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1.
Proc Natl Acad Sci U S A ; 121(25): e2401802121, 2024 Jun 18.
Artigo em Inglês | MEDLINE | ID: mdl-38865264

RESUMO

The spatial organization of gut microbiota is crucial for the functioning of the gut ecosystem, although the mechanisms that organize gut bacterial communities in microhabitats are only partially understood. The gut of the insect Riptortus pedestris has a characteristic microbiota biogeography with a multispecies community in the anterior midgut and a monospecific bacterial population in the posterior midgut. We show that the posterior midgut region produces massively hundreds of specific antimicrobial peptides (AMPs), the Crypt-specific Cysteine-Rich peptides (CCRs) that have membrane-damaging antimicrobial activity against diverse bacteria but posterior midgut symbionts have elevated resistance. We determined by transposon-sequencing the genetic repertoire in the symbiont Caballeronia insecticola to manage CCR stress, identifying different independent pathways, including AMP-resistance pathways unrelated to known membrane homeostasis functions as well as cell envelope functions. Mutants in the corresponding genes have reduced capacity to colonize the posterior midgut, demonstrating that CCRs create a selective barrier and resistance is crucial in gut symbionts. Moreover, once established in the gut, the bacteria differentiate into a CCR-sensitive state, suggesting a second function of the CCR peptide arsenal in protecting the gut epithelia or mediating metabolic exchanges between the host and the gut symbionts. Our study highlights the evolution of an extreme diverse AMP family that likely contributes to establish and control the gut microbiota.


Assuntos
Peptídeos Antimicrobianos , Microbioma Gastrointestinal , Simbiose , Animais , Peptídeos Antimicrobianos/metabolismo , Peptídeos Antimicrobianos/genética , Peptídeos Antimicrobianos/farmacologia , Bactérias/genética , Bactérias/metabolismo , Bactérias/efeitos dos fármacos , Trato Gastrointestinal/microbiologia
2.
Proc Natl Acad Sci U S A ; 120(40): e2304879120, 2023 10 03.
Artigo em Inglês | MEDLINE | ID: mdl-37769258

RESUMO

Many insects are dependent on microbial mutualists, which are often harbored in specialized symbiotic organs. Upon metamorphosis, insect organs are drastically reorganized. What mechanism regulates the remodeling of the symbiotic organ upon metamorphosis? How does it affect the microbial symbiont therein? Here, we addressed these fundamental issues of symbiosis by experimentally manipulating insect metamorphosis. The stinkbug Plautia stali possesses a midgut symbiotic organ wherein an essential bacterial symbiont resides. By RNAi of master regulator genes for metamorphosis, Kr-h1 over nymphal traits and E93 over adult traits, we generated precocious adults and supernumerary nymphs of P. stali, thereby disentangling the effects of metamorphosis, growth level, developmental stage, and other factors on the symbiotic system. Upon metamorphosis, the symbiotic organ of P. stali was transformed from nymph type to adult type. The supernumerary nymphs and the precocious adults, respectively, developed nymph-type and adult-type symbiotic organs not only morphologically but also transcriptomically, uncovering that metamorphic remodeling of the symbiotic organ is under the control of the MEKRE93 pathway. Transcriptomic, cytological, and biochemical analyses unveiled that the structural and transcriptomic remodeling of the symbiotic organ toward adult emergence underpins its functional extension to food digestion in addition to the original role of symbiont retention for essential nutrient production. Notably, we found that the symbiotic bacteria in the adult-type symbiotic organ up-regulated genes for production of sulfur-containing essential amino acids, methionine and cysteine, that are rich in eggs and sperm, uncovering adult-specific symbiont functioning for host reproduction and highlighting intricate host-symbiont interactions associated with insect metamorphosis.


