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1.
Artículo en Inglés | MEDLINE | ID: mdl-29024043

RESUMEN

The ants use their venom for predation, defense, and communication. The venom of these insects is rich in peptides and proteins, and compared with other animal venoms, ant venoms remain poorly explored. The objective of this study was to evaluate the protein content of the venom in the Ponerinae ant Pachycondyla striata. Venom samples were collected by manual gland reservoir dissection, and samples were submitted to two-dimensional gel electrophoresis and separation by ion-exchange and reverse-phase high-performance liquid chromatography followed by mass spectrometry using tanden matrix-assisted laser desorption/ionization with time-of-flight (MALDI-TOF/TOF) mass spectrometry and electrospray ionization-quadrupole with time-of-flight (ESI-Q/TOF) mass spectrometry for obtaining amino acid sequence. Spectra obtained were searched against the NCBInr and SwissProt database. Additional analysis was performed using PEAKS Studio 7.0 (Sequencing de novo). The venom of P. striata has a complex mixture of proteins from which 43 were identified. Within the identified proteins are classical venom proteins (phospholipase A, hyaluronidase, and aminopeptidase N), allergenic proteins (different venom allergens), and bioactive peptides (U10-ctenitoxin Pn1a). Venom allergens are among the most expressed proteins, suggesting that P. striata venom has high allergenic potential. This study discusses the possible functions of the proteins identified in the venom of P. striata.


Asunto(s)
Venenos de Hormiga/química , Hormigas/fisiología , Proteínas de Insectos/química , Proteómica , Animales
2.
J Exp Biol ; 219(Pt 1): 103-8, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26567344

RESUMEN

In the ant Ectatomma tuberculatum (Olivier 1792), workers have active ovaries and lay trophic eggs that are eaten by the queen and larvae. Vitellogenins are the main proteins found in the eggs of insects and are the source of nutrients for the embryo in the fertilized eggs and for adults in the trophic eggs. In social insects, vitellogenin titres vary between castes and affect reproductive social status, nursing, foraging, longevity, somatic maintenance, and immunity. In most insects, vitellogenin synthesis is mainly regulated by juvenile hormone. However, in non-reproductive worker ants, this relationship is poorly characterized. This study determined the effects of juvenile hormone on vitellogenin synthesis in non-reproductive E. tuberculatum workers. Juvenile hormone was topically applied onto workers, and the effect on vitellogenin synthesis in the fat body and vitellogenin titres in the haemolymph were analysed by ELISA and qPCR. Juvenile hormone downregulated protein synthesis and reduced vitellogenin titres in the haemolymph, suggesting that in workers of E. tuberculatum, juvenile hormone loses its gonadotrophic function.


Asunto(s)
Hormigas/fisiología , Hormonas Juveniles/fisiología , Vitelogeninas/metabolismo , Animales , Hormigas/efectos de los fármacos , Cuerpo Adiposo/metabolismo , Femenino , Hemolinfa/química , Hormonas Juveniles/farmacología , Óvulo/química
3.
Microsc Microanal ; 20(1): 285-95, 2014 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-24188829

RESUMEN

Bumblebees need to keep bodily homeostasis and for that have an efficient system of excretion formed by the Malpighian tubules, ileum, and rectum. We analyzed the excretory organs of Bombus morio, a bee without rectal pads. In addition, we analyzed the rectal epithelium of Melipona quadrifasciata anthidioides which has rectal pads. The Malpighian tubules exhibited two cell types and the ileum four types. However, comparative analysis of the rectum showed that only cells of the anterior region of the rectal epithelium of B. morio are structurally distinct. We suggest that cells of the Malpighian tubules of B. morio have an excretory feature and that cells of ileum have different functions, such as ion absorption and water, organic compound, and protein secretion. In addition, only the anterior region of the rectum of B. morio showed characteristic absorption. We suggest that Malpighian tubules participate in the excretion of solutes and that the ileum and rectal epithelium are responsible for homeostasis of water and solutes, compensating for the absence of rectal papillae. These results contribute to our understanding of the morphophysiology of the excretory organs of bees without rectal pads.


Asunto(s)
Abejas/ultraestructura , Túbulos de Malpighi/ultraestructura , Recto/ultraestructura , Animales , Íleon/ultraestructura , Microscopía Electrónica
4.
J Med Entomol ; 46(3): 435-41, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19496410

RESUMEN

This work studied the ultrastructure of the midgut cells of Cimex hemipterus Fabricius (Hemiptera: Cimicidae). The midgut of adult insects was analyzed on different days after a bloodmeal, and three anatomical regions with different digestive functions were apparent. In the anterior midgut, the digestive cells had many spherocrystals, lipid inclusions, and glycogen deposits, suggesting a role in water absorption, ion regulation, digestion, and storage of lipids and sugars. The digestive cells in the middle midgut contained secretory granules in the apical cytoplasm, lysosomes, and large amounts of rough endoplasmic reticulum, suggesting that this midgut region was active in digestive processes. The posterior midgut contained digestive cells with secretory vesicles, lysosomes, rough endoplasmic reticulum, and spherocrystals, suggesting digestion and ion/water absorption. Also, there was strong evidence that the posterior midgut may be the major site of nutrient absorption. The hematophagous heteropteran groups share many of these blood digestion mechanisms.


