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a muciniphila type strain muc t  (ATCC)


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    Structured Review

    ATCC a muciniphila type strain muc t
    Effect of the different extracts of O. biflora on the growth of A. <t>muciniphila</t> . The percentage relative growth yield of Akkermansia muciniphila cultured in Brain-Heart Infusion (BHI) medium, supplemented with Odontosoria biflora extract (OBE) obtained using different extraction solvents, namely aqueous (AQ), ethyl acetate (ETAC), methanol (MEOH), and hexane (HEX), is presented. The bacterial strain was cultivated in BHI medium, with and without glucose-supplemented OBE, at final concentrations of 250 mg/mL and 500 mg/mL, and its growth was assessed via OD620 measurements. The experiment was conducted in three independent trials, each performed in triplicate. Statistical significance relative to the control is indicated by asterisks (p ≤ 0.05).
    A Muciniphila Type Strain Muc T, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 806 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Differential in vitro and in vivo responses of Akkermansia muciniphila to Odontosoria biflora (Kaulf.) C.Chr. [ Lindsaeaceae ] hexane extract in diet- and alloxan-induced BALB/c mice"

    Article Title: Differential in vitro and in vivo responses of Akkermansia muciniphila to Odontosoria biflora (Kaulf.) C.Chr. [ Lindsaeaceae ] hexane extract in diet- and alloxan-induced BALB/c mice

    Journal: Acta Biochimica Polonica

    doi: 10.3389/abp.2026.16199

    Effect of the different extracts of O. biflora on the growth of A. muciniphila . The percentage relative growth yield of Akkermansia muciniphila cultured in Brain-Heart Infusion (BHI) medium, supplemented with Odontosoria biflora extract (OBE) obtained using different extraction solvents, namely aqueous (AQ), ethyl acetate (ETAC), methanol (MEOH), and hexane (HEX), is presented. The bacterial strain was cultivated in BHI medium, with and without glucose-supplemented OBE, at final concentrations of 250 mg/mL and 500 mg/mL, and its growth was assessed via OD620 measurements. The experiment was conducted in three independent trials, each performed in triplicate. Statistical significance relative to the control is indicated by asterisks (p ≤ 0.05).
    Figure Legend Snippet: Effect of the different extracts of O. biflora on the growth of A. muciniphila . The percentage relative growth yield of Akkermansia muciniphila cultured in Brain-Heart Infusion (BHI) medium, supplemented with Odontosoria biflora extract (OBE) obtained using different extraction solvents, namely aqueous (AQ), ethyl acetate (ETAC), methanol (MEOH), and hexane (HEX), is presented. The bacterial strain was cultivated in BHI medium, with and without glucose-supplemented OBE, at final concentrations of 250 mg/mL and 500 mg/mL, and its growth was assessed via OD620 measurements. The experiment was conducted in three independent trials, each performed in triplicate. Statistical significance relative to the control is indicated by asterisks (p ≤ 0.05).

    Techniques Used: Cell Culture, Extraction, Control

    Relative Akkermansia muciniphila -specific signal in fecal samples of BALB/c mice. Relative detection levels were quantified using a modified 2 − ΔΔCt approach with external A. muciniphila ATCC genomic DNA as reference and the normal group as biological calibrator. Data represented as mean ± SE. Statistical significance was determined by two-way repeated-measures ANOVA followed by Dunnett’s multiple comparisons test ( p < 0.05, p < 0.01, p < 0.001).
    Figure Legend Snippet: Relative Akkermansia muciniphila -specific signal in fecal samples of BALB/c mice. Relative detection levels were quantified using a modified 2 − ΔΔCt approach with external A. muciniphila ATCC genomic DNA as reference and the normal group as biological calibrator. Data represented as mean ± SE. Statistical significance was determined by two-way repeated-measures ANOVA followed by Dunnett’s multiple comparisons test ( p < 0.05, p < 0.01, p < 0.001).

