SciELO - Scientific Electronic Library Online

 
vol.33 issue4Change in genetic size of small-closed populations: lessons from a domestic mammal populationSociogenetic structure of Polistes (Aphanilopterus) versicolor Olivier, 1791 colonies (Hymenoptera, Vespidae, Polistini) author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

  • English (pdf)
  • Article in xml format
  • How to cite this article
  • SciELO Analytics
  • Curriculum ScienTI
  • Automatic translation

Indicators

Related links

Share


Genetics and Molecular Biology

Print version ISSN 1415-4757

Genet. Mol. Biol. vol.33 no.4 São Paulo  2010  Epub Sep 08, 2010

http://dx.doi.org/10.1590/S1415-47572010005000076 

Chromosomes of Theridiidae spiders (Entelegynae): Interspecific karyotype diversity in Argyrodes and diploid number intraspecific variability in Nesticodes rufipes

 

 

Leila Miguel StavaleI; Marielle Cristina SchneiderII; Douglas AraujoIII; Antonio Domingos BrescovitIV; Doralice Maria CellaI

IDepartamento de Biologia, Universidade Estadual Paulista "Júlio de Mesquita Filho", Rio Claro, SP, Brazil
IIDepartamento de Ciências Biológicas, Universidade Federal de São Paulo, Diadema, SP, Brazil
IIIUnidade Universitária de Mundo Novo, Universidade Estadual de Mato Grosso do Sul, Mundo Novo, MS, Brazil
IVLaboratório de Artrópodes, Instituto Butantan, São Paulo, SP, Brazil

Send correspondence to

 

 


ABSTRACT

Theridiidae is a derived family within the Araneoidea clade. In contrast to closely related groups, the 2n(male) = 20+X1X2 with acro/telocentric chromosomes is the most widespread karyotype among the theridiid spiders. In this work, the cytogenetic analysis of Argyrodes elevatus revealed original chromosome features different from those previously registered for Theridiidae, including the presence of 2n(male) = 20+X with meta/submetacentric chromosomes. Most individuals of Nesticodes rufipes showed family conserved karyotype characteristics. However, one individual had a 2n(male) = 24 due to the presence of an extra chromosome pair, which exhibited regular behavior and reductional segregation during meiosis. After silver staining, mitotic cells exhibited NORs localized on the terminal regions of the short arms of pairs 2, 3, and 4 of A. elevatus and on the terminal regions of long arms of pair 4 of N. rufipes. The comparative analysis with data from phylogenetically related species allowed the clarification of the origin of the interspecific and intraspecific chromosome variability observed in Argyrodes and in N. rufipes, respectively.

Key words: chromosome morphology, cytogenetic, meiosis, nucleolar organizer region, sex chromosome system.


 

 

Introduction

Theridiidae is among the largest families of the order Araneae, including 2.297 species subdivided into 112 genera (Platnick, 2010). The extreme diversity of foraging and lifestyle strategies, which range from solitary webless species to social spiders with maternal care, was certainly the factor that contributed to the diversification of the theridiids (Agnarsson, 2004; Arnedo et al., 2004). Within this family, the cosmopolitan species of the genus Argyrodes are famous for their kleptoparasite behavior. The kleptoparasite spiders invade the webs of unrelated and usually larger species to steal food or silk (Whitehouse et al., 2002; Agnarsson, 2004). Among the theridiids, most species of the genus Nesticodes have a synanthropic behavior, being frequently found in association with human habitations where it is easy to obtain food (Cushing and LeBeck, 1994; Rossi and Godoy, 2006).

The family Theridiidae belongs to the Araneoidea group, which includes almost one third of all taxonomically described spiders (Platnick, 2010). In contrast to the five other families of Araneoidea subjected to cytogenetic analyses (Araneidae, Linyphiidae, Nephilidae, Nesticidae, and Tetragnathidae), which exhibited a predominance of 2n(male) = 24 = 22+X1X2, 23 Theridiidae species showed a 2n(male) = 22, including a sex chromosome system of the X1X2 type and acro/telocentric chromosomes. Among eight other theridiids, the 2n(male) = 22+X1X2 was observed in Argyrodes gazingensis, Chrysso scintillans, and Parasteatoda tepidariorum, and chromosome numbers ranging from 2n(female) = 16 to 2n(female) = 28 were reported for five species of Latrodectus. The chromosome morphology was only described for three of these eight species, which exhibited acro/telocentric chromosomes (reviewed in Araujo et al., 2010).

