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. 2019 Jul 24;9(8):481. doi: 10.3390/ani9080481

Genomic Identification and Expression Analysis of the Cathelicidin Gene Family of the Forest Musk Deer

Long Zhang 1,2,*,†, Hang Jie 3,†, Yingping Xiao 4, Caiquan Zhou 1,2, Wentao Lyu 4, Wenke Bai 1,2,*
PMCID: PMC6719980  PMID: 31344924

Abstract

Simple Summary

Cathelicidins are a group of host defense peptides in vertebrates with both antimicrobial and immunomodulatory activities. In the present study, we identified the entire repertoire of the cathelicidin gene family from the forest musk deer genome. Sequence comparison, phylogenetic topology, and gene and genomic organizations collectively suggest that all cathelicidin genes have already been fixed in the genome of forest musk deer before the split of moschidae and bovidae, while independent pseudogenization events have occurred after species divergence. In addition, real-time PCR analysis suggested that all functional cathelicidins play important roles in the immune system. The results of this study will be helpful for further evolutionary and functional studies.

Abstract

The forest musk deer (Moschus berezovskii) is a small-sized artiodactyl species famous for the musk secreted by adult males. In the captive population, this species is under the threat of infection diseases, which greatly limits the increase of individual numbers. In the present study, we computationally analyzed the repertoire of the cathelicidin (CATHL) family from the genome of forest musk deer and investigated their expression pattern by real-time PCR. Our results showed that the entire genome of forest musk deer encodes eight cathelicidins, including six functional genes and two pseudogenes. Phylogenetic analyses further revealed that all forest musk deer cathelicidin members have emerged before the split of the forest musk deer and cattle and that forest musk deer CATHL3L2 and CATHL9 are orthologous with two cattle pseudogenes. In addition, the gene expression results showed that the six functional genes are not only abundantly expressed in the spleen and lung, but are also differently expressed in response to abscesses, which suggests that forest musk deer cathelicidins may be involved in infections. Taken together, identification and characterization of the forest musk deer cathelicidins provide fundamental data for further investigating their evolutionary process and biological functions.

Keywords: cathelicidin, forest musk deer, phylogenetic analysis, expression pattern

1. Introduction

The forest musk deer (Moschus berezovskii), also known as the dwarf musk deer, is a small-sized artiodactyl species that is mainly distributed in the forested and mountainous regions of South-West Asia [1]. As a result of overhunting and habitat destruction in the past, the size of the wild forest musk deer population has been sharply reduced. This species has been listed as a first-class key species of wildlife in the Chinese Wild Animal Protection Law and is listed in the Appendices of Convention on International Trade in Endangered Species of Wild Fauna and Flora, as well as on the International Union for Conservation of Nature’s Red List of Threatened Species [1,2,3]. Since the 1950s, musk deer farming has been widely used to increase the individual numbers of musk deer and provide sustainable musk resources in China [4]. However, restricted by insufficient space and other animals’ natural behavioral needs in the artificial environment, disease is becoming a bottleneck that prevents the increase of captive populations [5,6]. Consequently, understanding immunity, including the genetic information of immune genes, is urgently needed to enhance the disease resistance of forest musk deer.

Host defense peptides (HDPs) comprise a large and diverse group of cationic amphipathic short peptides in virtually all forms of life [7,8,9]. With potent antimicrobial and immunomodulatory activities and many additional functions, HDPs play multifunctional roles in both innate and adaptive immunity [10]. Cathelicidins (CATHLs) are a major family of HDPs that have been found in a large range of species ranging from hagfish to human [11,12,13,14]. Cathelicidins consist of a short signal peptide, a highly conserved cathelin-like domain and a mature peptide usually consisting of fewer than 40 amino acids [15,16]. The number of cathelicidin genes differs greatly between species, with pig, chicken and cattle having multiple cathelicidin family members, whereas only one gene has been found in humans and mice [16,17,18,19]. In addition, the cathelicidin family components in many clades, particularly in cetartiodactyla, are largely diverse in mature peptide structure. For instance, the mature peptide of human cathelicidin is α-helical [18], while the cattle cathelicidin repertoire includes peptides with linear, β-turn and proline-rich structures [20].

Although numerous cathelicidin genes with high diversity have been reported in a large number of phylogenetically divergent species, no information is available regarding the forest musk deer. Fortunately, the recent completion of the musk deer genome [21] has provided an unprecedented opportunity to conduct a genome-wide screening of the forest musk deer cathelicidin gene repertoire. In this study, we identified eight cathelicidin genes from the genome sequences of forest musk deer and systematic analyzed their phylogenetic relationships. Furthermore, we examined the expression of musk deer cathelicidins in four different tissues and compared the mRNA abundance of the functional members in the liver and spleen between healthy musk deer and those who died of abscess disease. Our findings in this work will be helpful in understanding the immunity of the forest musk deer and provide fundamental information for further studies.

