Skip to main content
  • ASM Journals
    • Antimicrobial Agents and Chemotherapy
    • Applied and Environmental Microbiology
    • Clinical Microbiology Reviews
    • Clinical and Vaccine Immunology
    • EcoSal Plus
    • Eukaryotic Cell
    • Infection and Immunity
    • Journal of Bacteriology
    • Journal of Clinical Microbiology
    • Journal of Microbiology & Biology Education
    • Journal of Virology
    • mBio
    • Microbiology and Molecular Biology Reviews
    • Microbiology Resource Announcements
    • Microbiology Spectrum
    • Molecular and Cellular Biology
    • mSphere
    • mSystems
  • Log in
  • My alerts
  • My Cart

Main menu

  • Home
  • Articles
    • Latest Articles
    • COVID-19 Research and News from ASM Journals
    • mSphere of Influence: Commentaries from Early Career Microbiologists
    • Archive
  • Topics
    • Applied and Environmental Science
    • Clinical Science and Epidemiology
    • Ecological and Evolutionary Science
    • Host-Microbe Biology
    • Molecular Biology and Physiology
    • Therapeutics and Prevention
  • For Authors
    • Getting Started
    • Submit a Manuscript
    • Scope
    • Editorial Policy
    • Submission, Review, & Publication Processes
    • Organization and Format
    • Errata, Author Corrections, Retractions
    • Illustrations and Tables
    • Nomenclature
    • Abbreviations and Conventions
    • Publication Fees
    • Ethics Resources and Policies
  • About the Journal
    • About mSphere
    • Editor in Chief
    • Board of Editors
    • For Reviewers
    • For the Media
    • For Librarians
    • For Advertisers
    • Alerts
    • RSS
    • FAQ
  • ASM Journals
    • Antimicrobial Agents and Chemotherapy
    • Applied and Environmental Microbiology
    • Clinical Microbiology Reviews
    • Clinical and Vaccine Immunology
    • EcoSal Plus
    • Eukaryotic Cell
    • Infection and Immunity
    • Journal of Bacteriology
    • Journal of Clinical Microbiology
    • Journal of Microbiology & Biology Education
    • Journal of Virology
    • mBio
    • Microbiology and Molecular Biology Reviews
    • Microbiology Resource Announcements
    • Microbiology Spectrum
    • Molecular and Cellular Biology
    • mSphere
    • mSystems

User menu

  • Log in
  • My alerts
  • My Cart

Search

  • Advanced search
mSphere
publisher-logosite-logo

Advanced Search

  • Home
  • Articles
    • Latest Articles
    • COVID-19 Research and News from ASM Journals
    • mSphere of Influence: Commentaries from Early Career Microbiologists
    • Archive
  • Topics
    • Applied and Environmental Science
    • Clinical Science and Epidemiology
    • Ecological and Evolutionary Science
    • Host-Microbe Biology
    • Molecular Biology and Physiology
    • Therapeutics and Prevention
  • For Authors
    • Getting Started
    • Submit a Manuscript
    • Scope
    • Editorial Policy
    • Submission, Review, & Publication Processes
    • Organization and Format
    • Errata, Author Corrections, Retractions
    • Illustrations and Tables
    • Nomenclature
    • Abbreviations and Conventions
    • Publication Fees
    • Ethics Resources and Policies
  • About the Journal
    • About mSphere
    • Editor in Chief
    • Board of Editors
    • For Reviewers
    • For the Media
    • For Librarians
    • For Advertisers
    • Alerts
    • RSS
    • FAQ
Observation | Host-Microbe Biology

Natural Transmission of Helicobacter saguini Causes Multigenerational Inflammatory Bowel Disease in C57/129 IL-10−/− Mice

Anthony Mannion, Zeli Shen, Yan Feng, Dylan Puglisi, Sureshkumar Muthupalani, Mark T. Whary, James G. Fox
Vincent B. Young, Editor
Anthony Mannion
aDivision of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Zeli Shen
aDivision of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Yan Feng
aDivision of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Dylan Puglisi
aDivision of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Sureshkumar Muthupalani
aDivision of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Mark T. Whary
aDivision of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
James G. Fox
aDivision of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Vincent B. Young
University of Michigan—Ann Arbor
Roles: Editor
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI: 10.1128/mSphere.00011-20
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

ABSTRACT

Cotton-top tamarins (CTTs) are an ideal model of human inflammatory bowel disease (IBD) because these animals develop multigenerational, lower bowel cancer. We previously isolated and characterized a novel enterohepatic Helicobacter species, Helicobacter saguini, from CTTs with IBD and documented that H. saguini infection in germfree C57BL IL-10−/− mice recapitulates IBD, suggesting that H. saguini influences IBD etiopathogenesis. In this study, we utilized a germfree IL-10−/− model to illustrate that H. saguini infection can naturally transmit and infect four generations and cause significant intestinal inflammatory pathology. Additionally, whole-genome sequencing of representative H. saguini isolates from each generation of IL-10−/− mice revealed gene mutations suggestive of multigenerational evolution. Overall, these results support that specific bacterial species with pathogenic potential, like H. saguini, are transmissible microorganisms in the etiopathogenesis of IBD in CTTs and reinforces the importance of specific microbiota in the pathogenesis of IBD in humans.

IMPORTANCE While family history is a significant risk factor for developing inflammatory bowel disease (IBD), it is unclear whether the microbiome from parents is a transmissible influence on disease in their offspring. Furthermore, it is unknown whether IBD-associated microbes undergo genomic adaptations during multigenerational transmission and chronic colonization in their hosts. Herein, we show that a single bacterial species, Helicobacter saguini, isolated from a nonhuman primate species with familial IBD, is transmissible from parent to offspring in germfree IL-10−/− mice and causes multigenerational IBD. Additionally, whole-genome sequence analysis of H. saguini isolated from different mouse generations identified microevolutions in environmental interaction, nutrient metabolism, and virulence factor genes that suggest that multigenerational transmission may promote adaptations related to colonization and survival in new hosts and chronic inflammatory environments. The findings from our study highlight the importance of specific bacterial species with pathogenic potential, like H. saguini, as transmissible microorganisms in the etiopathogenesis of IBD.

