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The Inner Jungle:
The Natural History of the Human Microbiome




                     Carl Zimmer
 Joint Summits on Translational Science Keynote Lecture
           San Francisco, CA, March 8, 2011
Linsley Pond
Branford, Connecticut
http://www.ct.gov/caes/cwp/view.asp?a=2799&q=381326
G. Evelyn Hutchinson
    (1903-1991)
http://apod.nasa.gov
Linsley Pond as an energy flow




                                Raymond Lindeman
                                www.cedarcreek.umn.edu/
Real food webs are even more complex than this...
The biodiversity of a little lake:

4 species of mammals
3 birds
20 fish
~200 zooplankton
~1,000 algae
~20,000 species total
Why so many species?




http://www.glerl.noaa.gov/pubs/brochures/foodweb/LMfoodweb.pdf
Hutchinson’s Niche   From The Art of Ecology, 2011
A complicated space   From The Art of Ecology, 2011
Heating of Linsley Pond   From The Art of Ecology, 2011
Dissolved substances   From The Art of Ecology, 2011
From The Art of Ecology, 2011
Time opens new niches
From The Art of Ecology, 2011
“The History of a Lake”
Transforming invasions: the alewife
Brooks and Dodson 1965, Science 150:28-35
Erosion and
eutrophication leave
     their mark




Brugham, Ecology 1979 59:19-36
Brugham, Ecology 1979 59:19-36
Max Delbruck
 (1906-1981)




http://en.wikipedia.org/wiki/
   File:Max_Delbruck.jpg
Max Delbruck
and Salvador Luria
Cold Spring Harbor Archives http://www.flickr.com/photos/cshlarchives/4276595071/
“Molecular genetics, our latest
wonder, has taught us to spell
out the connectivity of the tree
of life in such palpable detail that
we may say in plain words, ‘This
riddle of life has been solved.’
The ideas of information
storage, of the replication of the
stored information and of its            Max Delbruck,
programmed readout have                Nobel Lecture, 1969
become commonplace and have
filtered down into the popular
magazines and grade school
textbooks.”
blogs.discover
magazine.com/
    loom
It will unlock new insights into our
                                  origins and history as a species;
                                  and it points to new ways of
                                  combating disease. The people of
                                  many countries have invested in
                                  the Human Genome Project's
                                  determination of the sequence, and
                                  it is hard to see how that
                                  investment could have received
                                  better returns.




http://www.nature.com/nature/journal/v409/n6822/full/409745a0.html
A flood of data...
...and impatience




http://tech.fortune.cnn.com/2010/04/08/the-decade-of-the-human-genome-where-are-the-fab-four/
The Genomic Hype Cycle




 http://en.wikipedia.org/wiki/Hype_cycle
Yes, we’re like viruses...
...but we are also like lakes
“Wee animacules”
Diaper ecology
An undeserved fame
Wang et al, Appl Microbiol Biotechnol (2010) 88:1333–1342
Stalking the Wild Microbiome




Wang et al, Appl Microbiol Biotechnol (2010) 88:1333–1342
100 trillion
microbes in your
   body: more
microbes than all
the humans who
 have ever lived
             sigen.org
Imagine producing an elephant’s worth of microbes
Now multiply times five
Microbial abundance raises the
 question: how human are we?
                  Human:
                  10 trillion human cells
                  20,000 human genes




Microbiota:                                 Microbiota:
100 trillion microbial cells                20 million microbial genes
  99.9% of our genomes the same, but our microbes...?
The microbiome is like an extra organ




        Sekirov, I. et al. Physiol. Rev. 90: 859-904 2010;
               doi:10.1152/physrev.00045.2009

                Copyright ©2010 American Physiological Society
The microbiome
helps digest food &
  metabolize drugs




Annu. Rev. Nutr. 2002. 22:283–307
doi: 10.1146/annurev.nutr.22.011602.092259
The microbiome
manages the
immune system




Fraune and Bosch 2010
Bioessays 32: 571–580
The microbiome kills invading pathogens




The skin bacteria
Staphylococcus
epidermis makes
δ-toxin and kills
S. aureus


 Cogen et al, PLoS ONE 5(1): e8557. doi:10.1371/journal.pone.0008557
The microbiome heals wounds




Left ear: wound                                              Right ear: wound
without S. epidermis                                         with S. epidermis




                  Lai 2009 Nature Medicine 15, 1377 - 1382 (2009)
The microbiome: an
organ that works as
an ecosystem
Diversity from nose to nose




           Wos-Oxley et al, The ISME Journal (2010) 4, 839–851
Mouth to mouth: 818 bacterial species lives in three people’s
mouths, 387 shared by all three.