2. Materials and Methods

2.1. Discovery of Cathelicidin Genes in the Musk Deer

To identify the entire repertoire of the cathelicidin gene family in the forest musk deer, a genomic identification strategy was conducted by a combination of the hidden Markov model (HMM) and the BLAST program, as we previously described [22]. Briefly, the hidden Markov model file of cathelicidin (accession number: PF00666.16) was downloaded from the Pfam database [23] and then used as a query to search against the predicted protein databases by using the HMMer (V3.1) program with the default settings. All potential hits with both E-values (full sequence and best 1 domain) <0.1 were then extracted and examined for the presence of the characteristic cathelin-like sequence. For every sequence identified, iterative TBLASTN [24,25] searches were conducted in the genome of musk deer (E-value < 10) until no new sequences were identified. The 4000-bp genomic sequences up- and downstream of each identified cathelin-like sequence were extracted from the genome for prediction of the full coding sequence with GeneWise [26] or GeneScan [27].

2.2. Collection of Tissues

The tissue samples, including the muscle from left hind leg, heart, lung, and spleen, were collected from three male captive musk deer died of natural disaster (earthquake of 20 April 2013), and three male captive musk deer died of abscess disease (mainly occurred in the lung). Tissues were cut into small pieces and immediately frozen in liquid nitrogen, and then stored at −80 °C until RNA extraction. These six musk deer ranged from six months to six years old and were raised on a farm at the Chongqing Institute of Medicinal Plant Cultivation. All experiments were approved by the ethics committees of the Chongqing Institute of Medicinal Plant Cultivation and were performed in accordance with the approved guidelines (DXY-S20160907) [28].

2.3. RNA Extraction and Real-Time PCR

Total RNA was extracted with TRIzol (Ambion) from all four tissues, RNA concentrations were measured by Nanodrop, and the first-strand cDNA was synthesized from 300 ng of total RNA using the PrimeScript® RT reagent kit with gDNA eraser (Takara Bio Inc., Dalian, China) according to the manufacturer’s instructions. The integrity of RNA and absence of genomic DNA contamination of were verified as previously described [29,30]. Real-time PCR was conducted to examine the expression of genes, and the gene-specific primers were designed by Primer 5.0 software based on the predicted cathelicidin sequences and the conserved sequences in bovidae (Table 1). The relative expression levels of each cathelicidin gene in different tissues were analyzed using the 2−ΔΔCT method [31], with the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene being employed as the reference gene. Real-time PCR analysis of each sample was repeated in triplicate.

Table 1.

Primer sequences used for real-time PCR analysis.

Gene Forward Primer Reverse Primer Fragment Length (bp) Annealing Temperature (°C)
CATHL1p CTACAGGGACGCCGTGCTTT GGGCTTTCTGGGTCTTCATCAT 120 60
CATHL3L2 CAGAGCAATGTGACTTCAAGGAGA GGTCGTTTAGCCCTGACACTCTG 127 60
CATHL4 CCCGGAGCAGTGTGACTTCAA CTGGTCATTGGACGGGTTCAG 82 60
CATHL5 GGTCGGGAGTAACTTCGACATTAC GGCCATACCTCTTCCAACCAT 101 60
CATHL6 CCAAGGACGATGAGAACCCAA GTCCAGAGTGACTGTCCCCACA 152 60
CATHL7 CCCAGGCCCTCAGCTACAGT CTCACAGGCTTTCGAGCACCA 148 60
CATHL9 GGGGAACTCGAAAGCCTGTGA CACACTGTTTTACCAGCCCATTCT 114 60
GAPDH GCAAGTTCAACGGCACAGTCA CTGGTTCACGCCCATCACAA 249 60
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2.4. Multiple Sequence Alignment and Phylogenetic Analysis

All predicted amino acid sequences of the forest musk deer, as well as the reported amino acid sequences of cattle and sheep, were used for phylogenetic analysis. Sequences were aligned codon-to-codon using the MUSCLE program [32] and visualized with Boxshade (https://embnet.vital-it.ch/software/BOX_form.html). A neighbor-joining tree was constructed in Mega 7.0 [33] by calculating the p-distance among all sequences, and the reliability of each branch was tested by 1000 bootstrap replications.

2.5. Comparison of the CATHL3L2 C-Terminus of the Forest Musk Deer and Cattle

The DNA sequences of cattle CATHL3L2p C-terminus were retrieved from cattle genome (ARS-UCD1.2), and aligned with the corresponding region of the forest musk deer CATHL3L2 by Mega 7.0 [33].

2.6. Statistical Analysis

The expression levels of the cathelicidins between the tissues of healthy and purulent individuals were analyzed using unpaired Student’s t-test in GraphPad Prism 5 (GraphPad Software, La Jolla, CA, USA), p < 0.05 was considered significant between the healthy and purulent groups.

3. Results

3.1. Identification of the Forest Musk Deer Cathelicidin Genes

By using the HMMER program, a total of six sequences (scaffold41.3782, scaffold116.8830, scaffold204.11849, scaffold511.18163, scaffold511.18172, scaffold511.18173) were obtained from the predicted protein data of musk deer with the aforementioned settings. The subsequent confirmation workflows showed that scaffold116.8830 and scaffold204.11849 present secreted phosphoprotein 24 and cystatin domains, respectively, while scaffold511.18172 contains five cathelicidin domains. Therefore, the initial query file of the TBLASTN search contains the full amino acid sequences of scaffold 41.3782, scaffold 511.18163 and scaffold 511.18173, as well as the five sequence segments extracted from scaffold 511.18172, with each sequence containing one cathelicidin domain. In the end, nine genes, including eight cathelicidin genes and one neutrophilic granule protein (NGP) gene, were identified from the forest musk deer genome (Table S1). Subsequently, the eight cathelicidins were designated based on their orthologous relationships with their bovine counterparts.