OBSERVATION

While remaining idiopathic, inflammatory bowel disease (IBD) is the multifactorial result of genetic, environmental, and microbial interactions. Family history is the greatest risk factor (1, 2). The concordance rate of IBD in monozygotic twins is <50%, indicating incomplete genetic penetrance and reinforcing the importance of shared environmental factors, including the microbiome (3–6). Cotton-top tamarins (Saguinus oedipus) (CTTs) are nonhuman primates that, when in captivity, develop multigenerational, idiopathic IBD that progresses to colon cancer (7–10). These animals are considered an ideal model for IBD due to their clinical and histopathological similarities with human IBD; however, they are no longer used because they have been placed on the endangered species list. Interestingly, CTTs are more likely to develop colitis when cohoused in a colony with endemic IBD than when reared apart, suggesting transmission of specific microorganisms, which could be etiologically important (7). Our lab isolated Helicobacter saguini, a novel enterohepatic Helicobacter species (EHS), from the feces and colons of captive CTTs with IBD (9). Given that EHS infection has been associated with IBD in human patients and macaque species (11, 12) and that other EHS experimentally induce IBD in murine models (13), we hypothesized that H. saguini infection is associated with IBD in CTTs. Recently, we demonstrated that mono-associated H. saguini infection in germfree IL-10−/− mice caused typhlocolitis and argued that H. saguini contributes to IBD in CTTs (14). H. saguini, however, was unable to colonize specific-pathogen-free (SPF) IL-10−/− mice (14). In this study, we used the germfree IL-10−/− mouse model to test the hypothesis that H. saguini infection in captive CTT colonies is naturally transmitted through successive generations resulting in colitis in infected animals. Additionally, we studied how multigenerational H. saguini colonization yielded microevolutions in its genome that may have promoted chronic colonization and the sustained ability of H. saguini to induce pathogenicity.

Experimental results.To test whether H. saguini infection can be naturally transmitted to multiple generations, a male and female breeding pair (F0 generation) were orally dosed and colonized with H. saguini. Breeding of F0 yielded three pups (F1), one of which naturally acquired infection after being cohoused with its dam (Fig. 1A). Breeding of the infected F1 female with the F0 male yielded F2, and subsequent brother-sister mating produced F3 followed by F4 that also naturally acquired H. saguini infection (Fig. 1A). For all generations, pups remained cohoused with their dams for 5 to 6 weeks after weaning to promote natural transmission of H. saguini infection. Infected mice remained H. saguini PCR positive at necropsy. Fluorescence in situ hybridization (FISH) of the ceca of representative mice from each generation demonstrated that H. saguini localized at the mucosal surface, while no bacteria were present in the age-matched control mice (Fig. 1B). These data indicate that H. saguini infection chronically colonized germfree IL-10−/− mice for up to ∼40 weeks and that infection with H. saguini can be naturally transmitted from dams to offspring over four successive generations, likely via fecal-oral horizontal transmission.

FIG 1
  • Open in new tab
  • Download powerpoint
FIG 1

(A) Diagram showing experimental design for multigenerational infection study in germfree IL-10−/− mice. A male (♂) and female (♀) breeding pair (F0 generation) were orally dosed with H. saguini and then bred to produce the F1 generation. The infected F1 female was bred with the F0 male to yield F2, and brother-sister mating produced the sequential F3 and F4 generations. Pups remained with the dams for 5 to 6 weeks after weaning. Colonization with H. saguini was confirmed by PCR analysis of feces using the Helicobacter genus-specific primers and shown by a plus or minus sign within the gender symbol to designate which animals were positive or negative for infection, respectively. Mice were euthanized and necropsied from 5 to 40 weeks old (average ages of the mice in the different generations follow: F1, ∼40 weeks old; F2, ∼30 weeks old; F3, ∼25 weeks old; F4, ∼25 weeks old). Three cohorts of mice were included as age-matched controls (not shown in the diagram). (B) Fluorescence in situ hybridization (FISH) using a Helicobacter genus-specific probe in mouse ceca from representative mice of the different generations. H. saguini cells are labeled in red. 4′,6′-Diamidino-2-phenylindole (DAPI) stained the nuclei blue. (C) Histopathological scores for the ceca of germfree IL-10−/− mice from F1, F2, F3, and F4 generations compared to age-matched controls. Mice were separated based on sex and whether they were infected with H. saguini as determined by PCR [infected (PCR +) or not infected (PCR -)]. Values that are significantly different are indicated by bars and asterisks as follows: *, P value of <0.05; **, P value of <0.01. Values that are not significantly different (n.s.) are indicated. (D) Representative hematoxylin and eosin (H&E) staining images of cecum from H. saguini-infected IL-10−/− mouse from F4 generations compared to 40-week-old control mouse. H. saguini infection caused severe inflammation and architectural malformations to epithelial, mucosal, and submucosal layers of the cecum, not observed in the uninfected control mice. Images were taken at 40×, 100×, and ×200 magnifications, and bars represent 500, 200, and 100 μm distance, respectively. (E) Comparison of the colonization loads of H. saguini in feces from male and female mice from the F1, F2, F3, and F4 generations. *, P value of <0.05; n.s., not significant. (F) Histopathology scores in ceca versus colonization loads of H. saguini in feces from male and female mice from the F1, F2, F3, and F4 generations. (G) Inflammatory gene expression in cecal tissue in a representative litter from the F4 generation. Expression of each inflammatory gene was significantly greater in infected mice than in age-matched control mice (**, P value < 0.01; ***, P value < 0.001; n.s., not significant). The data are presented as the fold change compared to the mean gene expression of glyceraldehyde-3-phosphate dehydrogenase (GAPDH).

