Chromosomal homology of Uraeotyphlus oxyurus group of species (Amphibia, Gymnophiona, Ichthyophiidae).

Uraeotyphlus oxyurus (Dumeril et Bibron, 1841), Uraeotyphlus interruptus Pillai et Ravichandran, 1999, Uraeotyphlus narayani Seshachar, 1939 and Uraeotyphlus menoni Annandale, 1913 were cytogenetically analysed following conventional and differential staining techniques. These species show similar karyotypes with 2n=36 (FN=58). There were no traces of species-specific features in regard to C-banding and NOR staining. The comparative study of karyotypes shows chromosomal homologies among the four species. Chromosomal data seem to support the concept that two species groups exist in the genus Uraeotyphlus.

Introduction

The genus Peters, 1879is endemic to the Western Ghats region of peninsular India and constitutes one of the three genera within the family Ichthyophiidae Taylor, 1968 along with Taylor, 1968 and Fitzinger, 1826(Wilkinson et al. 2011). Its taxonomy had been uncertain till the publication of Nussbaum and Wilkinson (1989) which gave this group a family level status among the existing caecilians of India. However, after a lapse of a decade or so, this prevailing situation seemed to have recovered moderately and is sufficient in redefining interrelationships among other families of caecilians based on morphological and molecular evidence (Wilkinson and Nussbaum 1996, 2006, Frost et al. 2006, Gower and Wilkinson 2007, Roelants et al. 2007, Gower et al. 2008, Zhang and Wake 2009, Wilkinson et al. 2011).

On the basis of morphological features such as cylindrical body, annulation and of the presence or absence of phallodeum, and of limited molecular evidence, Gower and Wilkinson (2007) partitioned this supposedly monophyletic genus into two species groups: species complex and species group. Consequent upon this arrangement, (Dumeril & Bibron, 1841), Pillai & Ravichandran, 1999, Seshachar, 1939 and Annandale, 1913 were grouped as derived species, while of Gower, Rajendran, Nussbaum & Wilkinson, 2008, Gower & Wilkinson, 2007 and (Beddome, 1870) were considered as primitive ones (Gower et al. 2008).

Earlier, Seshachar (1939) presented the male meiotic chromosomal complement of with the dipoloid number of 36 and gave detailed descriptions based on chromosomal morphs observed such as V-shaped, rods and dots in the complement. Elayidom et al. (1963) have described the somatic and meiotic chromosomal complement of as consisting of diploid number of 36 for the species, but neither study presented karyotypic characteristics. Venkatachalaiah and Venu (2002) gave a detailed karyotypic characteristic of what was then mistakenly thought to be Taylor, 1960 (2n=36, FN= 60) but which was subsequently found to be prope interruptus of Ichthyophiidae. With this surge of interest to elucidate the phylogeny and evolution, Venu et al. (2011) have presented the chromosomes of a member of the species group, , bearing2n=42, FN=58, highest diploid number known thus far for a member of the genus of the family Ichthyophiidae.

In this study, we present the karyotypes of and and the results of reanalysis of chromosomes of and with a view to providing new insights into the intragenus relationships within the genus .

Material and methods

Specimens of both sexes, collected from different regions the Western Ghats (Table 1) a few days before the experiment, were kept in glass aquaria under suitable conditions. After in vivo colchicine treatment, chromosome preparations were obtained from the liver, the gut epithelium and the testis. Cell suspensions, hypotonic treatment and fixation of cells were performed as described earlier (Venkatachalaiah and Venu 2002, Venu et al. 2011). Chromosome number and standard karyotype (in respect of somatic metaphase and meiotic pachytene) morphology were determined by conventional Giemsa staining technique. Chromosome nomenclature was followed as proposed earlier by Levan et al. (1964) but adopted for the present situation as described earlier (Venkatachalaiah and Venu 2002).

Table 1.

Details of collection of , , and

Species	Locality	Habitat	Voucher number	No. of animals used	Geographical coordinates
Uraeotyphlus interruptus	Gudalur, Nilgiris (Dt), Tamil Nadu, India	Mixed plantations of tea, banana, pepper, orange, coffee	BUB114, 103BUB105, 111	2 males2 females	11°30'0"N, 76°30'00"E
Uraeotyphlus narayani	Changanssery,Kottayam (Dt), Kerala, India	Backyard garden with banana plantation	BUB101, 115BUB109, 116	2 males2 females	9°28'00"N, 76°33'00"E
Uraeotyphlus menoni	Mattathur, Thrissur (Dt), Kerala, India	Backyard garden with banana plantation	BUB107, 113BUB106, 102	2 males2 females	10°22'45"N, 76°19'15"E
Uraeotyphlus oxyurus	Agali, Palakkad (Dt), Kerala, India	Cultivated agricultural land with banana and coconut plantation	BUB104, 112BUB108, 110	2 males2 females	11°5'0"N, 76°35'0"E

Conventional C-banding was performed according to Sumner (1972) using Ba(OH)2 at 600C followed by staining in dilute Giemsa solution, with modifications in alkaline treatment.

Location of nucleolus organizer regions (NORs) was performed by applying the one-step silver nitrate method of Goodpasture and Bloom (1975).

