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  • Research article
  • Open Access

Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae): a case of chromosomal speciation?

  • 1,
  • 2,
  • 3,
  • 1,
  • 4,
  • 4,
  • 4,
  • 5,
  • 6,
  • 6 and
  • 4, 5Email author
BMC Evolutionary Biology201919:73

https://doi.org/10.1186/s12862-019-1393-4

  • Received: 2 May 2018
  • Accepted: 15 February 2019
  • Published:

Abstract

Background

Synbranchidae or swamp eels are fishes belonging to the order Synbranchiformes that occur in both freshwater and occasionally in brackish. They are worldwide distributed in tropical and subtropical rivers of four different continents. A large degree of chromosomal variation has been found in this family, mainly through the use of conventional cytogenetic investigations. Inside this group, a still almost unexplored species under the cytogenetic point of view is the Asian swamp eel Monopterus albus, a widely distributed species throughout Asia. Here, we tested the hypothesis of chromosomal speciation, where a case of sympatric speciation may occur as the primary consequence of chromosomal rearrangements. We performed a comparative chromosomal analysis of M. albus from 22 different localities in Thailand, using distinct staining methods (C-banding, Ag-NO3, and Chromomycin A3), and FISH with repetitive DNA probes (5S rDNA, 18S rDNA, Rex1 element and microsatellite repeats).

Results

This approach evidenced two contrasting karyotypes (named karyomorphs A and B) that varied concerning their 2n and repetitive DNAs distribution, where chromosomal fusions and pericentric inversions were involved in such differentiation. While the karyomorph A has 2n = 24 chromosomes, the karyomorph B has only 2n = 18, both with NF = 24. In addition, karyomorph A contains only acrocentric chromosomes, while karyomorph B contains three unique metacentric pairs. These features highlight that M. albus has already gone through a significant genomic divergence, and may include at least two cryptic species.

Conclusions

This marked chromosomal differentiation, likely linked to the lifestyle of these fishes, point to the occurrence of a chromosomal speciation scenario, in which fusions and inversions had a prominent role. This highlights the biodiversity of M. albus and justifies its taxonomic revision, since this nominal species may constitute a species complex.

Keywords

  • Tropical freshwater fish
  • Reproductive isolation
  • Repetitive DNAs
  • Centric fusion
  • Species complex

Background

Freshwater habitats make up less than 0.01% of available aquatic habitat but contain almost half of all 34,000 valid fish species, making freshwater fishes an excellent model for studying speciation events [1, 2]. However, although freshwater environments are largely fragmented and isolated, which means allopatric speciation events are more frequently found, several known cases of sympatric speciation have already been identified [3, 4].

In recent years, cytogenetic studies have made important contributions toward a better understanding of recent speciation events, since chromosomal rearrangements can act as genetic barriers to gene flow, thus facilitating reproductive isolation [58]. The chromosomal rearrangements promote the reorganization of the genetic structure, and the evolutionary impact and the consequences at the speciation level can vary according to the rearrangement type, that is, inversion, fusion, fission or translocation [712]. Such chromosomal rearrangements can facilitate adaptation to heterogeneous environments by limiting genomic recombination [10].

Molecular cytogenetic studies using fluorescence in situ hybridization (FISH) to map repetitive DNA sequences have provided important contributions to the characterization of chromosomal rearrangements and the evolution of distinct fish groups (reviewed in [13]). Repetitive DNAs, widely distributed in the eukaryotic genomes, are generally divided into two classes, one comprising tandem sequences (satellite DNAs, minisatellites and microsatellites), and the other comprising interspersed sequences, such as transposons and retrotransposons [14].

Synbranchidae or swamp eels are fishes belonging to the order Synbranchiformes; they occur in freshwater and occasionally in brackish water. They are distributed worldwide in tropical and subtropical Asia, the Indo-Australian Archipelago, West Africa (Liberia), Mexico and Central and South America (Fig. 1) [1]. This family comprises four genera: Macrotrema, Monopterus, Ophisternon and Synbranchus [15]. While Macrotrema, Monopterus and Ophisternon are found in the Old World, Ophisternon and Synbranchus occur in the New World. Thus, the genus Ophisternon is currently found in both the Old and New Worlds. Macrotrema is restricted to Asia and Synbranchus to the Neotropical region. At present, 23 valid species are recognized: Macrotrema (1); Monopterus (13), Ophisternon (6) and Synbranchus (3) [16]. Macrotrema caligans (Cantor, 1849), Monopterus albus (Zuiew, 1793) and Ophisternon bengalense (McClelland, 1844) are the three species recorded in Thailand [1].
Fig. 1
Fig. 1