    Techniques Used: Modification



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    ATCC a muciniphila type strain muc t
    Effect of the different extracts of O. biflora on the growth of A. <t>muciniphila</t> . The percentage relative growth yield of Akkermansia muciniphila cultured in Brain-Heart Infusion (BHI) medium, supplemented with Odontosoria biflora extract (OBE) obtained using different extraction solvents, namely aqueous (AQ), ethyl acetate (ETAC), methanol (MEOH), and hexane (HEX), is presented. The bacterial strain was cultivated in BHI medium, with and without glucose-supplemented OBE, at final concentrations of 250 mg/mL and 500 mg/mL, and its growth was assessed via OD620 measurements. The experiment was conducted in three independent trials, each performed in triplicate. Statistical significance relative to the control is indicated by asterisks (p ≤ 0.05).
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    ATCC m anserisalpingitidis atcc baa 2147 type strain
    Effect of the different extracts of O. biflora on the growth of A. <t>muciniphila</t> . The percentage relative growth yield of Akkermansia muciniphila cultured in Brain-Heart Infusion (BHI) medium, supplemented with Odontosoria biflora extract (OBE) obtained using different extraction solvents, namely aqueous (AQ), ethyl acetate (ETAC), methanol (MEOH), and hexane (HEX), is presented. The bacterial strain was cultivated in BHI medium, with and without glucose-supplemented OBE, at final concentrations of 250 mg/mL and 500 mg/mL, and its growth was assessed via OD620 measurements. The experiment was conducted in three independent trials, each performed in triplicate. Statistical significance relative to the control is indicated by asterisks (p ≤ 0.05).
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    ATCC a muciniphila type strain atcc baa 835
    ( a-b ) Validation of the chain of transmission of a strain of Akkermansia muciniphila SGB9226 (Fig. ) using a SGB-specific PCR assay; a , Sensitivity of the SGB9226-specific PCR assay, assessed by testing a SGB9226-negative human fecal DNA spiked with seven ten-fold dilutions of genomic DNA from A. muciniphila ATCC <t>BAA-835,</t> corresponding to an estimated 106 to 1 genome copies (“D1” to “D7”). Controls included the human fecal matrix alone (“Spike-in Matrix”) and a no-template control (NTC). b , Application of the SGB9226-specific PCR to fecal samples in Fig. . Sample IDs include the volunteer type and family number, while per volunteer longitudinal samples are identified by timepoint. Relative abundances according to MetaPhlAn 4 (“Rel. Abun., %”) and sample IDs are colored dark blue (positive) or grey (negative) based on strain identification according to StrainPhlAn (Fig. ). Genomic DNA from A. muciniphila ATCC BAA-835 is included as a positive control, alongside a NTC. ( c ) Phylogenetic tree of Alistipes finegoldii SGB2301 (left) and chain of transmission events of one strain in group 1 of nursery B (right). Participant types are identified by shape (educator, cross; baby, circle; mother, diamond) containing participant identifiers (with the initial identifying the participant type followed by specific family number). Familial relations are highlighted by same-color filling. Each circle represents a sample collected from participants depicted, with color filling indicating the identity of the strain of Alistipes finegoldii SGB2301 detected in the sample (except gray, used to indicate the SGB was not detected/typable) and arrows indicating the most likely transmission event. ( d-e ) Strain-sharing between pets ( n = 5) and human hosts within the same family (turquoise) and across different ones (gray). d , The average total number of strains shared between participant pairs across contemporaneous samples are reported above the connecting lines; in brackets are indicated the number of pet-human pairs with at least one strain shared over the total number of pet-human pairs. Statistical significance according to a two-sided Fisher’s exact test is depicted for the same family vs different family pet-baby comparison. All other comparisons are non significant. e , Average number shared strains between pet and human across contemporaneous samples, in different vs same family. In the box plots, box edges indicate the lower and upper quartiles, the center line represents the median, and whiskers extend to the most extreme data point within 1.5× the IQR. Statistical significance P -values refer to two-sided Mann-Whitney U tests, with n indicating the number of pet-human pairs. All other comparisons are non significant.
    A Muciniphila Type Strain Atcc Baa 835, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC reference strain american type culture collection
