Encyclopedia
Please note this is a comparison between Version 1 by Eliška Čermáková and Version 3 by Lindsay Dong.
Various methods, differing in their principle and detected target molecules, can be used for fish species identification and adulteration detection. PRecently, parvalbumin detection has been preferred, but this is quite demanding compared to other food allergens because of its high biochemical and immunological variability among fish species and differing thermostability. This in itself sidelines the use of some types of methods, e.g., proteomic ones, and favors DNA-based methods, whose target, DNA, is not destroyed by the processing. Using DNA analysis, for example, a common form of adulteration—replacing the species (a more expensive one with a cheaper one)—can be detected. Additionally, DNA-based methods have the potential to detect the consumer being misled about the fish’s origin, another common type of adulteration. This is even more relevant, since genetically modified (GM) fish can be bought on the world market. Even though GM organisms do not pose a threat to public health and their quality is no different, consumers should be informed about the content of GM products, and because the public can be skeptical about GM products, sellers may want to hide this information and deliberately deceive the consumer.
- DNA-based methods
- fish
- food fraud
1. Introduction
Food adulteration, the act of misleading customers for financial gain, is currently one of the most discussed topics in the field of food analysis. It is a substantial concern that poses significant risks to public health and reduces food quality and nutrition value [1]. Fish and fish products are among the most commonly adulterated foods, which is driven by their increasing consumption worldwide, and fish population decline due to overfishing, along with the subsequent commercial consequences. Additionally, fish are among the most easily adulterated foods because of the morphological changes that occur during processing, which make visual identification impossible [2][3][4][5][2,3,4,5].
Fish and fishery products are a highly valuable source of nutrients. Their muscle is rich in both macro- and micro-nutrients, especially (i) proteins, (ii) vitamins, (iii) polyunsaturated omega-3 and omega-6 fatty acids important for the human neural system, and (iv) minerals, such as calcium, iodine, zinc, iron, and selenium [6]. Simultaneously, fish meat is usually low in saturated fats, carbohydrates, and cholesterol, and low in purines compared to other types of meat. This all makes fish an irreplaceable dietary component.
Despite all of the benefits of fish consumption, it is necessary to mention some of its risks. In addition to the concern about eating small bones in meat, there is the major issue of food allergy. Fish-induced allergy is a severe worldwide problem, as evidenced by an estimated prevalence of 7% in the pediatric population, often persisting into adulthood with serious symptoms [7][8][7,8]. Fish allergy is a pathophysiological immune response to specific proteins mediated by IgE, commonly manifesting as oral allergy syndrome, diarrhea, abdominal pain, rhinitis, angioedema, and several other symptoms, even as life-threatening anaphylaxis [9]. Allergenicity differs across fish species due to the content of specific proteins (main allergens) [10][11][10,11]. Parvalbumins are the leading ones; enolases, aldolases and gelatin have also been identified as fish allergens, although their role in fish allergenicity is still not clearly understood [9][12][9,12].
Parvalbumins are highly stable proteins with a low molecular weight (10–12 kDa) common in fish muscle [13]. Fish contains both α and β parvalbumins, with most allergens belonging to the β line [14]. The expression of β parvalbumins occurs mainly in the sarcoplasmic part of fish white muscle tissue. This is directly related to the allergenicity of individual species; for example, carp, which is mainly composed of white tissue, contains an up to 100 times higher level of the parvalbumins than tuna (Thunnus) or mackerel (Scomber), which primarily contain red tissue and therefore have a lower allergenicity potential [9]. Furthermore, there are various known paralogs of parvalbumins which cause allergies differently and play a physiological role in fish muscle adaptation to environmental influences. For example, salmon (Salmo) contains only one allergenic parvalbumin isoform, parvalbumin β1 [15]. In addition, food processing may influence fish allergenicity by parvalbumin degradation or oligomerization, which may change the IgE epitope number [9][16][17][9,16,17]. Generally, two conclusions can be drawn on the allergenicity of parvalbumins based on current knowledge: (i) parvalbumins from different species can vary in allergenicity; and (ii) parvalbumin isoforms from the same species can vary [9]. This all encourages consumer demand for a verification of food identity, and food inspection authorities to implement reliable, strict quality control mechanisms [2].
