1. Introduction
The Large White pig is the most commonly raised commercial pig breed around the world, due to the fact that Yorkshire pigs in the USA and Canada are direct descendants of the Large White line [
1]. Today, a large majority of countries with developing or developed pig breeding have an imported Large White stock. The pedigree pigs of this breed are hardy, adaptable to climate, and can survive in various environments. Until the XIX century, local pigs occupied a prominent space in Europe. Various environmental conditions of certain regions impacted these animals [
2]. Since the end of the XVIII century, breed improvement of local pigs began by creating Romanov, Oriental, and later by introducing Chinese pigs. Significant breeding work has led to creating the Large White breed.
Large White pigs were brought to Russia in the in the second half of the XIX century; however, during the wars in the beginning of the XX century, the larger half of the pedigree pigs were killed. In 1923–1931, a livestock of Large White pigs was imported from England for developing domestic pedigree pig breeding. Long-term breeding and the impact of climate and feeding changed the English type of Large White pigs and a new type of local (Russian) Large White breed was created which, at that time, was superior to the English one for many indicators [
3]. Despite this, in the late XX to early XXI centuries, the pig livestock in Russia was almost completely replaced by imported pigs from leading breeding centers in Denmark, France, England, Holland, Ireland, etc.
One of the most effective approaches to assessing populations is studying mitochondrial DNA polymorphism. The mitochondrial genome is considered a mutation hotspot [
4]. The rate of recorded mutations in mitochondrial genomes of animals is approximately 10 times higher than that in equivalent sequences in a nuclear genome [
5]. For billions of years, the mitochondrial genome developed as organisms became adapted to the environment and selection pressure [
6]. As a result, mutations became fixed, and various mitochondrial lines clustered in groups known as mtDNA haplogroups. mtDNA haplotypes determine certain distinctions because genetic variations in the mitochondrial genome are sensitive both to natural and artificial selection [
7].
The mtDNA contains a non-coding (D-loop) sequence comprising regulatory sequences regulating both replication and transcription of the mtDNA [
8]. Many studies of farm animals, including pigs, have shown the effectiveness of applying the D-loop as a diversity marker when studying the mitochondrial genome [
9,
10,
11].
In connection with the above, a particular interest is represented by studies of pigs’ mtDNA bred at the breeding farms of the Russian Federation throughout the last two decades. This work includes studying variations of nucleotides in the field of a mtDNA D-loop in Large White pigs of various selections bred in the Russian Federation from 2000 to 2019 in order to define the presence of frequency distinctions of mtDNA haplotypes in Large White pigs of the Russian selection (created in the middle of the XX century) and the imported livestock of the Large White breed, which was the result of intensive selection work to increase productive traits (growth rate, reproduction, forage costs, etc.). On the other hand, assessment of current Large White pigs from various farms of the Russian Federation is also of interest as they represent the selection of different international genetic centers. The breeding lines belonging to these companies are the result of targeted selection based on their own technologies and know-how. In our study, we tried to define significant distinctions of genetic structure of mtDNA in different livestocks. In addition, the aim of our work was to define the relationship between the allocation of mtDNA haplotype frequencies with adaptation to different climatic conditions in Russian Large White pigs as far as breeding animals that were hardy to various environmental conditions had been one of the primary goals of that time. This research will allow us to obtain information about the genetic diversity of Large White pigs. The obtained results will contribute to the preservation and sustainable use of these resources and can also be used to improve the breed and create a Russian type of Large White breed.
3. Results
3.1. Genetic Diversity of Large White and Yorkshire Pig Populations in Russia
We studied 402 sequences of the D-loop fragment isolated from pigs kept in Russia from 2000 to 2020. The genetic diversity indicators of the Hd, Pi, and K of investigated pigs (
Table 2) were analyzed by using correlation analysis and PCA. All three parameters were positively correlated and the degree of correlation Pi and K was 1.0 (
Table 3).
