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m hominis atcc 23114  (ATCC)


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    Structured Review

    ATCC m hominis atcc 23114
    M Hominis Atcc 23114, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 166 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/m+hominis+strain+pg21/Mycoplasma+hominis%3B+Strain+PG21/pm40699317-59-4-6
    Average 95 stars, based on 166 article reviews
    m hominis atcc 23114 - by Bioz Stars, 2026-11
    95/100 stars

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    Related Articles

    other:

    Article Title: O -Linked Protein Glycosylation in Mycoplasma
    Article Snippet: For 13 C labeling, [U- 13 C]starch was obtained from Cambridge Isotopes Laboratories, Inc.

    Article Title: Interaction of Mycoplasma hominis PG21 with Human Dendritic Cells: Interleukin-23-Inducing Mycoplasmal Lipoproteins and Inflammasome Activation of the Cell
    Article Snippet: The cells were lysed by three 1-min bursts of sonication on ice at the maximum setting for the micro tip (Vibra-Cell sonicator; Branson).

    Control:

    Article Title: Clonal Spread of Tetracycline Resistance Among Mycoplasma hominis Clinical Strains, Tunisia
    Article Snippet: Out of 1180 samples, sixty-five (5,5%) M. hominis clinical strains isolated from outpatients (48 non-pregnant women and 17 men) presenting to the diagnostic center of the Pasteur Institute of Tunis (Grand Tunis, Tunisia), from January 2000 to December 2018, were included in this study. .. As control, M. hominis strain PG21 (ATCC 23,114) has been considered. ..

    Article Title: <p>Clonal Spread of Tetracycline Resistance Among <em>Mycoplasma hominis</em> Clinical Strains, Tunisia</p>
    Article Snippet: Out of 1180 samples, sixty-five (5,5%) M. hominis clinical strains isolated from outpatients (48 non-pregnant women and 17men) presenting to the diagnostic center of the Pasteur Institute of Tunis (Grand Tunis, Tunisia), from January 2000 to December 2018, were included in this study. .. As control, M. hominis strain PG21 (ATCC 23,114) has been considered. ..

    Isolation:

    Article Title: Interaction of Mycoplasma hominis PG21 with Human Dendritic Cells: Interleukin-23-Inducing Mycoplasmal Lipoproteins and Inflammasome Activation of the Cell
    Article Snippet: .. M. hominis strain PG21 (ATCC 23114) was cultivated, and membranes were isolated as described previously ( 8 ) with slight modifications. ..



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    M Hominis Atcc 23114, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC m hominis reference strain pg21
    COG classification of genes. (A) Clusters of orthologous genes (COGs) distribution among the 52 M. <t>hominis</t> strains associated with infertility. (B) COGs distribution among the 10 M. hominis strains associated with genital infections. Bars in green, red, and blue, represent the core genome, the accessory genes (shell genes), and unique genes (cloud genes), respectively.
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    ATCC m hominis reference strains atcc 23114 pg21
    COG classification of genes. (A) Clusters of orthologous genes (COGs) distribution among the 52 M. <t>hominis</t> strains associated with infertility. (B) COGs distribution among the 10 M. hominis strains associated with genital infections. Bars in green, red, and blue, represent the core genome, the accessory genes (shell genes), and unique genes (cloud genes), respectively.
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    ATCC uab diagnostic mycoplasma laboratory uses m hominis atcc 23114
    COG classification of genes. (A) Clusters of orthologous genes (COGs) distribution among the 52 M. <t>hominis</t> strains associated with infertility. (B) COGs distribution among the 10 M. hominis strains associated with genital infections. Bars in green, red, and blue, represent the core genome, the accessory genes (shell genes), and unique genes (cloud genes), respectively.
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    ATCC strain m hominis
    <t>Mycoplasma</t> <t>hominis</t> infection alters the growth and colony formation of primary human keratinocytes (PHKs) even at low inoculum concentrations. ( A ) Quantification of viable PHKs after 72 h of infection with M. hominis at different concentrations. Approximately 8000 PHKs/well were present at the time of infection. * Represents a statistically significant difference between the infection and control groups (one-tailed Mann–Whitney test, significance level of 95%, (*) p ≥ 0.05, (**) p ≥ 0.01, and (***) p ≥ 0.001). ( B ) PHK growth curves after M. hominis infection. Plating was performed with approximately 2.3 × 10 3 to 3.7 × 10 3 cells. After 12–24 h, M. hominis infection was induced at a multiplicity of infection (MOI) of 0.04–0.6. After 24, 48, 72, 96, 120,144, and 168 h of infection, the cells were trypsinised and counted using a haemocytometer. The assays were performed in triplicate. The points on the curves represent the average number of cells obtained with the respective standard deviations. From 48 h of M. hominis infection, a statistically significant difference was observed in the infection group compared with that in the control group (two-way ANOVA with Bonferroni post-test, significance level of 95%). ( C ) The clonogenic assay performed with PHKs after M. hominis infection. The number of PHKs initially plated was approximately 1000. The MOI for M. hominis was 4.44. Left: photograph of the petri dishes in one of the tests. The colonies were stained with crystal violet and counted using the Promega Colony Counter (Promega). Right: reduction in the colony formation percentage after 15 days of infection. One-tailed Mann–Whitney test, significance level of 95%.
    Strain M Hominis, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/m+hominis+strain+pg21/Mycoplasma+hominis%3B+Strain+PG21/pmc09608843-32-1-4
    Average 95 stars, based on 1 article reviews
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    Image Search Results


