Morphological Characteristics and Genetic Diversity of Fish Moolgarda cunnesius (Valenciennes, 1836) in Tam Giang Lagoon, Vietnam
Morphological Characteristics and Genetic Diversity of Fish
Moolgarda cunnesius (Valenciennes, 1836) in Tam Giang Lagoon, Vietnam
Ty Nguyen, Giang Thi Huong Phung, Lan Le Thuy Hoang and Giang Van Tran*
Department of Biology, Hue University of Education, Hue University, 49000, Vietnam.
Abstract | Moolgarda cunnesius, belongs to the Mugilidae family, is an important fish species in view of its immense contribution to the need of this country in terms of nutrition, economic growth and development. The results of morphometric and genetic analysis of M. cunnesius in this study contributed the documents for identification and the genetic diversity, which are the basis for further research about M. cunnesius in breeding, species conservation and management at the Tam Giang Cau Hai Wetland Reserve. Research results showed that this species distributed in the North has a size ranging from 101.7 to 160.7 mm, with an average of 137 mm, corresponding to a weight of 10.6 - 35.6 g, with an average of 25.2 g, the fish distributed in the South has a size ranging from 112.4 - 172.7 mm with an average of 144 mm, corresponding to a weight of 10.6 - 35.6 g, an average of 28.3 g. CO1 gene DNA barcoding was used to study the genetic diversity of M.cunnesius in two regions of the North and the South of Tam Giang lagoon. Amplified and sequenced 10 samples of CO1 gene of M. cunnesius sample in Tam Giang lagoon were recorded size of 650 bp. The average ratio of four types of nucleotides is A: 23.38%; T: 32.62%; G:18.15%; C: 25.85%. The rate of difference in CO1 sequences of the 2 samples is low compared to previous studies. The similarity coefficient of M. cunnesius in the two areas of Tam Giang lagoon is very high (0.9953).
Novelty Statement | The paper presented detailed morphological features and genetic diversity of Moolgarda cunnesius (Valenciennes, 1836) in Tam Giang Lagoon, Vietnam, which is the first study in this area to serve as a scientific basis for breeding and farming and conservation of this species in the future.
Article History
Received: May 28, 2021
Revised: July 15, 2022
Accepted: August 27, 2022
Published: November 08, 2022
Authors’ Contributions
TN and GTHP collected samples. LLTH, TN and GTHP processed the samples. TN and GVT planned the experiments. GTHP and TN performed experiments.TN and LLTH wrote the manuscript. GVT presented the idea, analyzed data and took the lead in writing the manuscript.
Keywords
Genetic diversity, Longarm mullet, Morphological characteristics, Moolgarda cunnesius, Tam Giang lagoon
Copyright 2022 by the authors. Licensee ResearchersLinks Ltd, England, UK. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Corresponding author: Giang Van Tran
To cite this article: Nguyen, T., Phung, T.H.G, Hoang, L.T.L. and Tran, V.G., 2022. Morphological characteristics and genetic diversity of fish Moolgarda cunnesius (Valenciennes, 1836) in Tam Giang Lagoon, Vietnam. Punjab Univ. J. Zool., 37(2): 113-119. https://dx.doi.org/10.17582/journal.pujz/2022.37.2.113.119
Introduction
Moolgarda cunnesius (Valenciennes, 1836) is the member of family Mugilidae, order Mugiliformes (Thomson, 1984), inhabiting in marine, freshwater and brackish water and distributed in Indo-West Pacific (Froese and Pauly, 2021), which is one of the commercial species in Tam Giang lagoon, Vietnam (Vu, 2009). Recently, (Qwabe and Cyrus, 2020) stated that M. cunnesius inhabited in the Mfolozi-Msunduzi estuary, South Africa, where the substrata with high component of fine sand was preferred. In Vietnam, Truong (1991) reported that the mullet living in Cua Be waters uses mainly floating plants and animals as food sources. Nguyen (2010) when researching on longarm mullet (Mugil kelaartii Gunther, 1861), found that it was caught in O Loan lagoon, Phu Yen province. The total production of longarm muller M. cunnesius exploiting in Thua Thien Hue in 2015 was 120.86 tons, in which, Phu Vang is the district with the largest total exploitation output (47.94 tons) (Dang and Vo, 2017). Nguyen