By aligning the deduced amino acid sequences of the eight forest musk deer cathelicidins (Figure 1), we observed a high level of conservation in the signal peptides and the cathelin-like domains but a large variation in the C-terminal mature peptides. Furthermore, two of the eight cathelicidin genes, termed CATHL1p and CATHL8p, were pseudogenes containing premature stop codons. Moreover, we noticed that CATHL8p was not an intact gene, which only contains the signal peptide and a part of the cathelin-like domain. The absence of the remaining parts of the CATHL8p gene could be caused by pseudogenization followed by sequence degeneration. Alternatively, the CATHL8p gene might have evolved from a partial gene copy event.

Figure 1.

Figure 1

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Multiple sequence alignment of forest musk deer cathelicidins. The positions of four exon boundaries are indicated by vertical lines, and conserved residues are shaded. The predicted C-terminal mature peptides are shown with the lengths and net charges (in parenthesis). The mature peptides of the forest musk deer cathelicidin genes were predicted based on the amino acid alignment of other cathelicidin genes, and the net charge of each mature peptide was estimated by using the on-line software at https://pepcalc.com/.

In an attempt to determine the cationicity of forest musk deer cathelicidins, we predicted the net charge of their deduced mature peptides. As shown in Figure 1, all of these cathelicidin peptides were positively charged due to the presence of an excess number of cationic residues. The net charges of the mature peptides range from 5.0 to 13.1, implying that these molecules are able to interact with the negative charges located on the bacterial surface.

3.2. Phylogenetic Analysis of the Forest Musk Deer Cathelicidins

To reveal the evolutionary relationships of the forest musk deer cathelicidins, a phylogenetic tree was constructed by using the neighbor-joining method together with the reported cathelicidin peptides from the sheep and cattle (File S1). As illustrated in Figure 2, the CATHL1p, CATHL3L2, CATHL4-7, and CATHL9 of the forest musk deer have an orthologous gene in the cattle, which suggests that these genes existed before the split of the cattle and musk deer before 24.6 million years ago [34]. However, the CATHL1p in the forest musk deer is a pseudogene, suggesting that the pseudogenization of the forest musk deer CATHL1 emerged after the species diverged. Interestingly, no sequence of the forest musk deer is located in the same subclade of the bovine CATHL3; instead, together with sheep Bac6, a cathelicidin gene of forest musk deer is clearly clustered with the cattle CATHL9p with a bootstrap value of 70. In addition, supported by a value of 72, the forest musk deer CATHL3L2 also shares the same branch with a pseudogene termed cattle CATHL3L2p. Given that multiple paralogs of CATHL3 exist in the genome of sheep and cattle, our results imply that gene duplication, diversification, pseudogenization, and even gene loss occurred in these three species.

Figure 2.

Figure 2

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Phylogenetic relationships of the forest musk deer cathelicidins. Amino acid sequences of the forest musk deer cathelicidins were compared with sequences from other representative species. The phylogenetic tree was conducted by the neighbor-joining method with bootstrapping (1000 iterations). Only the bootstrap values higher than 50 are shown above branches.

3.3. Comparison of the C-Terminus of the Forest Musk Deer CATHL3L2 and Cattle CATHL3L2p

Although the phylogenetic analysis suggested that forest musk deer CATHL3L2 may be an ortholog of cattle CATHL3L2p, the amino acid comparison of the genes exhibited low similarity in the C-terminus. The previously deduced cattle CATHL3L2p seem to lack a few sequences in the mature peptide [19]. To confirm that the forest musk deer CATHL3L2 is an ortholog of the cattle CATHL3L2p, we analyzed the C-terminal sequences of the cattle CATHL3L2p. As shown in Figure 3, a 28-amino-acid open reading frame was identified from the sequences immediately following the first stop codon of the cattle CATHL3L2p. Furthermore, the deduced amino acid sequences of this open reading frame are almost identical to the corresponding region of the forest musk deer CATHL3L2, which strongly indicates that the two cathelicidins are orthologous genes and that a previously unnoticed premature stop codon is also located in the putative mature peptide of the cattle CATHL3L2p.

Figure 3.

Figure 3

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Sequence comparison of C-terminal sequences of CATHL3L2 from the forest musk deer (Mb) cattle (Bt). Identical amino acids are shadowed, and the asterisk represents the termination codon. The nucleotide position that caused the pseudogenization of the cattle CATHL3L2 was boxed.

3.4. Gene and Genome Organization of the Forest Musk Deer Cathelicidin Gene Family

To evaluate the gene structure of the forest musk deer cathelicidins, we compared the deduced amino acid sequences with the genomic sequence data. Similar to cathelicidin genes in other species [17,19], the coding sequence of each functional forest musk deer cathelicidin gene consists of four exons separated by three introns (Table 2), suggesting a high conservation of gene structure in cathelicidins.

Table 2.

Gene and genomic organizations of forest musk deer cathelicidins.