Mice PCR positive for H. saguini infection in all four generations developed significant inflammatory pathology in the cecum and colon compared to their respective age-matched controls (Fig. 1C; see also Fig. S1A in the supplemental material), except generation F1 in which only 1/3 mice were positive for infection. Litter 3 from generation F4, which failed to naturally acquire infection, did not have statistically different histology scores compared to those of the controls. Pathology in the cecum and colon was characterized by marked infiltration of inflammatory cells in the mucosa and submucosa along with dysplasia, hyperplasia, and epithelial and crypt defects (Fig. 1D and Fig. S1B). Interestingly, male mice from the F3 and F4 generations had considerably higher median cecum and colon pathology scores compared to their female counterparts, although the difference did not reach statistical significance (Fig. 1C and Fig. S1A). Fecal colonization of H. saguini was statistically higher in females than in males in the F3 generation and when all generations were pooled (Fig. 1E). Furthermore, we observed that mice colonized with ≥∼105 copies of H. saguini have cecum and colon pathology scores of <10 and were primarily females, while the opposite trend was seen for males (Fig. 1F and Fig. S1C). This suggests that females may tolerate higher colonization densities and elicit less robust pathology responses to H. saguini compared to males in this model.

FIG S1

(A) Histopathological scores for the colons of germfree IL-10−/− mice from F1, F2, F3, and F4 generations compared to age-matched controls. Mice were separated based on sex and whether they were infected with H. saguini as determined by PCR (infected, PCR +; noninfected, PCR -). *, P value < 0.05; **, P value < 0.01; n.s., not significant. (B) Representative H&E staining images of a colon from a H. saguini-infected IL-10−/− mouse from F4 generation compared to a40-week-old control mouse. H. saguini infection caused severe inflammation and architectural malformations to epithelial, mucosal, and submucosal layers of the colon, not observed in the uninfected control mice. Images were taken at 40×, 100×, and 200× magnifications, and bars represent 500, 200, and 100 μm distance, respectively. (C) Histopathology scores in colon versus colonization loads of H. saguini in feces of male and female mice from the F1, F2, F3, and F4 generations. (D) Representative immunohistochemistry images of cecum stained for γ-H2AX (green) and nuclei (DAPI; blue) from two H. saguini-infected mice from the F4 generation and two age-matched control mice. (E) Quantification of γ-H2AX-positive cells located in crypt epithelium in a representative litter from the F4 generation compared to age-matched control mice. **, P value of < 0.01. Download FIG S1, TIF file, 2.6 MB.
Copyright © 2020 Mannion et al.

This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.

The levels of inflammatory cytokines for interleukin 22 (IL-22), gamma interferon (IFN-γ), inducible nitric oxide synthase 2 (iNOS2), IL-17a, IL-6, tumor necrosis factor alpha (TNF-α), IL-23a, and IL-4 expressed in the ceca of a representative F4 litter were also significantly higher than those for age-matched controls (Fig. 1G). Immunohistochemistry was performed for the DNA histone modification, γ-H2AX, a marker for DNA damage (15) and apoptotic cells (16). H. saguini-infected mice from a representative F4 litter demonstrated significantly higher levels of γ-H2AX in the cecum compared to age-matched controls (Fig. S1D and E). These results indicated that multigenerational, chronic H. saguini infection induces inflammatory gene pathways as well as DNA damage and cell death.

Genomic microevolutions have been reported for the gastric carcinogen Helicobacter pylori during chronic host colonization (17, 18) and transmission to family members (19–21) as well as for the gastroenteritis-causing pathogen Campylobacter jejuni (a close relative to EHS) during adaption to new host species (22–26). However, whether microbes associated with IBD undergo genomic microevolution within their hosts is unknown. We sought to address this question by performing comparative genomic analyses between multigenerational H. saguini isolates. Representative H. saguini isolates were cultured from F0, F2, F3, and F4 mice. Although the mouse from the F1 generation had high H. saguini colonization levels (Fig. 1E), an isolate could not be recovered possibly because the organism did not remain viable/culturable after sample collection and frozen storage. Genomes for F0 to F4 isolates were sequenced using Illumina MiSeq and PacBio for high-quality de novo contig assemblies (see Tables S1 and S2 in the supplemental material). Gross rearrangements in chromosomal regions were not detected in the isolates. Variant analysis identified synonymous, nonsynonymous, insertion, and deletion mutational differences between the multigenerational genomes (Table S3) that occurred throughout the chromosome (Fig. 2A). Overall, the number of variants increased in a generational manner (Fig. 2B and C).

FIG 2
  • Open in new tab
  • Download powerpoint
FIG 2

(A) Graphical circular maps of chromosomes from H. saguini F0, F2, F3, and F4 isolates. The rings from the outermost ring to the innermost ring designate forward protein coding sequences (CDS), reverse CDS, and locations of gene variants between generational pairwise comparisons. (B) Number of variant genes or total variant hits detected in F0 versus F2, F3, and F4 isolate genomes. (C) Number of synonymous, nonsynonymous, insertion, and deletion variants detected in F0 versus F2, F3, and F4 isolate genomes. (D) KEGG automatic annotation server (KAAS) analysis to determine the top 10 most frequent KEGG (Kyoto Encyclopedia of Genes and Genomes) metabolic/functional pathways associated with the variant genes detected for F0 versus F2, F3, and F4 isolate genomes.

