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  1. Article ; Online: Comparative analysis of the vaginal microbiome of pregnant women with either Trichomonas vaginalis or Chlamydia trachomatis.

    Masha, Simon Chengo / Owuor, Collins / Ngoi, Joyce Mwongeli / Cools, Piet / Sanders, Eduard J / Vaneechoutte, Mario / Crucitti, Tania / de Villiers, Etienne P

    PloS one

    2019  Volume 14, Issue 12, Page(s) e0225545

    Abstract: Background: Although the significance of the human vaginal microbiome for health and disease is increasingly acknowledged, there is paucity of data on the differences in the composition of the vaginal microbiome upon infection with different sexually ... ...

    Abstract Background: Although the significance of the human vaginal microbiome for health and disease is increasingly acknowledged, there is paucity of data on the differences in the composition of the vaginal microbiome upon infection with different sexually transmitted pathogens.
    Method: The composition of the vaginal bacterial community of women with Trichomonas vaginalis (TV, N = 18) was compared to that of women with Chlamydia trachomatis (CT, N = 14), and to that of controls (N = 21) (women negative for TV, CT and bacterial vaginosis). The vaginal bacterial composition was determined using high throughput sequencing with the Ion 16S metagenomics kit of the variable regions 2, 4 and 8 of the bacterial 16S ribosomal RNA gene from the vaginal swab DNA extract of the women. QIIME and R package "Phyloseq" were used to assess the α- and β-diversity and absolute abundance of the 16S rRNA gene per sample in the three groups. Differences in taxa at various levels were determined using the independent T-test.
    Results: A total of 545 operational taxonomic units (OTUs) were identified in all the three groups of which 488 occurred in all three groups (core OTUs). Bacterial α-diversity, by both Simpson's and Shannon's indices, was significantly higher, (p = 0.056) and (p = 0.001) respectively, among women with either TV or CT than among controls (mean α-diversity TV-infected > CT-infected > Controls). At the genus level, women infected with TV had a significantly (p < 0.01) higher abundance of Parvimonas and Prevotella species compared to both controls and CT-infected women, whereas women infected with CT had a significantly (p < 0.05) higher abundance of Anaerococcus, Collinsella, Corynebacterium and Dialister.
    Conclusion: The vaginal microbiomes of TV and CT-infected women were markedly different from each other and from women without TV and CT. Future studies should determine whether the altered microbiomes are merely markers of disease, or whether they actively contribute to the pathology of the two genital infections.
    MeSH term(s) Adolescent ; Adult ; Chlamydia Infections/immunology ; Chlamydia Infections/microbiology ; Chlamydia trachomatis/genetics ; Chlamydia trachomatis/immunology ; Chlamydia trachomatis/isolation & purification ; DNA, Bacterial/isolation & purification ; Female ; Humans ; Microbiota/genetics ; Microbiota/immunology ; Pregnancy ; Pregnancy Complications, Infectious/immunology ; Pregnancy Complications, Infectious/microbiology ; RNA, Ribosomal, 16S/genetics ; Trichomonas Vaginitis/immunology ; Trichomonas Vaginitis/microbiology ; Trichomonas vaginalis/genetics ; Trichomonas vaginalis/immunology ; Trichomonas vaginalis/isolation & purification ; Vagina/microbiology ; Young Adult
    Chemical Substances DNA, Bacterial ; RNA, Ribosomal, 16S
    Language English
    Publishing date 2019-12-12
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0225545
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Longitudinal Analysis of Infant Stool Bacteria Communities Before and After Acute Febrile Malaria and Artemether-Lumefantrine Treatment.

    Mandal, Rabindra K / Crane, Rosie J / Berkley, James A / Gumbi, Wilson / Wambua, Juliana / Ngoi, Joyce Mwongeli / Ndungu, Francis M / Schmidt, Nathan W

    The Journal of infectious diseases

    2019  Volume 220, Issue 4, Page(s) 687–698

    Abstract: Background: Gut microbiota were recently shown to impact malaria disease progression and outcome, and prior studies have shown that Plasmodium infections increase the likelihood of enteric bacteria causing systemic infections. Currently, it is not known ...

