Dietary and Flight Energetic Adaptations in a Salivary Gland Transcriptome of an Insectivorous Bat

We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory pr...

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Published inPloS one Vol. 9; no. 1; p. e83512
Main Authors Phillips, Carleton J., Phillips, Caleb D., Goecks, Jeremy, Lessa, Enrique P., Sotero-Caio, Cibele G., Tandler, Bernard, Gannon, Michael R., Baker, Robert J.
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 14.01.2014
Public Library of Science (PLoS)
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Online AccessGet full text
ISSN1932-6203
1932-6203
DOI10.1371/journal.pone.0083512

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Abstract We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary 'bursts' of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event.
AbstractList We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary ‘bursts’ of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event.
We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary 'bursts' of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event.We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary 'bursts' of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event.
Audience Academic
Author Phillips, Carleton J.
Lessa, Enrique P.
Baker, Robert J.
Tandler, Bernard
Gannon, Michael R.
Goecks, Jeremy
Phillips, Caleb D.
Sotero-Caio, Cibele G.
AuthorAffiliation 4 Departamento de Ecología y Evolución, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay
1 Department of Biological Sciences, Texas Tech University, Lubbock, Texas, United States of America
Louisiana State University, United States of America
2 Department of Biology, Emory University, Atlanta, Georgia, United States of America
5 Department of Biological Sciences, School of Dental Medicine, Case Western Reserve University, Cleveland, Ohio, United States of America
3 Department of Math and Computer Science, Emory University, Atlanta, Georgia, United States of America
6 Department of Biology, Pennsylvania State University, Altoona College, Altoona, Pennsylvania, United States of America
AuthorAffiliation_xml – name: 2 Department of Biology, Emory University, Atlanta, Georgia, United States of America
– name: 4 Departamento de Ecología y Evolución, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay
– name: 6 Department of Biology, Pennsylvania State University, Altoona College, Altoona, Pennsylvania, United States of America
– name: 3 Department of Math and Computer Science, Emory University, Atlanta, Georgia, United States of America
– name: Louisiana State University, United States of America
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– name: 1 Department of Biological Sciences, Texas Tech University, Lubbock, Texas, United States of America
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/24454705$$D View this record in MEDLINE/PubMed
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Copyright COPYRIGHT 2014 Public Library of Science
2014 Phillips et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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SourceType-Scholarly Journals-1
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: CJP RJB EPL. Performed the experiments: JG BT CDP CGS-C. Analyzed the data: CJP CDP CGS-C RJB. Contributed reagents/materials/analysis tools: BT JG MRG. Wrote the paper: CJP CDP BT RJB. Electron microscopy: BT. Bioinformatics: JG CDP CJP. Analysis of natural selection: EPL CDP. Moblile element: CJP CGS-C.
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Snippet We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among...
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SubjectTerms Adaptation
Adaptation, Physiological - genetics
Animal behavior
Animals
Apolipoprotein E
Apolipoproteins
Bats
Bats (Animals)
Bioinformatics
Biological evolution
Biological Transport
Biology
Chiroptera
Chiroptera - genetics
Chiroptera - metabolism
Chiroptera - physiology
Diet
Dietary Fats - metabolism
Energy Metabolism - genetics
Enzymes
Evolution
Evolution, Molecular
Flight
Flight, Animal - physiology
Forage
Gastric mucosa
Gene Dosage
Gene Duplication
Gene expression
Gene sequencing
Genes
Genomes
Genomics
Histology
Hydrolysis
Hyperlipidemias - genetics
Hypotheses
Insects
Insulin
Insulin resistance
Lipase
Lipid metabolism
Lipid Metabolism - genetics
Lipids
Mammals
Metabolic syndrome
Metabolism
Morphology
Muscles
Myotis lucifugus
Physiology
Proteins
Proteomes
Proteomics
Reproduction (copying)
Rodents
Salivary gland
Secretion
Submandibular Gland - metabolism
Transcriptome
Transport
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Title Dietary and Flight Energetic Adaptations in a Salivary Gland Transcriptome of an Insectivorous Bat
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