                                    Zaura et al BMC Microbiol (2009) vol. 9 (1) pp. 259
What is the shape of the core microbiome?




Hamady M , Knight R Genome Res. 2009;19:1141-1152
Or is it a core of genes, not of species?
Hamady M , Knight R Genome Res. 2009;19:1141-1152
Diversity within
    the core


    Periphery
(not in all people)




      Core
 (in all people)
                      Costello et al, Science Vol. 326 no. 5960 pp. 1694-1697
r                              Hair

                                                  The body has many niches
                                                                Hair
ehead                          Forehead
                                                                Forehead
ernal ear (L)                  External nose
                                                                External nose
ernal ear (R)                  External ear (R)
                                                                External ear (R)
 el                            External ear (L)                 External ear (L)
mpit (R)                       Palm (R)
                                                                Palm (R)
mpit (L)                       Index finger (R)
                                                                Index finger (R)
ernal nose                     Palm (L)                         Palm (L)
 tril (R)                      Index finger (L)                 Index finger (L)
 tril (L)                      Forearm (R)                      Forearm (R)
ex finger (R)                  Forearm (L)                      Forearm (L)
m (R)                          Nostril (R)                      Nostril (R)
ex finger (L)                  Nostril (L)                      Nostril (L)
earm (R)                       EAC (R)                          Armpit (R)
earm (L)                       EAC (L)                          Armpit (L)
m (L)                          Armpit (R)                       Sole of foot (R)
 k of knee (R)                 Armpit (L)                       Sole of foot (L)
 k of knee (L)                 Sole of foot (R)                 Back of knee (R)
e of foot (R)                  Sole of foot (L)                 Back of knee (L)
e of foot (L)                  Back of knee (R)                 Navel
C (R)                          Back of knee (L)                 EAC (R)
C (L)                          Navel                            EAC (L)
ns penis                       Glans penis                      Glans penis
 ia minora                     Labia minora                     Labia minora
 l cavity                      Oral cavity                      Oral cavity
 sal tongue                    Dorsal tongue                    Dorsal tongue
 (Sp)                          Gut (Sp)                         Gut (Sp)
 (Sw)                          Gut (Sw)                         Gut (Sw)
                 0.02                              0.05




                        weighted                  quantitative symmetric
                        UniFrac                       (Kulczynski)
                                                    Costello et al, Science Vol. 326 no. 5960 pp. 1694-1697
                                                                        Fig. S11
Detailed biogeography of the
human face
Detailed biogeography of the
human face
Wang et al, Appl Microbiol Biotechnol (2010) 88:1333–1342
From The Art of Ecology, 2011
Time opens new niches
Time opens new niches
A                          0.9



                           0.8
UniFrac distance




                           0.7



                           0.6                                                 variation within people
                                                                               (day-to-day)

                                                                               variation between people
                           0.5                                                 (on any given day)




                           0.4
                                  Oral     Gut   Skin   Nostril   Hair   EAC
                                 cavity
                                                   Habitat


B                          0.3
eighted UniFrac distance




                           0.2




                                                                               variation within people
                           0.1                                                 (day-to-day)
                                                                                       Costello et al, Science Vol. 326 no. 5960 pp. 1694-1697
                                                                               variation between people
Diversity through co-dependence:
the case of the elusive mouth resident, Synergistetes




 Vartoukian et al Environmental Microbiology (2010) 12(4), 916–928
Top: Synergistetes alone in culture grows
                                           extremely slowly




                                  Bottom: Parvimonas micra speeds up
                                    growth of Synergistetes (streak)


Vartoukian et al Environmental Microbiology (2010) 12(4), 916–928
It’s a jungle in there
Four mouth microbes that cannot grow alone


Actinomyces                                                                      Streptococcus
 naeshindii                                                                          oralis




Fusobacterium                                                                    Porphyromonas
  nucleatum                                                                          gigivalis
                Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
Four mouth microbes that cannot grow alone
                        supports the growth of

Actinomyces                                                                      Streptococcus
 naeshindii                                                                          oralis
                         supports the growth of




Fusobacterium                                                                    Porphyromonas
  nucleatum                                                                          gigivalis
                Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
Four mouth microbes that cannot grow alone
                        supports the growth of