and Nguyen (2012) revealed 18 orders with 73 families including 177 species which were recorded in Tam Giang – Cau Hai lagoon, Vietnam, in which Mugilidae have 5 species including Mugil cephalus (Lin., 1758), Valamugil cunnesius (Val., 1836), Moolgarda pedaraki (Val, 1836), Liza melinoptera (Val, 1836) and Chelon haematocheilus (Temm and Schlegel, 1845). Nevertheless, while studies on M. cunnesius have concentrated on reporting the occurrence of the species and the species composition in Tam Giang lagoon, the data on morphologic characteristic as well as genetic diversity of this species in Tam Giang lagoon is limited. Therefore, the documents of morphological and molecular analyses of M. cunnesius are essential for accurate identification. However, up to now, there have been no studies on the morphology and genetic polymorphism of Moolgarda cunnesius in Tam Giang lagoon, Thua Thien Hue province. According to Hebert et al. (2003a), DNA barcode basing on the use of gene sequences in the mtDNA cytochrome c oxidase 1 (CO1) can apply as the universal bioidentification systems for creatures. The species recognition is carried effectively through COI analysis (Hebert et al., 2003b). Also, using DNA barcodes to identify species is used more and more by the scientists in the studies on the ecological system and evolution species, which is the vital tool to quantify species diversity (Kress, 2015). Aaron et al. (2018) suggested that the integration of both approaches including morphological identification and molecular assessment is an important step to determine accurate identification. Durand and Borsa (2015) presented that their study used CO1 barcoding for specifing species in Mugilidae family and determing molecular detection for 24 species and for 25 cryptic creatures. In present study, the data will provide about morphologic perspectives and genetic diversity of assessment of longarm mullet, which is the scientific basic for future studies as well as for breeding and farming and conservation of this species.
Materials and Methods
Fish material
The speciments of M. cunnesius were collected in two areas north and south of Tam Giang lagoon (water area of Dien Hai commune, Quang Loi commune, Huong Phong commune, Hai Duong commune) with 53 samples from September 2020 to June 2021, in which the area north was 31 samples while the South was 24 samples (Figure 1). The sample collection was repeated in the sampling locations monthly for 10 months (around 5 individuals per month) by directly fishing with locals, or by buying fish samples from fishermen in the area. The pectoral fin samples were cut off and put in eppendorf tubes with 96% alcohol, then they were stored at -86°C for further analysis.
Morphological study
Fish samples were conducted to study as soon as the fish was caught and fixed with 40% formol solution; Photograph and convert to 4% formol solution. Descriptive observations of the external morphological characteristics of fish according to the fish research guidelines of Pravdin (1973), Thomson (1984) and Nguyen (2005). The total of 31 morphologic measurements were used in this study for each specimen including Standard length (SL, mm), Body length, Fork length, Head length, Body height at dorsal fin base 1, Body height at pelvic fin base, Tail stalk length, Tail stalk height, Dorsal fin length 1, Dorsal fin length 2, Pectoral fin length, Pelvic fin length, Tail fin length, Anal fin length, Dorsal fin height 1, Dorsal fin height 2, Pectoral fin height, Pelvic fin height, Tail fin height, Anal fin height, Head length behind eyes, Muzzle length, Length of snout to dorsal fin 1, Muzzle length to dorsal fin 2, Length of snout to ventral fins, Length of snout to anal fin, Head Width, Head Height, Distance between eyes, Eye Diameter, Mouth width.
Five Meristic charaters counted: the number of spines and first dorsal fin rays (D1); the number of rays and spines of second dorsal fin (D2); the number of rays and spines of pectoral fin (P), the number of rays and spines of ventral fin (V); the number of rays and caudal fin spines (C), the number of rays and spines of anal fin (A).
