Morphology of the spermatheca of Triatoma lecticularia (Hemiptera: Reduviidae) (Stal, 1859)/Morfologia da espermateca de Triatoma lecticularia (Hemiptera: Reduviidae) (Stal, 1859).
The Triatominae (Hemiptera: Reduviidae) are obligate hematophagous insects feeding on different hosts. Many representatives of Triatominae are potential vectors of Trypanosoma cruzi (Chagas, 1909), the etiological agent of Chagas's disease (Lent and Wygodzinsky, 1979).
Triatoma lecticularia (Hemiptera: Reduviidae) (Stal, 1859) is a forest dwelling species found in the United States and Mexico (Lent and Wygodzinsky, 1979; Jurberg and Costa 1989; Silva et al., 1993; Galvao et al., 2003) and is generally found infected with T. cruzi, being important for the maintenance of the wild cycle of this pathogen at North America (Silva et al., 1993; Bern et al., 2011).
The reproductive female tract of Hemiptera is formed by ovaries, lateral oviducts, a common oviduct, accessory glands and spermatheca (Jahnke et al., 2006; Chiang et al., 2012; Chapman, 2013). During mating the spermatozoa are transferred together with the secretion of the male accessory glands to the spermatheca (Chapman, 2013). The spermatheca is an organ of the female reproductive tract, responsible for storing and maintaining the viability of spermatozoa from mating until oocyte fecundation, reducing or eliminating the need for multiple matings and, consequently, the probability of the female being preyed upon (Thornhill and Alcock 1983; Souza et al., 2008, 2016).
In the spermatheca, the spermatozoa are protected from physical damage as well as from contact with hemolymph content and free radicals (Collins et al., 2004; Al-Lawati et al., 2009; King et al., 2011; Pascini and Martins, 2017). Generally, the spermatozoa are stored in a spermathecal bulb that is associated with a muscular duct, which controls spermatozoa release. The reservoir is lined by a layer epithelial cells in bees (Dallai, 1975; Martins and Serrao, 2002; Souza et al., 2008) or multiple layers with different cell types in Hemiptera and Diptera (Souza et al., 2016; Pascini and Martins, 2017). The reservoir epithelium seems to contribute to the transportation of the hemolymph molecules to the spermathecal lumen (Gobin et al., 2006; Martins et al., 2008). In some insects, there is a spermathecal gland containing a secretion rich in glycogen, glycoproteins, phospholipids and mucopolysaccharides (Bhatnagar and Musgrave, 1971; Wolfner, 2011; Pascini and Martins, 2017), which is released in the reservoir lumen to contribute to the maintenance of the spermatozoa viability.
The spermatheca is present in all orders of insect and generally, there is one spermatheca per individual, although in Rhodnius prolixus (Hemiptera, Reduviidae) and representatives of Culicidae and Caliphoridae (Diptera) have been reported multiple spermathecae with different morphologies (Pascini and Martins, 2017).
The control of the spermatozoa release from the spermatheca during oocytes fecundation is carried out by the muscular duct (King et al., 2011; Chapman, 2013), which can also show morphological variation according to species (Pendergrast, 1957; Kocorek and Danielczok-Demska, 2002).
Considering the importance of the spermatheca in the reproductive biology of insects, studies that provide morphological and physiological data regarding this organ are important for future research into population management of insects that are disease vectors. This study described the histology and histochemistry of the spermatheca of T. lecticularia, an insect directly related to the maintenance of the forest cycle of T. cruzi.
2. Material and Methods
Mated Triatoma lecticularia females in oviposition were obtained from colonies in the Insectary of the Parasitology Department at the Universidade Federal do Triangulo Mineiro (UFTM), Uberaba, Minas Gerais, Brazil (19[degrees]44'21" S, 47[degrees]57'26" W). The insects were maintained in acrylic cylindrical vials containing a cardboard strip with accordion folds to increase surface area, providing space and permitting access for food. The vials were sealed with fine cottonwool balls to allow the blood meal of the insects which was realized every seven days, using chickens (Mendes, 2014).
2.1. Histology and histochemistry
Six mated T. lecticularia females were cryo-anesthetized at 0 [degrees]C and dissected in presence of 125 mM NaCl. The spermatheca were transferred to Zamboni fixative solution (Stefanini et al., 1967) for four hours, dehydrated in a graded ethanol series (70, 80, 90 and 95%), and embedded in historesin (Leica). Slices 3 [micro]m thick were stained with toluidine blue and analyzed under a light microscope.