Assuntos
Heterópteros , Simbiose , Masculino , Animais , Simbiose/fisiologia , Sêmen , Sistema Digestório/microbiologia , Insetos , Heterópteros/fisiologia , Bactérias/genética , Metamorfose Biológica
3.
Photochem Photobiol ; 93(2): 466-472, 2017 03.
Artigo em Inglês | MEDLINE | ID: mdl-27716939

RESUMO

Fireflies are widespread all over the world and a numerous numbers of luciferases have been isolated and characterized. In this study, we identified and characterized the luciferase and luciferase-like genes from a Tibetan firefly collected in Shangri-La, China. The altitude of this area is more than 3300 m. We saw this Tibetan firefly flying with strong luminescence after sunset at ~10°C. We analyzed the transcriptome of Tibetan firefly using head, thorax, abdomen (without light organ), and light organ tissue by RNA sequencing. We identified one luciferase gene, which was almost identical to luciferase from fireflies Pyrocoelia species, and expressed specifically in the light organ. Interestingly, the optimal temperature of the Tibetan firefly recombinant luciferase was 10°C. The Km for D-luciferin and ATP of the recombinant luciferase was 23 and 154 µm, respectively. The optimal pH was around 7.0-7.5. The emission peak was 556 nm at pH 8.0, while it shifted to 606 nm at pH 6.0. We also found a luciferase-like gene with 43% identical amino acids to the Tibetan firefly luciferase, which was scarcely expressed in any portion of the adult body. No luciferase activity was detected for this luciferase-like protein.


Assuntos
Adaptação Fisiológica , Temperatura Baixa , Vaga-Lumes/fisiologia , Luciferases de Vaga-Lume/metabolismo , Trifosfato de Adenosina/metabolismo , Sequência de Aminoácidos , Animais , China , Vaga-Lumes/classificação , Vaga-Lumes/enzimologia , Luciferina de Vaga-Lumes/metabolismo , Concentração de Íons de Hidrogênio , Luciferases de Vaga-Lume/química , Luciferases de Vaga-Lume/genética , Substâncias Luminescentes/metabolismo , Masculino , Filogenia , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Análise de Sequência de RNA , Homologia de Sequência de Aminoácidos , Tibet , Transcriptoma
4.
PLoS One ; 8(5): e64557, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23691247

RESUMO

The bean bug Riptortus pedestris possesses a specialized symbiotic organ in a posterior region of the midgut, where numerous crypts harbor extracellular betaproteobacterial symbionts of the genus Burkholderia. Second instar nymphs orally acquire the symbiont from the environment, and the symbiont infection benefits the host by facilitating growth and by occasionally conferring insecticide resistance. Here we performed comparative transcriptomic analyses of insect genes expressed in symbiotic and non-symbiotic regions of the midgut dissected from Burkholderia-infected and uninfected R. pedestris. Expression sequence tag analysis of cDNA libraries and quantitative reverse transcription PCR identified a number of insect genes expressed in symbiosis- or aposymbiosis-associated patterns. For example, genes up-regulated in symbiotic relative to aposymbiotic individuals, including many cysteine-rich secreted protein genes and many cathepsin protease genes, are likely to play a role in regulating the symbiosis. Conversely, genes up-regulated in aposymbiotic relative to symbiotic individuals, including a chicken-type lysozyme gene and a defensin-like protein gene, are possibly involved in regulation of non-symbiotic bacterial infections. Our study presents the first transcriptomic data on gut symbiotic organ of a stinkbug, which provides initial clues to understanding of molecular mechanisms underlying the insect-bacterium gut symbiosis and sheds light on several intriguing commonalities between endocellular and extracellular symbiotic associations.


Assuntos
Burkholderia/fisiologia , Espaço Extracelular/microbiologia , Heterópteros/genética , Heterópteros/microbiologia , Mucosa Intestinal/metabolismo , Simbiose/genética , Transcriptoma , Sequência de Aminoácidos , Animais , Etiquetas de Sequências Expressas/metabolismo , Feminino , Ontologia Genética , Heterópteros/anatomia & histologia , Intestinos/microbiologia , Dados de Sequência Molecular
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