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bioRxiv Paper
April 30, 2017.
PNAS Paper
As an additional complication, many microbiome surveys do not
distinguish between dead or dormant passengers [“transients” (33)] and
persistent, living populations [“residents” (33) or “symbionts” sensu
(34)]. Furthermore, microbes in the latter category may be parasitic or
pathogenic, as well as beneficial.
Residents vs. Transients
Do caterpillars depend on gut microbes for feeding and development?
To answer this question, we first characterized gut microbial abundance and composition across
a taxonomically and geographically broad array of wild caterpillars
•Our analyses are focused on the digestive tract, the most likely habitat for microbial
colonization, as abundant microbes have not been observed elsewhere in the caterpillar
body
•We applied the same methods to 24 additional insect, bird, and mammal species that we
expected to have functional microbiomes to assess the reliability of our protocol and to
contextualize our findings
•We then conducted a field-based experiment testing whether gut bacteria impact larval
growth and survival of the model species
Low density of microbes
Using quantitative PCR and sequencing of the 16S rRNA gene, we found
that wild caterpillars representing a broad diversity of Lepidoptera had gut
bacterial densities multiple orders of magnitude lower than the
microbiomes of other insects and vertebrate feces measured using identical
methods
in most caterpillars over 80% of fecal 16S rRNA gene sequences were from
plant chloroplasts or mitochondria versus ∼0.1% for other herbivores or
omnivores with plant-rich diets
Most caterpillar gut sequences from plants
Animals with functionally important, resident microbiomes tend to host a
high abundance of microbial taxa shared among conspecific individuals
Indeed, within species of the other insects and vertebrates analyzed here,
microbiomes were largely made up of a common set of bacterial
phylotypes (Fig. 1C).
This observation hints that many of the core taxa found in caterpillar guts
may be transient, food-derived microbes.
Non Caterpillar Controls
Caterpillar gut microbiomes are dominated by leaf-associated bacteria,
further suggesting that resident, host-specific symbionts are sparse or
absent.
Other caterpillar gut sequences
mostly leaf associated
Low precision may partly explain the extensive variation in caterpillar
gut bacterial loads (Fig. 1A)
However, transient inputs of leaf microbes also generate variation
among caterpillar species and individuals
Lots of variation between individuals
Furthermore, bacterial densities dropped by a median of 214-fold from
leaves to feces (Fig. 2A), suggesting that any potential bacterial growth
within the gut is relatively minor.
Bacterial density: poop <<< leaves
Variation in bacterial taxonomic composition among leaves and caterpillar
feces was also correlated
In other words, caterpillars consuming leaves with more distinct bacterial
assemblages had more distinct bacterial assemblages in their feces, as would
be expected if gut microbes are diet-derived and only transiently present.
Variation correlated in poop and leaves
Moreover, this process can explain a relationship between host relatedness
and microbiome structure, a pattern sometimes termed “phylosymbiosis”
(48). Specifically, although confamilial caterpillars in Costa Rica had
marginally more similar gut bacterial assemblages than did caterpillars in
different families (PERMANOVA, pseudo-F6,43 = 1.47, P = 0.053), they
had also been feeding on plants with especially similar leaf microbiomes
(PERMANOVA, pseudo-F6,42 = 1.73, P = 0.005).
Variation correlated in poop and leaves
Supporting our claim that caterpillars lack resident gut microbiomes, we show experimentally
that the growth and survival of field-collected M. sexta caterpillars are not dependent on gut
bacterial activity
Given that antibiotics reduced fecal bacteria to a variable extent within and among treatments (SI
Appendix, Fig. S4A), we repeated the aforementioned analyses using gut bac- terial abundance
as the predictor variable. In all cases there was no significant relationship with host performance
(P > 0.1), further indicating that reducing or eliminating gut bacteria from caterpillars does not
reduce M. sexta fitness.
