Host susceptibility genes of asymptomatic malaria from South Central Timor, Eastern Indonesia
Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was t...
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Published in | Parasitology research (1987) Vol. 122; no. 1; pp. 61 - 75 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Berlin/Heidelberg
Springer Berlin Heidelberg
01.01.2023
Springer Springer Nature B.V |
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Abstract | Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was to investigate the association between both cytokine and adhesion molecule genotypes with susceptibility to malaria infection in humans. Ten cytokine polymorphism loci (
IL4
+
33
,
IL4-590
,
IL6-174
,
IL10-1082
,
IL10-1035
,
IL12p40
,
TNF-238
,
TNF-308
,
TNF-1031
, and
TNF-β
) and three adhesion molecule polymorphism loci (
CD36
exon 10,
ICAM-1 Kilifi
, and
ICAM-1
exon 6) were genotyped using PCR–RFLP analysis. We conducted this study on 178 asymptomatic malaria subjects and 122 uninfected subjects. Results showed that certain
CD36
exon 10 and
IL10
-3575 polymorphisms were associated with asymptomatic infection. The heterozygous (GT) and homozygous (GG) genotypes for
CD36
exon 10 are associated with an increased risk of malaria infection. On the other hand, the homozygous genotype (AA) for
IL10
-3575 reduced the risk of asymptomatic malaria infection. No significant differences were found for the other polymorphisms studied. We also found that a polymorphism in
CD36
exon 10 was strongly associated with asymptomatic malaria caused specifically by
Plasmodium vivax
. These findings suggest that the G allele of
CD36
exon 10 is associated with an increased risk of asymptomatic malaria infection. On the other hand, the genotype AA for
IL10
-3575 was associated with a reduced risk of malaria infection. |
---|---|
AbstractList | Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was to investigate the association between both cytokine and adhesion molecule genotypes with susceptibility to malaria infection in humans. Ten cytokine polymorphism loci (IL4 + 33, IL4-590, IL6-174, IL10-1082, IL10-1035, IL12p40, TNF-238, TNF-308, TNF-1031, and TNF-[beta]) and three adhesion molecule polymorphism loci (CD36 exon 10, ICAM-1 Kilifi, and ICAM-1 exon 6) were genotyped using PCR-RFLP analysis. We conducted this study on 178 asymptomatic malaria subjects and 122 uninfected subjects. Results showed that certain CD36 exon 10 and IL10-3575 polymorphisms were associated with asymptomatic infection. The heterozygous (GT) and homozygous (GG) genotypes for CD36 exon 10 are associated with an increased risk of malaria infection. On the other hand, the homozygous genotype (AA) for IL10-3575 reduced the risk of asymptomatic malaria infection. No significant differences were found for the other polymorphisms studied. We also found that a polymorphism in CD36 exon 10 was strongly associated with asymptomatic malaria caused specifically by Plasmodium vivax. These findings suggest that the G allele of CD36 exon 10 is associated with an increased risk of asymptomatic malaria infection. On the other hand, the genotype AA for IL10-3575 was associated with a reduced risk of malaria infection. Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was to investigate the association between both cytokine and adhesion molecule genotypes with susceptibility to malaria infection in humans. Ten cytokine polymorphism loci (IL4 + 33, IL4-590, IL6-174, IL10-1082, IL10-1035, IL12p40, TNF-238, TNF-308, TNF-1031, and TNF-β) and three adhesion molecule polymorphism loci (CD36 exon 10, ICAM-1 Kilifi, and ICAM-1 exon 6) were genotyped using PCR–RFLP analysis. We conducted this study on 178 asymptomatic malaria subjects and 122 uninfected subjects. Results showed that certain CD36 exon 10 and IL10-3575 polymorphisms were associated with asymptomatic infection. The heterozygous (GT) and homozygous (GG) genotypes for CD36 exon 10 are associated with an increased risk of malaria infection. On the other hand, the homozygous genotype (AA) for IL10-3575 reduced the risk of asymptomatic malaria infection. No significant differences were found for the other polymorphisms studied. We also found that a polymorphism in CD36 exon 10 was strongly associated with asymptomatic malaria caused specifically by Plasmodium vivax. These findings suggest that the G allele of CD36 exon 10 is associated with an increased