    ( a-b ) Validation of the chain of transmission of a strain of Akkermansia muciniphila SGB9226 (Fig. ) using a SGB-specific PCR assay; a , Sensitivity of the SGB9226-specific PCR assay, assessed by testing a SGB9226-negative human fecal DNA spiked with seven ten-fold dilutions of genomic DNA from A. muciniphila ATCC <t>BAA-835,</t> corresponding to an estimated 106 to 1 genome copies (“D1” to “D7”). Controls included the human fecal matrix alone (“Spike-in Matrix”) and a no-template control (NTC). b , Application of the SGB9226-specific PCR to fecal samples in Fig. . Sample IDs include the volunteer type and family number, while per volunteer longitudinal samples are identified by timepoint. Relative abundances according to MetaPhlAn 4 (“Rel. Abun., %”) and sample IDs are colored dark blue (positive) or grey (negative) based on strain identification according to StrainPhlAn (Fig. ). Genomic DNA from A. muciniphila ATCC BAA-835 is included as a positive control, alongside a NTC. ( c ) Phylogenetic tree of Alistipes finegoldii SGB2301 (left) and chain of transmission events of one strain in group 1 of nursery B (right). Participant types are identified by shape (educator, cross; baby, circle; mother, diamond) containing participant identifiers (with the initial identifying the participant type followed by specific family number). Familial relations are highlighted by same-color filling. Each circle represents a sample collected from participants depicted, with color filling indicating the identity of the strain of Alistipes finegoldii SGB2301 detected in the sample (except gray, used to indicate the SGB was not detected/typable) and arrows indicating the most likely transmission event. ( d-e ) Strain-sharing between pets ( n = 5) and human hosts within the same family (turquoise) and across different ones (gray). d , The average total number of strains shared between participant pairs across contemporaneous samples are reported above the connecting lines; in brackets are indicated the number of pet-human pairs with at least one strain shared over the total number of pet-human pairs. Statistical significance according to a two-sided Fisher’s exact test is depicted for the same family vs different family pet-baby comparison. All other comparisons are non significant. e , Average number shared strains between pet and human across contemporaneous samples, in different vs same family. In the box plots, box edges indicate the lower and upper quartiles, the center line represents the median, and whiskers extend to the most extreme data point within 1.5× the IQR. Statistical significance P -values refer to two-sided Mann-Whitney U tests, with n indicating the number of pet-human pairs. All other comparisons are non significant.
    Reference Strain American Type Culture Collection, 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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    ( a-b ) Validation of the chain of transmission of a strain of Akkermansia muciniphila SGB9226 (Fig. ) using a SGB-specific PCR assay; a , Sensitivity of the SGB9226-specific PCR assay, assessed by testing a SGB9226-negative human fecal DNA spiked with seven ten-fold dilutions of genomic DNA from A. muciniphila ATCC <t>BAA-835,</t> corresponding to an estimated 106 to 1 genome copies (“D1” to “D7”). Controls included the human fecal matrix alone (“Spike-in Matrix”) and a no-template control (NTC). b , Application of the SGB9226-specific PCR to fecal samples in Fig. . Sample IDs include the volunteer type and family number, while per volunteer longitudinal samples are identified by timepoint. Relative abundances according to MetaPhlAn 4 (“Rel. Abun., %”) and sample IDs are colored dark blue (positive) or grey (negative) based on strain identification according to StrainPhlAn (Fig. ). Genomic DNA from A. muciniphila ATCC BAA-835 is included as a positive control, alongside a NTC. ( c ) Phylogenetic tree of Alistipes finegoldii SGB2301 (left) and chain of transmission events of one strain in group 1 of nursery B (right). Participant types are identified by shape (educator, cross; baby, circle; mother, diamond) containing participant identifiers (with the initial identifying the participant type followed by specific family number). Familial relations are highlighted by same-color filling. Each circle represents a sample collected from participants depicted, with color filling indicating the identity of the strain of Alistipes finegoldii SGB2301 detected in the sample (except gray, used to indicate the SGB was not detected/typable) and arrows indicating the most likely transmission event. ( d-e ) Strain-sharing between pets ( n = 5) and human hosts within the same family (turquoise) and across different ones (gray). d , The average total number of strains shared between participant pairs across contemporaneous samples are reported above the connecting lines; in brackets are indicated the number of pet-human pairs with at least one strain shared over the total number of pet-human pairs. Statistical significance according to a two-sided Fisher’s exact test is depicted for the same family vs different family pet-baby comparison. All other comparisons are non significant. e , Average number shared strains between pet and human across contemporaneous samples, in different vs same family. In the box plots, box edges indicate the lower and upper quartiles, the center line represents the median, and whiskers extend to the most extreme data point within 1.5× the IQR. Statistical significance P -values refer to two-sided Mann-Whitney U tests, with n indicating the number of pet-human pairs. All other comparisons are non significant.
    Type Acinetobacter Baumannii Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC type strain atcc baa
