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Brazilian Archives of Biology and Technology - Ultrastructural and quantitative studies of hemocytes in the sugarcane borer, Diatraea saccharalis (Lepidoptera: Pyralidae)

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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913

Braz. arch. biol. technol. vol.46 no.2 Curitiba Mar. 2003

http://dx.doi.org/10.1590/S1516-89132003000200021 

Ultrastructural and quantitative studies of hemocytes in the sugarcane borer, Diatraea saccharalis (Lepidoptera: Pyralidae)

 

 

Ângela Maria Ferreira FalleirosI, *; Maria Terezinha Siqueira BombonatoII; Elisa Aparecida GregórioIII

IDepartamento de Histologia; Centro de Ciências Biológicas; Universidade Estadual de Londrina - UEL; C. P. 6001, CEP 86051-990; Londrina - PR - Brazil
IIUNESP; Bauru - SP - Brazil
IIICentro de Microscopia Eletrônica; Instituto de Biociências; UNESP; Botucatu - SP - Brazil

 

 


ABSTRACT

Six circulating hemocytes cell types from Diatraea saccharalis (Fabricius) (Lepidoptera: Pyralidae) larvae were identified by transmission and scanning electron microscope: prohemocytes (PR), plasmatocytes (PL) granulocytes (GR), spherulocytes (SP), oenocytoids (OE) and vermicytes (VE). The PR was the smallest cell type with a large nucleus, a cytoplasm with few organelles and a homogenous smooth surface. The PL was polymorphic and abundant, with a cytoplasm rich in organelles and a cellular surface with several cytoplasmic projections. The GR was abundant, showing two types of membrane-bounded granules (dense and structutered), glycogen, lipid droplets and a surface with philopodial projections. The SP was a large cell, with a cytoplasm full of intracytoplasmic spherules. The OE was the largest hemocyte type with a large and homogeneous cytoplasm and scarce organelles. The VE was discoid in shape and showed electron-dense granules.

Keywords: Insect; Lepidoptera; Hemocytes; Ultrastructural Morphology; Differential Hemocyte Count; Morphometry


RESUMO

Seis tipos de hemócitos circulantes foram caracterizados na hemolinfa de larvas de Diatraea saccharalis (Fabricius) (Lepidoptera: Pyralidae), através da microscopia eletrônica de transmissão e varredura: prohemócitos (PR), plasmatócitos (PL), granulócitos (GR), esferulócitos (ES), oenocitóides (OE) e vermiformes (VE). O PR foi o menor tipo celular; apresentando um núcleo grande, citoplasma com poucas organelas e superfície lisa e homogênea. O PL era polimórfico e abundante, com citoplasma rico em organelas e superfície celular com várias projeções citoplasmáticas. O GR era abundante, apresentando dois tipos de grânulos envoltos por membrana (denso e estruturado), glicogênio, gotas de lipídio e projeções citoplasmáticas filopodiais. O ES era uma célula grande, com citoplasma carregado de esférulas intracitoplasmáticas. O OE foi o maior tipo de hemócito encontrado, apresentando citoplasma grande, homogêneo e escassas organelas. O VE era discóide e apresentou grânulos elétrons-densos.


 

 

INTRODUCTION

Insect hemocytes, like vertebrate leucocytes, are a mixture of cell types with different morphological and biological functions. The hemocytes have the ability to discriminate stranger agents, mediate phagocytosis, cytotoxicity, encapsulation, wound repair and coagulation. These defense reactions were observed against pathogens, parasites and other foreign bodies, which entered in the hemocoel (Ratcliffe et al., 1985; Lackie, 1986; Ratcliffe and Rowley, 1987; Brookman et al., 1989; Rahmet-Alla and Rowley, 1989; Falleiros and Gregório, 1995; Hung and Boucias, 1996).

Seven types of hemocytes have been frequently described in various insects: prohemocytes, plasmatocytes, granulocytes, spherulocytes, adipohemocytes, oenocytoids and coagulocytes (Jones, 1979; Gupta, 1985; Brehélin and Zachary, 1986, among others).

The sugarcane borer, Diatraea saccharalis (Fabricius) is a serious destructive pest found in sugarcane and many other crops including maize, sorghum and rice. However, very little is known about their hemocytes. This paper aims at characterizing morphologically and morpho-metrically these cellular types, using the electron microscopy. It also quantifies, through differential counts (DCH), the types of hemocytes found in the hemolymph of Diatraea saccharalis, which were evaluated by phase contrast microscopy.

 

MATERIAL AND METHODS

D. saccharalis larvae were obtained from the Pest Control Laboratory at the Usina Barra Grande in Lençois Paulista, S.P., Brazil. The larvae were grown in the laboratory on artificial diet (Hensley and Hammond, 1968) at 25-27° C and 70% relative humidity. Late instars larvae aging from 17 to 23 days were used.