Gene Scaffold Gene Size (bp) 1
E 1 I 1 E 2 I 2 E 3 I 3 E 4
CATHL1p Scaffold41 198 115 107 150 72 561 117
CATHL3L2 Scaffold511 198 624 108 157 72 602 171
CATHL4 Scaffold511 198 106 108 137 72 603 66
CATHL5 Scaffold511 201 611 108 163 72 597 102
CATHL6 Scaffold511 201 614 108 139 72 600 99
CATHL7 Scaffold41 201 620 108 154 72 600 117
CATHL8p Scaffold511 198 579 108 NA NA NA NA
CATHL9 Scaffold511 198 623 108 165 72 601 111
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1 Each intact cathelicidin gene consists of four exons (E) separated by three introns (I). The sizes of the exons were predicted based on the deduced amino acid sequences.

Coupled with the cattle, we strategically analyzed the genomic structure of the forest musk deer cathelicidins. As illustrated in Figure 4, the forest musk deer cathelicidins are clustered densely in the chromosomal region, although they are located in two different scaffolds. Additionally, we noticed that the gene order and orientation of all the forest musk deer cathelicidin genes, including the functional genes and pseudogenes, are highly conserved in the cattle. Together with the phylogenetic relationship, these observations suggested that both the functional genes and pseudogenes already existed in the forest musk deer before the divergence of the forest musk deer and cattle, while no allele comprising duplicate genes has been fixed in the forest musk deer genome since 24.6 million years ago [34].

Figure 4.

Figure 4

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Genomic organization of the cathelicidin clusters in the cattle and forest musk deer. The position and transcriptional direction of each gene are represented by arrows. The solid arrows refer to functional genes, whereas open arrows refer to pseudogenes. A broken line in a gene cluster is an indication of a gap in the genomic DNA sequence. The orthologous genes are linked using solid lines, and paralogous genes are connected with dashed lines.

3.5. Tissue Expression Pattern of Forest Musk Deer Cathelicidins

As summarized in Figure 5, all six functional forest musk deer cathelicidins were ubiquitously expressed in all examined tissues from healthy animals, with the lowest expression level being observed in the leg muscle and relatively more abundant expression being detected in the other three tissues. The relatively higher mRNA levels in the spleen and lung indicated that cathelicidins might play critical roles in the immunity of forest musk deer. As expected, the expression of CATHL1p could not be detected in any of the tissues, which strongly suggests that CATHL1p is a pseudogene instead of a null allele in the forest musk deer (data not shown). At the same time, the detection of CATHL3L2 and CATHL9 within the cDNA of these tissues evidently suggests that they are functional genes in the forest musk deer.

Figure 5.

Figure 5

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Relative expression levels of functional cathelicidin (CATHL) genes in forest musk deer. The expression levels of the forest musk deer cathelicidins were calculated relative to that of CATHL3L2 using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a reference gene. The color elements represent average log2 ratios of fold change from three samples.

We further compared the transcript abundance of cathelicidin genes in the liver and spleen between healthy musk deer and those who died of abscess disease. The expression patterns of the six cathelicidins were all upregulated in these two tissues from purulent forest musk deer, except for CATHL4 in the lung (Figure 6). The marked expression patterns of cathelicidins between the two types of tissues suggest a possible involvement of musk deer cathelicidins in the immune response to abscesses.

Figure 6.

Figure 6

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Comparison of the relative expression levels of cathelicidins in spleen (A) and lung (B) of healthy and purulent individuals. The relative gene expression was measured by real-time PCR using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a reference gene. The bars represent the means ± standard error of mean (SEM). Differences between the healthy and purulent groups were determined by an unpaired Student’s two-tailed t-test, and * indicates p < 0.05.

4. Discussion

Although multiple cathelicidin peptides with a large range of structures have been characterized in cetartiodactyla, limited sequences can be retrieved from species other than food animals. In the present study, we reported the repertoire of forest musk deer cathelicidin genes for the first time. The results of sequence alignment, neighbor-joining tree and genomic structure collectively suggested that all of the cathelicidin genes in the forest musk deer, including the pseudogenes, have already emerged before the divergence of moschidae and bovidae. Similar to previous reports [19,35], the phylogenetic analysis performed in the present study indicated that a series of genes that have high similarity to CATHL3 are located in the cattle, sheep, and forest musk deer. In addition, we observed independent pseudogenization in the genomes of cattle and forest musk deer. In other words, CATHL1 lost its function in the forest musk deer, while the orthologous genes of forest musk deer CATHL3L2 and CATHL9 became pseudogenes in the cattle. For the CATHL8p, a two-exon pseudogene identified both from the forest musk deer and cattle is highly likely to have been fixed in the genome before the two species diverged. However, because only the forest musk deer CATHL8p contains a premature stop codon and the two genes are not clustered in the same subclade, we cannot exclude a pseudogenization or partial gene copy event that may have independently occurred in the genome of cattle and forest musk deer. Further genomic investigations in other species are needed to provide detailed evolutionary processes. Given the high sequence similarity presented among the CATHL3 paralogs, we speculated that the pseudogenization of some cathelicidin genes might be caused by functional redundancy. Interestingly, we noticed that the first intron of CATHL1p and CATHL4 are approximately 110 bp in length (Table 2), which are considerably shorter than the others. Along with the close location of these genes in the genome, these findings suggest that CATHL1 and CATHL4 have closely phylogenetic relationships and might diverge from a common ancestor. However, the mature peptides of CATHL1 and CATHL4 share a low level of similarity, while both topology of the phylogenetic tree in this research, as well as in other studies [19], indicate that CATHL1 tends to be grouped with CATHL5, and CATHL4 shares more similarity with CATHL2. It has been suggested that in addition to amino acid substitutions driven by positive selection, multiple kinds of evolutionary processes may be involved in the emergence of the distinct cathelicidin subfamilies [36]. For instance, both the protegrins and prophenins in pigs are evolved from a proline-arginine-rich cathelicidin peptide by sequence insertion and internal repeat [37]. It would be particularly interesting to unravel the process that diversified the forest musk deer cathelicidins after gene duplication by using new strategies.