Considering that only one Brazilian species of Theridiidae has been cytogenetically studied to date and the discrepant chromosome numbers found in this family in relation to other araneoids, this work aimed to characterize the mitotic and meiotic chromosomes of Argyrodes elevatus Taczanowski, 1873 and Nesticodes rufipes (Lucas, 1846). The chromosomal analyses were performed in gonadal and embryonic cells after standard staining with Giemsa and silver impregnation. The results were compared with those of related species to establish the main trends of chromosome evolution within Theridiidae.

 

Material and Methods

The sample of 58 individuals analyzed in this work comprised: A. elevatus - 13 adult males and 13 embryos (eight males and five females) from Rio Claro (22°23' S, 47°32' W), São Paulo (SP), Brazil, and 10 embryos (four males and six females) from Tupã (21°56' S, 50°30' W), SP; N. rufipes - 12 adults (five males and seven females) and four male embryos from Rio Claro, SP, and one adult male and five embryos (two males and three females) from Viçosa (20°45' S, 44°52' W), Minas Gerais, Brazil. The sex of the embryos was determined according to their karyotype. The adult specimens were deposited in the collection of the Laboratório de Artrópodes, Instituto Butantan (IBSP), São Paulo, SP. The chromosome preparations were obtained from adult gonads and from embryos, according to the methodology described by Araujo et al. (2008). Chromosome spreads were stained with Giemsa (3% of commercial Giemsa and 3% of phosphate buffer pH 6.8, in distilled water) for 15 min, followed by silver nitrate impregnation (Howell and Black, 1980) to reveal the nucleolar organizer regions (NORs). The chromosome analysis was performed under an Olympus BX51 light microscope and the images of the mitotic and meiotic cells were captured using the DP Controller software. The nomenclature for chromosome morphology followed Levan et al. (1964).

 

Results

Mitotic metaphase cells of A. elevatus showed a diploid number 2n = 21 for males and 2n = 22 for females with a sex chromosome system of the X/XX type and meta/submetacentric chromosomes (Figure 1a,b). The autosome pairs gradually decreased in size and the X chromosome was extremely large. In males, pachytene cells presented ten totally synapsed autosomal bivalents plus one highly condensed and strongly stained chromosome, which was identified as the univalent X chromosome (Figure 1c). Diplotene and diakinesis nuclei showed up to three autosomal bivalents with two terminal chiasmata. The other bivalents presented only one interstitial or terminal chiasma (Figure 1d,e). In these late prophase I stages, the X chromosome also revealed a higher degree of condensation in relation to the autosomes.

 



 

The karyotypes of 12 adults and 9 embryos of N. rufipes had a diploid number 2n = 22 in males and 2n = 24 in females, which were consistent with a sex chromosome system of the X1X2/X1X1 X2X2 type (Figure 2a-b). In this species, all chromosomes were acrocentric with gradually decreasing sizes. The medium-sized sex chromosomes were slightly more condensed than the autosomes. Male prophase I cells revealed two highly condensed stained blocks disposed side by side, confirming the X1X2 sex chromosome system in this species (Figure 2c). Diplotene nuclei had the meiotic formula 10II+X1X2 and all autosomal bivalents showed only one interstitial or terminal chiasma (Figure 2d). Metaphase II cells exhibited n = 10+X1X2 and n = 10 (Figure 2e).

 



 

Mitotic cells of one adult male of N. rufipes from Viçosa revealed 2n = 24 with acrocentric chromosomes, differing from all other males analyzed (Figure 3a). In these cells, the sex chromosomes did not exhibit differential cytological features that allowed their identification. Male diplotene and diakinesis nuclei showed 11 autosomal bivalents and two sex chromosomes arranged side by side or in close proximity (Figure 3b). Metaphase II cells revealed two kinds of haploid sets: n = 11+X1X2 and n = 11 (Figure 3c,d).