2. Identification of Fish Species
Traditional fish species identification has been based on the qualitative and quantitative analysis of morphological features. Qualitative evaluation is usually focused on elementary characteristics such as fish body shape, fin placement, color, or the position of the mouth and possibly whiskers; quantitative morphological features commonly include the length of various body parts, number of scales, number of vertebrae or bones, etc. All of the above-mentioned characteristics are specific for a certain group of fish, depending on the nature of the species’ environment and the trophic resource use of the species (especially on the method it uses to obtain food). For this reason, it is still one of the methods used for the fast determination of fish species. However, the application of these attributes is not possible for the majority of processed products, in which fish meat is usually mixed with other ingredients and the morphological characteristics cannot be evaluated. Additionally, it is not possible to determine the areas and/or geographical origin of fish in processed products. This all emphasizes the need for the development of reliable analytical methods that enable fish species identification and that can detect food adulteration and consumers being misled. In general, various methods for the detection of fish adulteration have been developed over the last few decades. These primarily include gas and liquid chromatography [18][19][20][18,19,20], mass spectrometry [21][22][21,22], infrared spectroscopy [23], nuclear magnetic resonance (NMR) [24][25][24,25], immunochemical methods (e.g., Enzyme-Linked Immuno Sorbent Assay—ELISA) [26], and electrophoresis [18][27][18,27]. Each of them is based on a different principle and thus provides certain possibilities for detecting different means of food adulteration. For example, to determine a fish origin region, stable isotopes of calcified structures can be analyzed [28]. Furthermore, the analysis of δ13C isotopes by NMR spectroscopy allows the differentiation between wild and farmed fish [24]. For instance, organically farmed and conventionally farmed salmonid fish can be distinguished by the isotopes δ15N and δ13C [29]. However, species substitution is one of the most common types of fish adulteration, and thus analytical methods enabling fish species identification are of critical importance. Currently, fish species identification is mostly performed by proteomic and/or genomic methods. Both approaches are reliable for the analysis of fresh or thawed tissue, but also have their specifications and limitations. Protein-based methods may fail to analyze heat-treated or dried samples due to the denaturation of proteins (occurring after the heating at 40–60 °C), causing the loss of their biological functions and changes in many of their properties. Physical and chemical conditions can also damage DNA molecules, but unlike proteins, DNA fragments contain sufficient differences in their sequence that allow species characterization [30][31][30,31]. Furthermore, the nucleotide sequence enables the identification of species from all cell types and is independent of the tissue source or sample damage. Other significant benefits of the DNA-based methods include their specificity, sensitivity, and speed [3][4][32][3,4,32]. This has all led to their frequent application and predominance over all of the above-mentioned methods [33][34][35][33,34,35].3. DNA-Based Methods
Various DNA-based methods are used for fish species identification. Although they are often based on different bases, their implementation includes several similar preparatory steps, such as DNA isolation and in silico analysis using available databases (e.g., designing specific primers). The general procedure is shown in Figure 1.
Figure 1.
Scheme of the general procedure using DNA-based methods.
3.1. Nucleic Acid Databases
The field of DNA sequencing technology has a rich history. In the past, DNA barcoding and FINS were widely employed, providing information mainly about mtDNA. This was followed by WGS, which together with mtDNA information was able to provide the complete information regarding the organisms studied. The overwhelming production of DNA sequences led to the necessary introduction of nucleic acid databases. The Fish Barcode of Life Initiative (FISH-BOL), a global effort to coordinate and standardize a reference sequence library for fish species, aimed to create a reliable, fast and cost-effective way to identify fish species based on DNA analysis. For this purpose, a public database of standardized mtDNA reference sequences was created in 2005 [46]. Although it is not complete, and the number of sequenced fish species is constantly growing [37][47][37,47], the FISH-BOL website is no longer available today; the obtained sequenced data are available in the Barcode of Life database (BOLD). Currently, there are several databases of nucleic acid sequences. The most important ones are (i) the European Molecular Biology Laboratory (EMBL), which was established in 1980 as the first nucleotide sequence