Some sections were submitted for histochemical testing with mercury bromophenol to detect total proteins and Periodic Acid-Schiff (P.A.S) to detect neutral polysaccharides and glycoconjugates (Bancroft and Gamble, 2008).
The female reproductive tract of T. lecticularia is formed by a pair of ovaries connected to lateral oviducts, a common oviduct and a pair of spermatheca (Figure 1).
Spermathecae are irregular shaped tubes with c.a. 3 mm width connected at the common oviduct by a narrow duct (Figure 2A). Glands associated with the spermatheca were no found in the T. lecticularia reproductive tract.
The lumen of the spermathecal reservoir was lined by a single layered columnar epithelium (Figure 2A, B) with the nucleus placed in the center of the cell with a predominance of decondensed chromatin (Figure 2B). The perinuclear and apical regions of the columnar cells were strongly basophil in comparison with the basal cell region.
The columnar epithelial cells were weakly positive for the P.A.S test, with homogenous distribution of glycoconjugates in whole cytoplasm (Figure 2C). The secretion in the spermathecal lumen was positive for the P.A.S (Figure 2C). The mercury bromophenol histochemical test showed strong reaction in the apical cell region (Figure 2D) as well as the secretion of the spermathecal lumen.
The connection of the spermathecal reservoir to the common oviduct is made via a short muscular duct with circular muscles (Figure 2E, F).
The presence of the two tubular spermathecae without associated glands in T. lecticularia is similar to what has been reported in other Triatominae (Davey, 1958; Chiang et al., 2012; Nascimento, 2015), except in Triatoma infestans which has oval espermatheca (Nascimento, 2015).
In T. lecticularia, the spermatheca are sinuous with the reservoir connected to the common oviduct with a narrower duct in comparison with the duct portion near to the reservoir, as found in the triatomines Panstrongylus megistus, P. lignarius and T. tibiamaculata (Nascimento, 2015).
The spermatheca of T. lecticularia has a single layer of columnar cells lining a lumen that stores the spermatozoa. These cells are basophils in the apical region, indicating that they can assume a secretory function, releasing molecules into the spermathecal lumen contributing to spermatozoa maintenance.
To reinforce the secretory role of the spermathecal epithelium of T. lecticularia, the histochemical tests show that both the cell cytoplasm and the lumen content are positive for the P.A.S test, suggesting that the epithelial cells release polysaccharides and/or glycoconjugates to the spermathecal lumen or transport them from the hemolymph. The transportation of molecules from the hemolymph to the spermathecal lumen has been reported in Hymenoptera, due to the basal region of the epithelial cells of the reservoir rich in invaginations associated with mitochondria, which characterizes the active transportation of molecules (Dallai, 1975; Wheeler and Krutzsch, 1994; Martins et al., 2008; Pascini and Martins, 2017).
The accumulation of total proteins in the apical cell cytoplasm of the T. lecticularia spermatheca suggests that the proteins synthesized by these cells may be released into the lumen of the organ. According to Souza et al. (2008), the epithelium of the spermatheca of stingless bee Melipona quadrifasciata anthidioides (Hymenoptera, Apidae) has a single layered epithelium and apical basophil indicating a secretory function. However, M. quadrifasciata anthidioides and other Hymenoptera have a pair of glands for the spermatheca that take on the main secretory role (Dallai, 1975; Martins and Serrao, 2002; Gobin et al., 2006; Souza et al., 2008; Gotoh et al., 2009), structures absent in T. lecticularia.
In Heteroptera, the spermatheca has morphology distinct from that found in Triatoma spp. (Kocorek and Danielczok-Demska, 2002; Stacconi and Romani, 2011; Candan et al., 2014; Souza et al., 2016), with only one spermatheca. In these species, the reservoir shows three types of cells: i) class III secretory cells, characterized by the presence of intracellular canaliculi, ii) cells that form ducts for the transportation of secretions to the lumen of the spermatheca and iii) epithelial cells associated with the cuticle (Noirot and Quennedey, 1991; Stacconi and Romani, 2011; Souza et al., 2016; Pascini and Martins 2017).