Actinomyces                                                                      Streptococcus
 naeshindii                                                                          oralis
                         supports the growth of


 supports the
  growth of




Fusobacterium                                                                    Porphyromonas
  nucleatum                                                                          gigivalis
                Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
Four mouth microbes that cannot grow alone
                        supports the growth of

Actinomyces                                                                      Streptococcus
 naeshindii                                                                          oralis
                         supports the growth of


 supports the
  growth of




                       supports the growth of
Fusobacterium                                                                    Porphyromonas
  nucleatum                                                                          gigivalis
                Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
Four mouth microbes that cannot grow alone
                        supports the growth of

Actinomyces                                                                      Streptococcus
 naeshindii                                                                          oralis
                         supports the growth of


 supports the                                                                    cannot support the
  growth of                                                                          growth of




                       supports the growth of
Fusobacterium                                                                    Porphyromonas
  nucleatum                                                                          gigivalis
                Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
Four mouth microbes that cannot grow alone
                        supports the growth of

Actinomyces                                                                      Streptococcus
 naeshindii                                                                          oralis
                         supports the growth of


 supports the             cannot support on its                                  cannot support the
  growth of                own, but can speed                                        growth of
                         growth if A. naeshindii is
                              also present


                       supports the growth of
Fusobacterium                                                                    Porphyromonas
  nucleatum                                                                          gigivalis
                Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
The Tangled Bank




Kolenbrander et al 2010 Nature Reviews Microbiology 8:471
“The History of a Lake”   From The Art of Ecology, 2011
The History of A Microbiome




  Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
From sterile to lush in a matter of weeks




      Fierer et al, Research in Microbiology 161 (2010) 635e642
Sampling of the microbiota 20
minutes after birth
Koenig et al, PNAS 2010
A baby’s microbiome
grows more diverse




                      Koenig et al, PNAS 2010
A lesson from ecology:
                                                   diversity is healthy




 Salmonella invades more
 successfully if mice are
 treated with antibiotics, have
 low-diversity microbiomes
 (LCM), or are germ-free

Photo- http://flic.kr/p/3vhoNg   Stecher and Hardt Current Opinion in Microbiology 2010, 14:1–10
Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
Two invaders that alter ecosystems




Alewife




              Helicobacter hepatica
As Helicobacter hepaticus
 becomes more common in
mouse cecae (A), microbiome
     diversity falls (B)




KUEHL ET AL, INFECTION AND IMMUNITY, Oct. 2005, p. 6952–6961
A Manmade Catastrophe (for the Microbiome)
Jernberg et al, Microbiology (2010), 156, 3216–3223
Antonopoulos et al, Infection and Immunity (2009) vol. 77 (6) pp. 2367-2375
Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
Microbes guide the flow of energy
Do My Bacteria Make Me Look Fat?




Ley RE, Backhed F, Turnbaugh P, et al. 2005. Proc Natl Acad Sci USA 102: 11070–5.
•   Germ-free mice given
                        ob/ob or wild-type gut
                        microbes
                    •   Chow consumption and
                        exercise the same for
                        both groups
                    •   Both sets of mice had
                        similar starting weight
                        and percentage of body
                        fat


Turnbaugh, et al. Nature 2006; 444:1027
Sandoval et al, Science 328, 179 (2010)
Kinross et al. Genome Medicine 2011, 3:14
Becoming Ecosystem Engineers




Alexander Khoruts, University of Minnestoa
Khoruts’s dilemma:


              61 year old patient
--Antibiotics for lung infection led to intestinal
               C. difficile infection
          Chronic Diarrhea - 8 months
   Loose bowel movements every 15 minutes
            Wore diapers at all times
            Confined to a wheel chair
                     Lost 27 Kg
   Antibiotic therapy for C. difficile uneffective
                     Khoruts, et al. J. Clin. Gastroenterol. 44, 354–360 (2010)
Microbiome transplant




        Khoruts, et al. J. Clin. Gastroenterol. 44, 354–360 (2010)
Patient had first solid bowel movement 2
          days after treatment
On 6 month follow up visit, reported daily
     stools that were well formed
                   Khoruts, et al. J. Clin. Gastroenterol. 44, 354–360 (2010)
Thanks to Jonathan Eisen, Karen Jansson, Rob Knight,
Sarkis Mazmanian, David Post, and David Skelly




                     For more information,
                      visit carlzimmer.com

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The Human Jungle: Exploring the Microbiome