database in the United Kingdom, and which to this day is publicly available at the website of the European Bioinformatics Institute (http://www.ebi.ac.uk, accessed on 20 October 2022); (ii) the DNA Data Bank of Japan (DDBJ), managed by the Center for Information Biology (CIB), which mainly collects data from Japanese research (publicly available at http://www.ddbj.nig.ac.jp, accessed on 20 October 2022); and (iii) the GenBank database, maintained by the National Center for Biotechnology Information (NCBI), available at http://www.ncbi.nlm.nih.gov, accessed on 20 October 2022. There are also databases that focus directly on fish nucleotide sequences, such as the European Union database FishTrace (https://fishtrace.jrc.ec.europa.eu/, accessed on 20 October 2022), which is limited to European marine fish species. Unlike FISH-BOL, which focused on COI sequences only, FishTrace includes sequences for both mitochondrial (cytb) and nuclear (rhodopsin) gene. All of the databases contain the same set of information, including species names, collection records or sample identifiers. Knowledge of a fish genome sequence can significantly facilitate progress in the development of DNA-based identification methods. The first sequenced fish genome was Fugu (Takifugu rubripes) in 2002 [48][49], and the number of newly sequenced species rose slowly over the next few years. A breakthrough came in 2020, when more than 300 fish genomes were published [49][50], and this trend has continued to this day. In April 2022, the whole genome sequence (WGS) was available for almost 900 fish species, mainly in the NCBI repository and to a lesser extent also in other repositories, e.g., GigaDB and the ENA. Even though this is an impressive number, it represents less than 3% of the 32,000 total fish species on record [50][51].3.2. Mitochondrial and Nuclear Identification Markers
Identification markers are defined as parts of DNA sequences unique to a given species. These markers must meet the basic requirements for analysis. First of all, they must have sufficient specificity for a particular species to be identified. The choice of a suitable marker for a given purpose depends on the requirements, in particular, whether a qualitative or quantitative analysis is being performed. Various mitochondrial and nuclear markers, with different advantages and disadvantages, are currently used for this purpose. For the identification of fish species, mitochondrial loci have been preferred to nuclear genes because of their features: mitochondrial genes belong to a haploid genome, they are present in high copy numbers (particularly in fish muscle tissues), which provides higher sensitivity of detection, and their mutation rate is greater than that of nuclear genes [51][52][53][55,56,57]. This means that the coalescence of neutral genes will be positively correlated with the adequate population size of the species [54][58]. Thus, according to population genetics theory, mtDNA should evolve four times faster than the average nuclear gene. Hence, mtDNA can be used to follow divergence in very closely related taxa and even within species. An undeniable advantage of mtDNA is the ability to identify the geographical origin of the individual [55][56][59,60]. The most common mitochondrial markers used for fish species identification are the following: (i) the gene for cytochrome-c-oxidase subunit I (COI; EC 7.1.1.9), whose 600-bp-long segment became the basis for taxonomic fish differentiation via DNA barcoding [57][58][61,62], and (ii) cytochrome b (cytb; EC 7.1.1.8) [59][60][61][63,64,65]. Due to the presence of a high copy number of mtDNA molecules in the cell (~1000× more than copies of nDNA), their occurrence is also expected in highly processed products [52][62][56,66]. Furthermore, mtDNA is thought to be more thermally stable due to the greater internal stability caused by its ring structure [63][67]. Another disadvantage of mitochondrial markers in comparison with nuclear ones is the impossibility of quantifying DNA, because mtDNA concentrations vary depending on the type of tissue [56][64][60,73]. The above-mentioned difficulties can be overcome by amplifying nuclear sequences instead, as they have the advantage of possessing a known haploid genome size and quite a high level of uniqueness, even in orthologs of such markers in closely related fish species [51][65][55,74]. This phenomenon, based on an absence of selection pressure on introns as they are spliced out and are not reflected in the resulting protein, allows for a high level of mutations, and therefore early diversification of their sequence after the split into new species [66][75]. As for nuclear markers, the most frequently used ones for fish authentication are β-actin, which has also become an often-used internal control for mRNA quantification [67][68][69][76,77,78], and parvalbumin [70][79]. Besides these markers, novel nuclear barcode regions have also been proposed for fish species identification [71][80]. The length of these nDNA barcodes is generally shorter than that of the mtDNA barcodes: this facilitates the amplification