Symbiont Digestive Range Reflects Host Plant Breadth in Herbivorous Beetles

Numerous adaptations are gained in light of a symbiotic lifestyle. Here, we investigated the obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pectinolytic Stammera symbionts to detail how changes to the bacterium’s streamlined metabolic range can shape the dig...

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Published inCurrent biology Vol. 30; no. 15; pp. 2875 - 2886.e4
Main Authors Salem, Hassan, Kirsch, Roy, Pauchet, Yannick, Berasategui, Aileen, Fukumori, Kayoko, Moriyama, Minoru, Cripps, Michael, Windsor, Donald, Fukatsu, Takema, Gerardo, Nicole M.
Format Journal Article
LanguageEnglish
Published England Elsevier Inc 03.08.2020
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ISSN0960-9822
1879-0445
1879-0445
DOI10.1016/j.cub.2020.05.043

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Abstract Numerous adaptations are gained in light of a symbiotic lifestyle. Here, we investigated the obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pectinolytic Stammera symbionts to detail how changes to the bacterium’s streamlined metabolic range can shape the digestive physiology and ecological opportunity of its herbivorous host. Comparative genomics of 13 Stammera strains revealed high functional conservation, highlighted by the universal presence of polygalacturonase, a primary pectinase targeting nature’s most abundant pectic class, homogalacturonan (HG). Despite this conservation, we unexpectedly discovered a disparate distribution for rhamnogalacturonan lyase, a secondary pectinase hydrolyzing the pectic heteropolymer, rhamnogalacturonan I (RG-I). Consistent with the annotation of rhamnogalacturonan lyase in Stammera, cassidines are able to depolymerize RG-I relative to beetles whose symbionts lack the gene. Given the omnipresence of HG and RG-I in foliage, Stammera that encode pectinases targeting both substrates allow their hosts to overcome a greater diversity of plant cell wall polysaccharides and maximize access to the nutritionally rich cytosol. Possibly facilitated by their symbionts’ expanded digestive range, cassidines additionally endowed with rhamnogalacturonan lyase appear to utilize a broader diversity of angiosperms than those beetles whose symbionts solely supplement polygalacturonase. Our findings highlight how symbiont metabolic diversity, in concert with host adaptations, may serve as a potential source of evolutionary innovations for herbivorous lineages. [Display omitted] •Stammera genomes are structurally conserved across Cassidinae species•Symbiont pectinases complement the host’s endogenous cellulases and xylanases•Stammera differentially encode pectinases in their reduced genomes•Symbiont pectinolytic range reflects host plant breadth Tortoise leaf beetles rely on the symbiotic bacterium, Stammera, to digest foliage rich in pectin. Salem et al. reveal that Stammera varies in the pectinases it encodes and supplements. Stammera encoding a more dynamic digestive range allows its host to overcome a greater diversity of plant polysaccharides, corresponding to a wider ecological distribution.
AbstractList Numerous adaptations are gained in light of a symbiotic lifestyle. Here, we investigated the obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pectinolytic Stammera symbionts to detail how changes to the bacterium's streamlined metabolic range can shape the digestive physiology and ecological opportunity of its herbivorous host. Comparative genomics of 13 Stammera strains revealed high functional conservation, highlighted by the universal presence of polygalacturonase, a primary pectinase targeting nature's most abundant pectic class, homogalacturonan (HG). Despite this conservation, we unexpectedly discovered a disparate distribution for rhamnogalacturonan lyase, a secondary pectinase hydrolyzing the pectic heteropolymer, rhamnogalacturonan I (RG-I). Consistent with the annotation of rhamnogalacturonan lyase in Stammera, cassidines are able to depolymerize RG-I relative to beetles whose symbionts lack the gene. Given the omnipresence of HG and RG-I in foliage, Stammera that encode pectinases targeting both substrates allow their hosts to overcome a greater diversity of plant cell wall polysaccharides and maximize access to the nutritionally rich cytosol. Possibly facilitated by their symbionts' expanded digestive range, cassidines additionally endowed with rhamnogalacturonan lyase appear to utilize a broader diversity of angiosperms than those beetles whose symbionts solely supplement polygalacturonase. Our findings highlight how symbiont metabolic diversity, in concert with host adaptations, may serve as a potential source of evolutionary innovations for herbivorous lineages.
