key: cord-0760654-29ohzeug
authors: Chen, Xiaolan; Ali Abdalla, Bahareldin; Li, Zhenhui; Nie, Qinghua
title: Epigenetic Regulation by Non-Coding RNAs in the Avian Immune System
date: 2020-08-12
journal: Life (Basel)
DOI: 10.3390/life10080148
sha: b6539c2cb63a332c963646e6645a720e5fa2a461
doc_id: 760654
cord_uid: 29ohzeug

The identified non-coding RNAs (ncRNAs) include circular RNAs, long non-coding RNAs, microRNAs, ribosomal RNAs, small interfering RNAs, small nuclear RNAs, piwi-interacting RNAs, and transfer RNAs, etc. Among them, long non-coding RNAs, circular RNAs, and microRNAs are regulatory RNAs that have different functional mechanisms and were extensively participated in various biological processes. Numerous research studies have found that circular RNAs, long non-coding RNAs, and microRNAs played their important roles in avian immune system during the infection of parasites, virus, or bacterium. Here, we specifically review and expand this knowledge with current advances of circular RNAs, long non-coding RNAs, and microRNAs in the regulation of different avian diseases and discuss their functional mechanisms in response to avian diseases.

About 1% of the mammalian genome has the potential to encode proteins, which means a huge amount of non-coding RNAs (ncRNAs) exist in mammalian transcripts [1] . The huge amount of ncRNAs indicated that they are very important biological molecules in epigenetic regulation. Although the current studies on ncRNAs are not elaborate, its important functions for various biological processes have been discovered, especially its extensive roles in different kind of diseases. As a pillar of the economy and people's livelihood, poultry industry becomes important for our life, the meat and egg of chicken is directly associated with the human health. But the threat of disease infection to poultry farming has never been absent, which means it requested from us to develop the poultry host immunity to prevent the infection of avian diseases. Many factors have an impact on the chicken innate and acquired immunity, such as environment, nutrition, and genetics. As the most complicated factor, genetics has its special power to improve the host defense. Genetic improvement is the most effective strategy to deal with disease invasion, and is a complex biological process of multilevel regulation, in which ncRNAs played their unique role. Numerous studies have been conducted on ncRNAs analysis in avian diseases; therefore, summarizing the roles of ncRNAs in the regulation of avian immunity is helpful for us to investigate the new potential function of ncRNAs in avian immunity.

The classical recognition of ncRNAs is that they are the products of genome DNA transcription but they lack the ability to encode a functional protein [2] . However, with the continuous development of the technology of high-throughput sequencing, the implementation of ribosome sequencing (Ribo-Seq) has given the evidence that most of the ncRNAs can be bound to ribosome, especially the large Circular RNAs are special endogenous ncRNA molecules that contain a closed loop structure. Previously, we knew that the majority of identified circRNAs were from only exonic region or only intronic region or both exonic and intronic region, and relatively fewer circRNAs produced by intergenic regions, antisense transcripts of known transcripts, untranslated regions (UTRs), and other regions in eukaryotes [25] . So circRNAs are mainly classified in exonic circular RNA (eciRNA), intronic circular RNA (ciRNA), and exon-intron circular RNA (EIciRNA). But recently, circRNAs from mitochondria DNA were newly investigated, this kind of circRNA was called mecciRNAs [26] . Because circRNAs have no free 5 cap and 3 poly A tail, it makes them not easily degraded by RNase. Sometimes, they are more stable than other RNAs and even expressed more abundantly than parental gene in eukaryotes [27] . As a kind of stably existing RNA, several circRNA functional mechanisms have been investigated, such as acting as miRNA sponges [28] (Figure 1g ), interacting with RNA binding protein (RBP) [29, 30] (Figure 1h ) and translating to a functional peptide (Figure 1i ) [31, 32] . Among them, circRNA as miRNA sponge is the most well studied. It is presented that circRNAs have a certain amount of miRNA biding cites and could arrest miRNA and then release miRNA targets [33] . The interaction with RBP makes circRNAs possess various regulatory functions. For instance, circRNA interacts with small nuclear ribonucleoprotein U1 subunit (U1 snRNP) in the nucleus to regulate the transcript of RNA [34] ; circRNA binds to eukaryotic initiation factor 4E (eIF4E) and eukaryotic initiation factor 4G (eIF4G) to regulate the translation of mRNA [29] ; quaking (QKI) protein interacts with the pre-mRNA of gene and promotes the biogenesis of circRNA [35] ; methylation-related protein-YTH N6-methyladenosine RNA binding protein 2 (YTHDF2) interacts with circRNA and activates the m(6)A-induced degradation of circRNA [30] . As the most novel functional mechanism, circRNA translation was mainly discovered in circRNA which has internal ribosome entry site (IRES) or m6A modification [36] . IRES allows direct recruitment of initiation factors and ribosomes on the RNA and initiates the circRNA translation through cap-independent manner [37, 38] . It is discovered that some endogenous circRNAs that have m (6) A motifs have the ability to translate and the abundance of m (6) A motifs could affect the translation efficiency of circRNA [36] . However, it requires the involvement of eukaryotic translation initiation factor 4 gamma 2 (eIF4G2) and m (6) A reader YTH N6-methyladenosine RNA binding protein 3 (YTHDF3) and will be affected by other m (6) A modification-related proteins. It can be enhanced by methyltransferase like 3/14 (METTL3/14) and suppressed by demethylase FTO [36] .