TABLE S1

Summary statistics for multigenerational H. saguini genome sequencing. Download Table S1, DOCX file, 0.01 MB.
Copyright © 2020 Mannion et al.

This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.

TABLE S2

Summary statistics for multigenerational H. saguini genome assembly and annotation. Download Table S2, DOCX file, 0.01 MB.
Copyright © 2020 Mannion et al.

This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.

TABLE S3

Variant sequences identified between the multigenerational genomes. Download Table S3, XLSX file, 0.2 MB.
Copyright © 2020 Mannion et al.

This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.

Based on functional and metabolic predictions, variant genes appeared to affect the interaction of H. saguini with its environment, as evidenced by mutations primarily occurring in two-component systems, such as chemotaxis, motility, and nutrient metabolism genes (Fig. 2D). Previous metabolic reconstructions predicted that H. saguini is dependent on amino/organic acid precursors and de novo biosynthetic pathways to meet carbon and nitrogen demands that fuel energetic needs (27). Alterations in chemotaxis and subsequent metabolism suggest that H. saguini may have adapted to the murine host and/or chronic inflammatory environment. Mutations were also detected in virulence factor genes associated with the biosynthesis and modification of lipopolysaccharide, lipooligosaccharides, and the polysaccharide capsule (Table S3). These mutations were often insertions and/or deletions in polynucleotide tracts that caused frameshifts and represent potential phase-variable genes. Mutations in phase-variable surface-associated genes, as described above, have been reported for H. pylori and C. jejuni and have been proposed to enable rapid adaptation to new or changing environments by altering pathogen-host cell interactions at the gastrointestinal mucosal/epithelial surface and antigenicity/detection by the host immune system (18, 21–23, 26, 28–33). The accumulation of gene variants indicated that H. saguini undergoes multigenerational microevolutions that may facilitate colonization and survival adaptations in its host. We hypothesized that multigenerational passage of H. saguini in germfree IL-10−/− mice yielded gene variants that would enhance its colonization in SPF IL-10−/− murine hosts. Therefore, SPF IL-10−/− mice were inoculated with the H. saguini F4 isolate. However, this strain failed to colonize (data not shown), possibly because the murine microbiota precluded H. saguini colonization, which was similar to our previous study attempting to infect SPF IL-10−/− mice with this organism (14).

Conclusion/summary.Here, we show that H. saguini infection can naturally transmit and persistently colonize several successive generations of germfree IL-10−/− mice to cause IBD. Given the coprophagic behavior of mice, horizontal transmission via the fecal-oral route is the likely mechanism for transmitting H. saguini infection from the dams to offspring. This is the primary mechanism by which EHS infection, such as H. hepaticus, are also transmitted to new hosts. Whole-genome comparative analyses identified host- and generation-dependent variant genes from H. saguini isolates, suggesting that IBD-associated microbes may adapt for colonization and survival in chronic inflammatory environments. However, in this study, in vitro culturing may have accounted for some genetic changes, although we attempted to minimize this potential by minimally passaging (≤4 times) H. saguini isolates before whole-genome sequencing. Future studies will be required to address the functional significance of the variant genes identified in the multigenerational H. saguini isolates. Nevertheless, our results support the hypothesis that transmission of specific microbiota (i.e., H. saguini) may be important in initiating and maintaining IBD in captive CTTs. In conclusion, the findings of this study warrant future investigations into the role of the microbiome in the etiopathogenesis of multigenerational IBD in other animal models and humans.

Methods.Germfree C57BL/6 (B6.129P2-IL-10tm1Cgn [IL-10−/−]) mice were infected with H. saguini MIT 97-6194-4 as previously described (14). Briefly, a male and female breeding pair (F0 generation) received 0.2 ml of fresh inoculum of H. saguini by gastric gavage every other day for three doses and then were bred to produce the F1 generation. The infected F1 female was bred with the F0 male to yield F2, and brother-sister mating produced the sequential F3 and F4 generations. Pups were cohoused with the dams for 5 to 6 weeks after weaning. Three cohorts of mice were included as age-matched controls. Colonization with H. saguini was confirmed by PCR of feces using the Helicobacter genus-specific primer pair C97/C05. Histopathological evaluation, fluorescence in situ hybridization (FISH), immunohistochemistry for γ-H2AX, and quantitative PCR (qPCR) for cytokine gene expression were performed as previously described (14). Colonization levels of H. saguini in fecal samples were quantified with qPCR targeting the 16s rRNA gene. Genomic copies were calculated from a standard curve of H. saguini genomic DNA in which 1 g of H. saguini genomic DNA (∼2.7 Mb) equals ∼3.43 × 1014 molecular copies (assuming 1 bp equals ∼650 g/mol and Avogadro’s number is ∼6.02 × 1023 molecules/mol). The levels of eukaryotic 18S rRNA from mouse DNA were determined using qPCR. Colonization levels were then normalized for each sample by reporting genomic copies of H. saguini per μg of mouse 18S rRNA. Cecal and colonic lesion scores, cytokine mRNA expression, H. saguini colonization levels, and γ-H2AX expression were analyzed using the Mann-Whitney U nonparametric test. Statistical analyses were performed using GraphPad Prism, version 5.0 (GraphPad Software, Inc., La Jolla, CA). Results were considered significant at a P value of <0.05.

H. saguini was cultured from fecal samples and intestinal samples as described previously (14). Isolates were repassaged ≤4 times to minimize potential genetic or phenotypic changes. Purified genomic DNA was sequenced by Illumina MiSeq (34) and Pacific Biosciences RSII (35). Spades version 3.10.1 was used for de novo hybrid assembly with the MiSeq reads and the PacBio filtered subreads as long-read scaffolds (36). Resulting contigs were annotated by RAST hosted by PATRIC (37). Sequence variants were identified using the Variation Analysis Service hosted by PATRIC with the BWA-mem aligner and FreeBayes single nucleotide polymorphism (SNP) caller. Further gene annotations and analyses for metabolic function and virulence factors were performed as previously described (27).