    ( a-b ) Validation of the chain of transmission of a strain of Akkermansia muciniphila SGB9226 (Fig. ) using a SGB-specific PCR assay; a , Sensitivity of the SGB9226-specific PCR assay, assessed by testing a SGB9226-negative human fecal DNA spiked with seven ten-fold dilutions of genomic DNA from A. muciniphila ATCC <t>BAA-835,</t> corresponding to an estimated 106 to 1 genome copies (“D1” to “D7”). Controls included the human fecal matrix alone (“Spike-in Matrix”) and a no-template control (NTC). b , Application of the SGB9226-specific PCR to fecal samples in Fig. . Sample IDs include the volunteer type and family number, while per volunteer longitudinal samples are identified by timepoint. Relative abundances according to MetaPhlAn 4 (“Rel. Abun., %”) and sample IDs are colored dark blue (positive) or grey (negative) based on strain identification according to StrainPhlAn (Fig. ). Genomic DNA from A. muciniphila ATCC BAA-835 is included as a positive control, alongside a NTC. ( c ) Phylogenetic tree of Alistipes finegoldii SGB2301 (left) and chain of transmission events of one strain in group 1 of nursery B (right). Participant types are identified by shape (educator, cross; baby, circle; mother, diamond) containing participant identifiers (with the initial identifying the participant type followed by specific family number). Familial relations are highlighted by same-color filling. Each circle represents a sample collected from participants depicted, with color filling indicating the identity of the strain of Alistipes finegoldii SGB2301 detected in the sample (except gray, used to indicate the SGB was not detected/typable) and arrows indicating the most likely transmission event. ( d-e ) Strain-sharing between pets ( n = 5) and human hosts within the same family (turquoise) and across different ones (gray). d , The average total number of strains shared between participant pairs across contemporaneous samples are reported above the connecting lines; in brackets are indicated the number of pet-human pairs with at least one strain shared over the total number of pet-human pairs. Statistical significance according to a two-sided Fisher’s exact test is depicted for the same family vs different family pet-baby comparison. All other comparisons are non significant. e , Average number shared strains between pet and human across contemporaneous samples, in different vs same family. In the box plots, box edges indicate the lower and upper quartiles, the center line represents the median, and whiskers extend to the most extreme data point within 1.5× the IQR. Statistical significance P -values refer to two-sided Mann-Whitney U tests, with n indicating the number of pet-human pairs. All other comparisons are non significant.
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    ATCC type strain atcc baa 2683
    ( a-b ) Validation of the chain of transmission of a strain of Akkermansia muciniphila SGB9226 (Fig. ) using a SGB-specific PCR assay; a , Sensitivity of the SGB9226-specific PCR assay, assessed by testing a SGB9226-negative human fecal DNA spiked with seven ten-fold dilutions of genomic DNA from A. muciniphila ATCC <t>BAA-835,</t> corresponding to an estimated 106 to 1 genome copies (“D1” to “D7”). Controls included the human fecal matrix alone (“Spike-in Matrix”) and a no-template control (NTC). b , Application of the SGB9226-specific PCR to fecal samples in Fig. . Sample IDs include the volunteer type and family number, while per volunteer longitudinal samples are identified by timepoint. Relative abundances according to MetaPhlAn 4 (“Rel. Abun., %”) and sample IDs are colored dark blue (positive) or grey (negative) based on strain identification according to StrainPhlAn (Fig. ). Genomic DNA from A. muciniphila ATCC BAA-835 is included as a positive control, alongside a NTC. ( c ) Phylogenetic tree of Alistipes finegoldii SGB2301 (left) and chain of transmission events of one strain in group 1 of nursery B (right). Participant types are identified by shape (educator, cross; baby, circle; mother, diamond) containing participant identifiers (with the initial identifying the participant type followed by specific family number). Familial relations are highlighted by same-color filling. Each circle represents a sample collected from participants depicted, with color filling indicating the identity of the strain of Alistipes finegoldii SGB2301 detected in the sample (except gray, used to indicate the SGB was not detected/typable) and arrows indicating the most likely transmission event. ( d-e ) Strain-sharing between pets ( n = 5) and human hosts within the same family (turquoise) and across different ones (gray). d , The average total number of strains shared between participant pairs across contemporaneous samples are reported above the connecting lines; in brackets are indicated the number of pet-human pairs with at least one strain shared over the total number of pet-human pairs. Statistical significance according to a two-sided Fisher’s exact test is depicted for the same family vs different family pet-baby comparison. All other comparisons are non significant. e , Average number shared strains between pet and human across contemporaneous samples, in different vs same family. In the box plots, box edges indicate the lower and upper quartiles, the center line represents the median, and whiskers extend to the most extreme data point within 1.5× the IQR. Statistical significance P -values refer to two-sided Mann-Whitney U tests, with n indicating the number of pet-human pairs. All other comparisons are non significant.
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    Image Search Results


