<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-24T11:41:19Z</responseDate><request verb="GetRecord" identifier="oai:univendspace.univen.ac.za:11602/2880" metadataPrefix="dim">https://univendspace.univen.ac.za/server/oai/request</request><GetRecord><record><header><identifier>oai:univendspace.univen.ac.za:11602/2880</identifier><datestamp>2025-08-21T01:01:30Z</datestamp><setSpec>com_11602_1926</setSpec><setSpec>com_11602_1914</setSpec><setSpec>com_11602_1897</setSpec><setSpec>com_11602_737</setSpec><setSpec>col_11602_2146</setSpec><setSpec>col_11602_738</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Traore, A. N.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Magwalivha, M.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Potgieter, N.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Molepo, Mmasehlare Stellah</dim:field>
   <dim:field mdschema="dc" element="date">2025</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2025-08-20T04:09:44Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2025-08-20T04:09:44Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2025-05-16</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="citation" lang="en_ZA">Molepo, M.S. 2025. The production and gene polymorphisms of tumor necrosis factor-alpha in patients with tuberculosis in the Vhembe District, Limpopo Province. . . </dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://univendspace.univen.ac.za/handle/11602/2880</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="vancouvercitation" lang="en_ZA">Molepo MS. The production and gene polymorphisms of tumor necrosis factor-alpha in patients with tuberculosis in the Vhembe District, Limpopo Province. []. , 2025 [cited yyyy month dd]. Available from: </dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="apacitation" lang="en_ZA">Molepo, M. S. (2025). &amp;lt;i&amp;gt;The production and gene polymorphisms of tumor necrosis factor-alpha in patients with tuberculosis in the Vhembe District, Limpopo Province&amp;lt;/i&amp;gt;. (). . Retrieved from </dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="chicagocitation" lang="en_ZA">Molepo, Mmasehlare Stellah. &amp;lt;i&amp;gt;&amp;quot;The production and gene polymorphisms of tumor necrosis factor-alpha in patients with tuberculosis in the Vhembe District, Limpopo Province.&amp;quot;&amp;lt;/i&amp;gt; ., , 2025. </dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="ris" lang="en_ZA">&#xd;
TY  - Dissertation&#xd;
AU  - Molepo, Mmasehlare Stellah&#xd;
AB  - Background: Tuberculosis (TB) is an old, irresistible infection caused by Mycobacterium tuberculosis (Mtb). The causative agent has antigens that can stimulate the production of cytokines via the mononuclear phagocyte system. Although mutations in immune-related genes may directly impact a host’s ability to control the infection when exposed to M.tb, the pro-inflammatory cytokine Tumor Necrosis Factor- α is crucial in host defence against TB and granuloma formation. Therefore, this study aimed to assess the production and gene polymorphisms of TNF-α in patients with TB in the Vhembe district, Limpopo province.
Methods: This study recruited thirteen TB patients from three healthcare facilities in the Vhembe district, Limpopo province. Collected samples (sputum) were analysed using the Allplex/Anyplex kit, to detect the presence of Mycobacterium tuberculosis. Serum was collected from the blood and used to determine the levels of TNF-α in the participants, using the DIAsource ELISA kit. Genomic DNA was extracted from blood samples and purified using the Zymo kit from Inqaba Biotec. The purified DNA was quantified using the Nanodrop 8 from Thermo Fischer. The quantified DNA was analyzed by MassARRAY system to sequence various TNF-α SNPs. Data analysis for this study was carried out using the Jamovi software for windows version 2.5.3.
Results: This study found that about 69% of the participants were male and 62% were ≤48 years of age. The majority of the participants (62%) were unemployed. Additionally, 46% of the sputum samples were positive for Mtb. There was a high prevalence (69%) in participants with moderate TNF-α levels. Furthermore, this study found ten SNPs namely: rs10242595, rs1524107, rs1799724, rs1799964, rs1800629, rs1800630, rs1800750, rs3093662, rs309376, and rs361525. The following alleles were reported to have higher frequency than the other: rs10242595 A* (58%), rs1524107 C* (58%), rs1799724 C* (100%), rs1799964 T* (93), rs1800629 G* (88), rs1800630 C* (92), rs1800750 G* (85), rs3093662 A* (73%) and rs361525 A* (100). The allele frequency in rs309376 was evenly distributed G* (50%) and A* (50%).