Ethics approval for animal studies.The protocols for use of animals were approved by the Committee on Animal Care of the Massachusetts Institute of Technology.

Data availability.All data and materials generated or analyzed during this study are included in this published article and its supplemental material files or are available from the corresponding author(s) upon request. DNA sequence and assembled genome data have been deposited in NCBI under the BioProject accession no. PRJNA449717.

ACKNOWLEDGMENTS

A.M. greatly acknowledges Greg Miller from Northeastern University and his thesis committee for their thoughtful insights and encouraging discussions.

This work was supported by the following NIH grants given to J.G.F.: T32-OD010978, P30-ES002109, P01-CA028848, and R35-CA210088.

We declare that we have no competing interests.

A.M. performed animal necropsies, tissue processing, bacterial culture, DNA isolation, genome assembly and analysis, data analysis and statistics, and wrote the manuscript. Z.S. performed tissue processing and bacterial culture, interpreted data, and reviewed the manuscript. Y.F. performed tissue processing for immunohistochemistry (IHC). D.G. performed animal necropsies and tissue processing. S.M. performed histopathological analysis. M.T.W. supervised germfree facility studies. J.G.F. conceived the project, supervised all studies, interpreted data, and reviewed and edited the manuscript. All authors read and approved the final manuscript.

FOOTNOTES

    • Received January 9, 2020.
    • Accepted March 7, 2020.
  • Copyright © 2020 Mannion et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