Antibiotics don’t do shit
Supplemental Figures
Discussion of "Caterpillars lack a resident gut microbiome"
Discussion of "Caterpillars lack a resident gut microbiome"
Discussion of "Caterpillars lack a resident gut microbiome"
Discussion of "Caterpillars lack a resident gut microbiome"
Discussion of "Caterpillars lack a resident gut microbiome"
Discussion of "Caterpillars lack a resident gut microbiome"

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Discussion of "Caterpillars lack a resident gut microbiome"

  • 3. As an additional complication, many microbiome surveys do not distinguish between dead or dormant passengers [“transients” (33)] and persistent, living populations [“residents” (33) or “symbionts” sensu (34)]. Furthermore, microbes in the latter category may be parasitic or pathogenic, as well as beneficial. Residents vs. Transients
  • 4. Do caterpillars depend on gut microbes for feeding and development? To answer this question, we first characterized gut microbial abundance and composition across a taxonomically and geographically broad array of wild caterpillars •Our analyses are focused on the digestive tract, the most likely habitat for microbial colonization, as abundant microbes have not been observed elsewhere in the caterpillar body •We applied the same methods to 24 additional insect, bird, and mammal species that we expected to have functional microbiomes to assess the reliability of our protocol and to contextualize our findings •We then conducted a field-based experiment testing whether gut bacteria impact larval growth and survival of the model species
  • 5. Low density of microbes Using quantitative PCR and sequencing of the 16S rRNA gene, we found that wild caterpillars representing a broad diversity of Lepidoptera had gut bacterial densities multiple orders of magnitude lower than the microbiomes of other insects and vertebrate feces measured using identical methods
  • 6.
  • 7. in most caterpillars over 80% of fecal 16S rRNA gene sequences were from plant chloroplasts or mitochondria versus ∼0.1% for other herbivores or omnivores with plant-rich diets Most caterpillar gut sequences from plants
  • 8. Animals with functionally important, resident microbiomes tend to host a high abundance of microbial taxa shared among conspecific individuals Indeed, within species of the other insects and vertebrates analyzed here, microbiomes were largely made up of a common set of bacterial phylotypes (Fig. 1C). This observation hints that many of the core taxa found in caterpillar guts may be transient, food-derived microbes. Non Caterpillar Controls
  • 9. Caterpillar gut microbiomes are dominated by leaf-associated bacteria, further suggesting that resident, host-specific symbionts are sparse or absent. Other caterpillar gut sequences mostly leaf associated
  • 10. Low precision may partly explain the extensive variation in caterpillar gut bacterial loads (Fig. 1A) However, transient inputs of leaf microbes also generate variation among caterpillar species and individuals Lots of variation between individuals
  • 11. Furthermore, bacterial densities dropped by a median of 214-fold from leaves to feces (Fig. 2A), suggesting that any potential bacterial growth within the gut is relatively minor. Bacterial density: poop <<< leaves
  • 12. Variation in bacterial taxonomic composition among leaves and caterpillar feces was also correlated In other words, caterpillars consuming leaves with more distinct bacterial assemblages had more distinct bacterial assemblages in their feces, as would be expected if gut microbes are diet-derived and only transiently present. Variation correlated in poop and leaves
  • 13. Moreover, this process can explain a relationship between host relatedness and microbiome structure, a pattern sometimes termed “phylosymbiosis” (48). Specifically, although confamilial caterpillars in Costa Rica had marginally more similar gut bacterial assemblages than did caterpillars in different families (PERMANOVA, pseudo-F6,43 = 1.47, P = 0.053), they had also been feeding on plants with especially similar leaf microbiomes (PERMANOVA, pseudo-F6,42 = 1.73, P = 0.005). Variation correlated in poop and leaves
  • 14.
  • 15. Supporting our claim that caterpillars lack resident gut microbiomes, we show experimentally that the growth and survival of field-collected M. sexta caterpillars are not dependent on gut bacterial activity Given that antibiotics reduced fecal bacteria to a variable extent within and among treatments (SI Appendix, Fig. S4A), we repeated the aforementioned analyses using gut bac- terial abundance as the predictor variable. In all cases there was no significant relationship with host performance (P > 0.1), further indicating that reducing or eliminating gut bacteria from caterpillars does not reduce M. sexta fitness. Antibiotics don’t do shit
  • 16.