miRNAs are a class of small ncRNAs that were~22 nucleotides in length. The classical role of miRNA is binding to the 3 UTR (Figure 1j ) of the mRNAs and then induce the degradation of mRNA or inhibit the translation of mRNA [39] . Notably, at the RNA world, miRNA plays a key role in the whole ncRNA regulatory network. It becomes the central of the ceRNA network and could bind lncRNAs/circRNAs with mRNAs as both circRNAs and lncRNAs have the miRNA response element (MRE site) and could act as a miRNA sponge [28] . LncRNA/circRNA-miRNA-mRNA axis is a powerful regulatory mechanism and was extensively investigated in various biological process of different species. With the deep study of molecular biology, miRNA was given several new functions. First, it could regulate the expression of circRNA by recruiting Argonaute (AGO) protein to interact with circRNA ( Figure 1k ). For instance, miR-671 regulates the production of a circCDR1 via cleaving the CDR1 antisense transcript in an Ago2-mediated manner [40] . miRNA-1224 negatively regulates circRNA-Filip1l expression through binding and splicing pre-circRNA-Filip1l, which also requires the Ago2 protein [41] . Additionally, the m7G methylation of miRNA showed another functional mechanism of miRNA. It is evidenced that the m7G methylation of let-7 miRNA induced by methyltransferase like 1 (METTL1) could regulate the process of lung cancer [42] . Moreover, it was investigated that some pri-miRNAs in plants have the ability to encode a peptide (Figure 1l ) that is termed as miRNA-encoded peptide (miPEP). The translation of the pri-miRNAs leads to the accumulation of their corresponding miRNAs, then causing the downregulation of miRNA targets. For instance, pri-miR-171b in Medicago truncatula (M. truncatula) contains two ORFs, ORF1 and ORF2; ORF1 could encode functional peptide, termed as miPEP171b. The overexpression of miPEP171b or the application of a synthetic miPEP171b could increase the abundance of miR-171b [43] . Similar functional mechanism was found in other pri-miRNAs, such as miR-160b, miR-164a, miR-169d, miR-171e, miR-319a, and miR-165a in M.truncatula or Arabidopsis thaliana (A. thaliana) [43, 44] . Lastly, miRNA-derived sequences that are identical with pre-miRNAs could regulate lncRNA splicing through overlapping the pre-transcript of lncRNA ( Figure 1m ). Specifically, hsa-miR-99b regulates the splicing of the primary transcript of LINC01129 through complementary combination with its exon-intron junction [45] . In spite of the underlying mechanisms of those newly identified miRNA functions warrant further analysis, these novel functions provided us the new area to study the potential role of miRNAs.