  • 1. The Inner Jungle: The Natural History of the Human Microbiome Carl Zimmer Joint Summits on Translational Science Keynote Lecture San Francisco, CA, March 8, 2011
  • 3.
  • 4. G. Evelyn Hutchinson (1903-1991)
  • 5.
  • 7.
  • 8. Linsley Pond as an energy flow Raymond Lindeman www.cedarcreek.umn.edu/
  • 9. Real food webs are even more complex than this...
  • 10. The biodiversity of a little lake: 4 species of mammals 3 birds 20 fish ~200 zooplankton ~1,000 algae ~20,000 species total
  • 11. Why so many species? http://www.glerl.noaa.gov/pubs/brochures/foodweb/LMfoodweb.pdf
  • 12. Hutchinson’s Niche From The Art of Ecology, 2011
  • 13. A complicated space From The Art of Ecology, 2011
  • 14. Heating of Linsley Pond From The Art of Ecology, 2011
  • 15. Dissolved substances From The Art of Ecology, 2011
  • 16. From The Art of Ecology, 2011 Time opens new niches
  • 17. From The Art of Ecology, 2011 “The History of a Lake”
  • 19.
  • 20. Brooks and Dodson 1965, Science 150:28-35
  • 21.
  • 22. Erosion and eutrophication leave their mark Brugham, Ecology 1979 59:19-36
  • 24.
  • 26.
  • 27.
  • 29.
  • 30. Cold Spring Harbor Archives http://www.flickr.com/photos/cshlarchives/4276595071/
  • 31. “Molecular genetics, our latest wonder, has taught us to spell out the connectivity of the tree of life in such palpable detail that we may say in plain words, ‘This riddle of life has been solved.’ The ideas of information storage, of the replication of the stored information and of its Max Delbruck, programmed readout have Nobel Lecture, 1969 become commonplace and have filtered down into the popular magazines and grade school textbooks.”
  • 33. It will unlock new insights into our origins and history as a species; and it points to new ways of combating disease. The people of many countries have invested in the Human Genome Project's determination of the sequence, and it is hard to see how that investment could have received better returns. http://www.nature.com/nature/journal/v409/n6822/full/409745a0.html
  • 34. A flood of data...
  • 36. The Genomic Hype Cycle http://en.wikipedia.org/wiki/Hype_cycle
  • 37. Yes, we’re like viruses...
  • 38. ...but we are also like lakes
  • 39.
  • 41.
  • 44. Wang et al, Appl Microbiol Biotechnol (2010) 88:1333–1342
  • 45. Stalking the Wild Microbiome Wang et al, Appl Microbiol Biotechnol (2010) 88:1333–1342
  • 46. 100 trillion microbes in your body: more microbes than all the humans who have ever lived sigen.org
  • 47. Imagine producing an elephant’s worth of microbes
  • 49. Microbial abundance raises the question: how human are we? Human: 10 trillion human cells 20,000 human genes Microbiota: Microbiota: 100 trillion microbial cells 20 million microbial genes 99.9% of our genomes the same, but our microbes...?
  • 50. The microbiome is like an extra organ Sekirov, I. et al. Physiol. Rev. 90: 859-904 2010; doi:10.1152/physrev.00045.2009 Copyright ©2010 American Physiological Society
  • 51. The microbiome helps digest food & metabolize drugs Annu. Rev. Nutr. 2002. 22:283–307 doi: 10.1146/annurev.nutr.22.011602.092259
  • 52. The microbiome manages the immune system Fraune and Bosch 2010 Bioessays 32: 571–580
  • 53. The microbiome kills invading pathogens The skin bacteria Staphylococcus epidermis makes δ-toxin and kills S. aureus Cogen et al, PLoS ONE 5(1): e8557. doi:10.1371/journal.pone.0008557
  • 54. The microbiome heals wounds Left ear: wound Right ear: wound without S. epidermis with S. epidermis Lai 2009 Nature Medicine 15, 1377 - 1382 (2009)
  • 55. The microbiome: an organ that works as an ecosystem
  • 56. Diversity from nose to nose Wos-Oxley et al, The ISME Journal (2010) 4, 839–851
  • 57. Mouth to mouth: 818 bacterial species lives in three people’s mouths, 387 shared by all three. Zaura et al BMC Microbiol (2009) vol. 9 (1) pp. 259
  • 58. What is the shape of the core microbiome? Hamady M , Knight R Genome Res. 2009;19:1141-1152
  • 59. Or is it a core of genes, not of species? Hamady M , Knight R Genome Res. 2009;19:1141-1152
  • 60. Diversity within the core Periphery (not in all people) Core (in all people) Costello et al, Science Vol. 326 no. 5960 pp. 1694-1697
  • 61. r Hair The body has many niches Hair ehead Forehead Forehead ernal ear (L) External nose External nose ernal ear (R) External ear (R) External ear (R) el External ear (L) External ear (L) mpit (R) Palm (R) Palm (R) mpit (L) Index finger (R) Index finger (R) ernal nose Palm (L) Palm (L) tril (R) Index finger (L) Index finger (L) tril (L) Forearm (R) Forearm (R) ex finger (R) Forearm (L) Forearm (L) m (R) Nostril (R) Nostril (R) ex finger (L) Nostril (L) Nostril (L) earm (R) EAC (R) Armpit (R) earm (L) EAC (L) Armpit (L) m (L) Armpit (R) Sole of foot (R) k of knee (R) Armpit (L) Sole of foot (L) k of knee (L) Sole of foot (R) Back of knee (R) e of foot (R) Sole of foot (L) Back of knee (L) e of foot (L) Back of knee (R) Navel C (R) Back of knee (L) EAC (R) C (L) Navel EAC (L) ns penis Glans penis Glans penis ia minora Labia minora Labia minora l cavity Oral cavity Oral cavity sal tongue Dorsal tongue Dorsal tongue (Sp) Gut (Sp) Gut (Sp) (Sw) Gut (Sw) Gut (Sw) 0.02 0.05 weighted quantitative symmetric UniFrac (Kulczynski) Costello et al, Science Vol. 326 no. 5960 pp. 1694-1697 Fig. S11
  • 62. Detailed biogeography of the human face
  • 63. Detailed biogeography of the human face
  • 64. Wang et al, Appl Microbiol Biotechnol (2010) 88:1333–1342