DNA extraction, PCR amplification and decoding
GeneJET Genomic DNA Purification Kit DNA Extraction Kit was applied to extract the total DNA of each pectoral fin following the producer’s procedure. The 650 bp DNA fragment (CO1) was amplified by PCR reaction with the using of universal primers: Fish F1 (5’- TCAACCAACCACAAAGACATTGGCAC-3’) and Fish R1 (5’-TAGACTTCTGGGTGGCCAAAGAATCA-3’) (Ward et al., 2005). The total reaction volume of 50 μl was composed of: 2 μl of total DNA (⁓50ng), 25 μl of GoTaq (2X), 2.5 μl of each primer (10pmol/μl) and 18 μl of Kit free-RNA/DNA water. PCR was carried out in a thermal cycler (ESCO-AERIS-BG096) following the thermal process: (1) DNA denaturation: 94°C/5 min; (2) 35 cycles: (94°C/ 1 minute; 54°C/ 30 seconds; 72°C/ 55 seconds); (3) final 72°C/ 5 min. The amplified product was examined by electrophoresing on a 1% agarose gel; the amplification bands were taken in the gel documentation system. Gel analysis software (UN-SCAN-IT gel version 6.1) was applied to analyze the gel images.
Diversity genetic analysis
BioEdit software v.7.2.5 was conducted to edit and arrange sequence. Search and compare research sequences with similar sequences on Genbank using BLAST program. Building phylogenetic tree by Test Maximum Likelihood method using MEGA version X software with bootstrap value repeated 1000 times for the each sample.
Data analysis
The data were processed by MS Excel v. 365 and SPSS (IBM v. 20) programming. A one-way analysis of variance (ANOVA) was used to compare the mean of the morphological parameters between water areas with the significance level (p<0.05).
Results and Discussion
Morphological characteristics of the M. cunnesius in Tam Giang lagoon
Morphological characteristics
When analyzing 31 indicators, 5 counts of 53 samples of M. cunnesius combined with identification documents, the samples were identified as M. cunnesius (Valenciennes, 1836) with the main morphological features: Head relatively short, the top of the head is flat; The muzzle is slightly broad but short; Eyes round and medium large; The eye fat membrane is especially thick, covering the whole eye except for the pupil, the dorsal fin has 2, the first dorsal fin consists of stiff spines, the beginning of the first dorsal fin is located near the tip of the pectoral fin; the origin of the second dorsal fin is behind the beginning of the anal fin base; Pectoral fin long, beyond first dorsal fin starting point, pectoral fin tip black dotted, pectoral fin base with axillary scale (Figure 2). Research results show that this species in the area north has a size ranging from 78.9 - 126.6 mm, corresponding to a weight of 10.6 - 35.6 g. In particular, the variation in size as well as mass of this species distributed in the area south has a difference, in detail, the size ranges from 90.3 - 138.8 mm, the mass fluctuates in the range of 13.4 – 47.7 g; the number of spines andrays of first dorsal fin D1 = 4.0; the number of spines andrays of second dorsal fin D2 = 1 – 2,7 – 8; the number of spines and rays and of pectoral fin P = 1 – 3, 12 – 15; the number of spinesand rays of ventral fin V = 1, 5 – 6; the number of spines and rays ofcaudal fin C = 0,14 – 17; the number of spines and rays of anal fin A = 1 – 3, 9 – 10.
The head length measured in the study was 25.9% of the SL for the northern fish and 26.1% of the SL for the southern fish. However, when analyzing ANOVA, there was no significant difference with p>0.05. Head width of leaf mullet in 2 regions is 60.2% compared to HL and 59.8% compared to HL, respectively and has no statistical significance (p>0.05); similarly, the measured head height is 79.6% compared to HL and 78 % compared to HL and has no statistical significance (p>0.05) (Table 1).
The results of differences in size, mass and tip length between the two distribution regions are only preliminary data. Within the framework of our study, the difference is due to the first reason that the age of fish in the two regions is different; the second is due to the characteristics of the water environment and different nutritional regimes.