The important roles of lncRNAs, circRNAs, and miRNAs in regulating the pathogenicity of many diseases have been mainly discovered in humans. The critical roles of ncRNAs in avian inflammation and autoimmune regulation were also investigated. This review sheds light on the regulatory mechanism of lncRNAs, circRNAs, and miRNAs on chicken immunity and be helpful for identifying potential ncRNA biomarkers for avian diseases

Avian invasion diseases are mainly caused by parasites, viruses, or bacterial infections. They infect chickens by specific manners and cause serious damage to chicken organs, thus influencing livability and body health of chickens. The direct consequence of this damage is the decrease of egg and meat production, which can bring huge financial losses to the poultry industry. According to the research progress on ncRNAs, we selected the related diseases researches in avian to summarize here. 

Avian leukosis virus (ALV) is a retrovirus belonging to a retroviridae family. ALV includes seven subgroups of A, B, C, D, E, J, and K, among which, ALV-J is the most pathogenic subgroup with high transmission and pathogenicity [46, 47] . The clinical manifestation of ALV-J-infected chicken including pathogenic tumors, immune tolerance, delayed growth and also higher susceptibility to a secondary infection [46, 48] .

Several studies have been focused on the expression profile and the molecular regulatory mechanisms of circRNAs during the infection of ALV. Thousands of circRNAs were identified in various types of ALV-infected organs, and the number of differentially expressed circRNAs (DEcircRNAs) are calculated, ranges from dozens to thousands [49] [50] [51] [52] . Gene ontology (GO) term and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that the DEcircRNAs were involved in immune-related GO items and KEGG pathways. Main GO terms include regulation of B-cell activation [49] , B-cell differentiation [49, 50] , alpha-beta T-cell activation [49] , and main KEGG pathways have signaling pathways of mTOR [49, 50] , TGF-beta [50] , Toll-like receptor [50] , RIG-I-like receptor [50] , Jak-STAT [50] , Insulin [50] and ErbB [50] , MAPK [52] , Wnt [52] , and B-cell receptor [52] . Many circRNA-miRNA-mRNA ceRNA networks were characterized [49] [50] [51] [52] . Even through so many circRNAs were identified, only few circRNAs were validated for their localization or functional mechanism. One exon-intron DEcircRNA, circHRH4 localizes in cytoplasm and was abundantly expressed in different chicken tissues and cells [50] . circ-Vav3 can interact with miR-375 and upregulate the expression of yes-associated protein 1 (YAP1), a target gene of miR-375. circ-Vav3/miR-375/YAP1 axis participated in tumorigenesis through activating epithelial-mesenchymal transition (EMT) by altering the expression of EMT markers, including Vimentin, zinc finger E-box binding homeobox 1 (ZEB1), matrix metallopeptidase 2 (MMP2), N-cadherin, Fibronectin, and E-cadherin [51] .

As we know from the current research process, the role of circRNAs related to the infection of ALV largely remain on the early stage of the characterization, expression profile, and associated pathways. Only a few researches have explored the single circRNA molecular function in response to the ALV-infection, which inspired us to study the specific functional mechanism of single circRNA in regulating ALV-infection.

Similar to circRNA, a few researches have been focused on the lncRNA expression during ALV infections. RNA-seq had been performed on both chicken tissues and cells to screen the ALV-associated lncRNAs. For instance, differentially expressed lncRNAs (DElncRNAs), differentially expressed miRNAs (DEmiRNAs), and differentially expressed mRNAs (DEmRNAs) between infected and non-infected tissues [53, 54] , chick embryo fibroblasts cells (CEF cells) [55] or chicken primary monocyte-derived macrophages (MDMs) [56] , were identified. Some important immune-related pathways were enriched, including Toll-like receptor, NODlike receptor, RIG-I receptor, and JAK-STAT signaling pathways [55] . The co-expression network analysis among those DEmRNAs, DEmiRNAs, and DElncRNAs revealed that the DElncRNAs could interact with immune-related miRNAs and genes to exhibit their role in diseases and cancers process [53] [54] [55] [56] . Specially, some lncRNA-miRNA-mRNA interaction networks participated in the regulation of cyclin D3 (CCND3) and suppressor of cytokine signaling 5 (SOCS5) through JAK -STAT signaling pathway [56] . In addition, several lncRNAs (XLOC_672329, ALDBGALG0000001429, XLOC_016500, and ALDBGALG0000000253) ( Table 1) were predicated to cis-regulate cholesterol 25-hydroxylase [CH25H)/cytokine inducible SH2 containing protein (CISH)/interleukin 1 beta (IL-1β)/CD80 molecule (CD80) to participate in host antiviral responses [56] . CD80 participate in host antiviral responses [56] The current findings of lncRNA involvement in the infection of ALV are just simply focused on the lncRNA characterization, expression profile, and associated pathways, however, still more proper investigations become necessary.