Results

Karyotypes of and

The karyotypes of (Fig. 1) and (Fig. 2) revealed a diploid chromosomal complement consisting of 2n=36, FN=58.

Figure 1.

Giemsa stained male karyotype and female metaphase complement of . Bar = 10 µm.

Figure 2.

Giemsa stained male karyotype and female metaphase complement of . Bar = 10 µm.

The somatic metaphase chromosomes in the karyotype could be divided into four groups, A, B, C and D, based on the decreasing order of total length and position of centromere of each chromosome. The first group (A) includes two pairs (1–2) of large metacentrics and one pair (3) of submetacentrics, while the B group consisted of three pairs (4–6) of medium sized metacentrics in which the pair four was slightly longer than other two pairs. The third group (C) included 5 pairs (7–11) of smaller submetacentrics, all in decreasing order of their total length. The fourth group (D) included mostly acrocentric (12–18) pairs.

Similar karyotypes were obtained for the species (Fig. 3) and (Fig. 4).

Figure 3.

Giemsa stained male karyotype and female metaphase complement of . Bar = 10 µm.

Figure 4.

Giemsa stained male karyotype and female metaphase complement of . Bar = 10 µm.

No detectable sex chromosome pair was observed in either sex in the metaphase chromosomal complement and karyotypes of , , and .

Meiosis

The meiotic chromosomes prepared from male individuals of revealed a good number of pachytene (Fig. 5), diplotene (Fig. 6), diakinetic and second meiotic metaphase configurations.

Figure 5.

Pachytene karyotype and complement of . Bar = 10 µm.

Figure 6.

Diplotene complement of . Bar = 10 µm.

Pachytene chromosome karyotype constructed as per the somatic metaphase chromosome karyotype revealed eighteen pachytene bivalents corresponding the eighteen pairs of somatic chromosomes.

PageBreakPageBreakPageBreakThe diplotene complement allowed the counting of eighteen individually identifiable bivalents. In each diplotene complement, the longer ones carried 4-6 chiasmata, whereas the smaller acrocentrics consisting of at least one chiasma.

Similar results were obtained for the other three species, , and .

C – Staining

The karyotype is characterized by discernible but faintly stained centromeric C-bands in the metacentric and submetacentric chromosomes, while the acrocentrics have very prominent C-bands at the centromeric region cumulatively highlighting both the centromeric regions and the proximal portions of each short arms of each chromosome (Fig. 7). In comparison with the C-staining characteristics of , typical C-bands were observed in the other three species karyotypes.

Figure 7.

C-stained male karyotype and female metaphase complement of . Bar = 10 µm.

Ag-NOR – Staining

Silver nitrate staining showed that in , Nucleolus Organizer Regions (NORs) are confined to chrormosomal pair 9 in the complement but were not consistently demonstrated in each and every cell. Whereas, interphase nuclei demonstrated 1 to 2 (or sometimes 3) numbers of silver nitrate (2–3) aggregates (Fig. 8). This situation is perhaps an indication of limited proportionality of rDNA sites that could not be elicited cytologically and those of transcriptionally silent NORs did not form any discrete Ag-NORs sites at metaphase chromosomes.

Figure 8.

Silver-stained interphase nucleus and mitotic metaphase complement of . Bar = 10 µm.

Similar kind of results could be drawn for the other three species, , and .

Discussion

Emphasizing on systematics of those Indian endemic uraeotyphlids, the morphological attributes as elicited by Gower and Wilkinson (2007) and Gower et al. (2008) are in congruence with the results of cytogenetic data that were available for determining their primacy and prevalence of bimodal karyotypic characteristics.

In the present study, the karyotype carrying a diploid number of 36 (2n=36) chromosomes was found consistently identical in each of the four species belonging to species complex. The cytogenetic data converged on chromosome morphology indicate that the genus is relatively well conserved with most chromosomal pairs classified as meta- and submetacentrics in size and shape. This observation, especially of all the four oxyurus type karyotypes having a homologous situation reveals a closer phylogenetic relationship. This, in turn, supports consideration for a monophyletic origin.

The same situation cannot be considered as applying to those species belonging to group. Until now, none of these species karyotypes were known except a publication citing a variable karyotype for the species belonging to the genus, , . Venu et al. (2011) have described the karyotype of bearing a different basic chromosomal number (2n=42) and morphology. A major attribute of karyotype is that it is similar to any of the known karyotypes of the species belonging to and of the family Ichthyophiidae (Venkatachalaiah and Venu 2002, Matsui et al. 2006, Venu 2008, Venu et al. 2011).

This karyolgical description lends support to Gower and Wilkinson’s (2007) contention that it is possible to draw conclusions as to the karyological affinities between the two taxa through a comparison of the primitive uraeotyphlid karyotype with that of ichthyophiid karyotypes. The karyogrammic and morphometric data on the karyotype of and that of representative karyotype of and (Nussbaum 1991; Venkatachalaiah and Venu 2002; Matsui et al. 2006; Venu 2008) lend support to the concept of closer phylogenetic affinity between the two taxa within the family (Wilkinson et al. 2011, Venu et al. 2011).