A significant feature of the spermatheca of insects is the presence of the cuticle, due to its ectodermal origin (Chapman, 2013; Pascini and Martins, 2017). However, the cuticle was not observed in the spermatheca of T. lecticularia. The spermathecal epithelium in T. lecticularia assumes the secretory function and the absence of the cuticle indicates that the secretion is quickly transported into the lumen.
In conclusion, the spermatheca of T. lecticularia is similar to the spermathecae of other Reduviidae. In addition, the histological data reveal the importance of reservoir epithelium for the spermatozoa maintenance stored in this organ.
This research was supported by Minas Gerais State Research Agency (FAPEMIG).
AL-LAWATI, H., KAMP, G. and BIENEFELD, K., 2009. Characteristics of the spermathecal contents of old and young honeybee queens. Journal of Insect Physiology, vol. 55, no. 2, pp. 116-121. http://dx.doi.org/10.1016/jjinsphys.2008.10.010. PMid:19027748.
BANCROFT, J.D. and GAMBLE, M., 2008. Theory and practice of histological techniques. 6th ed. London: Livingstone Churchill, 744 p.
BERN, C., KJOS, S., YABSLEY, M.J. and MONTGOMERY, S.P., 2011. Trypanossoma cruzi and Chagas' disease in the United States. Clinical Microbiology Reviews, vol. 24, no. 4, pp. 655-681. http://dx.doi.org/10.1128/CMR.00005-11. PMid:21976603.
BHATNAGAR, R.D. and MUSGRAVE, A., 1971. Aspects of histophysiology of the spermathecal gland of Sitophilus granarius (L.)(Coleoptera). Canadian Journal of Zoology, vol. 49, no. 2, pp. 275-277. http://dx.doi.org/10.1139/z71-038. PMid:5101971.
CANDAN, S., ERBEY, M., OZYURT, N. and SULUDERE, Z., 2014. Spermathecae morphology in Four Species of Eurydema Laporte, 1833 (Heteroptera: Pentatomidae) from Turkey: a scanning electron microscope study. Journal of Entomology and Zoology Studies, vol. 2, pp. 206-213.
CHAPMAN, R.F. 2013. The insects: structure and function. 5th ed. Cambridge: University Press, 929 p.
CHIANG, R.G., CHIANG, J.A., SARQUIS, O. and LIMA, M.M., 2012. Morphology of reproductive accessory glands in eight species of blood-feeding Hemiptera (Hemiptera, Reduviidae) insect vectors of Chagas disease. Acta Tropica, vol. 122, no. 2, pp. 196-204. http://dx.doi.org/10.1016/j.actatropica.2012.01.011. PMid:22314031.
COLLINS, A.M., WILLIAMS, V. and EVANS, J.D., 2004. Sperm storage and antioxidative enzyme expression in the honey bee, Apis mellifera. Insect Molecular Biology, vol. 13, no. 2, pp. 141-146. http://dx.doi.org/10.1111/j.0962-1075.2004.00469.x. PMid:15056361.
DALLAI, R., 1975. Fine structure of the spermatheca of Apis mellifera. Journal of Insect Physiology, vol. 21, no. 1, pp. 89-109. http://dx.doi.org/10.1016/0022-1910(75)90072-4.
DAVEY, K.G., 1958. The migration of spermatozoa in the femanle of Rhodnius prolixus Stal. The Journal of Experimental Biology, vol. 35, pp. 694-701.
GALVAO, C., CARCAVALLO, R., ROCHA, D.D.S. and JURBERG, J., 2003. A checklist of the current valid species of the subfamily Triatominae Jeannel, 1919 (Hemiptera, Reduviidae) and their geographical distribution, with nomenclatural and taxonomic notes. Zootaxa, vol. 202, no. 1, pp. 1-36. http://dx.doi. org/10.11646/zootaxa.202.1.1.
GOBIN, B., ITO, F., PEETERS, C. and BILLEN, J., 2006. Queenworker differences in spermatheca reservoir of phylogenetically basal ants. Cell and Tissue Research, vol. 326, no. 1, pp. 169-178. http://dx.doi.org/10.1007/s00441-006-0232-2. PMid:16773314.