In accordance with previous studies [19], relatively abundant transcripts of many cathelicidin mRNA were detected in the spleen and lung of forest musk deer by RT-PCR. However, we noticed that the expression of cattle CATHL3 and forest musk deer CATHL3L2 are largely different. The cattle CATHL3 was not reliably detected in the spleen [19], whereas a strong expression of CATHL3L2 was detected in the spleen of forest musk deer. This result could be attributed to the phylogenetic relationship of CATHL3s in these two species. As suggested in this research, the two genes are paralogs instead of orthologs, although they may have been duplicated from a common ancestor. However, given that the samples used for tissue expression analysis were obtained from three individuals that died of natural disasters of different ages and that the mRNA abundance of cathelicidins could be influenced by the living environment, we cannot exclude the possibility that the abundant expression level of CATHL3L2 in the spleen of forest musk deer is due to raising conditions, as well as other factors. Therefore, additional evidence is needed to confirm our observations in the future. On the other hand, our results showed that the expression of CATHL4 is decreased in the purulent lung, which was the opposite of the trend observed for the other five cathelicidins. Because several bacterial pathogens have evolved the ability to downregulate HDP expression to better establish themselves in the host [38], the downregulation of CATHL4 in the lung might be derived from the same mechanism.

Multiple studies have suggested that abscesses are the most prevalent causes of death in the captive population of forest musk deer [6,39,40]. As a widespread and common practice aiming to fight against infection, antibiotics have been routinely used in this species for decades. As a result, bacteria with antibiotic resistance genes have also been identified from captive forest musk deer. For instance, Arcanobacterium pyogenes, an opportunistic pathogen that is capable of causing surface or internal abscesses, has been found to have high rates of resistance to β-lactams or trimethoprim in the Miyaluo forest musk deer farm [6]. Alternatives to antibiotics are therefore urgently needed to ensure health and minimize the development of antimicrobial resistance in forest musk deer. Given that HDPs exert pleiotropic effects on both innate and adaptive immune responses, they are being developed into drugs that not only act directly against pathogens but also boost the immune system in unique ways [41]. In addition, because the cationicity of HDPs allows them to blind and kill negatively charged microorganisms through disruption of cell membranes and interaction with intracellular macromolecules, it is very difficult for microbes to develop resistance to HDPs [42]. Although lacking conceivable evidence on the antimicrobial and immune regulatory activities of the forest musk deer cathelicidin peptides, a large number of their orthologous and paralogous peptides from cattle and sheep have been found to be active against microorganisms and to possess immunomodulation activity [43,44]. The peptides thus appear to have the ability to be developed as antimicrobial agents to treat purulent diseases, as well as to combat the growing threat from antimicrobial resistance in captive populations. Alternatively, natural compounds that have the ability to boost endogenous cathelicidin synthesis may also provide a strategy for fighting infectious diseases and alleviating the negative effects caused by the use of antibiotics [45,46,47,48,49,50]. Further exploration of the in vivo and in vitro activities of these peptides may lead to better utilization of these peptides for therapeutic use.

5. Conclusions

In conclusion, we identified six functional genes and two pseudogenes from the forest musk deer genome for the first time. Evolutionary analyses indicated that all eight genes have already been fixed in the genome of forest musk deer before the split of moschidae and bovidae, and independent pseudogenization events have occurred after species divergence. On the other hand, the results of sequence comparison, net charge and expression pattern analyses showed a crucial role of forest musk deer cathelicidins in the immune system. These results have a potential application to combat infections with a low risk of developing resistance. This study increased our understanding of the cathelicidins and will be useful for further genetic studies, as well as for the discovery of novel antimicrobial agents in the future.

Supplementary Materials

The following are available online at https://www.mdpi.com/2076-2615/9/8/481/s1, Table S1: Locations and orientations of the forest musk deer cathelicidin genes, File S1: Sequence alignments of the cathelicidins used to create the neighbor-joining tree.

Click here for additional data file. (8.8KB, zip)

Author Contributions

Conceptualization, L.Z., C.Z., and W.B.; methodology, L.Z., H.J., and Y.X.; validation, L.Z., H.J., and W.B.; formal analysis, L.Z., Y.X., and W.L.; resources, H.J.; writing—original draft preparation, L.Z. and W.B.; writing—review and editing, L.Z., C.Z., and W.B.; project administration, L.Z., H.J., C.Z., and W.B.; funding acquisition, L.Z., H.J., C.Z., and W.B.