risk of asymptomatic malaria infection. On the other hand, the genotype AA for IL10-3575 was associated with a reduced risk of malaria infection. Abstract Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was to investigate the association between both cytokine and adhesion molecule genotypes with susceptibility to malaria infection in humans. Ten cytokine polymorphism loci (IL4 + 33, IL4-590, IL6-174, IL10-1082, IL10-1035, IL12p40, TNF-238, TNF-308, TNF-1031, and TNF-β) and three adhesion molecule polymorphism loci (CD36 exon 10, ICAM-1 Kilifi, and ICAM-1 exon 6) were genotyped using PCR–RFLP analysis. We conducted this study on 178 asymptomatic malaria subjects and 122 uninfected subjects. Results showed that certain CD36 exon 10 and IL10-3575 polymorphisms were associated with asymptomatic infection. The heterozygous (GT) and homozygous (GG) genotypes for CD36 exon 10 are associated with an increased risk of malaria infection. On the other hand, the homozygous genotype (AA) for IL10-3575 reduced the risk of asymptomatic malaria infection. No significant differences were found for the other polymorphisms studied. We also found that a polymorphism in CD36 exon 10 was strongly associated with asymptomatic malaria caused specifically by Plasmodium vivax. These findings suggest that the G allele of CD36 exon 10 is associated with an increased risk of asymptomatic malaria infection. On the other hand, the genotype AA for IL10-3575 was associated with a reduced risk of malaria infection. Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was to investigate the association between both cytokine and adhesion molecule genotypes with susceptibility to malaria infection in humans. Ten cytokine polymorphism loci ( IL4 + 33 , IL4-590 , IL6-174 , IL10-1082 , IL10-1035 , IL12p40 , TNF-238 , TNF-308 , TNF-1031 , and TNF-β ) and three adhesion molecule polymorphism loci ( CD36 exon 10, ICAM-1 Kilifi , and ICAM-1 exon 6) were genotyped using PCR–RFLP analysis. We conducted this study on 178 asymptomatic malaria subjects and 122 uninfected subjects. Results showed that certain CD36 exon 10 and IL10 -3575 polymorphisms were associated with asymptomatic infection. The heterozygous (GT) and homozygous (GG) genotypes for CD36 exon 10 are associated with an increased risk of malaria infection. On the other hand, the homozygous genotype (AA) for IL10 -3575 reduced the risk of asymptomatic malaria infection. No significant differences were found for the other polymorphisms studied. We also found that a polymorphism in CD36 exon 10 was strongly associated with asymptomatic malaria caused specifically by Plasmodium vivax . These findings suggest that the G allele of CD36 exon 10 is associated with an increased risk of asymptomatic malaria infection. On the other hand, the genotype AA for IL10 -3575 was associated with a reduced risk of malaria infection. Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was to investigate the association between both cytokine and adhesion molecule genotypes with susceptibility to malaria infection in humans. Ten cytokine polymorphism loci (IL4 + 33, IL4-590, IL6-174, IL10-1082, IL10-1035, IL12p40, TNF-238, TNF-308, TNF-1031, and TNF-β) and three adhesion molecule polymorphism loci (CD36 exon 10, ICAM-1 Kilifi, and ICAM-1 exon 6) were genotyped using PCR-RFLP analysis. We conducted this study on 178 asymptomatic malaria subjects and 122 uninfected subjects. Results showed that certain CD36 exon 10 and IL10-3575 polymorphisms were associated with asymptomatic infection. The heterozygous (GT) and homozygous (GG) genotypes for CD36 exon 10 are associated with an increased risk of malaria infection. On the other hand, the homozygous genotype (AA) for IL10-3575 reduced the risk of asymptomatic malaria infection. No significant differences were found for the other polymorphisms studied. We also found that a polymorphism in CD36 exon 10 was strongly associated with asymptomatic malaria caused specifically by Plasmodium vivax. These findings suggest that the G allele of CD36 exon 10 is associated with an increased risk of asymptomatic malaria infection. On the other hand, the genotype AA for IL10-3575 was associated with a reduced risk of malaria infection.Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria infection. Polymorphisms in host genes have been correlated with malaria infection in both African and Asian regions. The purpose of this study was to investigate the association between both cytokine and adhesion molecule genotypes with susceptibility to malaria infection in humans. Ten cytokine polymorphism loci (IL4 + 33, IL4-590, IL6-174, IL10-1082, IL10-1035, IL12p40, TNF-238, TNF-308, TNF-1031, and TNF-β) and three adhesion molecule polymorphism loci (CD36 exon 10, ICAM-1 Kilifi, and ICAM-1 exon 6) were genotyped using PCR-RFLP analysis. We conducted this study on 178 asymptomatic malaria subjects and 122 uninfected subjects. Results showed that certain CD36 exon 10 and IL10-3575 polymorphisms were associated with asymptomatic infection. The heterozygous (GT) and homozygous (GG) genotypes for CD36 exon 10 are associated with an increased risk of malaria infection. On the other hand, the homozygous genotype (AA) for IL10-3575 reduced the risk of asymptomatic malaria infection. No significant differences were found for the other polymorphisms studied. We also found that a polymorphism in CD36 exon 10 was strongly associated with asymptomatic malaria caused specifically by Plasmodium vivax. These findings suggest that the G allele of CD36 exon 10 is associated with an increased risk of asymptomatic malaria infection. On the other hand, the genotype AA for IL10-3575 was associated with a reduced risk of malaria infection. |
Audience | Academic |
Author | Hutagalung, Jontari Dewi, Rita Marleta Sunarno, Sunarno Chaijaroenkul, Wanna Handayani, Sarwo Na-Bangchang, Kesara Fitri, Nyoman Tjitra, Emiliana |
Author_xml | – sequence: 1 givenname: Nyoman surname: Fitri fullname: Fitri, Nyoman organization: Chulabhorn International College of Medicine (CICM), Thammasat University (Rangsit Campus), National Institute of Health Research and Development, Ministry of Health, Republic of Indonesia – sequence: 2 givenname: Kesara surname: Na-Bangchang fullname: Na-Bangchang, Kesara organization: Chulabhorn International College of Medicine (CICM), Thammasat University (Rangsit Campus) – sequence: 3 givenname: Emiliana surname: Tjitra fullname: Tjitra, Emiliana organization: St Carolus School of Health Sciences, Faculty of Medicine, Malahayati University – sequence: 4 givenname: Jontari surname: Hutagalung fullname: Hutagalung, Jontari organization: National Institute of Health Research and Development, Ministry of Health, Republic of Indonesia – sequence: 5 givenname: Sunarno surname: Sunarno fullname: Sunarno, Sunarno organization: National Research and Innovation Agency – sequence: 6 givenname: Rita Marleta surname: Dewi fullname: Dewi, Rita Marleta organization: National Research and Innovation Agency – sequence: 7 givenname: Sarwo surname: Handayani fullname: Handayani, Sarwo organization: National Research and Innovation Agency – sequence: 8 givenname: Wanna surname: Chaijaroenkul fullname: Chaijaroenkul, Wanna email: wn_ap39@yahoo.com organization: Chulabhorn International College of Medicine (CICM), Thammasat University (Rangsit Campus) |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36284023$$D View this record in MEDLINE/PubMed |
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Keywords | Host genetic factor Adhesion molecule Malaria Cytokine |
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Snippet | Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria... Abstract Host genetic factors, such as the genes for various cytokines and adhesion molecules, play a significant role in determining susceptibility to malaria... |
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SubjectTerms | adhesion alleles Analysis Asymptomatic Asymptomatic infection Biomedical and Life Sciences Biomedicine CD36 antigen Cytokines Cytokines - genetics Disease susceptibility exons Gene polymorphism Genes Genetic aspects Genetic factors Genetic polymorphisms Genetic Predisposition to Disease Genetic research Genotype genotyping Health aspects heterozygosity homozygosity Humans Immunology Indonesia Indonesia - epidemiology Infection Infections Intercellular adhesion molecule 1 Intercellular Adhesion Molecule-1 - genetics Interleukin 10 Interleukin-10 - genetics interleukin-12 interleukin-4 Interleukin-4 - genetics Malaria Malaria - epidemiology Medical Microbiology Microbiology Plasmodium vivax Polymorphism Polymorphism, Single Nucleotide risk risk reduction Timor Tumor necrosis factor |
Title | Host susceptibility genes of asymptomatic malaria from South Central Timor, Eastern Indonesia |
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