GOTOH, A., BILLEN, J., HASHIM, R. and ITO, F., 2009. Evolution of specialized spermatheca morphology in ant queens: Insight from comparative developmental biology between ants and polistine wasps. Arthropod Structure & Development, vol. 38, no. 6, pp. 521-525. http://dx.doi.org/10.1016Zj.asd.2009.08.003. PMid:19720157.
JAHNKE, S.M., REDAELLI, L.R. and DIEFENBACH, L.M.G., 2006. Internal reproductive organs of Cosmoclopius nigroannulatus (Hemiptera; Reduviidae). Brazilian Journal of Biology = Revista Brasileira de Biologia, vol. 66, no. 2A, pp. 509-512. http://dx.doi.org/10.1590/S1519-69842006000300017. PMid:16862306.
JURBERG, J. and COSTA, J.M., 1989. Estudos sobre a resistencia ao jejum e aspectos nutricionais de Triatoma lecticularia (Stal, 1859)(Hemiptera, Reduviidae, Triatominae). Memorias do Instituto Oswaldo Cruz, vol. 84, no. 3, pp. 393-399. http://dx.doi. org/10.1590/S0074-02761989000300016. PMid:2520831.
KING, M., EUBEL, H., MILLAR, A.H. and BAER, B., 2011. Proteins within the seminal fluid are crucial to keep sperm viable in the honeybee Apis mellifera. Journal of Insect Physiology, vol. 57, no. 3, pp. 409-414. http://dx.doi.org/10.1016/jjinsphys.2010.12.011. PMid:21192944.
KOCOREK, A. and DANIELCZOK-DEMSKA, T., 2002. Comparative morphology of the spermatheca within the family Dinidoridae (Hemiptera: Heteroptera). European Journal of Entomology, vol. 99, no. 1, pp. 91-98. http://dx.doi.org/10.14411/ eje.2002.016.
LENT, H. and WYGODZINSKY, P., 1979. Revision of the Triatominae (Hemiptera, Reduviidae), and their significance as vectors of Chagas' disease. Bulletin of the American Museum of Natural History, vol. 163, pp. 123-520.
MARTINS, G.F. and SERRAO, J.E., 2002. A comparative study of the spermatheca in bees (Hymenoptera; Apoidea). Sociobiology, vol. 40, pp. 711-720.
MARTINS, G.F., ZANUNCIO, J.C. and SERRAO, J.E., 2008. Spermatheca morphology of the social wasp Polistes erythrocephalus. Bulletin of Insectology, vol. 61, pp. 37-41.
MENDES, M.T., 2014. Avaliacao do efeito da saliva de triatomineos (Heteroptera: Reduviidae) sobre a biologia de celulas dendriticas murinas. Uberaba: Universidade Federal do Triangulo Mineiro, 99 p. Dissertacao de Mestrado em Medicina Tropical e Infectologia.
NASCIMENTO, J.D., 2015. Estudo histologico das espermatecas e traqueias de seis especies de Triatominae (Hemiptera, Reduviidae). Campinas: Universidade Estadual de Campinas, 60 p. Dissertacao de Mestrado em Biologia Animal.
NOIROT, C. and QUENNEDEY, A., 1991. Glands, gland cell, glandular units: some comments on terminology and classification. Annales de la Societe Entomologique de France, vol. 23, pp. 123-128.
PASCINI, T.V. and MARTINS, G.F., 2017. The insect spermatheca: an overview. Zoology, vol. 121, pp. 56-71. http:// dx.doi.org/10.1016/j.zool.2016.12.001. PMid:28089345.
PENDERGRAST, J.G., 1957. Studies on the reproductive organs of the Heteroptera with a consideration of their bearing on classification. Ecological Entomology, vol. 109, pp. 1-63.
SILVA, I.G., SANTOS, L.G.P. and NAKANO, R., 1993. Ciclo evolutivo de Triatoma lecticularia (Stal, 1859) (Hemiptera, Reduviidae). Revista de Patologia Tropical, vol. 22, pp. 259-263.
SOUZA, E.A., CAMPOS, L.A.O., NEVES, C.A., ZANUNCIO, J.C. and SERRAO, J.E., 2008. Effect of delayed mating on spermathecal activation in Melipona quadrifasciata anthidioides (Hymenoptera, Apidae) queens. Apidologie, vol. 39, no. 3, pp. 293-301. http://dx.doi.org/10.1051/apido:2008008.