    COG classification of genes. (A) Clusters of orthologous genes (COGs) distribution among the 52 M. hominis strains associated with infertility. (B) COGs distribution among the 10 M. hominis strains associated with genital infections. Bars in green, red, and blue, represent the core genome, the accessory genes (shell genes), and unique genes (cloud genes), respectively.

    Journal: Frontiers in Microbiology

    Article Title: A genome-wide investigation of Mycoplasma hominis genes associated with gynecological infections or infertility

    doi: 10.3389/fmicb.2025.1561378

    Figure Lengend Snippet: COG classification of genes. (A) Clusters of orthologous genes (COGs) distribution among the 52 M. hominis strains associated with infertility. (B) COGs distribution among the 10 M. hominis strains associated with genital infections. Bars in green, red, and blue, represent the core genome, the accessory genes (shell genes), and unique genes (cloud genes), respectively.

    Article Snippet: The genome size of M. hominis reference strain PG21 (ATCC 23114) was estimated to be around 665 kb (Calcutt and Foecking, ), thus exceeding Mycoplasma genitalium genome (580 kb), the smallest genome of any organism that can be grown in pure culture (Fookes et al., ), by only 85 kb.

    Techniques:

    Single nucleotide polymorphism (SNP) distribution among M. hominis strains associated with gynecological infections (red boxplot) and infertility (blue boxplot). Student's t -test was used to assess for statistical significant difference ( P < 0.05) between the mean SNPs count values of strains linked to infertility and gynecological infections. * Represents the mean SNP count of each boxplot.

    Journal: Frontiers in Microbiology

    Article Title: A genome-wide investigation of Mycoplasma hominis genes associated with gynecological infections or infertility

    doi: 10.3389/fmicb.2025.1561378

    Figure Lengend Snippet: Single nucleotide polymorphism (SNP) distribution among M. hominis strains associated with gynecological infections (red boxplot) and infertility (blue boxplot). Student's t -test was used to assess for statistical significant difference ( P < 0.05) between the mean SNPs count values of strains linked to infertility and gynecological infections. * Represents the mean SNP count of each boxplot.

    Article Snippet: The genome size of M. hominis reference strain PG21 (ATCC 23114) was estimated to be around 665 kb (Calcutt and Foecking, ), thus exceeding Mycoplasma genitalium genome (580 kb), the smallest genome of any organism that can be grown in pure culture (Fookes et al., ), by only 85 kb.

    Techniques:

    TreeWAS-based phylogenetic tree illustrating the relatedness between the 62 Tunisian M. hominis clinical strains based on pathotype association. Strains in red are associated with gynecological infections pathotype and strains in blue are associated with infertility pathotype.

