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Genetics and Molecular Biology

Print version ISSN 1415-4757

Genet. Mol. Biol. vol.30 no.3 São Paulo  2007

http://dx.doi.org/10.1590/S1415-47572007000400023 

MUTAGENESIS
RESEARCH ARTICLE

 

Astylus variegatus (Coleoptera, Melyridae): Cytogenetic study of a population exposed to agrochemical products

 

 

Marielle Cristina SchneiderI; Bianca Pierina CarraroII; Doralice Maria CellaI; Rodrigo Rodrigues MatielloIII; Roberto Ferreira ArtoniII; Mara Cristina AlmeidaII

IDepartamento de Biologia, Instituto de Biociências, Universidade Estadual Paulista, Rio Claro, São Paulo, Brazil
IIDepartamento de Biologia Estrutural, Molecular e Genética, Universidade Estadual de Ponta Grossa, Ponta Grossa, Paraná, Brazil
IIIDepartamento de Fitotecnia e Fitossanidade, Universidade Estadual de Ponta Grossa, Ponta Grossa, Paraná, Brazil

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ABSTRACT

In this work we describe the cytogenetic analyses performed in specimens of Astylus variegatus (Germar, 1824) collected in two localities: one area of natural vegetation and one of agricultural crops, where agrochemical products were used. Astylus variegatus had karyotypes with 2n(male) = 16+Xyp and 2n (female) = 16+XXp, with exclusively metacentric chromosomes. Pachytene spermatocytes showed synapsed autosomal bivalents and non-associated sex chromosomes. In diplotene, the autosomal bivalents exhibited one or two terminal chiasmata and the Xyp had a typical parachute configuration. In meiotic cells of some specimens, an extra chromosome, interpreted as a B chromosome, was observed. C-banding showed constitutive heterochromatin in the pericentromeric region of all chromosomes, with the exception of the yp. Silver nitrate staining revealed one nucleolus organizer region (NOR) on the terminal region of the short arm of the second autosome pair. Silver staining of meiotic cells confirmed the NOR pattern detected in mitotic cells and revealed an argentophilous material on the Xyp. A cytogenetic comparison between the two populations of A. variegatus showed a statistically significant divergence (c2 = 117.10; df = 1) in the number of aneuploid cells and a higher frequency of B chromosome in the population exposed to agrochemicals.

Key words: B chromosome, constitutive heterochromatin, karyotype, meiosis, Ag-NORs.


 

 

Introduction

Astylus variegatus is endemic to the Neotropical region and belongs to the superfamily Cleroidea (Lawrence and Newton, 1995). This superfamily comprises around 10.000 species included in eight families (Lawrence and Newton, 1995; Costa, 2003). Cytogenetic data, however, are restricted to 15 Cleroidea species of two families, Cleridae and Melyridae (Smith and Virkki, 1978; Yadav and Dange, 1989).

All the 12 species of the family Cleridae previously studied had the same diploid number (2n = 18) and a sex chromosome system of the Xyp type. In this system, the X and the y represent the sex chromosomes and the "p" indicates the meiotic configuration of the sex chromosomes, which was compared to a parachute by Stevens (1906). The chromosome morphology has been reported for six Cleridae species: Enoclerus sp., Necrobia ruficollis, Necrobia rufipes, Priocera spinosa, Thanasimus formicarius, and Trichodes apiarius. All these species presented exclusively meta/submetacentric chromosomes (Virkki, 1960, 1963; Smith and Virkki, 1978; Yadav and Dange, 1989). In contrast, the three studied species of the family Melyridae, which includes A. variegatus, presented different karyotypes: Endeodes collaris showed 2n = 18+X0, Collops sp. exhibited 2n = 16+X0, and Hoppingiana hudsonica revealed 2n = 12+Xyp. The chromosomes morphology has not been described in any of these species (Smith and Virkki, 1978).

Cytogenetic analyses of Cleroidea species are restricted to conventional staining. Therefore, there are no data on specific chromosome regions, such as constitutive heterochromatin and nucleolar organizer regions (NORs), for Cleroidea species, which could be useful in understanding the chromosome evolution strategies in the group.

Many beetle species are considered agricultural pests because they feed on cultivated plants or on stored grains. The control of these species is thus economically important. During its larval phase, Astylus variegatus can damage seeds in the soil before they germinate. This species is considered a minor agricultural pest because only a large population is capable of harming some cultivated plants, specially maize (Matioli et al., 1990; Viana et al., 2002). Nevertheless, agrochemical products, such as insecticides, have sporadically been required to control A. variegatus populations (Viana et al., 2002).