    Effect of the different extracts of O. biflora on the growth of A. muciniphila . The percentage relative growth yield of Akkermansia muciniphila cultured in Brain-Heart Infusion (BHI) medium, supplemented with Odontosoria biflora extract (OBE) obtained using different extraction solvents, namely aqueous (AQ), ethyl acetate (ETAC), methanol (MEOH), and hexane (HEX), is presented. The bacterial strain was cultivated in BHI medium, with and without glucose-supplemented OBE, at final concentrations of 250 mg/mL and 500 mg/mL, and its growth was assessed via OD620 measurements. The experiment was conducted in three independent trials, each performed in triplicate. Statistical significance relative to the control is indicated by asterisks (p ≤ 0.05).

    Journal: Acta Biochimica Polonica

    Article Title: Differential in vitro and in vivo responses of Akkermansia muciniphila to Odontosoria biflora (Kaulf.) C.Chr. [ Lindsaeaceae ] hexane extract in diet- and alloxan-induced BALB/c mice

    doi: 10.3389/abp.2026.16199

    Figure Lengend Snippet: Effect of the different extracts of O. biflora on the growth of A. muciniphila . The percentage relative growth yield of Akkermansia muciniphila cultured in Brain-Heart Infusion (BHI) medium, supplemented with Odontosoria biflora extract (OBE) obtained using different extraction solvents, namely aqueous (AQ), ethyl acetate (ETAC), methanol (MEOH), and hexane (HEX), is presented. The bacterial strain was cultivated in BHI medium, with and without glucose-supplemented OBE, at final concentrations of 250 mg/mL and 500 mg/mL, and its growth was assessed via OD620 measurements. The experiment was conducted in three independent trials, each performed in triplicate. Statistical significance relative to the control is indicated by asterisks (p ≤ 0.05).

    Article Snippet: Briefy, the A. muciniphila type strain Muc T (= ATCC BAA-835 T = CIP 107961 T ), obtained from the Japan Collection of Microorganisms (JCM) at the RIKEN BioResource Research Center, was cultured anaerobically in Brain Heart Infusion (BHI) medium, following the protocol of with modifications.

    Techniques: Cell Culture, Extraction, Control

    Relative Akkermansia muciniphila -specific signal in fecal samples of BALB/c mice. Relative detection levels were quantified using a modified 2 − ΔΔCt approach with external A. muciniphila ATCC genomic DNA as reference and the normal group as biological calibrator. Data represented as mean ± SE. Statistical significance was determined by two-way repeated-measures ANOVA followed by Dunnett’s multiple comparisons test ( p < 0.05, p < 0.01, p < 0.001).

    Journal: Acta Biochimica Polonica

    Article Title: Differential in vitro and in vivo responses of Akkermansia muciniphila to Odontosoria biflora (Kaulf.) C.Chr. [ Lindsaeaceae ] hexane extract in diet- and alloxan-induced BALB/c mice

    doi: 10.3389/abp.2026.16199

    Figure Lengend Snippet: Relative Akkermansia muciniphila -specific signal in fecal samples of BALB/c mice. Relative detection levels were quantified using a modified 2 − ΔΔCt approach with external A. muciniphila ATCC genomic DNA as reference and the normal group as biological calibrator. Data represented as mean ± SE. Statistical significance was determined by two-way repeated-measures ANOVA followed by Dunnett’s multiple comparisons test ( p < 0.05, p < 0.01, p < 0.001).

    Article Snippet: Briefy, the A. muciniphila type strain Muc T (= ATCC BAA-835 T = CIP 107961 T ), obtained from the Japan Collection of Microorganisms (JCM) at the RIKEN BioResource Research Center, was cultured anaerobically in Brain Heart Infusion (BHI) medium, following the protocol of with modifications.