REFERENCES

  1. 1.↵
    1. Russell RK,
    2. Satsangi J
    . 2008. Does IBD run in families? Inflamm Bowel Dis 14(Suppl 2):S20–S21. doi:10.1002/ibd.20573.
    OpenUrlCrossRef
  2. 2.↵
    1. Halme L,
    2. Paavola-Sakki P,
    3. Turunen U,
    4. Lappalainen M,
    5. Farkkila M,
    6. Kontula K
    . 2006. Family and twin studies in inflammatory bowel disease. World J Gastroenterol 12:3668–3672. doi:10.3748/wjg.v12.i23.3668.
    OpenUrlCrossRefPubMedWeb of Science
  3. 3.↵
    1. Albenberg LG,
    2. Lewis JD,
    3. Wu GD
    . 2012. Food and the gut microbiota in inflammatory bowel diseases: a critical connection. Curr Opin Gastroenterol 28:314–320. doi:10.1097/MOG.0b013e328354586f.
    OpenUrlCrossRefPubMed
  4. 4.↵
    1. Lane ER,
    2. Zisman TL,
    3. Suskind DL
    . 2017. The microbiota in inflammatory bowel disease: current and therapeutic insights. J Inflamm Res 10:63–73. doi:10.2147/JIR.S116088.
    OpenUrlCrossRef
  5. 5.↵
    1. Ni J,
    2. Wu GD,
    3. Albenberg L,
    4. Tomov VT
    . 2017. Gut microbiota and IBD: causation or correlation? Nat Rev Gastroenterol Hepatol 14:573–584. doi:10.1038/nrgastro.2017.88.
    OpenUrlCrossRef
  6. 6.↵
    1. Lepage P,
    2. Hasler R,
    3. Spehlmann ME,
    4. Rehman A,
    5. Zvirbliene A,
    6. Begun A,
    7. Ott S,
    8. Kupcinskas L,
    9. Dore J,
    10. Raedler A,
    11. Schreiber S
    . 2011. Twin study indicates loss of interaction between microbiota and mucosa of patients with ulcerative colitis. Gastroenterology 141:227–236. doi:10.1053/j.gastro.2011.04.011.
    OpenUrlCrossRefPubMedWeb of Science
  7. 7.↵
    1. Johnson LD,
    2. Ausman LM,
    3. Sehgal PK,
    4. King N
    . 1996. A prospective study of the epidemiology of colitis and colon cancer in cotton-top tamarins (Saguinus oedipus). Gastroenterology 110:102–115. doi:10.1053/gast.1996.v110.pm8536845.
    OpenUrlCrossRefPubMed
  8. 8.↵
    1. Wood JD,
    2. Peck OC,
    3. Tefend KS,
    4. Rodriguez MM,
    5. Rodriguez MJV,
    6. Hernandez CJ,
    7. Stonerook MJ,
    8. Sharma HM
    . 1998. Colitis and colon cancer in cotton-top tamarins (Saguinus oedipus oedipus) living wild in their natural habitat. Dig Dis Sci 43:1443–1453. doi:10.1023/a:1018842210330.
    OpenUrlCrossRefPubMedWeb of Science
  9. 9.↵
    1. Saunders KE,
    2. Shen Z,
    3. Dewhirst FE,
    4. Paster BJ,
    5. Dangler CA,
    6. Fox JG
    . 1999. Novel intestinal Helicobacter species isolated from cotton-top tamarins (Saguinus oedipus) with chronic colitis. J Clin Microbiol 37:146–151. doi:10.1128/JCM.37.1.146-151.1999.
    OpenUrlAbstract/FREE Full Text
  10. 10.↵
    1. Bertone ER,
    2. Giovannucci EL,
    3. King NWJ,
    4. Petto AJ,
    5. Johnson LD
    . 1998. Family history as a risk factor for ulcerative colitis-associated colon cancer in cotton-top tamarin. Gastroenterology 114:669–674. doi:10.1016/S0016-5085(98)70580-3.
    OpenUrlCrossRefPubMedWeb of Science
  11. 11.↵
    1. Castano-Rodriguez N,
    2. Kaakoush NO,
    3. Lee WS,
    4. Mitchell HM
    . 2017. Dual role of Helicobacter and Campylobacter species in IBD: a systematic review and meta-analysis. Gut 66:235–249. doi:10.1136/gutjnl-2015-310545.
    OpenUrlAbstract/FREE Full Text
  12. 12.↵
    1. Hansen R,
    2. Thomson JM,
    3. Fox JG,
    4. El-Omar EM,
    5. Hold GL
    . 2011. Could Helicobacter organisms cause inflammatory bowel disease? FEMS Immunol Med Microbiol 61:1–14. doi:10.1111/j.1574-695X.2010.00744.x.
    OpenUrlCrossRefPubMed
  13. 13.↵
    1. Whary MT,
    2. Fox JG
    . 2004. Natural and experimental Helicobacter infections. Comp Med 54:128–158.
    OpenUrlPubMedWeb of Science
  14. 14.↵
    1. Shen Z,
    2. Mannion A,
    3. Whary MT,
    4. Muthupalani S,
    5. Sheh A,
    6. Feng Y,
    7. Gong G,
    8. Vandamme P,
    9. Holcombe HR,
    10. Paster BJ,
    11. Fox JG
    . 2016. Helicobacter saguini, a novel helicobacter isolated from cotton-top tamarins with ulcerative colitis, has proinflammatory properties and induces typhlocolitis and dysplasia in gnotobiotic IL-10−/− mice. Infect Immun 84:2307–2316. doi:10.1128/IAI.00235-16.
    OpenUrlAbstract/FREE Full Text
  15. 15.↵
    1. Rogakou EP,
    2. Pilch DR,
    3. Orr AH,
    4. Ivanova VS,
    5. Bonner WM
    . 1998. DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139. J Biol Chem 273:5858–5868. doi:10.1074/jbc.273.10.5858.
    OpenUrlAbstract/FREE Full Text
  16. 16.↵
    1. Rogakou EP,
    2. Nieves-Neira W,
    3. Boon C,
    4. Pommier Y,
    5. Bonner WM
    . 2000. Initiation of DNA fragmentation during apoptosis induces phosphorylation of H2AX histone at serine 139. J Biol Chem 275:9390–9395. doi:10.1074/jbc.275.13.9390.
    OpenUrlAbstract/FREE Full Text
  17. 17.↵
    1. Lundin A,
    2. Bjorkholm B,
    3. Kupershmidt I,
    4. Unemo M,
    5. Nilsson P,
    6. Andersson DI,
    7. Engstrand L
    . 2005. Slow genetic divergence of Helicobacter pylori strains during long-term colonization. Infect Immun 73:4818–4822. doi:10.1128/IAI.73.8.4818-4822.2005.
    OpenUrlAbstract/FREE Full Text
  18. 18.↵
    1. Nell S,
    2. Kennemann L,
    3. Schwarz S,
    4. Josenhans C,
    5. Suerbaum S
    . 2014. Dynamics of Lewis b binding and sequence variation of the babA adhesin gene during chronic Helicobacter pylori infection in humans mBio 5:e02281-14. doi:10.1128/mBio.02281-14.
    OpenUrlAbstract/FREE Full Text
  19. 19.↵
    1. Didelot X,
    2. Nell S,
    3. Yang I,
    4. Woltemate S,
    5. van der Merwe S,
    6. Suerbaum S
    . 2013. Genomic evolution and transmission of Helicobacter pylori in two South African families. Proc Natl Acad Sci U S A 110:13880–13885. doi:10.1073/pnas.1304681110.
    OpenUrlAbstract/FREE Full Text
  20. 20.↵
    1. Morelli G,
    2. Didelot X,
    3. Kusecek B,
    4. Schwarz S,
    5. Bahlawane C,
    6. Falush D,
    7. Suerbaum S,
    8. Achtman M
    . 2010. Microevolution of Helicobacter pylori during prolonged infection of single hosts and within families. PLoS Genet 6:e1001036. doi:10.1371/journal.pgen.1001036.
    OpenUrlCrossRefPubMed
  21. 21.↵
    1. Furuta Y,
    2. Konno M,
    3. Osaki T,
    4. Yonezawa H,
    5. Ishige T,
    6. Imai M,
    7. Shiwa Y,
    8. Shibata-Hatta M,
    9. Kanesaki Y,
    10. Yoshikawa H,
    11. Kamiya S,
    12. Kobayashi I
    . 2015. Microevolution of virulence-related genes in Helicobacter pylori familial infection. PLoS One 10:e0127197. doi:10.1371/journal.pone.0127197.
    OpenUrlCrossRef
  22. 22.↵
    1. Jerome JP,
    2. Bell JA,
    3. Plovanich-Jones AE,
    4. Barrick JE,
    5. Brown CT,
    6. Mansfield LS
    . 2011. Standing genetic variation in contingency loci drives the rapid adaptation of Campylobacter jejuni to a novel host. PLoS One 6:e16399. doi:10.1371/journal.pone.0016399.
    OpenUrlCrossRefPubMed
  23. 23.↵
    1. Thomas DK,
    2. Lone AG,
    3. Selinger LB,
    4. Taboada EN,
    5. Uwiera RRE,
    6. Abbott DW,
    7. Inglis GD
    . 2014. Comparative variation within the genome of Campylobacter jejuni NCTC 11168 in human and murine hosts. PLoS One 9:e88229. doi:10.1371/journal.pone.0088229.
    OpenUrlCrossRefPubMed
  24. 24.↵
    1. Bell JA,
    2. St Charles JL,
    3. Murphy AJ,
    4. Rathinam VAK,