    Abstract Background: Gut microbiota were recently shown to impact malaria disease progression and outcome, and prior studies have shown that Plasmodium infections increase the likelihood of enteric bacteria causing systemic infections. Currently, it is not known whether Plasmodium infection impacts human gut microbiota as a prelude to bacteremia or whether antimalarials affect gut microbiota. Our goal was to determine to what degree Plasmodium infections and antimalarial treatment affect human gut microbiota.
    Methods: One hundred Kenyan infants underwent active surveillance for malaria from birth to 10 months of age. Each malaria episode was treated with artemether-lumefantrine (AL). Any other treatments, including antibiotics, were recorded. Stool samples were collected on an approximately biweekly basis. Ten children were selected on the basis of stool samples having been collected before (n = 27) or after (n = 17) a malaria episode and without antibiotics having been administered between collections. These samples were subjected to 16S ribosomal ribonucleic acid gene (V3-V4 region) sequencing.
    Results: Bacterial community network analysis revealed no obvious differences in the before and after malaria/AL samples, which was consistent with no difference in alpha and beta diversity and taxonomic analysis at the family and genus level with one exception. At the sequence variant (SV) level, akin to bacterial species, only 1 of the top 100 SVs was significantly different. In addition, predicted metagenome analysis revealed no significant difference in metagenomic capacity between before and after malaria/AL samples. The number of malaria episodes, 1 versus 2, explained significant variation in gut microbiota composition of the infants.
    Conclusions: In-depth bioinformatics analysis of stool bacteria has revealed for the first time that human malaria episode/AL treatment have minimal effects on gut microbiota in Kenyan infants.
    MeSH term(s) Antimalarials/administration & dosage ; Artemether, Lumefantrine Drug Combination/administration & dosage ; Computational Biology ; Dysbiosis ; Feces/microbiology ; Female ; Fever ; Gastrointestinal Microbiome ; Humans ; Infant ; Kenya ; Longitudinal Studies ; Malaria/drug therapy ; Malaria/pathology ; Male ; Plasmodium/drug effects ; RNA, Ribosomal, 16S/genetics
    Chemical Substances Antimalarials ; Artemether, Lumefantrine Drug Combination ; RNA, Ribosomal, 16S
    Language English
    Publishing date 2019-01-27
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiy740
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Individual-level variations in malaria susceptibility and acquisition of clinical protection.

    Valletta, John Joseph / Addy, John W G / Reid, Adam J / Ndungu, Francis M / Bediako, Yaw / Mwacharo, Jedida / Mohammed, Khadija Said / Musyoki, Jennifer / Ngoi, Joyce Mwongeli / Wambua, Joshua / Otieno, Edward / Berriman, Matt / Bejon, Philip / Marsh, Kevin / Langhorne, Jean / Newbold, Chris I / Recker, Mario

    Wellcome open research

    2021  Volume 6, Page(s) 22

    Abstract: After decades of research, our understanding of when and why individuals infected ... ...

    Abstract After decades of research, our understanding of when and why individuals infected with
    Language English
    Publishing date 2021-09-13
    Publishing country England
    Document type Journal Article
    ISSN 2398-502X
    ISSN 2398-502X
    DOI 10.12688/wellcomeopenres.16524.2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: 10-year longitudinal study of malaria in children: Insights into acquisition and maintenance of naturally acquired immunity.

    Addy, John W G / Bediako, Yaw / Ndungu, Francis M / Valetta, John Joseph / Reid, Adam J / Mwacharo, Jedida / Ngoi, Joyce Mwongeli / Wambua, Joshua / Otieno, Edward / Musyoki, Jennifer / Said, Khadija / Berriman, Matthew / Marsh, Kevin / Bejon, Philip / Recker, Mario / Langhorne, Jean

    Wellcome open research

    2021  Volume 6, Page(s) 79

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2021-12-03
    Publishing country England
    Document type Journal Article
    ISSN 2398-502X
    ISSN 2398-502X
    DOI 10.12688/wellcomeopenres.16562.2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Author Correction: Airway response to respiratory syncytial virus has incidental antibacterial effects.

    Sande, Charles J / Njunge, James M / Ngoi, Joyce Mwongeli / Mutunga, Martin N / Chege, Timothy / Gicheru, Elijah T / Gardiner, Elizabeth M / Gwela, Agnes / Green, Christopher A / Drysdale, Simon B / Berkley, James A / Nokes, D James / Pollard, Andrew J

    Nature communications

    2019  Volume 10, Issue 1, Page(s) 3291

    Abstract: An amendment to this paper has been published and can be accessed via a link at the top of the paper. ...

    Abstract An amendment to this paper has been published and can be accessed via a link at the top of the paper.
    Language English
    Publishing date 2019-07-18
    Publishing country England
    Document type Published Erratum
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-019-11222-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The effect of declining exposure on T cell-mediated immunity to Plasmodium falciparum - an epidemiological "natural experiment".