SOUZA, E.A., LISBOA, L.C.O., ARAUJO, V. A. and SERRAO, J.E., 2016. Morphology of the spermathecae of Leptoglossus zonatus (Heteroptera: Coreidae). Annals of the Entomological Society of America, vol. 109, no. 1, pp. 106-111. http://dx.doi. org/10.1093/aesa/sav097.
STACCONI, M. and ROMANI, R., 2011. Ultrastructural and functional aspects of the spermatheca in the American Harlequin Bug, Murgantia histrionica (Hemiptera: Pentatomidae). Neotropical Entomology, vol. 40, no. 2, pp. 222-230. http://dx.doi.org/10.1590/ S1519-566X2011000200011. PMid:21584404.
STEFANINI, M., DE MARTINO, C. and ZAMBONI, L., 1967. Fixation of ejaculated spermatozoa for electron microscopy. Nature, vol. 216, no. 5111, pp. 173-174. http://dx.doi.org/10.1038/216173a0. PMid:4862079.
THORNHILL, R. and ALCOCK, J., 1983. The evolution of insect mating systems. Cambridge: Harvard University Press.
WHEELER, D.E. and KRUTZSCH, P., 1994. Ultrastructure of the spermatheca and its associated gland in the ant Crematogaster opuntiae (Hymenoptera, Formicidae). Zoomorphology, vol. 114, no. 4, pp. 203-212. http://dx.doi.org/10.1007/BF00416859.
WOLFNER, M.F., 2011. Precious essences : female secretions promote sperm storage in Drosophila. PLoSBiology, vol. 9, no. 11, pp. e1001191. http://dx.doi.org/10.1371/journal.pbio.1001191. PMid:22087072.
M. F. Monteiro (a), L. C. O. Lisboa (a), T. M. Carvalho-Costa (b), J. C. Nevoa (b), C. J. F. Oliveira (b), J. E. Serrao (c) andE. A. Souz (a)*
(a) Instituto de Ciencias Biologicas e da Saude, Universidade Federal de Vicosa--UFV, Campus Rio Paranaiba, Rodovia MG 230, Km 7, CEP 38810-000, Rio Paranaiba, MG, Brasil
(b) Laboratorio de Imunologia, Universidade Federal do Triangulo Mineiro--UFTM, Campus I, Praca Manoel Terra, 330, 1 Piso, N.Sa. da Abadia, CEP 38025-015, Uberaba, MG, Brasil
(c)Departamento de Biologia Geral, Universidade Federal de Vicosa--UFV, Avenida Peter Henry Rolfs, s/no, Campus Universitario, CEP 36570-000, Vicosa, MG, Brasil
Received: June 2, 2017--Accepted: August 22, 2017--Distributed: February 28, 2019 (With 2 figures)
Caption: Figure 1. Female reproductive tract of Triatoma lecticularia showing ovaries (OV), lateral oviducts (LO), common oviduct (CO) and two spermathecae (Sp). Bar: 3mm.
Caption: Figure 2. Histology section of the spermathecae of Triatoma lecticularia. A: General view of the spermatheca showing its elongated shape and the single layered epithelium (Ep) lining the lumen (L). Bar: 200[micro]m; B: Columnar epithelial cells (Ep) with basophil cytoplasm (*) and nucleus with predominate decondensed chromatin. Note lumen (L) filled with spermathozoa. Bar: 20[micro]m; C: Spermatheca submitted to the P.A.S test with positive reaction into the lumen (L) and epithelial cells (Ep) with homogenously positive cytoplasm. Bar: 20[micro]m; D: Spermatheca submitted to the mercury bromophenol test for proteins showing positive reaction into the lumen (L) and epithelium (Ep). Bar: 20[micro]m; E: Muscular duct (md) opening in the common oviduct (Co). Bar: 200[micro]m; F: Detail of the muscle layers (m) of the spermathecal duct. Bar: 50 [micro]m. n: nucleus.
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|Title Annotation:||Original Article|
|Author:||Monteiro, M.F.; Lisboa, L.C.O.; Carvalho-Costa, T.M.; Nevoa, J.C.; Oliveira, C.J.F.; Serrao, J.E.; S|
|Publication:||Brazilian Journal of Biology|
|Date:||Feb 1, 2019|
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