3.2. Polymorphic Sites, Haplotypes, and Haplogroups
In the studied sample, we defined 46 polymorphic sites and 42 haplotypes (
Figure 1). The table with haplotype pigs is presented in
Supplementary Materials. The haplotype distribution by clusters corresponding to the Asian (A, B, C) and European (D, E) haplogroups is shown in
Figure 2. Construction of the phylogenetic tree by the maximum likelihood method showed that the haplotypes belonged to haplogroups A, B, C, D, E, and we highlighted a separate cluster near haplogroup E, which we contingently named E1.
Hap_11, determined in 28.9% of pigs (n = 116), had the highest frequency in the studied sample, while in the Old group, its frequency was 21.8% (n = 17), in Imp, 19.5% (n = 24), and in New, 31.3% (n = 75). High frequency (11.9%, n = 48) and representation in three groups (Old, 12.8%, n = 10; Imp, 7.3%, n = 9; New, 14.4%, n = 29) was defined for Hap_7. In total, only four haplotypes were present in all groups—these are the abovementioned Hap_11 and Hap_7, as well as Hap_1 and Hap_8.
3.3. Haplotype and Haplogroup Frequencies between the Old, Imp, and New Groups of Pigs
Despite the presence of common haplotypes, there were haplotypes found only in one of the groups. When comparing haplotype frequencies between the Old, Imp, and New groups, significant differences were found (
Table 5).
Therefore, the Нар_12 haplotype was found only in LW_2_Old, Нар_13, and Hap_14 in LW_4_Old. In the Imp group, we identified 11 unique haplotypes, five of which (Нар_18, 23, 25, 27, 29) were identified in only one animal and six (Hap_20–22, 26, 30.31) in more than one animal but also only on one farm. In the New group, 11 unique haplotypes were found, seven of which (Нар_33–37, 41, 42) were found in only one animal and four (Hap_32, 38–40) in more than one animal.
Figure 3 shows the frequency distribution of mtDNA haplotypes and haplogroups in pigs of the Old, Imp, and New groups.
The distribution of haplogroups also differed between the Old, Imp, and New groups. In the Old group, haplotype D had the highest frequency, and, in general, the distribution for Asian and European haplotypes was 50/50. European haplogroups prevailed in the Imp group (n = 70; 56.9%) and haplogroup D had the highest frequency. Asian haplogroups prevailed in the New group (n = 151; 75%) and group B haplotypes had the highest frequency.
3.4. Haplotypes and Haplogroups in Pigs of the New Group
The diversity of haplotypes and haplogroups in pigs of the New group was associated with the farms in which they were bred (
Figure 4). Despite the fact that Asian haplotypes prevailed in this group, it is possible to distinguish farms (LW_1, LW_4, LW_6, LW_9, and LW_11) where European haplotypes constitute 50% or more.
3.5. Frequencies of Haplotypes and Haplogroups in Old_Center, Old_Siberia, and Old_South Groups of Pigs
Furthermore, according to stated objectives, we found that, in the Old group, the frequency distribution of haplotypes was associated with pigs’ adaptation to different climatic conditions. To evaluate this, the pigs of the Old group were divided into three clusters corresponding to the Southern region of the Russian Federation (South), the Central region of the Russian Federation (Center) and Siberia (Siberia). In total, we identified 15 haplotypes in the Old group pigs, which were distributed among Asian (A, B, C) and European (D, E, E1) haplotypes (
Figure 5).
The results showed that haplotype frequencies significantly differed between the Old_Center, Old_Siberia, and Old_South clusters (
Table 6).
Significant differences in the haplogroup frequencies were defined only between the Old_Center and Old_Siberia groups. In the Old_Center pigs, haplogroup D prevailed (52%), while in the Old_Siberia, haplogroup C dominated (39%). Altogether, 70% of the Old_Siberia pigs had Asian haplogroups, compared to the Old_Center pigs with 64% of European haplogroups. In the Old_South cluster, the distribution for Asian and European haplogroups was 47% and 53%, respectively.
4. Discussion
Mitochondria are responsible for 95% of the energy of a eukaryotic cell through oxidative phosphorylation of ADP (adenosine diphosphate) forming ATP (adenosine triphosphate). Thus, some variations in mtDNA can have important consequences for animals when adapting to different environmental conditions [
20,
21,
22]. Evidence of adaptive evolution affecting mtDNA is presented by Niu et al. [
23], Slimen et al. [
24], Xu et al. [
25], and others.