    Bediako, Yaw / Ngoi, Joyce Mwongeli / Nyangweso, George / Wambua, Juliana / Opiyo, Michael / Nduati, Eunice Wambui / Bejon, Philip / Marsh, Kevin / Ndungu, Francis Maina

    BMC medicine

    2016  Volume 14, Issue 1, Page(s) 143

    Abstract: Background: Naturally acquired immunity to malaria may be lost with lack of exposure. Recent heterogeneous reductions in transmission in parts of Africa mean that large populations of previously protected people may lose their immunity while remaining ... ...

    Abstract Background: Naturally acquired immunity to malaria may be lost with lack of exposure. Recent heterogeneous reductions in transmission in parts of Africa mean that large populations of previously protected people may lose their immunity while remaining at risk of infection.
    Methods: Using two ethnically similar long-term cohorts of children with historically similar levels of exposure to Plasmodium falciparum who now experience very different levels of exposure, we assessed the effect of decreased parasite exposure on antimalarial immunity. Peripheral blood mononuclear cells (PBMCs) from children in each cohort were stimulated with P. falciparum and their P. falciparum-specific proliferative and cytokine responses were compared.
    Results: We demonstrate that, while P. falciparum-specific CD4
    Conclusion: Considered in the context of existing knowledge, these data suggest a model explaining how immunity is lost in absence of continuing exposure to P. falciparum.
    Language English
    Publishing date 2016-09-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 2131669-7
    ISSN 1741-7015 ; 1741-7015
    ISSN (online) 1741-7015
    ISSN 1741-7015
    DOI 10.1186/s12916-016-0683-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Repeated clinical malaria episodes are associated with modification of the immune system in children.

    Bediako, Yaw / Adams, Rhys / Reid, Adam J / Valletta, John Joseph / Ndungu, Francis M / Sodenkamp, Jan / Mwacharo, Jedidah / Ngoi, Joyce Mwongeli / Kimani, Domtila / Kai, Oscar / Wambua, Juliana / Nyangweso, George / de Villiers, Etienne P / Sanders, Mandy / Lotkowska, Magda Ewa / Lin, Jing-Wen / Manni, Sarah / Addy, John W G / Recker, Mario /
    Newbold, Chris / Berriman, Matthew / Bejon, Philip / Marsh, Kevin / Langhorne, Jean

    BMC medicine

    2019  Volume 17, Issue 1, Page(s) 60

    Abstract: Background: There are over 200 million reported cases of malaria each year, and most children living in endemic areas will experience multiple episodes of clinical disease before puberty. We set out to understand how frequent clinical malaria, which ... ...

    Abstract Background: There are over 200 million reported cases of malaria each year, and most children living in endemic areas will experience multiple episodes of clinical disease before puberty. We set out to understand how frequent clinical malaria, which elicits a strong inflammatory response, affects the immune system and whether these modifications are observable in the absence of detectable parasitaemia.
    Methods: We used a multi-dimensional approach comprising whole blood transcriptomic, cellular and plasma cytokine analyses on a cohort of children living with endemic malaria, but uninfected at sampling, who had been under active surveillance for malaria for 8 years. Children were categorised into two groups depending on the cumulative number of episodes experienced: high (≥ 8) or low (< 5).
    Results: We observe that multiple episodes of malaria are associated with modification of the immune system. Children who had experienced a large number of episodes demonstrated upregulation of interferon-inducible genes, a clear increase in circulating levels of the immunoregulatory cytokine IL-10 and enhanced activation of neutrophils, B cells and CD8
    Conclusion: Transcriptomic analysis together with cytokine and immune cell profiling of peripheral blood can robustly detect immune differences between children with different numbers of prior malaria episodes. Multiple episodes of malaria are associated with modification of the immune system in children. Such immune modifications may have implications for the initiation of subsequent immune responses and the induction of vaccine-mediated protection.
    MeSH term(s) Child ; Child, Preschool ; Humans ; Immune System Diseases/immunology ; Malaria/immunology
    Language English
    Publishing date 2019-03-13
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2131669-7
    ISSN 1741-7015 ; 1741-7015
    ISSN (online) 1741-7015
    ISSN 1741-7015
    DOI 10.1186/s12916-019-1292-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Addressing pandemic-wide systematic errors in the SARS-CoV-2 phylogeny