Numerous adaptations are gained in light of a symbiotic lifestyle. Here, we investigated the obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pectinolytic Stammera symbionts to detail how changes to the bacterium’s streamlined metabolic range can shape the digestive physiology and ecological opportunity of its herbivorous host. Comparative genomics of 13 Stammera strains revealed high functional conservation, highlighted by the universal presence of polygalacturonase, a primary pectinase targeting nature’s most abundant pectic class, homogalacturonan (HG). Despite this conservation, we unexpectedly discovered a disparate distribution for rhamnogalacturonan lyase, a secondary pectinase hydrolyzing the pectic heteropolymer, rhamnogalacturonan I (RG-I). Consistent with the annotation of rhamnogalacturonan lyase in Stammera, cassidines are able to depolymerize RG-I relative to beetles whose symbionts lack the gene. Given the omnipresence of HG and RG-I in foliage, Stammera that encode pectinases targeting both substrates allow their hosts to overcome a greater diversity of plant cell wall polysaccharides and maximize access to the nutritionally rich cytosol. Possibly facilitated by their symbionts’ expanded digestive range, cassidines additionally endowed with rhamnogalacturonan lyase appear to utilize a broader diversity of angiosperms than those beetles whose symbionts solely supplement polygalacturonase. Our findings highlight how symbiont metabolic diversity, in concert with host adaptations, may serve as a potential source of evolutionary innovations for herbivorous lineages. [Display omitted] •Stammera genomes are structurally conserved across Cassidinae species•Symbiont pectinases complement the host’s endogenous cellulases and xylanases•Stammera differentially encode pectinases in their reduced genomes•Symbiont pectinolytic range reflects host plant breadth Tortoise leaf beetles rely on the symbiotic bacterium, Stammera, to digest foliage rich in pectin. Salem et al. reveal that Stammera varies in the pectinases it encodes and supplements. Stammera encoding a more dynamic digestive range allows its host to overcome a greater diversity of plant polysaccharides, corresponding to a wider ecological distribution.
Numerous adaptations are gained in light of a symbiotic lifestyle. Here, we investigated the obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pectinolytic Stammera symbionts to detail how changes to the bacterium's streamlined metabolic range can shape the digestive physiology and ecological opportunity of its herbivorous host. Comparative genomics of 13 Stammera strains revealed high functional conservation, highlighted by the universal presence of polygalacturonase, a primary pectinase targeting nature's most abundant pectic class, homogalacturonan (HG). Despite this conservation, we unexpectedly discovered a disparate distribution for rhamnogalacturonan lyase, a secondary pectinase hydrolyzing the pectic heteropolymer, rhamnogalacturonan I (RG-I). Consistent with the annotation of rhamnogalacturonan lyase in Stammera, cassidines are able to depolymerize RG-I relative to beetles whose symbionts lack the gene. Given the omnipresence of HG and RG-I in foliage, Stammera that encode pectinases targeting both substrates allow their hosts to overcome a greater diversity of plant cell wall polysaccharides and maximize access to the nutritionally rich cytosol. Possibly facilitated by their symbionts' expanded digestive range, cassidines additionally endowed with rhamnogalacturonan lyase appear to utilize a broader diversity of angiosperms than those beetles whose symbionts solely supplement polygalacturonase. Our findings highlight how symbiont metabolic diversity, in concert with host adaptations, may serve as a potential source of evolutionary innovations for herbivorous lineages.Numerous adaptations are gained in light of a symbiotic lifestyle. Here, we investigated the obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pectinolytic Stammera symbionts to detail how changes to the bacterium's streamlined metabolic range can shape the digestive physiology and