World map highlighting the actual distribution of Synbranchidae fish family. This map was created using the following softwares: QGis 3.4.3 and Inkscape 0.92

Monopterus albus, commonly known as the Asian swamp eel or rice field eel, is widely distributed throughout Asia, from northern India and Burma to China, Asiatic Russia, Japan and the Indo-Malayan Archipelago. However, cytogenetic studies conducted on this species are scarce. There are only three karyotype reports for M. albus from Thailand and China, showing 24 chromosomes and the fundamental number NF = 24 [1719]. However, Donsakul and Magtoon [17] have also reported that M. albus from the central part of Thailand differs from the other populations, as it has 2n = 18 and NF = 24 (Table 1). Similarly, the Venezuelan Ophisternon aenigmaticum also highlights a karyotype diversification, including 2n = 45 and NF = 51 and 2n = 46 and NF = 52 [20], as well as the Synbranchus marmoratus species from Brazil and Argentina, which presents 2n ranging from 42 to 46 [2125]. The Synbranchidae family has high karyotype diversity among its species, with 2n ranging from 18 to 46, mainly due to extensive chromosomal rearrangements (fusions/fissions and inversions) (Table 1).
Table 1

Comparative cytogenetic data of Symbranchidae species

Species

Site sampling

2n

NF

Karyotype

Reference

Monopterus albus

Central of Thailand

18

24

6 m + 12a

[6]

Northeast of Thailand

24

24

24a

[6]

Central of Thailand

24

24

24a

[8]

China

24

24

24a

[7]

M. cuchia

India

42

46

4sm + 38a

[33]

Ophisternon aenigmaticum

La Vega, Garcia, Venezuela

45

51

6 m + 39a

[9]

EL Valle, Garcia, Venezuela

46

52

6 m + 40a

 

O. bangalense

Southeast coast of India

46

 

42 m + 4sm

[34]

Synbranchus lampreia

Lago Catalão

44

50

6 m + 2st + 36a

[19]

S. madeirae

Lago Catalão

46

52

6 m + 2st + 38a

 

S. marmoratus

Bataguassu – MS, Igaraçu do Tietê – SP, Pirassununga – SP, Icém – SP, Cáceres – MT, BR

42

46

4 m + 12st + 26a

[14]

Synbranchus marmoratus

Coxim, MS, BR

42

46

4 m,sm + 38st,a

[10]

São Simão, GO, BR

42

46

4 m,sm + 38st,a

Nova Granada, SP, BR

42

46

4 m,sm + 38st,a

Botucatu, SP, BR

42

46

4 m,sm + 38st,a

[11]

Birigui, SP, BR

42

46

4 m,sm + 38st,a

ParaguaçuPaulista, SP, BR

42

46

4 m,sm + 38st,a

Pirassununga, SP, BR

42

48

6 m,sm + 36st,a

RibeirãoPreto, SP, BR

42

48

6 m,sm + 36st,a

Bataguaçu, MS, BR

42

48

6 m,sm + 36st,a

Guaíra – PR, BR

42

48

6 m + 10st + 26a

[14]

Londrina, PR, BR

42

52

4 m + 2sm + 8st + 28a

[13]

Guairá, PR, BR

42

52

4 m + 2sm + 8st + 28a

Miranda, MS, BR

42

52

4 m + 2sm + 8st + 28a

Pereiras, SP, BR

42

52

4 m + 6sm + 8st + 24a

PresidenteEpitácio, SP, BR

42

52

4 m + 6sm + 8st + 24a

Rio Claro, SP, BR

44

48

4 m,sm + 40st,a

[10]

Pentecostes, CE, BR

44

48

4 m,sm + 40st,a

 

Botucatu, SP, BR

44

48

4 m,sm + 40st,a

[11]

Birigui, SP, BR

44

48

4 m,sm + 40st,a

Bataguaçu, MS, BR

44

48

4 m,sm + 40st,a

Ituzaingó, Corrientes, AR

44

48

4 m,sm + 40st,a

[12]

Reconquista, Santa Fé, AR

44

48

4 m,sm + 40st,a

Garabato, Santa Fé, AR

44

48

4 m,sm + 40st,a

Cerrito – RS, Rio Branco – AC, BR

44

48

4 m + 10st + 30a

[14]