    Hunt, Martin / Hinrichs, Angie S / Anderson, Daniel / Karim, Lily / Dearlove, Bethany L / Knaggs, Jeff / Constantinides, Bede / Fowler, Philip W / Rodger, Gillian / Street, Teresa L / Lumley, Sheila F / Webster, Hermione / Sanderson, Theo / Ruis, Christopher / De Maio, Nicola / Amenga-Etego, Lucas N / Amuzu, Dominic SY / Avaro, Martin / Awandare, Gordon A /
    Ayivor-Djanie, Reuben / Bashton, Matthew / Batty, Elizabeth M / Bediako, Yaw / De Belder, Denise / Benedetti, Estefania / Bergthaler, Andreas / Boers, Stefan A / Campos, Josefina / Carr, Rosina Afua Ampomah / Cuba, Facundo / Dattero, Maria Elena / Dejnirattisai, Wanwissa / Dilthey, Alexander T / Duedu, Kwabena Obeng / Endler, Lukas / Engelmann, Ilka / Francisco, Ngiambudulu M / Fuchs, Jonas / Gnimpieba Z., Etienne / Groc, Soraya / Gyamfi, Jones / Heemskerk, Dennis / Houwaart, Torsten / Hsiao, Nei-yuan / Huska, Matthew / Hoelzer, Martin / Iranzadeh, Arash / Jarva, Hanna / Jeewandara, Chandima / Jolly, Bani / Joseph, Rageema / Kant, Ravi / Ki, Karrie Ko Kwan / Kurkela, Satu / Lappalainen, Maija / Lataretu, Marie / Liu, Chang / Malavige, Gathsaurie Neelika / Mashe, Tapfumanei / Mongkolsapaya, Juthathip / Montes, Brigitte / Molina-Mora, Jose Arturo / Morang'a, Collins M / Mvula, Bernard / Nagarajan, Niranjan / Nelson, Andrew / Ngoi, Joyce Mwongeli / da Paixao, Joana Paula / Panning, Marcus / Poklepovich, Tomas / Quashie, Peter Kojo / Ranasinghe, Diyanath / Russo, Mara / San, James E / Sanderson, Nicholas D / Scaria, Vinod / Screaton, Gavin / Sironen, Tarja / Sisay, Abay / Smith, Darren / Smura, Teemu / Supasa, Piyada / Suphavilai, Chayaporn / Swann, Jeremy / Tegally, Houriiyah / Tegomoh, Bryan / Vapalahti, Olli / Walker, Andreas / Wilkinson, Robert / Williamson, Carolyn / IMSSC2 Laboratory Network Consortium / de Oliveira, Tulio / Peto, Timothy EA / Crook, Derrick / Corbett-Detig, Russ / Iqbal, Zamin

    bioRxiv

    Abstract: The SARS-CoV-2 genome occupies a unique place in infection biology -- it is the most highly sequenced genome on earth (making up over 20% of public sequencing datasets) with fine scale information on sampling date and geography, and has been subject to ... ...

    Abstract The SARS-CoV-2 genome occupies a unique place in infection biology -- it is the most highly sequenced genome on earth (making up over 20% of public sequencing datasets) with fine scale information on sampling date and geography, and has been subject to unprecedented intense analysis. As a result, these phylogenetic data are an incredibly valuable resource for science and public health. However, the vast majority of the data was sequenced by tiling amplicons across the full genome, with amplicon schemes that changed over the pandemic as mutations in the viral genome interacted with primer binding sites. In combination with the disparate set of genome assembly workflows and lack of consistent quality control (QC) processes, the current genomes have many systematic errors that have evolved with the virus and amplicon schemes. These errors have significant impacts on the phylogeny, and therefore over the last few years, many thousands of hours of researchers time has been spent in "eyeballing" trees, looking for artefacts, and then patching the tree. Given the huge value of this dataset, we therefore set out to reprocess the complete set of public raw sequence data in a rigorous amplicon-aware manner, and build a cleaner phylogeny. Here we provide a global tree of 3,960,704 samples, built from a consistently assembled set of high quality consensus sequences from all available public data as of March 2023, viewable at https://viridian.taxonium.org. Each genome was constructed using a novel assembly tool called Viridian (https://github.com/iqbal-lab-org/viridian), developed specifically to process amplicon sequence data, eliminating artefactual errors and mask the genome at low quality positions. We provide simulation and empirical validation of the methodology, and quantify the improvement in the phylogeny. Phase 2 of our project will address the fact that the data in the public archives is heavily geographically biased towards the Global North. We therefore have contributed new raw data to ENA/SRA from many countries including Ghana, Thailand, Laos, Sri Lanka, India, Argentina and Singapore. We will incorporate these, along with all public raw data submitted between March 2023 and the current day, into an updated set of assemblies, and phylogeny. We hope the tree, consensus sequences and Viridian will be a valuable resource for researchers.
    Keywords covid19
    Language English
    Publishing date 2024-04-30
    Publisher Cold Spring Harbor Laboratory
    Document type Article ; Online
    DOI 10.1101/2024.04.29.591666
    Database COVID19

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