Unlike circRNAs and lncRNAs, many studies have been conducted to explore not only the expression profile but also the underlying functional mechanism of miRNAs involved in ALV infection. miRNA microarray or small RNA sequencing revealed many miRNAs were aberrantly expressed after ALV infection [57] [58] [59] [60] . Among the DEmiRNAs, several of them were verified by qRT-PCR analysis in one or more kinds of ALV-infected materials, including miR-221 [57] [58] [59] [60] , miR-222 [57, 59, 60] , miR-1456 [57] , miR-1704 [57] , miR-1777 [57] , miR-1790 [57] , miR-2127 [57] , let-7b [57, 60, 61] , let-7i [57, 60, 61] , miR-125b [57] [58] [59] [60] , miR-375 [57, 60] , miR-458 [57] , miR-193a [58] , miR-193b [58, 59] , miR-148a [59] , miR-27b [59] , miR-34a [59] , miR-130a [59] , miR-23b [62] and miR-34b-5p [63] . Obviously, the expression of miR-221/miR-222, let-7b/i, miR-375, miR-125b, and miR-193b were changed in not only one type of materials after ALV-infection, indicating their important roles in response to the ALV.

The qRT-PCR-verified DEmiRNAs were involved in immune-related pathways by analyzing the target genes of the DEmiRNAs. Of which, miR-221/222 may have effect on oncogenicity [57] and exist in several common pathways (MAPK [58] , oocyte meiosis [58] , Wnt [58] , and the chronic myeloid leukemia pathway [61] ). In addition, miR-221 was also involved in antigen presentation and apoptosis pathways [59] . miR-1456, miR-1704, miR-1777, miR-1790, and miR-2127 may have effect on oncogenicity [57] . miR-125b was related to the oocyte meiosis and MAPK signaling [58] , and may have effect on tumor suppression [57] . miR-193a was involved in Wnt signaling and oocyte meiosis pathway, while miR-193b was included in Wnt signaling and oocyte meiosis pathway [58] . let-7b/i was related to the chronic myeloid leukemia pathway [61] . let-7b/i, miR-375, and miR-458 may be involved in tumor suppression [57] .

The underlying mechanisms of some DEmiRNAs involved in ALV infection were revealed ( Table 2 ). For miR-221 and miR-222, they have multiple roles in the regulation of ALV infection. On one hand, miR-221/miR-222 could facilitate DF1 (chicken fibroblast cell line) cell proliferation and migration, and could inhibit the expression of apoptosis-related gene, BCL-2 modifying factor (BMF), leading DF1 cells not easy to undergo apoptosis [64] . On the other hand, miR-221/222 could promote cell proliferation to help ALV replication in DF1 cells. Because the depression of G1/S switch and over proliferation induced by ALV-J for DF1 cells required high expression of miR-221 and miR-221, miR-221 and miR-221 can downregulate the expression of CDKN1B (cyclin dependent kinase inhibitor 1B)], which have the ability to arrest the cell cycle and inhibit the cell proliferation process via the CDKN1B-CDK2 (cyclin dependent kinase 2) /CDK6 (cyclin dependent kinase 6) pathway [65] . To sum up, miR-221 and miR-222 could promote the ALV progression in DF1 cells through inhibiting apoptosis and facilitating cell proliferation, migration, and growth. In addition, the expression of miR-23b is up-regulated in spleen after ALV-J infection. Moreover, miR-23b could enhance ALV-J replication by regulating interferon regulatory factor 1 (IRF1) [62] . Meanwhile, miR-34b-5p is another validated DEmiRNA in spleen after ALV-infection and it could target melanoma differentiation-associated gene 5 (MDA5) to promote ALV-J replication by facilitating the cell migration and proliferation [63] . 