In our study, we chose Large White pigs, which were selected after long-term targeted selection work for pig farming in Southern region, Central region and Siberia. For Southern region, dry and very hot summers and mild winters are inherent (the temperature can reach 35—40 °C); for the Central region, mildly cold winters and humid, moderately warm summers; for Siberia, cold winters with temperature reaching 40 °C and moderate–warm summers. Due to the fact that pigs of the Old group were distinguished by good productivity despite very high summer temperatures (Old_South) and quite severe winters (Old_Siberia), we suggested that this might be connected with mtDNA haplotypes.
Our findings do not fully prove that any genotypes are more or less preferable for different climatic conditions. However, they show local evidence that the distribution of haplotype frequencies is related to the geographical locations of zones with different climatic conditions and can be the basis for further research connected with searching loci of supposedly neutral and adaptive components of genetic diversity in mitochondrial and nuclear DNA.
Despite the high adaptation and good productivity of local pigs in the late XX–early XXI centuries, Russia began to import pigs of other selections which were significantly superior in growth rate and reproductive performance. The import pigs were too exacting to keep and feed, but despite this, they quickly replaced the local.
Our results showed that Large White pigs of the Old group had both European and Asian haplotypes. In 2008–2010, Large White pigs imported to the Russian Federation had predominantly European haplotypes. However, currently, in Large White pigs (from leading genetic centers), Asian haplotypes prevail. Perhaps this is due to targeted breeding aimed at increasing productivity, including sow fertility [
26]. In European pig farming, we can observe a steady increase in litter size during the last three decades [
27]. Currently, litters can reach up to 18–20 piglets [
26,
28]. To some extent, this is due to the introduction of Chinese genes to commercial European breeds [
29,
30].
Chinese breeds are highly fertile. The role of the mitochondrial genome in this process is still not clear today. Mitochondrial diversity has long been considered neutral or almost neutral [
31]. However, an increasing amount of research with animal models and humans suggests that mtDNA variants may be associated with some phenotypic traits [
32,
33,
34,
35,
36,
37,
38]. Given this, we can assume that further intensification of pig production can lead to a significant spread of some haplotypes and disappearance of others.
Over the past decade, the global commercial pig breeding industry has provoked significant business consolidation. The mergers and acquisitions of small genetic centers has led to a small number of remaining internationally operating breeding companies [
39]. Hence, the breeding lines belonging to these companies also have undergone a high degree of consolidation. Each of these companies uses its own selection technologies and target indices while improving the breeds and this in its turn makes a significant difference in the breed genetic structure.
Regarding Large White pigs raised in Russia, we can note that, alongside consolidating enough livestock in separate farms, other farms demonstrate high genetical diversity, with some farms having mainly European haplotypes and others, on the contrary, having Asian ones. Genetic variation in Large White pigs inside the farms may depend on the strategy of the economy, preferring either a rigid consolidated frame (in the case of working only with a certain selection center) or a more variable one allowing farmers to variate and improve their livestock.
5. Conclusions
The results of studying the mtDNA of pigs have shown the intrapedigree genetical diversity of the Large White breed. Peculiar properties of the genetical structure of mtDNA are bound to the period of their breeding in Russia; particularly, it is seen in Large White pigs of the Russian selection and the modern (commercial) livestock of the Large White breed. Along with this, we can trace certain distinctions of mtDNA haplotypes and haplogroups caused by differences in farming in the Russian Federation. This directly is bound to the selection strategy of international genetic centers where, in spite of significant consolidation of genetical structure inside the center, a significant general genetical diversity of the breed is provided. Besides the above, the obtained results indicate a connection between the frequency distribution of mtDNA haplotypes and adaptation to various climatic conditions in Large White pigs of the Russian selection.
As a whole, the presented results are an impetus for further investigations of mtDNA, and, with consideration of the functional importance of certain peptides encoded by mitochondrial genes, they introduce an interest in understanding the processes which are stimulating and sustaining variations in mtDNA.