 

 

 

After silver impregnation, mitotic metaphase cells of A. elevatus revealed NORs on the terminal regions of the short arms of pairs 2, 3, and 4. The number of active NORs varied from two to six per cell (Figure 4a,b). In N. rufipes, the NORs were localized on the terminal regions of the long arms of pair 4 (Figure 4c,d).

 


 

Discussion

The chromosomal characteristics observed in A. elevatus were extremely discrepant from those described for 30 species of Theridiidae previously studied, including five representatives of the genus Argyrodes (see Araujo et al., 2010). Thus, this is the first record of the karyotype formula 2n(male) = 21 = 20+X with biarmed chromosomes for a theridiid spider. In contrast, the karyotype with 2n(male) = 22, the X1X2 sex chromosome system and acrocentric chromosomes found in most N. rufipes studied herein is similar to that predominantly found in the family.

Theridiidae and its sister-group Nesticidae constitute the theridioids, a derived branch within the Araneoidea clade (Griswold et al., 1998; Agnarsson, 2004). The karyotype 2n(male) = 22+X1X2 with acro/telocentric chromosomes is highly conserved among the Araneoidea spiders, considering that, with the exception of Theridiidae, it was observed in approximately 80% of the species belonging to five different families (Araujo D, PhD Thesis, Instituto de Biociências de Rio Claro, UNESP, São Paulo, 2007). Nevertheless, among the theridiids, the karyotype with 2n(male) = 20+X1X2, and acro/telocentric chromosomes is the most widespread and was already observed in species of all subfamilies already investigated (Araujo et al., 2010). It appears thus that the main trend of chromosome evolution within Araneoidea was the reduction of the diploid number with the conservation of the sex chromosome system. In Theridiidae, diploid numbers higher than 2n(male) = 22, such as the 2n(male) = 24 observed in one species of Argyrodes, Chrysso, and in some individuals of Parasteatoda tepidariorum (Montgomery, 1907; Kageyama and Seto, 1979; Datta and Chatterjee, 1983), 2n(female) = 28 and 2n(female) = 26 found in species of Latrodectus, as well as diploid numbers lower than 2n(male) = 22, such as 2n(female) = 16 and 2n(female) = 18 also reported in Latrodectus (Araujo et al., 2010) and the 2n(male) = 21 of A. elevatus, probably correspond to a derived condition originated from the 2n(male) = 22.

Considering that the 2n(male) = 20+X1X2 could represent a basal condition for Theridiidae, the karyotype with 2n(male) = 20+X of A. elevatus would not have originated through changes in the number of autosomal pairs, but rather by a change in the sex chromosome system and in the morphology of the autosomes. The X type sex chromosome system probably derived from the X1X2 system after a Robertsonian translocation between the acro/telocentric X1 and X2 chromosomes. This hypothesis is reinforced by the fact that the X chromosome of A. elevatus is a large biarmed element. Additionally, the morphological change of all autosomes from acro/telocentric to meta/submetacentric probably resulted from pericentric inversions. An alternative mechanism would be the addition of constitutive heterochromatin.

In Entelegynae, a derived lineage within the suborder Araneomorphae, the X sex chromosome system also seems to have evolved secondarily from an X1X2 system with independent origins in different species or families (Král et al., 2006; Araujo D, PhD Thesis, Instituto de Biociências de Rio Claro, UNESP, São Paulo, 2007). The presence of metacentric or submetacentric chromosomes such as observed in A. elevatus is extremely sporadic among the entelegyne spiders. In this group, the change from acro/telocentric to meta/submetacentric chromosomes has been generally attributed to centric fusions involving all chromosomes of the complement. This proposition of chromosome evolution via "all or nothing" fusion (Rowell, 1990) has been corroborated by the fact that the species with a predominance of biarmed chromosomes have a lower diploid number than those with acro/telocentric chromosomes (Mittal, 1966; Rowell, 1988, 1990, 1991; Amalin et al., 1993). Nevertheless, the mechanism of pericentric inversions observed in A. elevatus may also be responsible for the dramatic karyotype evolution of the Entelegynae.