Funding

This research was funded by the Department of Science and Technology of Sichuan Province, grant number 2019YJ0338; the Doctoral Scientific Research Funds of China West Normal University, grant number 17E077 and 17E074; the Fundamental Research Funds of China West Normal University, grant number 18B030 and CXTD2017-4; and the Chongqing Research Program of Basic Research and Frontier Technology, grant number cstc2018jcyjAX0238.

Conflicts of Interest

The authors declare no conflict of interest.

References

  • 1.Gang Y., Wang B.B. Low population density of the endangered forest musk deer, Moschus berezovskii, in China. Pak. J. Zool. 2015;47:325–333. [Google Scholar]
  • 2.Guha S., Goyal S., Kashyap V. Molecular phylogeny of musk deer: A genomic view with mitochondrial 16S rRNA and cytochrome b gene. Mol. Phylogenet. Evol. 2007;42:585–597. doi: 10.1016/j.ympev.2006.06.020. [DOI] [PubMed] [Google Scholar]
  • 3.Zhou C., Zhang W., Wen Q., Bu P., Gao J., Wang G., Jin J., Song Y., Sun X., Zhang Y., et al. Comparative Genomics Reveals the Genetic Mechanisms of Musk Secretion and Adaptive Immunity in Chinese Forest Musk Deer. Genome Boil. Evol. 2019;11:1019–1032. doi: 10.1093/gbe/evz055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Meng X., Gong B., Ma G., Xiang L. Quantified Analyses of Musk Deer Farming in China: A Tool for Sustainable Musk Production and Ex situ Conservation. Asian Australas. J. Anim. Sci. 2011;24:1473–1482. doi: 10.5713/ajas.2011.11111. [DOI] [Google Scholar]
  • 5.Lv X.-H., Qiao J.-Y. A Review of Mainly Affected on Musk-Deer Diseases: Purulent, Respiratory System and Parasitic Diseases. J. Econ. Anim. 2009;13:104–106. [Google Scholar]
  • 6.Zhao K.-L., Wang H.-N., Yue B.-S., Liu Y., Zhang X.-Y., Palahati P. Detection and characterization of antibiotic-resistance genes in Arcanobacterium pyogenes strains from abscesses of forest musk deer. J. Med. Microbiol. 2011;60:1820–1826. doi: 10.1099/jmm.0.033332-0. [DOI] [PubMed] [Google Scholar]
  • 7.Ganz T. Defensins: Antimicrobial peptides of vertebrates. C. R. Boil. 2004;327:539–549. doi: 10.1016/j.crvi.2003.12.007. [DOI] [PubMed] [Google Scholar]
  • 8.Thomma B.P., Cammue B.P. Plant defensins. Planta. 2002;216:193–202. doi: 10.1007/s00425-002-0902-6. [DOI] [PubMed] [Google Scholar]
  • 9.Yu L.-T., Xiao Y.-P., Li J.-J., Ran J.-S., Yin L.-Q., Liu Y.-P., Zhang L. Molecular characterization of a novel ovodefensin gene in chickens. Gene. 2018;678:233–240. doi: 10.1016/j.gene.2018.08.029. [DOI] [PubMed] [Google Scholar]
  • 10.Hilchie A.L., Wuerth K., Hancock R.E.W. Immune modulation by multifaceted cationic host defense (antimicrobial) peptides. Nat. Methods. 2013;9:761–768. doi: 10.1038/nchembio.1393. [DOI] [PubMed] [Google Scholar]
  • 11.Uzzell T., Stolzenberg E.D., E Shinnar A., Zasloff M. Hagfish intestinal antimicrobial peptides are ancient cathelicidins. Peptides. 2003;24:1655–1667. doi: 10.1016/j.peptides.2003.08.024. [DOI] [PubMed] [Google Scholar]
  • 12.Agerberth B., Gunne H., Odeberg J., Kogner P., Boman H.G., Gudmundsson G.H. FALL-39, a putative human peptide antibiotic, is cysteine-free and expressed in bone marrow and testis. Proc. Natl. Acad. Sci. USA. 1995;92:195–199. doi: 10.1073/pnas.92.1.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Zhao H., Gan T.-X., Liu X.-D., Jin Y., Lee W.-H., Shen J.-H., Zhang Y. Identification and characterization of novel reptile cathelicidins from elapid snakes. Peptides. 2008;29:1685–1691. doi: 10.1016/j.peptides.2008.06.008. [DOI] [PubMed] [Google Scholar]
  • 14.Ishige T., Hara H., Hirano T., Kono T., Hanzawa K. Characterization of the cathelicidin cluster in the Japanese quail (Coturnix japonica) Anim. Sci. J. 2017;88:1249–1257. doi: 10.1111/asj.12752. [DOI] [PubMed] [Google Scholar]
  • 15.Zanetti M. Cathelicidins, multifunctional peptides of the innate immunity. J. Leukoc. Biol. 2004;75:39–48. doi: 10.1189/jlb.0403147. [DOI] [PubMed] [Google Scholar]
  • 16.Kosciuczuk E.M., Lisowski P., Jarczak J., Strzałkowska N., Jozwik A., Horbańczuk J.O., Krzyżewski J., Zwierzchowski L., Bagnicka E. Cathelicidins: Family of antimicrobial peptides. A review. Mol. Boil. Rep. 2012;39:10957–10970. doi: 10.1007/s11033-012-1997-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Xiao Y., Cai Y. Identification and functional characterization of three chicken cathelicidins with potent antimicrobial activity. J. Biol. Chem. 2006;281:2858–2867. doi: 10.1074/jbc.M507180200. [DOI] [PubMed] [Google Scholar]