of the DNA even for highly processed food products, as well as their compatibility with the current next-generation sequencing (NGS) technologies, which also allow the identification of species in a mixture [52][56]. Another frequently used marker for species identification are microsatellites, also called STRs (short tandem repeats) [72][81] or SSR (simple sequence repeats) [73][74][82,83]. Microsatellites are short stretches of DNA composed of repeating specific motifs of nucleotide sequences. These motifs are 1–10 nucleotides long. The majority of microsatellites in the genome (30–60%) are probably dinucleotide repeats; the most common motifs in the vertebrate genome are (AC)n or (AT)n [74][83]. Microsatellites are considered to be one of the most suitable genetic markers due to their extreme variability (polymorphism), multiallelic nature and codominant inheritance (this makes it possible to distinguish heterozygotes). Another advantage is their abundance across the genome, which requires a small amount of DNA to collect data [73][75][82,86].3.3. DNA-Based Methods
3.3.1. Polymerase Chain Reaction (PCR)
The PCR method is used for the selective amplification of a short region of nucleic acid. It has become very popular and, therefore, has been constantly evolving and improving since its discovery in 1983 [76][148]. The method has gradually developed into several variants, namely end-point PCR, quantitative PCR with fluorescence detection in real time (qPCR), and digital PCR (dPCR) [77][78][79][149,150,151]. The basic principle of the method remains the same for all variants. In general, specific sequence amplification is based on in vitro enzymatic replication that is repeated cyclically. The amplified region (amplicon) is defined by two short oligonucleotides—PCR primers. Each primer binds to single strand of DNA and, subsequently, allows DNA polymerase to begin synthesizing a strand complementary to it. This creates a double-stranded DNA, which is separated into two single-stranded molecules by following denaturation at high temperature. The amplification process is exponential in nature. After the amplification, the detection of the PCR product depends on the type of PCR used. The end-point PCR requires post-PCR electrophoretic detection on an agarose gel, which allows identification of amplicons by size. After qPCR, agarose electrophoresis is possible if needed, but not required. The qPCR, and also dPCR, allow the detection and quantification of target DNA in the reaction through the detection of fluorescence signals, which increases the sensitivity of the method. The fluorescence signal is produced by intercalating dye, such as SYBR Green I or Eva Green, or by a fluorescent dye-labeled probe. The result of each qPCR is an amplification curve showing the increase in fluorescence, and thus the amount of product, in time. In the case of intercalating dye, the specificity can be lower because the dye binds to all double-strand products present in the reaction [78][150]. Therefore, post-PCR identification of fish species using High-Resolution Melting (HRM) analysis of the amplified gene segment (amplicons) is widely used [39][80][81][39,152,153]. HRM relies on the different melting temperatures (Tm) of amplicons that occur due to minor variations in nucleotide composition, especially on the number of guanine and cytosine, and the length of the sequences. The dsDNA melts as the temperature increases. Thus, the DNA-binding fluorescent intercalation dye is released, and the melting profiles can be recorded and systematically and statistically processed using specific HRM software. Based on the different Tm values and/or the shape of the curve, it is possible to distinguish between closely related species even when a single base variation is present between their dsDNA sequences [82][83][84][154,155,156]. HRM is an advanced method that provides a high level of confidence and accuracy, but it lacks the determination of the precise nucleotide differences in the analyzed amplicons [80][81][84][85][86][152,153,156,157,158].3.3.2. Sequencing Methods
Today, many sequencing technologies exist. Traditional Sanger sequencing, which is limited by its ability to sequence only one DNA fragment at a time and lower sensitivity, has been overtaken by modern approaches using massive parallel sequencing based on NGS. NGS platforms can be roughly divided into long-reading (about 1 kb and above), such as MinION, and short-reading (usually <300 bases/read) sequencing platforms, e.g., Illumina, Ion Torrent, or Pyrosequencing, that provide higher throughput and are most suitable for PCR amplicon sequencing [87][88][89][90][163,164,165,166]. For fish species identification, Sanger sequencing and the Illumina platform are the most commonly used sequencing techniques. Both sequencing techniques, the Sanger dideoxy method (also known as capillary electrophoresis sequencing) and Illumina NGS, use the principle of amplification, in which DNA polymerase adds fluorescently labeled nucleotides to the growing strand one after the other, and the inserted nucleotide is subsequently