For transmission electron microscopy (TEM), hemolymph of at least 15 insects of the same age was collected from a punctured abdomen and pulled into an Eppendorff tube containing the insect anticoagulant solution described by Leonard et al., (1985). The hemocyte pellet was obtained by centrifugation at 6500 rpm for 2 min, suspended again and fixed in cacodylate buffer (0.1 M, pH 7.2) with glutaraldehyde solution (2.5%) for 2 h. The fixed pellets were embedded in 2.5% Bacto-agar (DIFCO), prepared in phosphate buffer (0.1 M, pH 7.2) at 45° C, cooled in ice and sliced into small fragments with a razor blade. The materials were post fixed in cacodylate buffer with osmium tetroxide solution (1%) for 2 h, dehydrated in graded acetone solution and embedded in Araldite®. The ultrathin sections were stained in uranil acetate and lead citrate.

For the scanning electron microscopy (SEM), the hemolymph was dropped directly on coverslips covered by 0.1% poly-l-lysine for 5 min in a moist chamber. After the adhesion of the hemocytes, the monolayers were fixed in cacodylate buffer (0.1 M, pH 7.3) with glutaraldehyde solution (2.5%), post-fixed in osmium tetroxide, dehydrated in graded acetone and dried at the critical point. The preparations were mounted on stubs, gold coated in a sputter coater and analyzed by SEM. The morphometric analysis of the different hemocyte types was performed on photomicrographs magnified 10,000 times, using a microprocessor-controlled measuring system (Mini-Mop, Kontron).

For the differential hemocyte counts (DHC), unfixed hemolymph was diluted in an insect anticoagulant solution. The percentage of each hemocyte type was determined by using 5insects /age, 200cells/insect count, in a 1000cells/age performance.

 

RESULTS

Six hemocyte types were ultrastructurally identified in the hemolymph of D. saccharalis larvae: prohemocytes, plasmatocytes, granulo-cytes, spherulocytes, oenocytoids and vermicytes.

Prohemocytes (PR) were the less frequently found hemocyte in the hemolymph, representing 4.1% of the 17 day-old larvae, showing a decrease in percentage terms and undetected in 20 day-old larvae (Table 1). PR was a small rounded cell with variable sizes (Table 2). Plasma membrane was generally smooth, and nucleus was large, centrally located, almost filling up the whole cell. The nuclear/cytoplasmic ratio was 84% (Table 2) with scattered chromatin and evident nucleoli. The cytoplasm showed a large amount of free ribosome, but only a small rough endoplasmic reticulum (RER) cisternae. Few mitochondria and rare Golgi complex were observed (Fig. 4). Plasmatocytes (PL) represented up to 29% of the circulating hemocytes, showing a decrease in 23 day-old larvae percentage (Table 1). These were polymorphic cells, generally oval and variable in size (Table 2). The plasma membrane may exhibit irregular processes, as micro papillae, philopodia or invaginations (Figs. 1, 4, 5, 6). The elongate or lobate nucleus present variable sizes and was centrally localized, showing scattered chromatin masses and up to two nucleoli (Fig. 4). The nuclear/cytoplasmic ratio was 36% (Table 2). Binuclear PL was occasionally observed. The cytoplasm showed well-developed RER, Golgi system, mitochondria and polymorphic vacuoles (Fig. 4). There were many cells with intermediate characteristics between PR and PL, interpreted as young PL.

 

 

Granulocytes (GR) were the most frequently observed cell type in larvae aging from 17 to 23 day-old (Table 1) and were spherical cells with variable sizes (Table 2). Plasma membrane showed projections, mainly philopodial (Figs.1, 2, 7, 8). The nucleus was either round or elongated, centrally located, with scattered chromatin masses and nucleolus, and the nuclear/cytoplasmic ratio was 27% (Table 2). Two types of membrane-bound granules were observed: dense granules, containing electron-dense and homogenous content, and structured granules, with crystalloid content (Figs.1, 2). Vacuoles of variable sizes and shapes were also present, with moderately electron-dense and flocculent material. The developed RER, the Golgi apparatus, mitochondria and glycogen particles were dispersed in the cytoplasm. Lipid droplets of various sizes, associated with either glycogen particles or dense granules (Fig. 1), were detected in the oldest larvae. Cells with intermediate features between PL and GR were observed. The percentage of spherulocytes (SP) in the hemolymph varied presenting values close to those of the PL, showing, however, an increase in the 23rd day-old larvae (Table 1). SP was spherical cell with variable sizes (Table 2), generally larger than the PL and GR. These hemocytes were characterized by their inclusions and membrane-bound spherules took up almost all the cytoplasm. The cellular surface was homogenous but exhibit cytoplasmic protrusion corresponding to the spherules (Figs. 2, 7). The nucleus was small, centrally located or eccentric, mostly deformed by the spherules (Fig. 2). The nuclear/cytoplasmic ratio was low, 9% (Table 2). The spherules contained moderate electron-dense and flocculent material, with a quite electron-dense core region (Fig. 2). Besides the spherules, the cytoplasm contained few organelles around the nucleus, such as ribosome, Golgi complex, RER and few mitochondria (Fig. 2).