Pirassununga, SP, BR

44

50

4 m + 2sm + 8st + 30a

[13]

Pirassununga, SP, BR

46

50

4 m,sm + 42st,a

[11]

RibeirãoPreto, SP, BR

46

50

4 m,sm + 42st,a

Bandeirantes, PR, BR

46

52

4 m + 2sm + 8st + 32a

[13]

Igaraçu do Tietê – SP, Pirassununga – SP, BR

46

52

4 m + 10st + 32a

[14]

Pirassununga – SP, Icém – SP, BR

46

52

6 m + 10st + 30a

 

Miranda, MS, BR

46

54

6 m + 2sm + 6st + 32a

[13]

Notes: BR Brazil, AR Argentina, 2n diploid number, NF fundamental number, m metacentric, sm submetacentric, st subtelocentric and a acrocentric chromosomes

This study presents a comparative chromosomal analysis of Monopterus albus from 22 different localities in Thailand (Fig. 2), using distinct staining methods (C-banding, Ag-NO3, and chromomycin A3) as well as FISH with repetitive DNA probes (5S rDNA, 18S rDNA, Rex1 element and microsatellite repeats). We tested the hypothesis of chromosomal speciation, where a case of sympatric speciation may occur as the primary consequence of chromosomal rearrangements. This approach provided an in-depth karyotype characterization of this taxon, evidencing the presence of two contrasting karyotypes occurring in sympatry and the occurrence of likely distinct species in this nominal species. This marked chromosomal differentiation, likely linked to the lifestyle of these fishes and their population fragmentation, protects from gene flow and therefore promotes speciation.
Fig. 2
Fig. 2

Map of Thailand highlighting the sample sites and specimens of two karyomorphs of the Asian swamp eel Monopterus albus. Red squares = karyomorph A (2n = 24) and blue circles = karyomorph B (2n = 18). Sympatry of both karyomorphs is indicated by circles. This map was created using the following software: Adobe Photoshop 7.0

Results

Karyotypes

M. albus from the populations analyzed presented two distinct karyotype forms, one with 2n = 24 (24a) and NF = 24 (karyomorph A) and the other with 2n = 18 (6 m + 12a) and NF = 24 (karyomorph B) (Fig. 3a). The first karyomorph was present in 21 localities (183 specimens), while the latter was found in five (17 specimens). Sympatry of both karyomorphs was observed in four localities, namely Nakhon Nayok, Kanchanaburi (Sri Yok), Chon Buri and Sa Kaeo Provinces (Table 2 and Fig. 2). No heterozygous karyotype forms were observed in the four localities of sympatry.
Fig. 3
Fig. 3

Karyotypes of the two Asian swamp eel Monopterus albus karyomorphs analyzed by (a) conventional staining and C-banding and (b) fluorescence in situ hybridization (FISH) with 5S (green) and 18S (red) rDNA probes. Inserted boxes indicate NOR-bearing chromosomes and CMA3 positive chromosomes. In (c) idiograms highlight the distribution of 18S rDNA (red) and 5S rDNA (green) in both karyomorphs. In the middle, the panel label highlights the main rearrangements related to karyotype differentiations, where centric fusions have played a major role. Scale bar = 5 μm

Table 2

Chromosomal data for Monopterus albus populations from different Thailand regions

Region

Population/Province

Number of specimen

2n

NF

Karyotype

NORs

Central

Nakhon Nayok

5

18

24

6 m + 12a

2 (near telomere)

 

7

24

24

24a

2 (near cetromere)

Nakhon Pathom

15

24

24

24a

2 (near cetromere)

Bangkok

8

24

24

24a

2 (near cetromere)

Sing Buri

10

24

24

24a

2 (near cetromere)

South

Nakhon Si Thammarat

8

18

24

6 m + 12a

2 (near telomere)

Chumphon

8

24

24

24a

2 (near cetromere)

West

Kanchanaburi

6

18

24

6 m + 12a

2 (near telomere)

(Sri Yok)

8

24

24

24a

2 (near cetromere)

Kanchanaburi (Sri Sawat)

11

24

24

24a

2 (near cetromere)

East

Chon Buri

6

18

24

6 m + 12a

2 (near telomere)

10

24

24

24a

2 (near cetromere)

Sa Kaeo (including

9

18

24

6 m + 12a

2 (near telomere)

Campodia)

6

24

24

24a

2 (near cetromere)

Chanthaburi

15

24

24

24a

2 (near cetromere)

PrachinBuri

12

24

24

24a

2 (near cetromere)