Conclusion: Our findings suggest that there’s a correlation between TNF-α levels and risk factors and also, there’s a significant association between TNF-α SNPs and TNF-α expression levels.&#xd;
DA  - 2025-05-16&#xd;
DB  - ResearchSpace&#xd;
DP  - Univen&#xd;
KW  - Tuberculosis&#xd;
KW  - Granuloma&#xd;
KW  - Cytokine&#xd;
KW  - Tumor necrosis factor&#xd;
KW  - Polymorphism&#xd;
KW  - Risk factors&#xd;
LK  - https://univendspace.univen.ac.za&#xd;
PY  - 2025&#xd;
T1  - The production and gene polymorphisms of tumor necrosis factor-alpha in patients with tuberculosis in the Vhembe District, Limpopo Province&#xd;
TI  - The production and gene polymorphisms of tumor necrosis factor-alpha in patients with tuberculosis in the Vhembe District, Limpopo Province&#xd;
UR  - &#xd;
ER  - &#xd;
</dim:field>
   <dim:field mdschema="dc" element="description">M.Sc. (Microbiology)</dim:field>
   <dim:field mdschema="dc" element="description">Department of Biochemistry and Microbiology</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">Background: Tuberculosis (TB) is an old, irresistible infection caused by Mycobacterium tuberculosis (Mtb). The causative agent has antigens that can stimulate the production of cytokines via the mononuclear phagocyte system. Although mutations in immune-related genes may directly impact a host’s ability to control the infection when exposed to M.tb, the pro-inflammatory cytokine Tumor Necrosis Factor- α is crucial in host defence against TB and granuloma formation. Therefore, this study aimed to assess the production and gene polymorphisms of TNF-α in patients with TB in the Vhembe district, Limpopo province.
Methods: This study recruited thirteen TB patients from three healthcare facilities in the Vhembe district, Limpopo province. Collected samples (sputum) were analysed using the Allplex/Anyplex kit, to detect the presence of Mycobacterium tuberculosis. Serum was collected from the blood and used to determine the levels of TNF-α in the participants, using the DIAsource ELISA kit. Genomic DNA was extracted from blood samples and purified using the Zymo kit from Inqaba Biotec. The purified DNA was quantified using the Nanodrop 8 from Thermo Fischer. The quantified DNA was analyzed by MassARRAY system to sequence various TNF-α SNPs. Data analysis for this study was carried out using the Jamovi software for windows version 2.5.3.
Results: This study found that about 69% of the participants were male and 62% were ≤48 years of age. The majority of the participants (62%) were unemployed. Additionally, 46% of the sputum samples were positive for Mtb. There was a high prevalence (69%) in participants with moderate TNF-α levels. Furthermore, this study found ten SNPs namely: rs10242595, rs1524107, rs1799724, rs1799964, rs1800629, rs1800630, rs1800750, rs3093662, rs309376, and rs361525. The following alleles were reported to have higher frequency than the other: rs10242595 A* (58%), rs1524107 C* (58%), rs1799724 C* (100%), rs1799964 T* (93), rs1800629 G* (88), rs1800630 C* (92), rs1800750 G* (85), rs3093662 A* (73%) and rs361525 A* (100). The allele frequency in rs309376 was evenly distributed G* (50%) and A* (50%).
Conclusion: Our findings suggest that there’s a correlation between TNF-α levels and risk factors and also, there’s a significant association between TNF-α SNPs and TNF-α expression levels.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent">1 online resource (iii, 81 leaves)</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso">en</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="requires">PDF</dim:field>
   <dim:field mdschema="dc" element="rights">University of Venda</dim:field>
   <dim:field mdschema="dc" element="subject">Tuberculosis</dim:field>
   <dim:field mdschema="dc" element="subject">Granuloma</dim:field>
   <dim:field mdschema="dc" element="subject">Cytokine</dim:field>
   <dim:field mdschema="dc" element="subject">Tumor necrosis factor</dim:field>
   <dim:field mdschema="dc" element="subject">Polymorphism</dim:field>
   <dim:field mdschema="dc" element="subject">Risk factors</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_ZA">UCTD</dim:field>
   <dim:field mdschema="dc" element="title">The production and gene polymorphisms of tumor necrosis factor-alpha in patients with tuberculosis in the Vhembe District, Limpopo Province</dim:field>
   <dim:field mdschema="dc" element="type">Dissertation</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
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