    5. Plovanich-Jones AE,
    6. Stanley EL,
    7. Wolf JE,
    8. Gettings JR,
    9. Whittam TS,
    10. Mansfield LS
    . 2009. Multiple factors interact to produce responses resembling spectrum of human disease in Campylobacter jejuni infected C57BL/6 IL-10-/- mice. BMC Microbiol 9:57. doi:10.1186/1471-2180-9-57.
    OpenUrlCrossRefPubMed
  25. 25.↵
    1. Wilson DL,
    2. Rathinam VAK,
    3. Qi W,
    4. Wick LM,
    5. Landgraf J,
    6. Bell JA,
    7. Plovanich-Jones A,
    8. Parrish J,
    9. Finley RL,
    10. Mansfield LS,
    11. Linz JE
    . 2010. Genetic diversity in Campylobacter jejuni is associated with differential colonization of broiler chickens and C57BL/6J IL10-deficient mice. Microbiology 156:2046–2057. doi:10.1099/mic.0.035717-0.
    OpenUrlCrossRefPubMedWeb of Science
  26. 26.↵
    1. Kim J-S,
    2. Artymovich KA,
    3. Hall DF,
    4. Smith EJ,
    5. Fulton R,
    6. Bell J,
    7. Dybas L,
    8. Mansfield LS,
    9. Tempelman R,
    10. Wilson DL,
    11. Linz JE
    . 2012. Passage of Campylobacter jejuni through the chicken reservoir or mice promotes phase variation in contingency genes Cj0045 and Cj0170 that strongly associates with colonization and disease in a mouse model. Microbiology 158:1304–1316. doi:10.1099/mic.0.057158-0.
    OpenUrlCrossRefPubMedWeb of Science
  27. 27.↵
    1. Mannion A,
    2. Shen Z,
    3. Fox JG
    . 2018. Comparative genomics analysis to differentiate metabolic and virulence gene potential in gastric versus enterohepatic Helicobacter species. BMC Genomics 19:830. doi:10.1186/s12864-018-5171-2.
    OpenUrlCrossRef
  28. 28.↵
    1. Alm RA,
    2. Ling LS,
    3. Moir DT,
    4. King BL,
    5. Brown ED,
    6. Doig PC,
    7. Smith DR,
    8. Noonan B,
    9. Guild BC,
    10. deJonge BL,
    11. Carmel G,
    12. Tummino PJ,
    13. Caruso A,
    14. Uria-Nickelsen M,
    15. Mills DM,
    16. Ives C,
    17. Gibson R,
    18. Merberg D,
    19. Mills SD,
    20. Jiang Q,
    21. Taylor DE,
    22. Vovis GF,
    23. Trust TJ
    . 1999. Genomic-sequence comparison of two unrelated isolates of the human gastric pathogen Helicobacter pylori. Nature 397:176–180. doi:10.1038/16495.
    OpenUrlCrossRefPubMedWeb of Science
  29. 29.↵
    1. Salaun L,
    2. Linz B,
    3. Suerbaum S,
    4. Saunders NJ
    . 2004. The diversity within an expanded and redefined repertoire of phase-variable genes in Helicobacter pylori. Microbiology 150:817–830. doi:10.1099/mic.0.26993-0.
    OpenUrlCrossRefPubMedWeb of Science
  30. 30.↵
    1. Tomb JF,
    2. White O,
    3. Kerlavage AR,
    4. Clayton RA,
    5. Sutton GG,
    6. Fleischmann RD,
    7. Ketchum KA,
    8. Klenk HP,
    9. Gill S,
    10. Dougherty BA,
    11. Nelson K,
    12. Quackenbush J,
    13. Zhou L,
    14. Kirkness EF,
    15. Peterson S,
    16. Loftus B,
    17. Richardson D,
    18. Dodson R,
    19. Khalak HG,
    20. Glodek A,
    21. McKenney K,
    22. Fitzegerald LM,
    23. Lee N,
    24. Adams MD,
    25. Hickey EK,
    26. Berg DE,
    27. Gocayne JD,
    28. Utterback TR,
    29. Peterson JD,
    30. Kelley JM,
    31. Cotton MD,
    32. Weidman JM,
    33. Fujii C,
    34. Bowman C,
    35. Watthey L,
    36. Wallin E,
    37. Hayes WS,
    38. Borodovsky M,
    39. Karp PD,
    40. Smith HO,
    41. Fraser CM,
    42. Venter JC
    . 1997. The complete genome sequence of the gastric pathogen Helicobacter pylori. Nature 388:539–547. doi:10.1038/41483.
    OpenUrlCrossRefPubMedWeb of Science
  31. 31.↵
    1. Appelmelk BJ,
    2. Martin SL,
    3. Monteiro MA,
    4. Clayton CA,
    5. McColm AA,
    6. Zheng P,
    7. Verboom T,
    8. Maaskant JJ,
    9. van den Eijnden DH,
    10. Hokke CH,
    11. Perry MB,
    12. Vandenbroucke-Grauls CM,
    13. Kusters JG
    . 1999. Phase variation in Helicobacter pylori lipopolysaccharide due to changes in the lengths of poly(C) tracts in alpha3-fucosyltransferase genes. Infect Immun 67:5361–5366. doi:10.1128/IAI.67.10.5361-5366.1999.
    OpenUrlAbstract/FREE Full Text
  32. 32.↵
    1. Solnick JV,
    2. Hansen LM,
    3. Salama NR,
    4. Boonjakuakul JK,
    5. Syvanen M
    . 2004. Modification of Helicobacter pylori outer membrane protein expression during experimental infection of rhesus macaques. Proc Natl Acad Sci U S A 101:2106–2111. doi:10.1073/pnas.0308573100.
    OpenUrlAbstract/FREE Full Text
  33. 33.↵
    1. Bayliss CD,
    2. Bidmos FA,
    3. Anjum A,
    4. Manchev VT,
    5. Richards RL,
    6. Grossier J-P,
    7. Wooldridge KG,
    8. Ketley JM,
    9. Barrow PA,
    10. Jones MA,
    11. Tretyakov MV
    . 2012. Phase variable genes of Campylobacter jejuni exhibit high mutation rates and specific mutational patterns but mutability is not the major determinant of population structure during host colonization. Nucleic Acids Res 40:5876–5889. doi:10.1093/nar/gks246.
    OpenUrlCrossRefPubMedWeb of Science
  34. 34.↵
    1. Mannion A,
    2. Fabian N,
    3. Stair M,
    4. Dzink-Fox J,
    5. Carrasco SE,
    6. Buckley-Jordan E,
    7. Annamalai D,
    8. Fox JG
    . 2019. Draft genome sequences of Klebsiella pneumoniae strains isolated from immunocompromised NOD-scid gamma research mice. Microbiol Resour Announc 8:e00869-19. doi:10.1128/MRA.00869-19.
    OpenUrlAbstract/FREE Full Text
  35. 35.↵
    1. Mannion AJ,
    2. Martin HR,
    3. Shen Z,
    4. Buckley EM,
    5. Dzink-Fox JL,
    6. Garcia A,
    7. Marini RP,
    8. Patterson MM,
    9. Fox JG
    . 2018. Plasmid-mediated quinolone resistance in Shigella flexneri isolated from macaques. Front Microbiol 9:311. doi:10.3389/fmicb.2018.00311.
    OpenUrlCrossRef
  36. 36.↵
    1. Nurk S,
    2. Bankevich A,
    3. Antipov D,
    4. Gurevich AA,
    5. Korobeynikov A,
    6. Lapidus A,
    7. Prjibelski AD,
    8. Pyshkin A,
    9. Sirotkin A,
    10. Sirotkin Y,
    11. Stepanauskas R,
    12. Clingenpeel SR,
    13. Woyke T,
    14. McLean JS,
    15. Lasken R,
    16. Tesler G,
    17. Alekseyev MA,
    18. Pevzner PA
    . 2013. Assembling single-cell genomes and mini-metagenomes from chimeric MDA products. J Comput Biol 20:714–737. doi:10.1089/cmb.2013.0084.
    OpenUrlCrossRefPubMed
  37. 37.↵
    1. Wattam AR,
    2. Davis JJ,
    3. Assaf R,
    4. Boisvert S,
    5. Brettin T,
    6. Bun C,
    7. Conrad N,
    8. Dietrich EM,
    9. Disz T,
    10. Gabbard JL,
    11. Gerdes S,
    12. Henry CS,
    13. Kenyon RW,
    14. Machi D,
    15. Mao C,
    16. Nordberg EK,
    17. Olsen GJ,
    18. Murphy-Olson DE,
    19. Olson R,
    20. Overbeek R,
    21. Parrello B,
    22. Pusch GD,
    23. Shukla M,
    24. Vonstein V,
    25. Warren A,
    26. Xia F,
    27. Yoo H,
    28. Stevens RL
    . 2017. Improvements to PATRIC, the all-bacterial Bioinformatics Database and Analysis Resource Center. Nucleic Acids Res 45:D535–D542. doi:10.1093/nar/gkw1017.
    OpenUrlCrossRefPubMed
PreviousNext
Back to top
Download PDF
Citation Tools
Natural Transmission of Helicobacter saguini Causes Multigenerational Inflammatory Bowel Disease in C57/129 IL-10−/− Mice
Anthony Mannion, Zeli Shen, Yan Feng, Dylan Puglisi, Sureshkumar Muthupalani, Mark T. Whary, James G. Fox
mSphere Mar 2020, 5 (2) e00011-20; DOI: 10.1128/mSphere.00011-20