The karyotype of most N. rufipes specimens was similar to the one considered conserved for Theridiidae. However, the mitotic and meiotic cells of one adult male showed two extra chromosomes. The diploid number variation in this individual was certainly not due to chromosome fission as the chromosomes were of uniform size, i.e., no autosomal pair exhibited a remarkable difference in size that could result from fission. Slight intraspecific variations in chromosome numbers have been frequently reported for spiders (Araujo D, PhD Thesis, Instituto de Biociências de Rio Claro, UNESP, São Paulo, 2007); but no further explanation for these variation has been put forward as yet. The 2n(male) = 24 in N. rufipes probably resulted from the presence of one additional autosome pair, considering that in diplotene and diakinesis nuclei, 11 instead of ten autosomal bivalents were invariably observed. Moreover, the metaphase II cells always showed the haploid sets n = 11+X1X2 and n = 11. Taking into account that the extra chromosome pair was seen in all cells of this individual, it is possible to infer that it originated by a meiotic non-disjunction during the formation of the maternal or paternal gametes. Alternatively, considering the haploid numbers verified in the metaphase II nuclei, this extra chromosome pair could correspond to B chromosomes with a regular meiotic behavior following a Mendelian transmission rate.

There are no previous records on the NOR distribution pattern in theridiid spiders in the literature. Nucleolar organizer regions on autosomes, such as those observed in A. elevatus and N. rufipes, are also the most frequent condition in Entelegynae, in which they were observed in all investigated species (Wise 1983; Barrion et al., 1989; Araujo et al., 2005; Rodriguez-Gil et al., 2007). Although the two theridiids exhibited great karyotypic differences, it is interesting to note that both species showed NORs on the terminal regions of one medium-sized autosomal pair (pair 4). The analysis of a larger number of Theridiidae spiders could reveal if NORs on medium-sized autosomal elements are a shared feature of the family. The increase of NORs numbers in A. elevatus may be a derived condition originated by duplications followed by translocations. In Oxyopidae spiders (Entelegynae), we also observed a relationship between a large number of NORs and an extremely derived karyotype.

 

Acknowledgments

This research was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo, FAPESP (06/53275-3, 08/55633-0) and Conselho Nacional de Desenvolvimento Científico e Tecnológico, CNPq (ADB, DA).

 

References

Agnarsson I (2004) Morphological phylogeny of cobweb spiders and their relatives (Araneae, Araneoidea, Theridiidae). Zool J Linn Soc 141:447-626.         [ Links ]

Amalin DM, Barrion AA and Jayoma M (1993) Comparative karyomorphology of two Neoscona species (Araneae, Araneidae). Philipp Entomol 9:1-6.         [ Links ]

Araujo D, Cella DM and Brescovit AD (2005) Cytogenetic analysis of the Neotropical spider Nephilengys cruentata (Araneomorphae, Tetragnathidae): Standard staining, NORs, C-bands and base-specific fluorochromes. Braz J Biol 65:193-202.         [ Links ]

Araujo D, Rheims CA, Brescovit AD and Cella DM (2008) Extreme degree of chromosome number variability in species of the spider genus Scytodes (Araneae, Haplogynae, Scytodidae). J Zoolog Syst Evol Res 46:89-95.         [ Links ]

Araujo D, Maia UM and Brescovit AD (2010) The first cytogenetic characterization of the poisonous black widow spider Latrodectus gr. curacaviensis from Brazil, with chromosomal review of the family Theridiidae (Arachnida, Araneae). Micron 41:165-168.         [ Links ]

Arnedo MA, Coddington J, Agnarsson I and Gillespie RG (2004) From a comb to a tree: Phylogenetic relationships of the comb-footed spiders (Araneae, Theridiidae) inferred from nuclear and mitochondrial genes. Mol Phylogenet Evol 31:225-245.         [ Links ]

Barrion AA, Amalian DM and Casal CV (1989) Morphology and cytology of the lynx spider Oxyopes javanus (Thorell). Philipp J Sci 118:229-237.         [ Links ]