  • 65. From The Art of Ecology, 2011 Time opens new niches
  • 66. Time opens new niches A 0.9 0.8 UniFrac distance 0.7 0.6 variation within people (day-to-day) variation between people 0.5 (on any given day) 0.4 Oral Gut Skin Nostril Hair EAC cavity Habitat B 0.3 eighted UniFrac distance 0.2 variation within people 0.1 (day-to-day) Costello et al, Science Vol. 326 no. 5960 pp. 1694-1697 variation between people
  • 67. Diversity through co-dependence: the case of the elusive mouth resident, Synergistetes Vartoukian et al Environmental Microbiology (2010) 12(4), 916–928
  • 68. Top: Synergistetes alone in culture grows extremely slowly Bottom: Parvimonas micra speeds up growth of Synergistetes (streak) Vartoukian et al Environmental Microbiology (2010) 12(4), 916–928
  • 69. It’s a jungle in there
  • 70. Four mouth microbes that cannot grow alone Actinomyces Streptococcus naeshindii oralis Fusobacterium Porphyromonas nucleatum gigivalis Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
  • 71. Four mouth microbes that cannot grow alone supports the growth of Actinomyces Streptococcus naeshindii oralis supports the growth of Fusobacterium Porphyromonas nucleatum gigivalis Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
  • 72. Four mouth microbes that cannot grow alone supports the growth of Actinomyces Streptococcus naeshindii oralis supports the growth of supports the growth of Fusobacterium Porphyromonas nucleatum gigivalis Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
  • 73. Four mouth microbes that cannot grow alone supports the growth of Actinomyces Streptococcus naeshindii oralis supports the growth of supports the growth of supports the growth of Fusobacterium Porphyromonas nucleatum gigivalis Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
  • 74. Four mouth microbes that cannot grow alone supports the growth of Actinomyces Streptococcus naeshindii oralis supports the growth of supports the cannot support the growth of growth of supports the growth of Fusobacterium Porphyromonas nucleatum gigivalis Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
  • 75. Four mouth microbes that cannot grow alone supports the growth of Actinomyces Streptococcus naeshindii oralis supports the growth of supports the cannot support on its cannot support the growth of own, but can speed growth of growth if A. naeshindii is also present supports the growth of Fusobacterium Porphyromonas nucleatum gigivalis Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
  • 76. The Tangled Bank Kolenbrander et al 2010 Nature Reviews Microbiology 8:471
  • 77. “The History of a Lake” From The Art of Ecology, 2011
  • 78. The History of A Microbiome Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
  • 79. From sterile to lush in a matter of weeks Fierer et al, Research in Microbiology 161 (2010) 635e642
  • 80. Sampling of the microbiota 20 minutes after birth
  • 81. Koenig et al, PNAS 2010
  • 82. A baby’s microbiome grows more diverse Koenig et al, PNAS 2010
  • 83. A lesson from ecology: diversity is healthy Salmonella invades more successfully if mice are treated with antibiotics, have low-diversity microbiomes (LCM), or are germ-free Photo- http://flic.kr/p/3vhoNg Stecher and Hardt Current Opinion in Microbiology 2010, 14:1–10
  • 84. Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
  • 85. Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
  • 86. Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
  • 87. Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
  • 88. Reid et al Nat Rev Micro (2011) vol. 9 (1) pp. 27-38
  • 89. Two invaders that alter ecosystems Alewife Helicobacter hepatica
  • 90. As Helicobacter hepaticus becomes more common in mouse cecae (A), microbiome diversity falls (B) KUEHL ET AL, INFECTION AND IMMUNITY, Oct. 2005, p. 6952–6961
  • 91. A Manmade Catastrophe (for the Microbiome)
  • 92. Jernberg et al, Microbiology (2010), 156, 3216–3223
  • 93. Antonopoulos et al, Infection and Immunity (2009) vol. 77 (6) pp. 2367-2375
  • 94. Robinson et al, Microbiol Mol Biol Rev. 2010 Sep;74(3):453-76.
  • 95. Microbes guide the flow of energy
  • 96. Do My Bacteria Make Me Look Fat? Ley RE, Backhed F, Turnbaugh P, et al. 2005. Proc Natl Acad Sci USA 102: 11070–5.
  • 97. Germ-free mice given ob/ob or wild-type gut microbes • Chow consumption and exercise the same for both groups • Both sets of mice had similar starting weight and percentage of body fat Turnbaugh, et al. Nature 2006; 444:1027
  • 98. Sandoval et al, Science 328, 179 (2010)
  • 99. Kinross et al. Genome Medicine 2011, 3:14
  • 100. Becoming Ecosystem Engineers Alexander Khoruts, University of Minnestoa
  • 101. Khoruts’s dilemma: 61 year old patient --Antibiotics for lung infection led to intestinal C. difficile infection Chronic Diarrhea - 8 months Loose bowel movements every 15 minutes Wore diapers at all times Confined to a wheel chair Lost 27 Kg Antibiotic therapy for C. difficile uneffective Khoruts, et al. J. Clin. Gastroenterol. 44, 354–360 (2010)
  • 102. Microbiome transplant Khoruts, et al. J. Clin. Gastroenterol. 44, 354–360 (2010)
  • 103. Patient had first solid bowel movement 2 days after treatment On 6 month follow up visit, reported daily stools that were well formed Khoruts, et al. J. Clin. Gastroenterol. 44, 354–360 (2010)
  • 104.
  • 105.
  • 106. Thanks to Jonathan Eisen, Karen Jansson, Rob Knight, Sarkis Mazmanian, David Post, and David Skelly For more information, visit carlzimmer.com