  • 18.Zelezetsky I., Pontillo A. Evolution of the primate cathelicidin. Clin. Microbiol. Infect. Suppl. 2005;11:83–84. [Google Scholar]
  • 19.Whelehan C.J., Barry-Reidy A., Meade K.G., Eckersall P.D., Chapwanya A., Narciandi F., Lloyd A.T., O’Farrelly C. Characterisation and expression profile of the bovine cathelicidin gene repertoire in mammary tissue. BMC Genom. 2014;15:128. doi: 10.1186/1471-2164-15-128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Young-Speirs M., Drouin D., Cavalcante P.A., Barkema H.W., Cobo E.R. Host defense cathelicidins in cattle: Types, production, bioactive functions and potential therapeutic and diagnostic applications. Int. J. Antimicrob. Agents. 2018;51:813–821. doi: 10.1016/j.ijantimicag.2018.02.006. [DOI] [PubMed] [Google Scholar]
  • 21.Fan Z., Li W., Jin J., Cui K., Yan C., Peng C., Jian Z., Bu P., Price M., Zhang X., et al. The draft genome sequence of forest musk deer (Moschus berezovskii) GigaScience. 2018;7:1–6. doi: 10.1093/gigascience/giy038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Zhang L., Chen D., Yu L., Wei Y., Li J., Zhou C. Genome-wide analysis of the ovodefensin gene family: Monophyletic origin, independent gene duplication and presence of different selection patterns. Infect. Genet. Evol. 2019;68:265–272. doi: 10.1016/j.meegid.2019.01.001. [DOI] [PubMed] [Google Scholar]
  • 23.El-Gebali S., Mistry J., Bateman A., Eddy S.R., Luciani A., Potter S.C., Qureshi M., Richardson L.J., A Salazar G., Smart A., et al. The Pfam protein families database in 2019. Nucleic Acids Res. 2018;47:D427–D432. doi: 10.1093/nar/gky995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Altschul S.F., Gish W. Basic local alignment search tool. J. Mol. Biol. 1990;215:403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  • 25.Yan H., Zhang L., Guo Z., Zhang H., Liu J. Production Phase Affects the Bioaerosol Microbial Composition and Functional Potential in Swine Confinement Buildings. Animals. 2019;9:90. doi: 10.3390/ani9030090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Birney E., Clamp M. GeneWise and Genomewise. Genome Res. 2004;14:988–995. doi: 10.1101/gr.1865504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Burge C.B., Karlin S. Finding the genes in genomic DNA. Curr. Opin. Struct. Biol. 1998;8:346–354. doi: 10.1016/S0959-440X(98)80069-9. [DOI] [PubMed] [Google Scholar]
  • 28.Chen M., Jie H., Xu Z., Ma T., Lei M., Zeng D., Zhao G., Feng X., Zheng C., Zhang C., et al. Isolation, primary culture, and morphological characterization of gland epithelium from forest musk deer (Moschus berezovskii) Vitr. Cell. Dev. Boil. Anim. 2018;54:545–548. doi: 10.1007/s11626-018-0268-0. [DOI] [PubMed] [Google Scholar]
  • 29.Yan H., Cao S., Li Y., Zhang H., Liu J. Reduced meal frequency alleviates high-fat diet-induced lipid accumulation and inflammation in adipose tissue of pigs under the circumstance of fixed feed allowance. Eur. J. Nutr. 2019:1–14. doi: 10.1007/s00394-019-01928-3. [DOI] [PubMed] [Google Scholar]
  • 30.Liu J., Zhang Y., Li Y., Yan H., Zhang H. L-tryptophan Enhances Intestinal Integrity in Diquat-Challenged Piglets Associated with Improvement of Redox Status and Mitochondrial Function. Animals. 2019;9:266. doi: 10.3390/ani9050266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Livak K.J., Schmittgen T.D. Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods. 2001;25:402–408. doi: 10.1006/meth.2001.1262. [DOI] [PubMed] [Google Scholar]
  • 32.Edgar R.C. MUSCLE: Multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004;32:1792–1797. doi: 10.1093/nar/gkh340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Kumar S., Stecher G., Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol. Boil. Evol. 2016;33:1870–1874. doi: 10.1093/molbev/msw054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Hedges S.B., Marin J., Suleski M., Paymer M., Kumar S. Tree of Life Reveals Clock-Like Speciation and Diversification. Mol. Boil. Evol. 2015;32:835–845. doi: 10.1093/molbev/msv037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Sang Y., Ortega M.T., Rune K., Xiau W., Zhang G., Soulages J.L., Lushington G.H., Fang J., Williams T.D., Blecha F. Canine cathelicidin (K9CATH): Gene cloning, expression, and biochemical activity of a novel pro-myeloid antimicrobial peptide. Dev. Comp. Immunol. 2007;31:1278–1296. doi: 10.1016/j.dci.2007.03.007. [DOI] [PubMed] [Google Scholar]