Cushingi B and Lebeck LM (1994) Foraging in cockroach sticky traps by the spider Nesticodes rufipes Lucas (Araneae, Theridiidae): A super food resource. Acta Arachnol 43:49-55.         [ Links ]

Datta SN and Chartterjee K (1983) Chromosome number and sex-determining system in fifty-two species of spiders from North-East India. Chromosome Inf Serv 35:6-8.         [ Links ]

Griswold CE, Coddington JA, Hormiga G and Scharff N (1998) Phylogeny of the orb-web building spiders (Araneae, Orbiculariae, Deinopidae, Araneoidea). Zool J Linn Soc 123:1-99.         [ Links ]

Howell WM and Black DA (1980) Controlled silver staining of nucleolus organizer regions with protective colloidal developer: A 1-step method. Experientia 36:1014-1015.         [ Links ]

Kageyama A and Seto T (1979) Chromosomes of seven species of Japanese theridiid spiders. Chromosome Inf Serv 27:10-12.         [ Links ]

Král J, Musilová J, St'áhlavsky F, Rezác M, Akan Z, Edwards RL, Coyle FA and Almerje CR (2006) Evolution of the karyotype and sex chromosome systems in basal clades of araneomorph spiders (Araneae, Araneomorphae). Chromosome Res 14:859-880.         [ Links ]

Levan A, Fredga K and Sandberg AA (1964) Nomenclature for centromeric position on chromosomes. Hereditas 52:201-220.         [ Links ]

Mittal OP (1966) Karyological studies on the Indian spiders V. Chromosomes cycle in three species of the family Clubionidae. Caryologia 19:385-394.         [ Links ]

Montgomery TH (1907) On the maturation mitoses and fertilization of the egg of Theridium. Zool Jahrb Abt Anat Ontogenie Tiere 25:237-250.         [ Links ]

Rodriguez-Gil SG, Merani MS, Scioscia CL and Mola LM (2007) Cytogenetics in three species of Polybetes Simon 1897 from Argentina (Araneae, Sparassidae). I. Karyotype and chromosome banding pattern. J Arachnol 35:227-237.         [ Links ]

Rossi MN and Godoy WAC (2006) Prey choice by Nesticodes rufipes (Araneae, Theridiidae) on Musca domestica (Diptera, Muscidae) and Dermestes ater (Coleoptera, Dermestidae). J Arachnol 34:186-193.         [ Links ]

Rowell DM (1988) The chromosomal constitution of Delena cancerides Walck. (Araneae, Sparassidae) and its role in the maintenance of social behaviour. Aust Entomol Soc Misc Publ 5:107-111.         [ Links ]

Rowell DM (1990) Fixed fusion heterozygosity in Delena cancerides Walck. (Araneae, Sparassidae): An alternative to speciation by monobrachial fusion. Genetica 80:139-157.         [ Links ]

Rowell DM (1991) Chromosomal fusion and meiotic behaviour in Delena cancerides (Araneae, Sparassidae). I. Chromosome pairing and X-chromosome segregation. Genome 34:561-566.         [ Links ]

Whitehouse M, Agnarsson I, Miyashita T, Smith D, Cangialosi K, Masumoto T, Li D and Henaut Y (2002) Argyrodes: Phylogeny, sociality and interspecific interactions - a report on the Argyrodes symposium, Badplaas 2001. J Arachnol 30:238-245.         [ Links ]

Wise D (1983) An electron microscope study of the karyotypes of two wolf spiders. Can J Genet Cytol 25:161-168.         [ Links ]

 

Internet Resources

Platnick NI (2010) The world spider catalogue version 10.5, American Museum of Natural History. http://research.amnh.org/entomology/spiders/catalog/ (June 25, 2010).         [ Links ]

 

 

Send correspondence to:
Marielle C. Schneider
Departamento de Ciências Biológicas
Universidade Federal de São Paulo
Avenida Prof. Artur Riedel 275
09972-270 Diadema, SP, Brazil
E-mail: maricb@rc.unesp.br

Received: February 23, 2010; Accepted: May 20, 2010.

 

 

Associate Editor: Yatiyo Yonenaga-Yassuda
License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License