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  58. Models of a core microbiome. The circles represent the microbial communities in different individuals and can be thought of as either representing different taxa (species, genera, etc.) or representing different genes. (A) “Substantial core” model. Most individuals share most components of the microbiota. (B) “Minimal core” model. All individuals share a few components, and any individual shares many components with a few other individuals, but very little is shared across all individuals. (C) “No core” model. Nothing is shared by all individuals, and most diversity is unique to a given individual. (D) “Gradient” model. Individuals next to each other on a gradient, for example, age or obesity, share many components, but individuals at opposite ends share little or nothing. (E) “Subpopulation” model. Different subpopulations, for example, those defined by geography or disease, have different cores, but nothing is shared across subpopulations. Scenarios C–E would represent situations in which the strategy of identifying core species for sequencing, then using these as a scaffold for “omics” studies, would be problematic.\n
  59. Models of a core microbiome. The circles represent the microbial communities in different individuals and can be thought of as either representing different taxa (species, genera, etc.) or representing different genes. (A) “Substantial core” model. Most individuals share most components of the microbiota. (B) “Minimal core” model. All individuals share a few components, and any individual shares many components with a few other individuals, but very little is shared across all individuals. (C) “No core” model. Nothing is shared by all individuals, and most diversity is unique to a given individual. (D) “Gradient” model. Individuals next to each other on a gradient, for example, age or obesity, share many components, but individuals at opposite ends share little or nothing. (E) “Subpopulation” model. Different subpopulations, for example, those defined by geography or disease, have different cores, but nothing is shared across subpopulations. Scenarios C–E would represent situations in which the strategy of identifying core species for sequencing, then using these as a scaffold for “omics” studies, would be problematic.\n
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