The four species karyotypes (2n=36) may be considered as derived ones from that of karyotype (2n=42), which serves as a modal karyotype for the group species which could be considered a basal one among uraeotyphlids. Besides, based on the pronounced chromosomal homogeneity among the said species groups’ karyotypic specificities, this may be considered as of cytogenetic importance while placing emphasis on species differentiation within the genus. Uraeotyphlid chromosome complements belonging to family Ichthyophiidae seem to present bimodal diploid numbers: 2n=42 chromosomes in the basal type group and 2n=36 chromosomes in the case of derived species belonging to species complex.

Presently, chromosomal data on ichthyophiid taxa indicate that they are all well-conserved among the species whose karyotypes are known, bearing identical chromosomal set in each case (Venkatachalaiah and Venu 2002; Venu 2008). The characteristics of the four karyotypes and of karyotype are unique in possessing most chromosomal pairs as conserved. The centromeric position of the lowerset of chromosomes in the karyotype makes all the more significant for consideration of their karyotypic specificities.

During the course of drawing karyological relationships prevailing between the two taxa (for e.g., ichthyophiids and uraeotyphlids) it is possible to infer that most submeta and metacentrics are conserved to a maximum extent and only acrocentrics mayhave paved the way for chromosome speciation events.

There are instances that exhibit very little variation in their karyological features. Marked karyological homogeneity seems prevalent in many taxa of cyprinid fishes PageBreak(Caputo et al. 2003, Rabova et al. 2003, Mesquita et al. 2008) and in some salamanders (Sessions 2008) and anuran amphibians (Kasahara et al. 2003, Aguiar et al. 2004, Rodrigues et al. 2011) and evidently in cryptodire reptilians (Olmo 2005, Castiglia et al. 2009). Karyological uniformity as demonstrated by some of these studies (including the present report) seems to point towards eliciting closer affiliation in their respective lineages. Moreover, this kind of situation in the context of phylogenetic assessment reflects upon their initial stages of evolutionary consequences.

Any attempt on comparison of karyotypes from the present study to that of other representative karyotypes for type (although only one species karyotype is available) makes clear the occurrence of a succession of chromosomal rearrangements, mainly through pericentric inversion and / or fusion. This appears necessary in order to create the karyotype found in described karyotype from those of ancestral ones. This sequence of events could account for the appearance of reduction in basic chromosome numbers from 2n=42 chromosome to 2n=36 chromosomes (Venkatachalaiah and Venu 2002).

The C-banding profile and NOR localization seems to be a homologous feature in oxyurus uraeotyphlids. C-banding pattern was found identical in the four species of oxyurus group within the genus. The variation illustrated by the two species group (viz., oxyurus and malabaricus) in which there is an enormous interspecific variation was evident in the distribution and amount of heterochromatin (Venu 2008; Venu et al. 2011). The NOR location is a conserved characteristic within the oxyurus group species. This view is in accordance with that of Schmid et al. (1990) opinion that in closely related species, the NORs are always almost located in the same chromosome regions within the complement.

Based on certain molecular analysis, it is possible to ascribe that the basal group is closely aligned in its affinity to primitive ichthyophid lineages. However, in order to expend linealogical connections between these two broader groups, Gower et al. (2002) and Frost et al. (2006) have proposed a possibility of an intermediate taxon.

Phylogeny of the Indian endemic genus is still poorly known. But a combined approach based on morphology, biochemistry, molecular biology and cytogenetics might help to resolve a revised classification of Ichthyophiidae and thus to understand better of their phylogenetic relationships with other caecilians. Towards that effect, San Mauro et al. (2004) have attempted to provide intrafamily relationships of extant caecilians mainly based on mitochondrial genomes since they found them offering a more reliable data set for comparison. Subsequently, Zhang and Wake (2009) have extended this type of molecular analyses to include multiple gene data sets and more number of taxa. Their work on the key species uncovered findings favoring sisterly relationships between the genera i.e., and and thereby supporting the view that they are to a certain extent, paraphyletic in nature. The latter study have offered support to the proposition of Gower and Wilkinson (2007) that the genus may be divided into the plesiomorphic group and apomorphic PageBreakgroup. The results of present study strengthen support to the derived status of group species.

Maddin et al. (2012) have attempted to explore the possibility of utilizing morphology based upon microcomputed tomographic pictures of brain case and stape of several caecilian taxa, as an additional criterion to other morphological features that ascribed during the course of their phylogenetic assessment. However, this study seems to point towards reaching congruence thereby limiting its extent to generic level classification but not at species specificity.

While exploring probable phylogenetic relationships and rapport, it also seems possible to infer that karyological data fall in line with those of recently assimilated molecular analyses (San Mauro et al. 2004, Zhang and Wake 2009).

In conclusion, the cytogenetic study based on conventional Giemsa staining including C- and NOR bandings, upon four oxyurus group species of taxa, indicate that they are more similar in their karyotypic profile (if not identical) which might form a monophyletic group. In the light of extensive chromosomal homology incurred, that does not preclude minor karyotypic differences necessitating in the use of other banding techniques for the improvement of karyological characterization.