    Journal: Frontiers in Microbiology

    Article Title: A genome-wide investigation of Mycoplasma hominis genes associated with gynecological infections or infertility

    doi: 10.3389/fmicb.2025.1561378

    Figure Lengend Snippet: TreeWAS-based phylogenetic tree illustrating the relatedness between the 62 Tunisian M. hominis clinical strains based on pathotype association. Strains in red are associated with gynecological infections pathotype and strains in blue are associated with infertility pathotype.

    Article Snippet: The genome size of M. hominis reference strain PG21 (ATCC 23114) was estimated to be around 665 kb (Calcutt and Foecking, ), thus exceeding Mycoplasma genitalium genome (580 kb), the smallest genome of any organism that can be grown in pure culture (Fookes et al., ), by only 85 kb.

    Techniques:

    Mycoplasma hominis infection alters the growth and colony formation of primary human keratinocytes (PHKs) even at low inoculum concentrations. ( A ) Quantification of viable PHKs after 72 h of infection with M. hominis at different concentrations. Approximately 8000 PHKs/well were present at the time of infection. * Represents a statistically significant difference between the infection and control groups (one-tailed Mann–Whitney test, significance level of 95%, (*) p ≥ 0.05, (**) p ≥ 0.01, and (***) p ≥ 0.001). ( B ) PHK growth curves after M. hominis infection. Plating was performed with approximately 2.3 × 10 3 to 3.7 × 10 3 cells. After 12–24 h, M. hominis infection was induced at a multiplicity of infection (MOI) of 0.04–0.6. After 24, 48, 72, 96, 120,144, and 168 h of infection, the cells were trypsinised and counted using a haemocytometer. The assays were performed in triplicate. The points on the curves represent the average number of cells obtained with the respective standard deviations. From 48 h of M. hominis infection, a statistically significant difference was observed in the infection group compared with that in the control group (two-way ANOVA with Bonferroni post-test, significance level of 95%). ( C ) The clonogenic assay performed with PHKs after M. hominis infection. The number of PHKs initially plated was approximately 1000. The MOI for M. hominis was 4.44. Left: photograph of the petri dishes in one of the tests. The colonies were stained with crystal violet and counted using the Promega Colony Counter (Promega). Right: reduction in the colony formation percentage after 15 days of infection. One-tailed Mann–Whitney test, significance level of 95%.

    Journal: Microorganisms

    Article Title: Mycoplasma hominis Causes DNA Damage and Cell Death in Primary Human Keratinocytes

    doi: 10.3390/microorganisms10101962

    Figure Lengend Snippet: Mycoplasma hominis infection alters the growth and colony formation of primary human keratinocytes (PHKs) even at low inoculum concentrations. ( A ) Quantification of viable PHKs after 72 h of infection with M. hominis at different concentrations. Approximately 8000 PHKs/well were present at the time of infection. * Represents a statistically significant difference between the infection and control groups (one-tailed Mann–Whitney test, significance level of 95%, (*) p ≥ 0.05, (**) p ≥ 0.01, and (***) p ≥ 0.001). ( B ) PHK growth curves after M. hominis infection. Plating was performed with approximately 2.3 × 10 3 to 3.7 × 10 3 cells. After 12–24 h, M. hominis infection was induced at a multiplicity of infection (MOI) of 0.04–0.6. After 24, 48, 72, 96, 120,144, and 168 h of infection, the cells were trypsinised and counted using a haemocytometer. The assays were performed in triplicate. The points on the curves represent the average number of cells obtained with the respective standard deviations. From 48 h of M. hominis infection, a statistically significant difference was observed in the infection group compared with that in the control group (two-way ANOVA with Bonferroni post-test, significance level of 95%). ( C ) The clonogenic assay performed with PHKs after M. hominis infection. The number of PHKs initially plated was approximately 1000. The MOI for M. hominis was 4.44. Left: photograph of the petri dishes in one of the tests. The colonies were stained with crystal violet and counted using the Promega Colony Counter (Promega). Right: reduction in the colony formation percentage after 15 days of infection. One-tailed Mann–Whitney test, significance level of 95%.

    Article Snippet: The strain M. hominis (ATCC 23114-PG-21) was obtained from the ICB/USP Mycoplasma laboratory and grown in 100 mL of SP4 medium [ ] until the mid-log phase.

    Techniques: Infection, Control, One-tailed Test, MANN-WHITNEY, Clonogenic Assay, Staining