None of the species of Brazilian Melyridae has been cytogenetically analyzed and A. variegatus specimens are found on cultivated plants and consequently exposed to agrochemical products. In this work, we performed a cytogenetic study of A. variegatus, including the description of its karyotype, C-banding, nucleolus organizer regions (NORs) distribution and meiosis. We also analyzed mitotic and meiotic chromosomes of specimens collected on cultivated plants, such as beans, maize, soybean, and sunflower, which have been exposed to agrochemical products.

 

Material and Methods

Forty adult specimens of A. variegatus were collected in two localities of Ponta Grossa, state of Paraná, Brazil: 20 specimens in an area of natural vegetation (Bairro Sabará - 25°04'57" S, 50°12'38" W) and 20 specimens in an agricultural area (Fazenda Escola Capão da Onça - 25°05'41" S, 50°03'40" W) from the Universidade Estadual de Ponta Grossa (Table 1). Chromosome preparations were obtained from gonads of adult male and female specimens. The testes were removed in insect saline solution (128.3 mM NaCl, 16.7 mM Na2HPO4, 19.9 mM KH2PO4), incubated in tap water as an hypotonic treatment for five minutes, and fixed in Carnoy I (3 methanol: 1 acetic acid) for 30 min. In order to obtain a large number of mitotic metaphases, some dissected gonads (testes and ovaries) were immersed in a colchicine solution (0.05% in insect saline solution) for two hours before the hypotonic treatment. After fixation, the gonads were macerated in 45% acetic acid and the slides were dried on a hot plate at 35-40 °C. All chromosome preparations were stained with a 3% Giemsa solution (94 mL of distilled water, 3 mL of Giemsa-Merck, and 3 mL of phosphate buffer - pH 6.8) for 15 min. Constitutive heterochromatin and NORs were detected by C-banding (Sumner, 1972) and with silver nitrate (Howell and Black, 1980), respectively. Chromosomes were morphologically classified according to Levan et al. (1964).

 

 

The chromosome data of the specimens collected in the two different localities (area of natural vegetation - control population and area of agricultural crops - population exposed to agrochemical products) were compared. A total of 1693 conventionally stained cells per population were analyzed. The significance of the cytogenetic differences observed between the two populations of A. variegatus were statistically evaluated by the chi-square test.

 

Results

Conventional staining

Spermatogonial and oogonial metaphases of A. variegatus showed 2n = 18. The male karyotype consisted of eight homomorphic pairs and two unpaired elements identified as the sex chromosomes, whereas the female karyotype was composed of nine homomorphic pairs, that is, eight autosomal and one sexual pair. The analyses of male meiotic cells and a comparison between the male and female karyotypes revealed a sex chromosome system of the Xyp type. All the chromosomes were metacentric. The autosome pairs gradually decreased in size and the Xp chromosome was slightly smaller than the smallest autosome pair. The yp chromosome was a dot-like negative heteropycnotic structure (Figures 1 and 4A).

 

 

 

Figure 2

 

 

 

 


 

Positively heteropycnotic material was observed as a block and some dots in interphase testes cells (Figure 2A). These regions probably correspond to the sexual chromatin and heterochromatic regions, respectively. Pachytene spreads showed eight autosomal bivalents regularly synapsed along their entire length and two univalent sex chromosomes (Figures 2B and 5B). One or two terminal chiasmata were observed in the autosomal bivalents during diplotene, while the sex chromosomes were associated in a typical parachute configuration (Figure 2C). Prophase I and metaphase I cells revealed the meioformula 2n = 8II+Xyp, in agreement with the diploid number and sex chromosome system observed in mitotic cells (Figure 2C-D). Metaphase II cells showed n = 8+Xp or n = 8+yp (Figure 2E-F). The Xp and yp sex chromosomes were positively and negatively heteropycnotic, respectively, during most of the meiosis.

 



 

Specimens of A. variegatus collected in the areas of natural vegetation and of agricultural crops showed the same cytogenetic features. In all the individuals from both populations some cells were aneuploid with a variable number of missing chromosomes ranging from one to seven, but differences in the quantity of hypoploid cells were observed between both populations.