    Techniques: Modification

    ( a-b ) Validation of the chain of transmission of a strain of Akkermansia muciniphila SGB9226 (Fig. ) using a SGB-specific PCR assay; a , Sensitivity of the SGB9226-specific PCR assay, assessed by testing a SGB9226-negative human fecal DNA spiked with seven ten-fold dilutions of genomic DNA from A. muciniphila ATCC BAA-835, corresponding to an estimated 106 to 1 genome copies (“D1” to “D7”). Controls included the human fecal matrix alone (“Spike-in Matrix”) and a no-template control (NTC). b , Application of the SGB9226-specific PCR to fecal samples in Fig. . Sample IDs include the volunteer type and family number, while per volunteer longitudinal samples are identified by timepoint. Relative abundances according to MetaPhlAn 4 (“Rel. Abun., %”) and sample IDs are colored dark blue (positive) or grey (negative) based on strain identification according to StrainPhlAn (Fig. ). Genomic DNA from A. muciniphila ATCC BAA-835 is included as a positive control, alongside a NTC. ( c ) Phylogenetic tree of Alistipes finegoldii SGB2301 (left) and chain of transmission events of one strain in group 1 of nursery B (right). Participant types are identified by shape (educator, cross; baby, circle; mother, diamond) containing participant identifiers (with the initial identifying the participant type followed by specific family number). Familial relations are highlighted by same-color filling. Each circle represents a sample collected from participants depicted, with color filling indicating the identity of the strain of Alistipes finegoldii SGB2301 detected in the sample (except gray, used to indicate the SGB was not detected/typable) and arrows indicating the most likely transmission event. ( d-e ) Strain-sharing between pets ( n = 5) and human hosts within the same family (turquoise) and across different ones (gray). d , The average total number of strains shared between participant pairs across contemporaneous samples are reported above the connecting lines; in brackets are indicated the number of pet-human pairs with at least one strain shared over the total number of pet-human pairs. Statistical significance according to a two-sided Fisher’s exact test is depicted for the same family vs different family pet-baby comparison. All other comparisons are non significant. e , Average number shared strains between pet and human across contemporaneous samples, in different vs same family. In the box plots, box edges indicate the lower and upper quartiles, the center line represents the median, and whiskers extend to the most extreme data point within 1.5× the IQR. Statistical significance P -values refer to two-sided Mann-Whitney U tests, with n indicating the number of pet-human pairs. All other comparisons are non significant.

    Journal: Nature

    Article Title: Baby-to-baby strain transmission shapes the developing gut microbiome

    doi: 10.1038/s41586-025-09983-z

    Figure Lengend Snippet: ( a-b ) Validation of the chain of transmission of a strain of Akkermansia muciniphila SGB9226 (Fig. ) using a SGB-specific PCR assay; a , Sensitivity of the SGB9226-specific PCR assay, assessed by testing a SGB9226-negative human fecal DNA spiked with seven ten-fold dilutions of genomic DNA from A. muciniphila ATCC BAA-835, corresponding to an estimated 106 to 1 genome copies (“D1” to “D7”). Controls included the human fecal matrix alone (“Spike-in Matrix”) and a no-template control (NTC). b , Application of the SGB9226-specific PCR to fecal samples in Fig. . Sample IDs include the volunteer type and family number, while per volunteer longitudinal samples are identified by timepoint. Relative abundances according to MetaPhlAn 4 (“Rel. Abun., %”) and sample IDs are colored dark blue (positive) or grey (negative) based on strain identification according to StrainPhlAn (Fig. ). Genomic DNA from A. muciniphila ATCC BAA-835 is included as a positive control, alongside a NTC. ( c ) Phylogenetic tree of Alistipes finegoldii SGB2301 (left) and chain of transmission events of one strain in group 1 of nursery B (right). Participant types are identified by shape (educator, cross; baby, circle; mother, diamond) containing participant identifiers (with the initial identifying the participant type followed by specific family number). Familial relations are highlighted by same-color filling. Each circle represents a sample collected from participants depicted, with color filling indicating the identity of the strain of Alistipes finegoldii SGB2301 detected in the sample (except gray, used to indicate the SGB was not detected/typable) and arrows indicating the most likely transmission event. ( d-e ) Strain-sharing between pets ( n = 5) and human hosts within the same family (turquoise) and across different ones (gray). d , The average total number of strains shared between participant pairs across contemporaneous samples are reported above the connecting lines; in brackets are indicated the number of pet-human pairs with at least one strain shared over the total number of pet-human pairs. Statistical significance according to a two-sided Fisher’s exact test is depicted for the same family vs different family pet-baby comparison. All other comparisons are non significant. e , Average number shared strains between pet and human across contemporaneous samples, in different vs same family. In the box plots, box edges indicate the lower and upper quartiles, the center line represents the median, and whiskers extend to the most extreme data point within 1.5× the IQR. Statistical significance P -values refer to two-sided Mann-Whitney U tests, with n indicating the number of pet-human pairs. All other comparisons are non significant.

    Article Snippet: Assay sensitivity was independently evaluated using a spike-in approach with DNA from the A. muciniphila type strain ATCC BAA-835 (from 1 M down to 1 single genome copy) into an A. muciniphila -negative faecal test sample.

    Techniques: Biomarker Discovery, Transmission Assay, Control, Positive Control, Comparison, MANN-WHITNEY