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Print
Alerts
Sign In to Email Alerts with your Email Address
Email

Thank you for sharing this mSphere article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Natural Transmission of Helicobacter saguini Causes Multigenerational Inflammatory Bowel Disease in C57/129 IL-10−/− Mice
(Your Name) has forwarded a page to you from mSphere
(Your Name) thought you would be interested in this article in mSphere.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
Natural Transmission of Helicobacter saguini Causes Multigenerational Inflammatory Bowel Disease in C57/129 IL-10−/− Mice
Anthony Mannion, Zeli Shen, Yan Feng, Dylan Puglisi, Sureshkumar Muthupalani, Mark T. Whary, James G. Fox
mSphere Mar 2020, 5 (2) e00011-20; DOI: 10.1128/mSphere.00011-20
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Top
  • Article
    • ABSTRACT
    • OBSERVATION
    • ACKNOWLEDGMENTS
    • FOOTNOTES
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • PDF

KEYWORDS

DNA damage
Helicobacter
cotton-top tamarins
germfree IL-10−/− mice
inflammatory bowel disease
microbiome
microevolutions
multigenerational
whole-genome sequencing

Related Articles

Cited By...

About

  • About mSphere
  • Board of Editors
  • Policies
  • For Reviewers
  • For the Media
  • Embargo Policy
  • For Librarians
  • For Advertisers
  • Alerts
  • RSS
  • FAQ
  • Permissions
  • Journal Announcements

Authors

  • ASM Author Center
  • Submit a Manuscript
  • Author Warranty
  • Types of Articles
  • Getting Started
  • Ethics
  • Contact Us

Follow #mSphereJ

@ASMicrobiology

       

 

Website feedback

ASM Journals

ASM journals are the most prominent publications in the field, delivering up-to-date and authoritative coverage of both basic and clinical microbiology.

About ASM | Contact Us | Press Room

 

ASM is a member of

Scientific Society Publisher Alliance

 

American Society for Microbiology
1752 N St. NW
Washington, DC 20036
Phone: (202) 737-3600

Copyright © 2021 American Society for Microbiology | Privacy Policy | Website feedback

Online ISSN: 2379-5042