identified due to its fluorescent label. The advantage of Sanger sequencing is its speed and the ability to sequence relatively long fragments (up to 1000 bp). It is also cost effective for low numbers (1–20) of samples. However, it has a lower throughput, detection limit (15–20%) and ability to identify novel variants (so-called discovery power) compared to NGS. Thus, the Sanger method is an effective approach for variant screening studies when the total number of samples is low [91][92][167,168]. Illumina has higher mutation resolution, from large chromosomal rearrangements to single nucleotide variants, and better discovery power. This is due to the higher sequencing depth, i.e., the number of times that a given nucleotide in the genome has been read, which provides the higher sensitivity (up to 1%) of the technique. The disadvantages of NGS include the need to analyze multiple samples at once to make the method less time consuming and expensive and the provision of shorter fragments (usually 150–300 bp, depending on the sequencing platform used) [91][93][167,169]. Therefore, NGS is a suitable technique for analysis where the massive sequencing of fragments per run or the performance of deeper sequencing to detect novel or rare variants is required. Other NGS platforms that is possible use for fish species identification include Ion Torrent [94][95][170,171] and pyrosequencing [96][97][172,173].3.3.3. DNA Hybridization
Nucleic acid hybridization is based on the specific association (hybridization or renaturation) of complementary nucleotide sequences derived from different molecules of DNA. The basis of hybridization is usually a fluorescently or radioactively (e.g., 32P) labeled probe with a known nucleotide sequence that allows the detection of a complementary sequence. Hybridization is most often performed on carriers (Southern blotting), but hybridization to nucleic acid in intact cells (“in situ” hybridization) is also possible [98][99][180,181]. DNA–DNA hybridization is still an important method used in the analysis of evolutionary relationships between organisms. The method uses the reassociation of ssDNA fragments, where heteroduplexes can be formed in a mixture of DNA of different species. Reassociation conditions (e.g., salt concentration, temperature, viscosity, fragment size) affect the possibility of hybrid molecules formation. Under strict conditions (low salt concentration, high temperature), only very similar sequences can be joined; as the conditions are gradually relaxed, more distinct sequences can pair. The greater evolutionary distance between species leads to more differences in the sequences of their DNA.3.3.4. Methods Using Restriction Enzyme Cleavage
Restriction Fragment Length Polymorphism (RFLP)
RFLP is one way to study species diversity. It refers to variations in their DNA sequences at sites recognized by restriction enzymes. Such variation results in unique patterns of DNA fragments caused by their different lengths between restriction sites. DNA fragments are separated electrophoretically on the basis of length, size or molecular weight, and then transferred to a membrane by Southern blotting. DNA fragments on the membrane hybridize with a labeled DNA probe, allowing visualization of DNA profiles. In the absence of restriction sites, no DNA cleavage occurs. RFLP thus makes it possible to detect both the absence and the presence of such sites. With PCR expansion, the development of methods combining PCR and restriction digestion (PCR-RFLP) began. The first step in the PCR-RFLP method is to amplify the fragment containing the variation. This is followed by treatment of the PCR products with the appropriate restriction enzyme. Depending on the presence or absence of a restriction site, restriction fragments of different sizes form. Nested PCR can be used to amplify the target region to avoid false-negative results. Thanks to the use of external and nested primers in two consecutive PCRs, this method has higher specificity, and high sensitivity and efficiency. This also allows amplification of the required fragments even at low DNA concentrations [36][100][101][36,184,185].Amplified Fragment Length Polymorphism (AFLP)
AFLP is a highly sensitive PCR-based method suitable for population studies and for finding genetic variation between closely related species. It is based on four steps: (i) restriction (specific cleavage of total DNA by two restriction endonucleases, most often MseI and EcoRI); (ii) ligation (adapters are attached to all fragments by T4 ligase); (iii) amplification (pre-selective and selective amplification to reduce the number of fragments); and (iv) fragment visualization. AFLP requires initial screening to find the optimal primer combination; specific primers are complementary to the adapters and have an overhang of one to three bases within the studied fragment. Obtained fragments can be separated by electrophoresis on a polyacrylamide gel and visualized autoradiographically. The final visualization can also be performed in an automatic sequencer if fluorescently labeled EcoRI primers are used.