  • 36.Zhu S. Did cathelicidins, a family of multifunctional host-defense peptides, arise from a cysteine protease inhibitor? Trends Microbiol. 2008;16:353–360. doi: 10.1016/j.tim.2008.05.007. [DOI] [PubMed] [Google Scholar]
  • 37.Zhu S., Gao B. A fossil antibacterial peptide gives clues to structural diversity of cathelicidin-derived host defense peptides. FASEB J. 2009;23:13–20. doi: 10.1096/fj.08-114579. [DOI] [PubMed] [Google Scholar]
  • 38.Islam D., Bandholtz L., Nilsson J., Wigzell H., Christensson B., Agerberth B., Gudmundsson G.H. Downregulation of bactericidal peptides in enteric infections: A novel immune escape mechanism with bacterial DNA as a potential regulator. Nat. Med. 2001;7:180–185. doi: 10.1038/84627. [DOI] [PubMed] [Google Scholar]
  • 39.Sun X., Cai R., Jin X., Shafer A.B.A., Hu X., Yang S., Li Y., Qi L., Liu S., Hu D. Blood transcriptomics of captive forest musk deer (Moschus berezovskii) and possible associations with the immune response to abscesses. Sci. Rep. 2018;8:599. doi: 10.1038/s41598-017-18534-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Zhao W., Tian Q., Luo Y., Wang Y., Yang Z.-X., Yao X.-P., Cheng J.-G., Zhou X., Wang W.-Y. Isolation, identification, and genome analysis of lung pathogenic klebsiella pneumoniae (lpkp) in forest musk deer. J. Zoo Wildl. Med. 2017;48:1039–1048. doi: 10.1638/2016-0241.1. [DOI] [PubMed] [Google Scholar]
  • 41.Ashby M., Petkova A. Cationic antimicrobial peptides as potential new therapeutic agents in neonates and children: A review. Curr. Opin. Infect. Dis. 2014;27:258–267. doi: 10.1097/QCO.0000000000000057. [DOI] [PubMed] [Google Scholar]
  • 42.Brogden K.A. Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria? Nat. Rev. Genet. 2005;3:238–250. doi: 10.1038/nrmicro1098. [DOI] [PubMed] [Google Scholar]
  • 43.Baumann A., Kiener M.S., Haigh B., Perreten V., Summerfield A. Differential Ability of Bovine Antimicrobial Cathelicidins to Mediate Nucleic Acid Sensing by Epithelial Cells. Front. Immunol. 2017;8:173. doi: 10.3389/fimmu.2017.00059. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Shamova O., Brogden K.A., Zhao C., Nguyen T., Kokryakov V.N., Lehrer R.I., McGhee J.R. Purification and Properties of Proline-Rich Antimicrobial Peptides from Sheep and Goat Leukocytes. Infect. Immun. 1999;67:4106–4111. doi: 10.1128/iai.67.8.4106-4111.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Robinson K., Ma X., Liu Y., Qiao S., Hou Y., Zhang G. Dietary modulation of endogenous host defense peptide synthesis as an alternative approach to in-feed antibiotics. Anim. Nutr. 2018;4:160–169. doi: 10.1016/j.aninu.2018.01.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Cai S., Qiao X., Feng L., Shi N., Wang H., Yang H., Guo Z., Wang M., Chen Y., Wang Y., et al. Python Cathelicidin CATHPb1 Protects against Multidrug-Resistant Staphylococcal Infections by Antimicrobial-Immunomodulatory Duality. J. Med. Chem. 2018;61:2075–2086. doi: 10.1021/acs.jmedchem.8b00036. [DOI] [PubMed] [Google Scholar]
  • 47.Feng F., Chen C., Zhu W., He W., Guang H., Li Z., Wang D., Liu J., Chen M., Wang Y., et al. Gene cloning, expression and characterization of avian cathelicidin orthologs, Cc-CATHs, from Coturnix coturnix. FEBS J. 2011;278:1573–1584. doi: 10.1111/j.1742-4658.2011.08080.x. [DOI] [PubMed] [Google Scholar]
  • 48.Liu J.B., Yan H.L., Zhang Y., Hu Y.D., Zhang H.F. Effects of dietary energy and protein content and lipid source on growth performance and carcass traits in Pekin ducks. Poult. Sci. 2019 doi: 10.3382/ps/pez217. [DOI] [PubMed] [Google Scholar]
  • 49.Xue P., Cao S., Chen L., Zhang H., Liu J. Effects of dietary phosphorus concentration and body weight on postileal phosphorus digestion in pigs. Anim. Feed. Sci. Technol. 2018;242:86–94. [Google Scholar]
  • 50.Yan H., Cao S., Zhang H., Liu J., Liu J. Effect of feed intake level on the determination of apparent and standardized total tract digestibility of phosphorus for growing pigs. Anim. Feed. Sci. Technol. 2018;246:137–143. [Google Scholar]

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