North

Tak

8

24

24

24a

2 (near cetromere)

Phayao

10

24

24

24a

2 (near cetromere)

Sukhothai

10

24

24

24a

2 (near cetromere)

Northeast

KhonKaen

12

24

24

24a

2 (near cetromere)

Loei

8

24

24

24a

2 (near cetromere)

Roi Et

8

24

24

24a

2 (near cetromere)

Kalasin

5

24

24

24a

2 (near cetromere)

Buri Ram

6

24

24

24a

2 (near cetromere)

UdonThani

8

24

24

24a

2 (near cetromere)

Mahasarakham

4

24

24

24a

2 (near cetromere)

Notes: 2n diploid number, NF fundamental number, m metacentric and a acrocentric chromosomes

C-banding, ag-NORs and Chromomycin A3 staining

C-positive heterochromatic bands were observed in the centromeric/pericentromeric region of all chromosomes as well as in the telomeric region of several pairs in both karyomorphs. Interstitial heterochromatic blocks were also found in chromosome pair no. 4 in both karyomorphs (Fig. 3a). Ag-NORs sites were present in the centromeric region of pair no. 7 and on the telomeric region of pair no. 3 in karyomorphs A and B, respectively. These Ag-NORs were the only observed GC-rich regions in the karyotype (Fig. 3a, boxed).

Chromosome mapping of 5S and 18S rDNAs

5S rDNA sequences were found in the pericentromeric region of the q arms of chromosome pair no. 7 in karyomorph A and in the pericentromeric region of the p arms of chromosome pair no. 3 in karyomorph B (Fig. 3b). Concerning the 18S rDNA sequences, chromosome pair no. 7 of karyomorph A also displayed sites in the pericentromeric region of the q arms, while in karyomorph B, in addition to the signals in the pericentromeric region, chromosomal pair no. 3 also showed telomeric markings (Fig. 3b). Therefore, the 5S and 18S rDNAs are located together in one chromosome pair in both karyomorphs.

Microsatellites and Rex1 distribution

The (GC)15, (CAA)10, (CAC)10, (CAG)10, (CAT)10, (CGG)10, (GAA)10 and (GAG)10 repeats displayed scattered hybridization signals throughout the genome of both karyomorphs, some showing more concentrated signals. However, while the (CA)15 and (TA)15 sequences also show a scattered distribution in karyomorph B, they clearly accumulate at the centromeric region of several chromosomes in karyomorph A. In turn, the (GA)15 and the retroelement Rex1 sequences present a strong, dispersed distribution without preferential accumulation in any chromosome pairs of either karyomorph (Figs. 4 and 5).
Fig. 4
Fig. 4

Metaphase plates of Monopterus albus karyomorph A mapped with di- and trinucleotide microsatellites and Rex1 as probes. Scale bar = 5 μm

Fig. 5
Fig. 5

Metaphase plates Monopterus albus karyomorph B mapped with di- and trinucleotide microsatellites and Rex1 as probes. Scale bar =5 μm

Discussion

The occurrence of distinct M. albus karyomorphs living in sympatry with the absence of natural hybrids, as found in the present study in Nakhon Nayok, Kanchanaburi (Sri Yok), Chon Buri and Sa Kaeo Provinces, reinforces the hypothesis that these karyomorphs represent two reproductively isolated biological units. Although easily distinguishable through cytogenetic analysis, specimens from both karyomorphs have the same morphology, making difficult the identification of such probable new species.

The integration of both conventional and molecular cytogenetic approaches allowed the proposal of some chromosomal rearrangements probably related to the differentiation of both M. albus karyomorphs, where centric fusions appear as the main evolutionary sources shaping such a process (Fig. 3c). The different karyotype composition among individuals allowed us to identify two distinct karyomorphs, named A and B, which presented 2n of 24 and 18 chromosomes, respectively, both with NF = 24. The chromosomal divergence as well as the relation between the karyomorphs is clearly evidenced by their same NF and different karyotype formulas. This indicates that karyomorph B originated from karyomorph A (with only acrocentric chromosomes), where centric fusions were the most probable mechanism behind the presence of six metacentric chromosomes in karyomorph B (Fig. 3c). However, another scenario can also not be ruled out, in which fission-type rearrangements would have originated the additional 12 acrocentric chromosomes in karyomorph A. Once the majority of chromosomal rearrangements involve heterochromatic regions, especially in fish species [26, 27], this explains the centromeric rearrangements in M. albus. The co-localization of CMA3 positive heterochromatin with the NOR loci also occurs in other synbranchids [25, 28], probably because of local changes in base composition (increase in GC content) due to the so-called GC-biased gene conversion that involves rDNA in many vertebrates, including ray-finned fishes [29].

