective against schistosomiasis infection. The IL-10-819 TT genotype is potentially protective against infection through its association with lower IL-10 levels.

Sections du résumé

BACKGROUND BACKGROUND
Knowledge gaps exist between host genetic factors and susceptibility to schistosomiasis.
OBJECTIVE OBJECTIVE
This study determined cytokine levels and single nucleotide polymorphisms of tumour necrosis factor (TNF)-α (rs1800629) and interleukin (IL)-10 (rs1800871) and their possible impact on susceptibility to schistosomiasis in preschool-age children in the Madziva area of Shamva district, Mashonaland Central province, Zimbabwe.
METHODS METHODS
Urogenital schistosomiasis was diagnosed using the urine filtration method, while a sandwich enzyme-linked immunosorbent assay was used for cytokine level determination. The survey was done in August 2015 and reinfection levels post treatment were assessed at 3, 6 and 12 months. Amplification refractory mutation system polymerase chain reaction with visualisation on 2% agarose gel electrophoresis was used for genotyping.
RESULTS RESULTS
Schistosomiasis prevalence was found to be 10.5% (59/563). Reinfections were detected in only six children at 3 months and only one was reinfected at 12 months. There were no significant differences in TNF-α-308 G/A allele or genotype frequencies between the
CONCLUSION CONCLUSIONS
Higher TNF-α levels and lower IL-10 levels are potentially protective against schistosomiasis infection. The IL-10-819 TT genotype is potentially protective against infection through its association with lower IL-10 levels.

Identifiants

pubmed: 34007813
doi: 10.4102/ajlm.v10i1.1138
pii: AJLM-10-1138
pmc: PMC8111665
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1138

Informations de copyright

© 2021. The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.

Références

PLoS Negl Trop Dis. 2014 Aug 14;8(8):e3014
pubmed: 25121489
Immunol Cell Biol. 2007 Feb-Mar;85(2):148-54
pubmed: 17160074
Trop Med Int Health. 2018 Jan;23(1):45-52
pubmed: 29131459
PLoS Pathog. 2011 Aug;7(8):e1002171
pubmed: 21829367
J Infect Dis. 2004 Dec 1;190(11):2020-30
pubmed: 15529268
Acta Derm Venereol. 2008;88(2):113-6
pubmed: 18311435
Asian Pac J Trop Med. 2017 Nov;10(11):1065-1071
pubmed: 29203103
Parasit Vectors. 2011 Feb 21;4:21
pubmed: 21338486
J Parasitol Res. 2012;2012:353768
pubmed: 22655171
Tropenmed Parasitol. 1982 Dec;33(4):227-8
pubmed: 7164164
Zhonghua Zhong Liu Za Zhi. 2010 Nov;32(11):845-9
pubmed: 21223691
PLoS Negl Trop Dis. 2018 Feb 8;12(2):e0006144
pubmed: 29420537
Rev Inst Med Trop Sao Paulo. 1972 Nov-Dec;14(6):397-400
pubmed: 4675644
Int J Parasitol. 2004 Jan;34(1):27-36
pubmed: 14711587
Am J Trop Med Hyg. 2006 Oct;75(4):720-6
pubmed: 17038701
Ann Trop Med Parasitol. 1985 Jun;79(3):287-99
pubmed: 4026440
Biol Res. 2001;34(3-4):237-41
pubmed: 11715861
Parasit Vectors. 2014 Apr 01;7:153
pubmed: 24690282
Ann Trop Med Parasitol. 1983 Dec;77(6):587-94
pubmed: 6660966
Am J Trop Med Hyg. 2015 May;92(5):945-51
pubmed: 25758654
Parasit Vectors. 2019 Sep 2;12(1):427
pubmed: 31477172

Auteurs

Amos Marume (A)

Department of Infection Prevention and Control, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.
Paraclinical Department, Faculty of Veterinary Sciences, University of Zimbabwe, Harare, Zimbabwe.

Theresa Chimponda (T)

Department of Biochemistry, Faculty of Science, University of Zimbabwe, Harare, Zimbabwe.

Arthur Vengesai (A)

Department of Biochemistry, Faculty of Science, University of Zimbabwe, Harare, Zimbabwe.

Caroline Mushayi (C)

Department of Biochemistry, Faculty of Science, University of Zimbabwe, Harare, Zimbabwe.

Jaclyn Mann (J)

Department of Infection Prevention and Control, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.

Takafira Mduluza (T)

Department of Infection Prevention and Control, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.
Department of Biochemistry, Faculty of Science, University of Zimbabwe, Harare, Zimbabwe.

Classifications MeSH