The length of the ventral fins of M. cunnesius was 12 % SL for fish from the northern region and larger than that of southern fish at 9.8% SL. When analyzing ANOVA, this dissimilarity was statistically significant with p<0.05. This showed that the length of the pelvic fins of fish in the North is different from the length of the pelvic fins of fish living in the South. The length of the caudal fin in the northern region with 27 % SL was higher than that in the southern region (25.4% SL) with a statistically significant difference with p<0.05. The length of snout to dorsal fin 2 of M. cunnesius in the northern region was 73% higher than that in the southern region with 72.2% SL and this difference reached statistical significance (p<0.05) (Table 1).
The length-weight relationship (LWR) is the criterion to evaluate the growth and development of M. cunnesius (Figures 3 and 4). The linear equation between standard dimension and body mass in the two areas shows that the relationship is positive (all R > 0.8, linear upward).
Specifically, the area north region has a linear equation y = 1.7027x + 65.605 (R² = 0.8888), the area south has a linear equation y = 1.2171x + 4.5103 (R² = 0.9832). From the above analysis results, it shows that the LWR of most of the analyzed individuals in the two areas are individuals with large length often having large sizes and vice versa. Neves et al. (2020) studied about 5 species in Mugil from the Tropical Southwestern Atlantic that suggested morphological features were extremely preserved because of resemblances in the environment that species inhabited and their biographical features. The integrative taxonomy (including DNA barcoding) plays a vital role in conserving and sustainably using the resources of nature.
The correlation between the standard length and body weight of northern and south fish of Tam Giang Lagoon shows that the Northern fish has a more close relationship. This difference is due to the first reason that the age of fish in the two areas is different; the second is due to the characteristics of the water environment and different nutritional regimes. However, this is just a preliminary data, to get accurate results and confirm the difference, it is necessary to study on a larger number of samples and more repetitions.
Genetic polymorphism of Moolgarda cunnesius in Tam Giang lagoon, Vietnam
Total DNA extraction
The total DNA was extracted with high quality, which is tested on 1% gel electrophoresis, the electrophoresis image gave a fairly clear dark band (Figure 5). Regarding the quality of the total DNA, further studies can be carried out.
Table 1: Morphological measurements (mm) of mullet species M. cunnesius distributed in Tam Giang lagoon, Vietnam. Means sharing a different letter in the same row differ statistically significantly p<0.05.
Targets |
Area north |
Area south |
||
min-max |
M ± SD |
min-max |
M ± SD |
|
Standard length (SL, mm) |
78.9 – 126.6 |
108.4 ± 12a |
90.3 – 138.8 |
114.6 ± 12.8a |
Body length |
101.7 - 160.7 |
137 ± 14.8a |
112.4 – 172.7 |
144 ± 15.7a |
Fork length |
13.2 – 148.4 |
112.2 ± 45a |
106.1 – 161.9 |
134.7 ± 14.7b |
Head length |
20.4 – 27.8 |
25.9 ± 1.3a |
24 – 28.2 |
26.1 ± 1.1a |