Oenocytoids (OE) represented up to 5.3% of the circulating hemocytes (Table 1). OE was a rounded cell, larger than all the other hemocyte types (Table 2). The cellular membrane was smooth (Figs. 5, 6, 7, 8); vesicles were observed in close association with the plasmalem (Fig. 5). The nucleus was small, eccentric, with a nuclear/cytoplasmic ratio of 11% (Table 2) and showed a distribution pattern with alternate condensed and discondensed chromatin. The cytoplasm was homogenous and poor in organelles, with the exception of the free ribosome, that were abundant (Fig. 6). Dense mitochondria, generally ring-shaped was observed (Fig. 5).

Vermicytes (VE) represented up to 9.3% of the circulating hemocytes (Table 1). VE was fusiform in shape and variable in size (Table 2). The cell membrane was generally smooth (Figs.1, 5). The nucleus was elongated, centrally located and the nuclear/cytoplasmic ratio was 32% (Table 2). Besides cell shape, this type cell was characterized by the rounded, electron-dense and homogenous cytoplasmic granules (Figs. 1, 5).

 

DISCUSSION

Among the cellular types observed in Diatraea saccharalis (Fabricius) larvae, PR, PL, GR, SP and OE presented ultrastructural morphological features similar to those found in other Lepidoptera species (Akai and Sato, 1973; Lai-Fook, 1973; Beaulaton and Monpeyssin, 1976; Raina, 1976; Beeman et al., 1983; Essawy et al., 1985; Wago and Kitano, 1985; Saxena, 1992; Ribeiro et al., 1996), except Wago and Kitano (1985), who recognized only three types of hemocytes present in the hemolymph of Pieris rapae crucivora (Boisduval). In addition, the hemocytes of D. saccharalis described in this study presented, for each type of hemocyte, and in different insect species, morphometric values within the numerical intervals reported by Gupta (1985) which were numerically very close to the data obtained by Raina (1976).

The identification of VE cell as a distinct cellular type has not been pointed out in many of the insects studied, being included as a functional variant of PL. Although some authors have reported behavioral differences in this cell, which distinguished them from the PL, they were classified as PL in Prodenia (Jones, 1959) and in Calpodes ethlius (Stoll) (Lai-Fook, 1973). Kurihara et al. (1992), analyzed hemocytes of Spodoptera litura (Fabricius) by phase contrast microscopy and were able to find adhesive character of forms, different from the PL. They proposed that these cells and the so-called coagulocytes (CO) were of the same cellular kind, naming them Podocytes (PO).

In the D. saccharalis larvae, these cells showed quite individualized morphological characteristics, which permitted us to distinguish them as a cellular type and not only a transitional, a variant of the PL functional state. Our morphological description for this cellular type was similar to Ribeiro et al. (1996).

AD has not been considered a cellular type in the present work since, ultrastructurally, they showed similar morphology to that of GR, except in the large amount of lipid droplets in the cytoplasm. The word "adipohemocyte" has been applied to cells of different morphologies, being functional variants of other cellular types with lipid droplets, according to Lea and Gilbert (1966). Thus, the use of synonymies for these different cells which accumulated lipid, as observed in GR of various insects (Price and Ratcliffe, 1974; Kaaya and Ratcliffe, 1982; Gupta, 1985; Ratcliffe et al. 1985, Fenoglio et al. 1993, among others), including the D. saccharalis larvae, was not recommended as it generated controversies, which made the characterization of insect hemocytes even more difficult.

The identification of cells with intermediate features between PR-PL and between PL-GR suggested a possible cell differentiation of those hemocyte types in the circulation. The decrease in the number of PR and PL, simultaneously with the increase of PL and GR, respectively, suggested that a transformation of PR in PL and of PL in GR took place, as reported by Gupta (1979, 1985) and Ratcliffe et al. (1985).

Although the results of this study referred to the presence of transitional stages among types of hemocytes, they did not reach any conclusion the differentiation of the blood cells. Probably PR was an undifferentiated cell that would be transformed in PL, which then would give origin to the GR. No morphological transitional stage among any other type of the D. saccharalis hemocytes (ES, OE and VE) was found, which led us to believe that the cellular types had a different origin from that mentioned earlier. Further studies are needed to contribute to this discussion.

Results of this work may help in the investigation of the role played by the different cell types on the defense mechanisms of the sugarcane borer. They may also contribute to the improvement of the techniques used in the control of this plague, mainly the biological control that takes place when the parasitoid deceives successfully the defense system of the host.

 

ACKNOWLEDGEMENTS

The authors are grateful to Nivalde Basso, Maria H Moreno and Maria Euleda Perez, for the technical support. This work was partially supported by CPG/UEL and CNPq.

 

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Received: February 15, 2001
Revised: September 19, 2001
Accepted: August 08, 2002

 

 

* Author for correspondence