Asunto(s)
Chinches/ultraestructura , Animales , Chinches/citología , Chinches/fisiología , Digestión/fisiología , Sistema Digestivo/citología , Sistema Digestivo/ultraestructura , Microscopía Electrónica de Transmisión
5.
Protoplasma ; 253(3): 815-820, 2016 May.
Artículo en Inglés | MEDLINE | ID: mdl-26077636

RESUMEN

Vitellogenins are the major yolk proteins, synthesized in the fat body, released into the hemolymph and captured by the developing oocytes, but the mechanisms by which these proteins cross the follicular cell layer are still poorly understood. This study describes the actin distribution in follicular cells during vitellogenin transport to the oocyte in social Hymenoptera represented by bees Apis mellifera and Melipona quadrifasciata, the wasp Mischocyttarus cassununga and the ant Pachycondyla curvinodis. In oocytic chambers of vitellogenic follicles, vitellogenin was found within the follicular cells, perivitelline space and oocyte, indicating a transcellular route from the hemolymph to the perivitelline space. The cortical actin cytoskeleton in follicular cells underwent reorganization during transport of vitellogenin across this epithelium suggesting that in the ovary of social hymenopterans, vitellogenin delivery to oocytes requires a dynamic cytoskeletal rearrangement of actin filaments in the follicular cells.


Asunto(s)
Himenópteros/metabolismo , Ovario/citología , Ovario/metabolismo , Vitelogeninas/metabolismo , Citoesqueleto de Actina/metabolismo , Citoesqueleto de Actina/ultraestructura , Animales , Hormigas , Abejas , Femenino , Himenópteros/citología , Microscopía Electrónica de Transmisión , Oocitos/metabolismo , Transporte de Proteínas , Avispas
6.
Protoplasma ; 252(2): 619-27, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25269629

RESUMEN

Fat body, typically comprising trophocytes, provides energy during metamorphosis. The fat body can be renewed once the larval phase is complete or recycled and relocated to form the fat body of the adult insect. This study aims to identify the class of programmed cell death that occurs within the fat body cells during the metamorphosis of the stingless bee Melipona quadrifasciata. Using immunodetection techniques, the fat body of the post-defecating larvae and the white-, pink-, brown-, and black-eyed pupae were tested for cleaved caspase-3 and DNA integrity, followed by ultrastructural analysis and identification of autophagy using RT-PCR for the Atg1 gene. The fat body of M. quadrifasciata showed some apoptotic cells positive for cleaved caspase-3, although without DNA fragmentation. During development, the fat body cells revealed an increased number of mitochondria and free ribosomes, in addition to higher amounts of autophagy Atg1 mRNA, than that of the pupae. The fat body of M. quadrifasciata showed few cells which underwent apoptosis, but there was evidence of increased autophagy at the completion of the larval stage. All together, these data show that some fat body cells persist during metamorphosis in the stingless bee M. quadrifasciata.


Asunto(s)
Autofagia , Abejas/citología , Cuerpo Adiposo/fisiología , Animales , Apoptosis , Secuencia de Bases , Abejas/crecimiento & desarrollo , Cuerpo Adiposo/citología , Proteínas de Insectos/genética , Larva/citología , Larva/crecimiento & desarrollo , Metamorfosis Biológica , Datos de Secuencia Molecular , Proteínas Serina-Treonina Quinasas/genética
7.
Protoplasma ; 251(6): 1441-7, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-24756368

RESUMEN

Nectar used by bees as a food source is collected and stored in the crop, where it is transported and converted into honey. The production of honey involves water uptake from nectar. However, the crop is a portion of the insect foregut that has been characterized solely as a food storage organ. Aquaporins are integral membrane proteins that function as specific canal for water transport and are abundant in tissues with high water permeability. In this study, we detected five predicted genes for aquaporins in the gut of the honeybee Apis mellifera. We evaluated the aquaporins' localization in the crop by using an anti-aquaporin antibody produced against the peptide sequence from one of the expressed genes, which was detected in the crop epithelium, particularly in the apical portions of the cells. Furthermore, we also showed an increase in sugar concentration in a sucrose solution collected from the crop lumen a few minutes after feeding, indicating that water uptake occurs during storage of nectar in the crop, suggesting a previously unidentified function for the honeybee crop.


Asunto(s)
Acuaporinas/metabolismo , Abejas/anatomía & histología , Abejas/metabolismo , Sistema Digestivo/metabolismo , Miel , Animales , Acuaporinas/genética , Abejas/genética , Epitelio/metabolismo , Genes de Insecto , Jerarquia Social , Inmunohistoquímica , Especificidad de Órganos , Reacción en Cadena de la Polimerasa , Sacarosa/metabolismo
8.
J Insect Physiol ; 57(7): 972-7, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-21536045

RESUMEN

Workers of the ant species Ectatomma tuberculatum (Ectatomminae) have active ovaries and lay eggs that are eaten by the queen and larvae (trophic eggs). Vitellogenins are the main proteins found in the eggs of insects and are a source of nutrients. The aim of this study was to characterize the period of vitellogenin production in workers of E. tuberculatum. The vitellogenin was identified from queen and worker eggs by SDS-PAGE. Anti-vitellogenin antibodies were obtained and used to detect this protein in the fat body and haemolymph of workers at different ages. Vitellogenin from E. tuberculatum consists of two polypeptides of 31 and 156 kDa. In the eggs of queens, the 156 kDa polypeptide is cleaved into two subunits of 36 and 123 kDa. The analysis of the haemolymph of workers showed that the secretion of vitellogenin varies with age. The secretion is initiated around the fifth day after emergence, with peak production from days 20 to 60, and stops around day 100. The variation in production is related to the different activities performed by the workers within the colony, suggesting that vitellogenin may have an important role in maintaining age polyethism.


Asunto(s)
Hormigas/química , Hormigas/fisiología , Vitelogeninas/análisis , Envejecimiento , Animales , Western Blotting , Electroforesis en Gel de Poliacrilamida , Cuerpo Adiposo/química , Femenino , Hemolinfa/química , Óvulo/química , Vitelogeninas/química
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