Body height at dorsal fin base 1 |
17.1 – 29.3 |
24.9 ± 1.9a |
23 – 27.4 |
24.7 ± 1.3a |
Body height at pelvic fin base |
17.1 – 26.8 |
23.4 ± 1.5a |
21.7 – 26.1 |
23.4 ± 1.2a |
Tail stalk length |
11.6 – 21.1 |
17.4 ± 2a |
15.3 – 20.9 |
17.6 ± 1.3a |
Tail stalk height |
10.8 – 17.9 |
11.7 ± 1.3a |
10.6 – 12.1 |
11.3 ± 0.4a |
Dorsal fin length 1 |
9.1 – 14.1 |
11.4 ± 1.1a |
10 – 12.7 |
11.5 ± 0.7a |
Dorsal fin length 2 |
11.5 - 14 |
12.5 ± 0.5a |
11.4 – 13.8 |
12.5 ± 0.6a |
Pectoral fin length |
6.5 - 30 |
10.8 ± 7.4a |
6.5 – 29 |
7.3 ± 0.7a |
Pelvic fin length |
8 – 18.5 |
12 ± 3.5a |
8.4 – 12.2 |
9.8 ± 0.9b |
Tail fin length |
24.8 – 32.5 |
27 ± 1.6a |
21.9 – 29.4 |
25.4 ± 1.7b |
Anal fin length |
13.7 – 20.8 |
16.5 ± 1.3a |
14.1 – 17.7 |
16.1 ± 0.8a |
Dorsal fin height 1 |
9.3 - 19 |
11.5 ± 1.9a |
9.9 – 13.1 |
11.3 ± 0.9a |
Dorsal fin height 2 |
9 – 19.8 |
12.6 ± 1.7a |
10.4 – 13.7 |
12.3 ± 0.8a |
Pectoral fin height |
21.6 –26.5 |
20.6 ± 6.2a |
19.6 – 24.6 |
22.3 ± 1.3a |
Pelvic fin height |
7.4 – 35.4 |
14.5 ± 4.4a |
13.6 – 16 |
14.5 ± 0.5a |
Tail fin height |
20.8 – 36.1 |
26.4 ± 3.8a |
21.1 – 32.2 |
27.5 ± 3.3a |
Anal fin height |
6.9 – 18.8 |
15.6 ± 1.9a |
14.1 – 17.7 |
15.9 ± 0.9a |
Head length behind eyes |
7.8 – 16.7 |
13.5 ± 1.3a |
10.9 – 15 |
13.5 ± 0.9a |
Muzzle length |
6.5 – 52.7 |
8.8 ± 8.2a |
6.4 – 8.4 |
7.2 ± 0.5a |
Length of snout to dorsal fin 1 |
39.5 – 53.7 |
49.5 ± 2.3a |
46.6 – 52.4 |
49.6 ± 1.3a |
Muzzle length to dorsal fin 2 |
69.5 – 75.4 |
73 ± 1.5a |
70 – 76.1 |
72.2 ± 1.5b |
Length of snout to ventral fins |
35.6 – 41.5 |
38.7 ± 1.3a |
36.4 - 41 |
38.1 ± 1.2a |
Length of snout to anal fin |
66.8 – 74.7 |
69.5 ± 1.7a |
67.3 – 71.2 |
66.1 ± 12.6a |
Head Width |
54 – 84.4 |
60.2 ± 5a |
55.4 – 68.5 |
59.8 ± 2.8a |
Head Height |
59.9 – 114.1 |
79.6 ± 7.9a |
58.7 – 86.7 |
78 ± 5.1a |
Distance between eyes |
39.7 – 65.2 |
45.3 ± 4.6a |
38.9 – 81.2 |
46 ± 7.9a |
Eye diameter |
25.1 – 42.3 |
27.4 ± 3.1a |
23.7 – 26.2 |
37.1 ± 48.1a |
Mouth width |
26.3 – 51.5 |
31.7 ± 4.4a |
27.7 – 35.6 |
32.3 ± 2.1a |
PCR performance product
The results of PCR product analysis on 1% agarose gel showed that specific DNA fragments with size of about 650-750 bp were amplified (Figures 5B and 6).
The results of the analysis of the CO1 gene sequence of Moolgarda cunnesius in Tam Giang lagoon, Vietnam
After sequencing and editing, all sequences were conducted to search and compare with matched sequences on Genbank. As a result, these two samples have a high similarity with M. cunnesius (Valenciennes, 1836).
When conducting genetic diversity analysis, all CO1 mitochondrial DNA gene sequences of the 2 samples were checked by comparing with the corresponding CO1 gene sequences on Genbank. The results show that the samples in this study belong to the species of longarm mullet M. cunnesius with more than 99.5% similarity, which is similar to the results of (Dang et al., 2021, Table 2).
After processing, the CO1 gene fragment is 650 bp in size. The results showed that the average rate of four types of nucleotides in was A: 23.38%; T: 32.62%; G:18.15%; C: 25.85%. This rate is quite similar to the results of studies on 143 bony fish species in Australia (Ward et al., 2005).