ecological opportunity of its herbivorous host. Comparative genomics of 13 Stammera strains revealed high functional conservation, highlighted by the universal presence of polygalacturonase, a primary pectinase targeting nature's most abundant pectic class, homogalacturonan (HG). Despite this conservation, we unexpectedly discovered a disparate distribution for rhamnogalacturonan lyase, a secondary pectinase hydrolyzing the pectic heteropolymer, rhamnogalacturonan I (RG-I). Consistent with the annotation of rhamnogalacturonan lyase in Stammera, cassidines are able to depolymerize RG-I relative to beetles whose symbionts lack the gene. Given the omnipresence of HG and RG-I in foliage, Stammera that encode pectinases targeting both substrates allow their hosts to overcome a greater diversity of plant cell wall polysaccharides and maximize access to the nutritionally rich cytosol. Possibly facilitated by their symbionts' expanded digestive range, cassidines additionally endowed with rhamnogalacturonan lyase appear to utilize a broader diversity of angiosperms than those beetles whose symbionts solely supplement polygalacturonase. Our findings highlight how symbiont metabolic diversity, in concert with host adaptations, may serve as a potential source of evolutionary innovations for herbivorous lineages.
Author Fukatsu, Takema
Cripps, Michael
Berasategui, Aileen
Pauchet, Yannick
Windsor, Donald
Salem, Hassan
Moriyama, Minoru
Kirsch, Roy
Gerardo, Nicole M.
Fukumori, Kayoko
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  orcidid: 0000-0002-4135-7407
  surname: Salem
  fullname: Salem, Hassan
  email: hassan.salem@tuebingen.mpg.de
  organization: Department of Biology, Emory University, Atlanta, GA 30322, USA
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  givenname: Roy
  surname: Kirsch
  fullname: Kirsch, Roy
  organization: Department of Entomology, Max Planck Institute for Chemical Ecology, Jena 07745, Germany
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  surname: Pauchet
  fullname: Pauchet, Yannick
  organization: Department of Entomology, Max Planck Institute for Chemical Ecology, Jena 07745, Germany
– sequence: 4
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  surname: Berasategui
  fullname: Berasategui, Aileen
  organization: Department of Biology, Emory University, Atlanta, GA 30322, USA
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  givenname: Kayoko
  surname: Fukumori
  fullname: Fukumori, Kayoko
  organization: National Institute for Advanced Industrial Science and Technology, Tsukuba 305-8566, Japan
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  organization: National Institute for Advanced Industrial Science and Technology, Tsukuba 305-8566, Japan
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  organization: AgResearch, Lincoln Research Centre, Lincoln 7608, New Zealand
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  organization: Smithsonian Tropical Research Institute, Panama City 0843-03092, Panama
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  organization: National Institute for Advanced Industrial Science and Technology, Tsukuba 305-8566, Japan
– sequence: 10
  givenname: Nicole M.
  surname: Gerardo
  fullname: Gerardo, Nicole M.
  organization: Department of Biology, Emory University, Atlanta, GA 30322, USA
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Keywords herbivore-microbe interactions
herbivory
adaptation
beetles
symbiosis
co-evolution
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Snippet Numerous adaptations are gained in light of a symbiotic lifestyle. Here, we investigated the obligate partnership between tortoise leaf beetles (Chrysomelidae:...
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SubjectTerms adaptation
beetles
co-evolution
herbivore-microbe interactions
herbivory
symbiosis
Title Symbiont Digestive Range Reflects Host Plant Breadth in Herbivorous Beetles
URI https://dx.doi.org/10.1016/j.cub.2020.05.043
https://www.ncbi.nlm.nih.gov/pubmed/32502409
https://www.proquest.com/docview/2410363726
Volume 30
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