Although the 18S and 5S sites are located in an acrocentric pair in karyomorph A and in a metacentric pair in karyomorph B, it is possible to infer that both pairs are related in both karyomorphs. As karyomorph B contains additional 18S rDNA signals in the telomeric region in pair no. 3, it is likely that a pericentric inversion has divided the pericentromeric 18S rDNA loci into two parts and has transposed one of them near the telomere. Centric fusions would be the most suitable rearrangements to illustrate this scenario.

The differential distribution of the microsatellite motifs (CA)15 and (TA)15 between the two karyomorphs reinforces the interpretation that they represent, in fact, different species. A genome-wide analysis found that microsatellites have a repeat- and chromosome-biased distribution in M. albus from China, mainly located in noncoding regions (98,602, 99%) [30]. Differences both in the abundance and in the chromosomal location of several microsatellite motifs have been reported among closely related fish species also involved in recent speciation events [31, 32]. Similar to microsatellites, the Rex1 sequences are also resolutive markers for comparative genomic studies, as was already shown for several Asian fish species [19, 30, 31]. In the present study, the interspersed distribution of the retroelement Rex1 contrasts with that reported by [19].

Inter- and/or intrapopulation diversity has also been found in the karyotypes of other Synbranchidae species. For example, Ophisternon aenigmaticum and Synbranchus marmoratus possess high karyotype variability, with several karyomorphs described among their populations; they are also considered species complexes, where independent and bidirectional rearrangements, such as fusion and fission events, were responsible for the distinct 2n and karyotypic characteristics observed (Table 1). Biological, physiological and/or reproductive characteristics of Synbranchidae fishes may facilitate the intra- and interspecific karyotype variability observed among species and populations, especially in Monopterus and Synbranchus. These species tolerate a wide range of water oxygen levels, being able to obtain up to 25% of air oxygen by the cutaneous surface, allowing them to survive up to nine months in a drying burrow [33]. They also form small populations, and although they prefer freshwater habitats, these fishes tolerate brackish and saline conditions [1]. On the other hand, as many individuals can be isolated in small lakes during dry years, the capacity of sex reversal observed in synbranchids could contribute to the viability of such populations, increasing the probability of the fixation of genetic differences and speciation processes [25, 28].

Conclusions

In summary, the present scenario points to the occurrence of a chromosomal speciation scenario, in which fusions and inversions had a prominent role in the diversification of two distinct karyomorphs that differ with respect to diploid number, chromosome features and repetitive DNA distributions. However, this does not necessarily mean that a sympatric speciation is the only viable alternative, since such karyomorphs could have been established in allopatry, where a secondary join between them originated the present distribution. The karyotypic features highlight the biodiversity of M. albus and justify a taxonomic revision, since this nominal species may actually constitute a species complex.

Methods

Individuals examined

Two hundred specimens of M. albus were collected in 22 localities from distinct Thai regions (Fig. 2 and Table 2). The specimens were caught using traps, and after capture, the animals were placed in sealed plastic bags containing oxygen and were transported to the research station. The specimens were deposited in the fish collection of the Cytogenetic Laboratory, Department of Biology, Faculty of Science, Khon Kaen University. All the experiments followed ethical protocols, and anesthesia with clove oil was used prior to sacrificing the animals to minimize suffering. The fishes were then immersed in an ice-slurry to achieve death by hypothermia. The process was approved by the Animal Ethics Committee of Khon Kaen University based on the Ethics of Animal Experimentation of the National Research Council of Thailand AEKKU23/2558.

Chromosome preparation and C-banding, ag- and CMA3 staining

Mitotic chromosomes were obtained from the cell suspensions of the anterior kidney, using the conventional air-drying method [34]. Conventional staining was done using 5% Giemsa solution in phosphate buffer, pH 6.8, for 10 min. Chromosomes were analyzed after silver nitrate staining [35] in order to visualize the nucleolar organizing regions (Ag-NORs), and C-banding was also employed to detect the C-positive heterochromatin [36]. GC-specific fluorochrome chromomycin A3 (CMA3) was carried out following the method of Amemiya and Gold [37] to detect CG-rich regions on the chromosomes.