Table 2: The similarity of the Mooc_017 gene sequence in the study with the 10 COI sequences of M. cunnesius on the GeneBank.
No. |
Species |
Gene |
Code |
Gene size (bp) |
Query cover (%) |
Proportion (%) of homologous nucleotides |
1 |
Moolgarda cunnesius |
CO1 |
MW336954.1 |
704 |
98% |
99.53% |
2 |
Moolgarda cunnesius |
CO1 |
MF628290.1 |
655 |
95% |
99.84% |
3 |
Moolgarda cunnesius |
CO1 |
JQ045777.1 |
649 |
95% |
99.68% |
4 |
Moolgardacunnesius |
CO1 |
KT231793.1 |
611 |
94% |
99.84% |
5 |
Moolgarda cunnesius |
CO1 |
KX834271.1 |
588 |
90% |
99.83% |
6 |
Moolgarda cunnesius |
CO1 |
EU595339.1 |
652 |
95% |
99.84% |
7 |
Moolgarda cunnesius |
CO1 |
FJ238048.1 |
652 |
95% |
99.68% |
8 |
Moolgarda perusii |
CO1 |
KY315413.1 |
655 |
95% |
99.84% |
9 |
Moolgarda perusii |
CO1 |
LC484868.1 |
655 |
95% |
99.68% |
10 |
Moolgarda perusii |
CO1 |
LC484868.1 |
655 |
95% |
99.68% |
Table 3: Genetic distance of M. cunnesius.
MW336954.1 M. cunnesius |
KY315413.1 M. perusii |
Mooc_018 |
Mooc_017 |
|
MW336954.1_M. cunnesius |
*** |
0.0016 |
0.0016 |
0.0016 |
KY315413.1_M. perusii |
*** |
0.0016 |
0.0016 |
|
Mooc_018 |
*** |
0.0033 |
||
Mooc_017 |
*** |
Mooc_017 and Mooc_018 = Moolgarda cunnesius.
The results of comparing the two samples analyzed with the sequence MW336954.1 (Dang et al., 2021) have differences at 4 positions: 385, 402, 631, 634, showing that the similarity between the studied sample and the sequence MW336954.1 is very high (Figure 7).
Genetic distance of leaf mullet in two waters of Tam Giang lagoon calculated by Kimura 2-parameter ratio is shown in Table 3.
The genetic distance between the two populations of mullet in Tam Giang lagoon is low (0.0033). This result is quite similar to the study of Dang et al. (2021) (0.0057). When building the phylogenetic tree of 2 samples of longarm mullet with 2 CO1 gene of 2 species of the Moolgarda genus (downloaded from Genbank). The results show that all specimen are in the same branch as M. cunnesius with 100% bootstrap value.
Conclusions and Recommendations
The M. cunnesius (Valenciennes, 1836) was distributed in the northern and southern areas of Tam Giang lagoon, Vietnam. This group of fish distributed in the north ranges in size from 101.7 to 160.7 mm, on average reaching 137 mm, corresponding to a weight of 10.6 - 35.6 g, an average of 25.2 g, fish distributed in the south range in size from 112.4 - 172.7 mm average 144 mm corresponding to the weight from 10.6 - 35.6 g, average 28.3 g. Extracting 10 total DNA samples of leaf mullet in the two regions of the North and the South, 10 specimens were amplified and sequenced the CO1 gene. Amplified and sequenced 2 samples of CO1 gene of mullet sample in Tam Giang lagoon with the size of 650. The average ratio of four types of nucleotides is A: 23.38%; T: 32.62%; G: 18.15%; C: 25.85%. The rate of difference in CO1 sequences of the 2 samples is low compared to previous studies. The similarity coefficient of the mullet in the two Tam Giang lagoon waters is very high (0.9953).
Acknowledgments
The authors would like to express the sincere gratitude to the project, Vietnam “Research on building DNA barcodes of some fish species with economic value in Tam Giang lagoon” –No.: B2020-DHH-17 for sponsoring the financial support in work research.
Conflict of interest
The authors have declared no conflict of interest.
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