3.3.5. Polymerase Chain Reaction–Single-Strand Conformation Polymorphism (PCR-SSCP)
In PCR-SSCP analysis, the target sequence is amplified and radiolabeled with primers or nucleotides. Subsequently, the amplified fragments are denatured and subjected to polyacrylamide gel electrophoretic analysis under non-denaturing conditions. Alternatively, the products are visualized on a gel using silver staining. Single-stranded DNA (ssDNA) tends to collapse into a spatial structure due to internal complementarity. Even a very small change in sequence can cause a different structural arrangement. Depending on the conformation of the ssDNA molecule, it migrates through the gel at different speeds during electrophoresis. The efficiency of SSCP decreases with increasing length of the analyzed fragment; the highest efficiency of the method is for up to 200 bp [36][102][36,191].3.3.6. Random Amplification of Polymorphic DNA (RAPD)
As the name of the method suggests, RAPD amplifies random sections of DNA. This is a significant difference compared to classical PCR, where a predetermined target fragment is amplified. Another difference is that the RAPD method uses only one short primer prier for amplification, usually 10 nucleotides long. This arbitrary primer often serves as both a forward and reverse primer, and during PCR amplification anneals at random sites in DNA. Variations in the genetic code give rise to unique patterns of DNA fragments in individual species. The obtained amplicons are analyzed by gel electrophoresis. The profile of the unknown sample is then compared with the profiles of species-specific bands, the so-called DNA fingerprints of the species, obtained with the same primer.3.3.7. Loop-Mediated Isothermal Amplification (LAMP)
LAMP is a gene amplification method that combines speed, high specificity, and simplicity. Due to the constant temperature amplification, the LAMP method, unlike other methods, does not require expensive laboratory equipment. The use of LAMP can thus greatly simplify routine analysis, although primer design is more complex than for PCR. The method uses a combination of two or three primer pairs (outer F3, B3; inner FIP, BIP; loop primers), which allows the reaction to possess high specificity. Both outer and inner primer pairs are necessary for the initial amplification, but only inner primers are important for the cyclic amplification and elongation of emerging DNA. The amount of the target sequence is thus tripled during each half of the cycle. The result of the reaction in the presence of target DNA are lamplicons of various lengths. Loop primers are not necessary for the reaction to work properly, but they increase the rate of exponential amplification, thus reducing the time required for analysis by up to half (approximately 30 min). Unlike the PCR method, which uses a wide range of polymerases, the LAMP method generally recommends Bst polymerase, which has a higher tolerance to inhibitors.3.3.8. Multi-Analyte Profiling (xMAP)
xMAP technology can be used for high-throughput multiplexing and the simultaneous detection and quantification of a large number of different analytes in a single reaction. Various biomarkers, such as proteins, nucleic acids, and polysaccharides, can be analyzed, as indicated by the “x” in the method name. xMAP is based on the same principles as PCR, ELISA, and flow cytometry. The fluorescence of molecules bound to polystyrene or magnetic microspheres labeled with up to five hundred different fluorescent dyes (so-called spectral code) is measured. A target molecule is bound to each type of microsphere, which can be, inter alia, a DNA probe or an antibody. The beads are read individually using an xMAP instrument. In each of them, the fluorescence is measured after excitation with two lasers in a silica glass cuvette. The first laser excites the red fluorochrome in the bead at 635 nm, thus determining the spectral code, i.e., the type of analyte. The second laser excites the fluorochrome phycoerythrin at 532 nm; the fluorescence intensity is measured, and the amount of analyte can be determined [103][199].3.4. Data Analysis
A combination of PCR with subsequent sequencing of the products is often used to identify species. Using this procedure, primer annealing in the expected gene region can be verified, and other nucleotide sequence analyses can be performed, e.g., the detection of nucleotide variations. Methods using this principle include forensic informative nucleotide sequencing and DNA barcoding [3][57][104][3,61,206]. A significant advantage of these methods is that only one universal pair of primers, specific for a selected marker, can be used for multiple animal species. Among the suitable markers, the mitochondrial genes cytb and COI are widely used for fish species identification [105][106][133,207]; thus, their sequences are well known, and primer design is relatively fast. On the other hand, complex databases of reference sequences and the amplification of relatively long stretches of DNA (compared to qPCR, for example) are needed for the identification of species in processed products.3.4.1. DNA Barcoding
