In nature, DNA is ubiquitous, existing not only inside but also outside of the cells of organisms. Intracellular DNA (iDNA) plays an essential role in different stages of biological growth, and it is defined as the carrier of genetic information. In addition, extracellular DNA (eDNA) is not enclosed in living cells, accounting for a large proportion of total DNA in the environment. Both the lysis-dependent and lysis-independent pathways are involved in eDNA release, and the released DNA has diverse environmental functions.
1. Introduction
A general consensus has risen that the total DNA in a natural environment is comprised of intracellular DNA (iDNA) and extracellular DNA (eDNA). DNA has been thought to exist only inside the cell for long periods of time. However, an increasing amount of evidence has shown the presence of DNA in the extracellular space, and these eDNA outside the cell may account for a large proportion of the total DNA [
1]. Compared with iDNA that is located in living cells, eDNA is outside the cell, and it is widely distributed in soil, sediments, feces and aquatic ecosystems and other ecological niches, and it has also been discovered in tissue cultures and in the blood of the human body and some other animals [
2,
3,
4,
5]. Moreover, the ratio of eDNA:iDNA could provide valuable information about the microbial activity in different environments [
6,
7], although the activity of different microorganisms is not completely correlated with the ratio [
8]. These results indicate that eDNA has the potential to be a proxy for specific microbial activities [
9].
Initially, eDNA was thought to be derived from lysed cells. Nowadays, it has been well documented that both the lysis-dependent and lysis-independent pathways were involved in eDNA release in prokaryotic and eukaryotic cells [
10]. There are two general forms of eDNA, which are single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA), and the latter accounts for a significant portion of the total eDNA in the environment due to the instability of ssDNA [
11]. The increasing amount of evidence has shown that eDNA plays a significant role in multiple biological processes such as biofilm formation and maturation, horizontal gene transfer (HGT), and multiple element cycling including for carbon, nitrogen, and phosphate [
12,
13,
14,
15]. However, the biological roles of eDNA are different across different species, and they even vary with the different life stages in the same organism. For example, in
Neisseria meningitidis, eDNA has different roles in early and late biofilm formation [
16].
During the past decades, biodiversity is disappearing at an alarming rate, and the large-scale assessment and monitoring of biodiversity has become a priority. Therefore, eDNA-based biomonitoring has emerged as an effective tool for detecting biodiversity changes at a large scale, and it offers us a better understanding of the microbial community composition as well as the community function [
9].
eDNA is widely distributed in the soil, sediments, feces, and other environments (Figure 3).
Figure 3. eDNA in different ecological environments. eDNA is widely distributed in soil, sediments, feces, and liquid environments. The left side of the picture represents the soil, and above the soil are the feces, and on the right side of the picture are the liquid environments, and under these is the sediment.
2. eDNA in Soil
eDNA widely exists in soil, and it accounts for about 40% of the total DNA pool. Its content of eDNA varies significantly in different soil regions, types, and layers, and most of the eDNA is concentrated in the upper layers of the soil [
15]. The range of eDNA content in soil is about 0.03–200 μg/g [
53]. At the increasing depth of the soil layer, the eDNA content tends to decrease, and its reduction is much more obvious than that of organic carbon [
1]. In addition, it has been found that the higher the fertilizer supply is, then the lower the eDNA concentration is [
62]. It is estimated that more than 70% of the DNA molecules present in soil are derived from fungi [
63].
The eDNA in soil can be divided into two fractions with one that is tightly bound to the soil particles and the other that is weakly bound [
64] so that the eDNA can be protected against degradation by nucleases in the soil, thus, stably persisting in the soil for a long time [
53]. Therefore, eDNA can serve as a historical microbial gene reservoir, reflecting the diachronic biodiversity of the investigated environments. The long-term stable existence of eDNA in soil can lead to the accumulation of exogenous genes such as antibiotic resistance genes (ARGs) which may be passed between cells, meanwhile soil microorganisms acquire ARGs through homologous recombination, thus, potentially generating new resistance strains, especially resistant pathogenic bacteria. These strains have strong resistance and are not easily subjected to environmental stresses, which pose great threats to the environments [
65]. In addition, eDNA occupies a large proportion (about 10%) of the soil P pool, which enables the microbes to take up DNA as a nutrition source of carbon, nitrogen, phosphorus, and nucleic acid precursors [
66]. Surprisingly, adding eDNA to a culture medium has been reported to promote the growth of the lateral roots and root hairs in
Arabidopsis [
67]. However, it has been found that conspecific eDNA treatment can inhibit the growth of plants and the soil microbe, whereas heterologous eDNA treatment cannot, indicating that this inhibitory effect might be due to the maintenance of the microbial diversity [
68]. However, more research is needed to further explore the underlying mechanism. In addition, plants can release NETs in which eDNA is able to enhance the resistance of root tip to soil pathogens, but the resistance of these pathogens would be lost with a DNaseI treatment [
69].
3. eDNA in Sediments
eDNA can be found in various types of sediments, such as marine sediments, river sediments and freshwater sediments. Among them, the marine sediments are the largest sediment eDNA reservoir. Increasing evidence suggests that more than 90% of DNA in sediments is extracellular, and it has been estimated that the content of eDNA ranges from 0.30 to 0.45 Gt in deep-sea sediments [
70]. The content of eDNA varies in the different sediments. A study of Haihe River sediments has demonstrated that the concentration of eDNA (96.8 ± 19.8 μg/g) is much higher that of iDNA (76.7 ± 13.0 μg/g) [
71]. In ferruginous sediments from Lake Towuti of Indonesia, the eDNA concentration is at around 0.5–0.6 μg/g in the surface layer of the sediments, and the concentration of eDNA has the same trends in the sediments and soil, namely, it decreases with the increasing depth [
72]. Apart from the eDNA concentration, the eDNA fragment size also decreases as the depth increases [
5].
The most of the eDNA in the sediments is bound or adsorbed to particles to fight against nuclease degradation [
73]. Additionally, the eDNA in sediments possesses multiple roles. For example, the eDNA in the marine sediments can not only reflect the biogenesis processes on different time scales, but also provide information on biodiversity and genetic diversity of different ecosystems in both ancient and modern times [
74]. In addition, eDNA could be used to obtain past climate and environmental information through a taxa analysis, and it promises to be a very powerful tool for predicting future environmental changes and the function of the ecosystem [
75].
4. eDNA in Feces
eDNA can be extracted from cattle feces, and its content is about 202.4 μg/g from fresh excrements [
76]. Additionally, the content of eDNA in swine mature ranges from 9.6 to 9.7 μg/g dw (dry weight) [
77]. There findings indicate that eDNA is an essential ARGs reservoir. eDNA receives increasing attention since the ARG pool in mature animals poses a threat to the ecological environments and human health. Livestock and poultry manure is generally considered to be a natural host for ARGs, and the environment exposure of manure from farms may drive the circulation of ARGs [
78]. In humans, gut microbiome dysregulation may lead to the occurrence of a series of diseases, and thus, extracellular viral-like particles (eVLPs) and virus DNA from human feces could be extracted for metagenome and morphology analyses [
79,
80].
5. eDNA in Other Ecological Environments
eDNA exists in various liquid environments such as seawater, freshwater, river water, and lake water. The eDNA concentration in aquatic environments can reach up to 88 μg/L [
81]. The concentration of eDNA is always associated with the trophic status and the season with its concentrations ranging from 2.5 to 46 μg/L in mesotrophic water, while it ranged from 11.5 to 72 μg/L in eutrophic water [
82].
This entry is adapted from the peer-reviewed paper 10.3390/ijms232213690