From a total of 1693 mitotic and meiotic cells of the 20 individuals collected in the natural vegetation area, 1472 cells had the normal chromosome number for the species (2n = 18 or n = 9) and 221 cells were hypoploid. In the 20 specimens collected in the area of agricultural crops, 1322 cells had normal chromosome numbers and 371 cells were hypoploid. The chi-square test showed that the difference in the quantity of cells with typical and atypical chromosome numbers between both A. variegatus populations was statistically significant (c2 = 117.10; df = 1).

In some specimens, metaphase I spermatocytes showed an extra chromosome similar in size to the Xp (Figure 3A). This chromosome, probably a B chromosome, was highly condensed during metaphase I, which prevented us from determining if it was bivalent or univalent. In the same specimens, a late segregating chromosome, probably corresponding to the B chromosome, was observed in some anaphase cells (Figure 3B). The B chromosome was detected in individuals of both A. variegatus populations, although with different frequencies: 5% in the control population and 10% in the population exposed to agrochemical products.

C-banding

After C-banding of spermatogonial metaphases of A. variegatus, small and well-defined dots of constitutive heterochromatin were evidenced in the pericentromeric region of all chromosomes, with the exception of the yp (Figure 4B).

Silver staining

After Ag-NORs staining, testicular mitotic cells of A. variegatus presented tenuous and small NORs on the terminal region of the short arm of pair 2 (Figure 5A). In pachytene spermatocytes, nucleolar material was associated to one autosomal bivalent, in agreement with the spermatogonial cells results (Figure 5B-C). During metaphase I, only an argentophilic block between the sex chromosomes was observed (Figure 5D-E).

 

Discussion

Some cytogenetic features of A. variegatus herein described, such as the Xyp sex chromosome system and the metacentric chromosome morphology, are similar to those considered ancestral for beetles of the suborder Polyphaga. Nevertheless, the 2n = 18 of A. variegatus differs from the 2n = 20 proposed as basic for Polyphaga by Smith and Virkki (1978). The reduction of one autosome pair and the conservation of the metacentric morphology verified in the karyotype of A. variegatus probably results from a centric fusion between autosomes, which was preceded by fission and loss of entirely heterochromatic autosomal arms or, alternatively, by pericentric inversions.

Chromosome evolution involving diploid number reduction is evident not only in A. variegatus, but also in all previously studied species of the superfamily Cleroidea (Smith and Virkki, 1978; Yadav and Dange, 1989). The karyotype with 2n = 16+Xyp of A. variegatus is shared with all 12 related species of the family Cleridae, but it is the first time that it is reported among Melyridae. Only four Melyridae species have already been cytogenetically analyzed (Smith and Virkki, 1978; present work) and the data reported for this family (2n = 18+X0; 2n = 16+X0; 2n = 16+Xyp; 2n = 12+Xyp) indicate that the chromosome variation can occur through the loss of the yp, giving rise to the X0 sex chromosome system, and/or through autosomes fusions, reducing the chromosome number.

The study of meiotic cells of A. variegatus allowed observing that all chromosomes showed regular patterns of heteropycnosis, synapsis, orientation, and segregation. Nevertheless, some peculiarities regarding the number of chiasmata and the association of the Xyp sex bivalent were detected in this species. The occurrence of bivalents with two chiasmata, such as verified in A. variegatus, has occasionally been described in coleopterans (Smith and Virkki, 1978). In species of Cleroidea, it was only reported in Enoclerus sp. and Necrobia ruficolis (Virkki, 1963; Yadav and Dange, 1989). In Coleoptera, biquiasmatic bivalents seem to be more frequent in species which present chromosome differentiation through fusions, such as representatives of the family Elateridae (Smith, 1956a; Agarwal, 1962; Kacker, 1963; Ferreira et al., 1984; Yadav and Vyas, 1994). The presence of two chiasmata in these bivalents may be explained by the fact that the number of chiasmata partly depends on the chromosome length, as postulated by John (1990).

The parachute configuration of the Xyp bivalent during meiosis has been found in the great majority of beetle species of the Polyphaga suborder (Smith and Virkki, 1978) and it may result from a biquiasmatic association between the sex chromosomes (Smith, 1951), terminal heterochromatic non-specific association (Drets et al., 1983), or presence of nucleolar material on the sexual bivalent (John and Lewis, 1960). Contrarily to the proposal of Smith (1951), the Xyp pairing in A. variegatus was certainly aquiasmatic as the sex chromosomes were univalent elements during pachytene. C-banding revealed that the Xp of A. variegatus only had pericentromeric heterochromatin and the yp was entirely C-band negative. Thus, the Xyp association in A. variegatus probably did not occur through the pairing of constitutive heterochromatic segments, as postulated by Drets et al. (1983) for Epilachna paenulata. The use of other methodologies to detect heterochromatin, such as the staining with base-specific fluorochromes, can be useful to confirm this hypothesis. On the other hand, the Xyp parachute configuration and the concomitant presence of an argentophilous material between these chromosomes in late prophase I and metaphase I cells suggests that the sex chromosomes association is related to the presence of this argentophilous material.