Within the sphere of DNA-based fish species identification approaches, a great deal of attention has been devoted to DNA barcoding, which relies on sequence variations within a short and standardized region of the genome. This selected region, designated a “DNA barcode”, is amplified by PCR and then sequenced. The barcoding method takes advantage of the high rate of mutations in mtDNA, which leads to a divergence of mtDNA between species and at the same time small differences in DNA within one species [56][107][60,208]. Currently, the mitochondrial genes coding COI and cytb are the most commonly used because they are considered reliable DNA barcodes for the discrimination of animal species [57][83][107][108][109][61,103,155,208,209]. Additionally, the Consortium for the Barcode of Life (BOL; www.ibol.org, accessed on 20 October 2022) is focused on COI gene sequencing to create a barcode database for all eukaryotic species to standardize the species identification process; the selected reference sequence is about 650 bp in length for most species group [57][107][61,208]. The functionality of DNA barcoding for fish species identification has been verified in many studies [58][83][110][111][112][62,155,211,212,213]. However, this method also has certain limitations. The most serious disadvantage is that it cannot be used for the identification of fish in mixed samples and, further, as with all mitochondrial markers, the inability to quantify the fish DNA content in the sample. When using markers with a longer sequence (>600 bp), identification in processed products can also be problematic due to DNA degradation. Sequencing reliability is also still being discussed [62][66]. On the other hand, it is a dependable, fast, and cost-effective way to identify fish based on DNA analysis. For the field of ichthyology, FISH-BOL is a powerful tool for a better understanding of the natural history and ecological interactions of different fish species [113][114][115][210,214,215].3.4.2. Forensically Informative Nucleotide Sequencing (FINS)
The FINS technique, which combines DNA sequencing and phylogenetic analysis, uses a similar principle to that of DNA barcoding. The amplified specific DNA fragment is sequenced, and this informative nucleotide sequence is subsequently identified by phylogenetic analysis using a database of reference sequences which should be obtained from properly identified fresh samples or authentic preserved samples [116][216]. The results of the analysis are displayed as a phylogenetic tree, where sequences of the same species are grouped into clades. Based on the calculated distances from the reference sequences of known species, unknown species are also included in the phylogenetic tree. This method thus allows the detection of new unexplored species [117][217]. To achieve high-resolution results, DNA regions with high inter-specific, but low intra-specific, variation are essential. Thus, rapidly evolving regions with many informative sites in DNA sequences, for example, cytb, COI, or 16S rRNA, are usually used as genetic targets [116][118][216,218].3.5. Advantages and Limitations
The methods using restriction cleavage (RFLP, AFLP) benefit from their simplicity, reliability and robustness. However, the high risk of incorrect identification needs to be taken into account due to the insufficient study of related species, which may form the same restriction profile or polymorphism in the analyzed DNA, leading to a change in the restriction site and thus incorrect evaluation of the analysis. As a result, some authors tend to recommend the use of sequencing and phylogenetic analysis techniques [60][119][64,219], such as DNA barcoding or FINS. These methods provide a high power of diagnosis, which minimizes the risk of misidentification of the species. When analyzing a species that has not been studied yet, it will be included in the appropriate node in the phylogenetic tree based on its nucleotide sequence. The phylogenetic tree also contains reference sequences of several species; the assignment to a node corresponding to a certain species thus allows the identification of blank samples [117][217]. However, sequencing-based methods run into limitations in the analysis of processed and/or pooled samples. In this case, species-specific PCR or LAMP seems appropriate. The advantages of the LAMP method compared to PCR are the lower demand for lab equipment and the possibility of shortening the amplification time by up to a third [120][220], but PCR is a more robust method. PCR and FINS also have high potential for building nucleotide databases. However, the above-mentioned methods (PCR, LAMP, FINS, RFLP) require prior knowledge of the DNA sequence of the analyzed species for the analysis itself, unlike RAPD and AFLP, for example. Next, RAPD and AFLP can be used for the analysis of multiple loci at once. AFLP markers also exhibit much higher variability than, for example, isozymes. However, neither method is very robust against DNA degradation, and they both have low potential for interlaboratory reproducibility. Compared to AFLP and RFLP, RAPD is considered the most reliable method for species identification when the genome sequence is unknown [63][121][67,221]. However, for both RAPD and RFLP, intraspecific variation can be problematic, in contrast to the SSCP method, for example. On the other hand, SSCP is more demanding and always requires the presence of a reference sample on the gel together with the analyzed samples. Despite the high sensitivity of SSCP or PCR-SSCP and its capability of intraspecific differentiation, the amount of information obtained from these methods is much lower than with sequencing [30][122][123][124][30,192,193,222].