Preparation of FISH probes derived from repetitive sequences

Two tandemly arrayed rDNA sequences isolated from the genome of an Erythrinidae fish species, Hoplias malabaricus, were used as probes, as described in details in [38, 39]. The 5S and 18S rDNA probes were labeled with Spectrum Green dUTP and Spectrum Orange dUTP, respectively, using nick translation according to the manufacturer’s recommendations (Roche, Mannheim, Germany).

The microsatellites (CA)15, (GA)15,(GC)15, (TA)15, (CAA)10, (CAC)10, (CAG)10, (CAT)10, (CGG)10, (GAA)10 and (GAG)10 were synthesized according to Kubat et al. [40]. During synthesis by Sigma (St. Louis, MO, USA), these sequences were directly labeled with Cy3 at the 5’terminus. The retrotransposable element Rex1 sequence was prepared by PCR, using primers described in Volff et al. [41]. The Rex1 probe was directly labeled with Spectrum Orange dUTP by nick translation, according to the manufacturer’s recommendations (Roche, Mannheim, Germany).

Detection of repetitive DNA sequences by FISH

All FISH experiments with repetitive DNA probes were essentially carried out according to the protocol described in Yano et al. [42]. The first post-hybridization wash was performed with 2x SSC for 5 min at 42 °C, and a final wash was performed at room temperature in 1x SSC for 5 min. Finally, the slides were counterstained with DAPI and mounted in an antifade solution (Vectashield from Vector Laboratories).

Microscopic analysis and image processing

At least 30 metaphase spreads per individual were analyzed to confirm the 2n, karyotype structure and FISH results. Images were captured using an Olympus BX50 microscope (Olympus Corporation, Ishikawa, Japan) with Cool SNAP, and the images were processed using Image Pro Plus 4.1 software (Media Cybernetics, Silver Spring, MD, USA). Chromosomes were classified as acrocentric (a) or metacentric (m), according to their arm ratios [43].

Abbreviations

2n: 

Diploid chromosome number

a: 

Acrocentric chromosome

CMA3

Chromomycin A3

DAPI: 

4′,6-diamidino-2-phenylindole

dUTP: 

2′-Deoxyuridine-5′-Triphosphate

FISH: 

Fluorescence in situ hybridization

FN: 

Fundamental number

m: 

Metacentric chromosome

NOR: 

Nucleolar organizer region

NTS: 

Non-transcribed spacer

PCR: 

Polymerase chain reaction

rDNA: 

ribosomal DNA

sm: 

Submetacentric chromosome

st: 

Subtelocentric chromosome

Declarations

Acknowledgements

Not applicable.

Funding

This study had financial support by the Young Researcher Development Project of Khon Kaen University (Year 2015); Toxic Substances in Livestock; Aquatic Animals Research Group; Post-Doctoral Training Program from Research Affairs and Graduate School (Grant no 59255), Khon Kaen University, Thailand; by the Conselho Nacional de Desenvolvimento Científico e Tecnológico- CNPq (Proc. nos 304992/2015–1 and 401962/2016–4) and CAPES/Alexander von Humboldt (Proc. No. 88881.136128/2017–01). This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001. These funding sources had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

Availability of data and materials

The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.

Authors’ contributions

WS, CFY, EAO and MBC carried out the molecular cytogenetic analysis and drafted the manuscript. KP, KS, PS,TL and SP helped in analysis and drafted the manuscript. LACB, TL, MBC and AT coordinated the study, drafted and revised the manuscript. All authors read and approved the final version of the manuscript.

Ethics approval

All the experiments followed ethical protocols and anesthesia with clove oil was used prior to sacrificing the animals to minimize suffering. The process was approved by the Animal Ethics Committee of Khon Kaen University based on the Ethic of Animal Experimentation of National Research Council of Thailand AEKKU23/2558.

Consent for publication

Not applicable

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
Faculty of Applied Science and Engineering, Khon Kaen University, Nong Khai Campus, Muang, Nong Khai, 34000, Thailand
(2)
Department of Fundamental Science, Faculty of Science and Technology, Surindra Rajabhat University, Muang, Surin, 32000, Thailand
(3)
School of Agriculture and Natural Resources, University of Phayao, Tumbol Maeka, Muang, Phayao, 56000, Thailand
(4)
Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, São Paulo, Brazil
(5)
Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Kollegiengasse 10, D-07743 Jena, Germany
(6)
Toxic Substances in Livestock and Aquatic Animals Research Group, Khon Kaen University, Muang, Khon Kaen, 40002, Thailand

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