B chromosomes have already been described in approximately 50 Coleoptera species and subspecies (Smith and Virkki, 1978), belonging to some families, such as Chrysomelidae, Coccinellidae, and Lampyridae (Smith and Virkki, 1978; Nokkala and Nokkala, 1989; Maffei et al., 2000; Schneider et al., 2002). Nevertheless, this is the first time that B chromosomes are recorded for a representative of the superfamily Cleroidea. Smith (1956b) verified an increase in the frequency of supernumerary chromosomes in one population of Diabrotica undecimpunctata howardi (Coleoptera, Chrysomelidae) exposed to insecticides and suggested that a higher number of supernumeraries could provide advantageous effects to specimens from that population. A detailed investigation of the B chromosome synaptic behavior in A. variegatus may shed light on its origin, as it may share homology with some A chromosome. An analysis of the meiotic behavior of the B chromosome in A. variegatus may also help in elucidating how it accumulates and what causes its interpopulational frequency difference.

C-banding and Ag-NOR were very useful in establishing Xyp pairing during meiosis and in obtaining data on specific chromosome regions in a Melyridae species. The pericentromeric constitutive heterochromatin pattern observed in A. variegatus is similar to that reported for most polyphagan species (Almeida et al., 2000; Rozek et al., 2004). Moreover, chromosomes with small amounts of constitutive heterochromatin were observed in many coleopteran families, e.g. Anthicidae, Attelabidae, Cerambycidae, Chrysomelidae, and Curculionidae (Rozek et al., 2004). Most beetles of the suborders Adephaga and Polyphaga have NORs restricted to the autosomes, which were described in 81% of the species studied (Schneider et al., in press). In many species with the Xyp sex chromosome system, an argentophilous material, usually interpreted as nucleolar, has been frequently detected during meiosis (Virkki et al., 1990; Juan et al., 1993), as was the case in A. variegatus herein studied. According to Juan et al. (1993), the rDNA genes in these species may be exclusively located on autosomes and the product of the active autosomal NORs may be imported by the sex bivalent, where it could have a role in the association and disjunction of these chromosomes during meiosis. Ag-NORs were not observed in the sex chromosomes in mitotic cells of A. variegatus. It is thus possible that there is only an autosomal NOR, a hypothesis that could be confirmed by fluorescent in situ hybridization with an rDNA probe.

The comparison between individuals of the two A. variegatus populations revealed that, in addition to the difference in B chromosome frequency, these populations differ in the number of hypoploid cells. Although the aneuploidies could result from some experimental problem, the number of hypoploid cells was higher in the population exposed to agrochemical products and the chi-square test showed a statistically significant difference between both A. variegatus populations. Therefore, the aneuploidy may result from the use of agrochemical products, which may interfere with spindle fiber polymerization. This, in turn, could trigger alterations in the chromosome distribution during cell division leading to aneuploidies (Rabello-Gay et al., 1991). It is worth to point out that the agrochemicals used in the Fazenda Escola Capão da Onça are non-specific for A. variegatus, which is frequently controlled with carbofuran. In conclusion, the high number of hypoploid gonadal cells in A. variegatus may reduce the number of viable gametes, leading to a decline in the population of the agricultural area. The use of agrochemical products may also be harmful to other ecologically important invertebrates.

 

Acknowledgments

The authors are grateful to Silvia D. Schneider for collecting some A. variegatus specimens and to Carlos Campaner, Museu de Zoologia, USP, São Paulo, SP, Brazil, for the identification of the specimens.

 

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Send correspondence to:
Marielle Cristina Schneider
Departamento de Biologia
Instituto de Biociências
Universidade Estadual Paulista
Av. 24-A, 1515, Caixa Postal 199
13506-900 Rio Claro, SP, Brazil
E-mail: maricb@rc.unesp.br

Received: September 19, 2006; Accepted: January 22, 2007.

 

 

Associate Editor: Catarina S. Takahashi