Marek's disease virus (MDV) has three serotypes: serotype 1 (MDV-1), serotype 2 (MDV-2), and turkey herpesvirus (HVT) [66] . Only MDV-1 has an oncogenic /pathogenic/tumorigenic effect [48] .

Marek's disease (MD) is caused by MDV. The chickens infected by MDV will cause immunologic suppression, T-cell lymphoma, and neurologic diseases, resulting in tissue or cell damage in chickens. If the MDV susceptible chickens are infected with MDV, the mortality can reach up to 100%, which brings massive loss to the poultry industry [67] .

To our knowledge, one circRNA sequencing research has been performed with three types of spleens: First, spleens from MDV infection-induced tumors; second, spleens from the survivors (without any lesion) after MDV infection; third, spleens from non-infected chickens. About 2169 circRNAs were detected in this research, of which, 113 circRNAs were differentially expressed. circRNA-miRNA-mRNA networks showed circZMYM3 could not only interact with 7 miRNAs but also target immune-related genes, such as SWAP70 and CCL4, because SWAP70 and CCL4 shared the same target site with miR-214 and circZMYM3. miR-155 was predicted to interact with circGTDC1, circMYO1B, GATA binding protein 4 (GATA4), peripherin 2 (PRPH2), eomesodermin (EOMES), Rho related BTB domain containing 1 (RHOBTB1), and serine palmitoyltransferase, small subunit B (SPTSSB) [68] .

Chicken MD resistant line 6 3 and MD susceptible line 7 2 are model animals for the investigation of responsible biomarkers or clinical diagnosis during the infection of MDV [69] . Expression analysis and bioinformatical functional annotation through RNA sequence by using line 6 3 and line 7 2 showed that lncRNAs were aberrantly expressed and were involved in immune-related pathways that indicate that lncRNAs participate in regulating MDV infection [70] . Comparing the expression of the RNAs between infected and noninfected chicken bursa, 425 DElincRNAs and 387 DE genes were found in line 6 3 , while 636 DElincRNAs and 2383 DE genes were identified in line 7 2 . Co-location analysis for the 30 DElincRNAs associated with immune response found that most of the neighboring genes of these lincRNAs were also associated with immune response. Of them, one candidate lincRNA, termed linc-satb1, was positively related to inflammatory/defense/external stimulus response and lymphocyte activation. In addition, the expression of linc-satb1 was correlated with Special AT-rich binding protein-1 (SATB1), which is known to have the ability to regulate chromatin structure and T-cell development/activation [71] . It implies that lnc-satb1 may participate in immune response to MD by regulating SATB1 [70] .

LncRNA could participate in MDV through interacting with both host MDV susceptible/resistant gene. For example, linc-GALMD1 was a DElincRNA of MDV non-infected and infected chickens [72] . IGLL1 (immunoglobulin lambda-like polypeptide 1) has distinct expression between line 6 3 and line 7 2 . It has lower expression in line 6 3 chickens but higher expression in line 7 2 chickens after infection of MDV, which implies that IGLL1 could be a line-specific or susceptible gene in response to MD [72] . Meanwhile, linc-GALMD1 expression level had a positive correlation with IGLL1 which indicated that linc-GALMD1 could potentially regulate MD by interacting with IGLL1 [72] . Some lncRNAs were predicted to interact with MD-resistant candidate genes [73] . MSTRG.360.1 was correlated with C-X-C motif chemokine ligand 12 (CXCL12), TNF receptor superfamily member 6b (TNFRSF6B), SWAP70, cytotoxic T-lymphocyte associated protein 4 (CTLA4), and histone deacetylase 9 (HDAC9) [73] . MSTRG.6725.1 may interact with CTLA4 and joining chain of multimeric IgA and IgM (JCHAIN). MSTRG.6754.1 was associated with JCHAIN and CTLA4 [73] . MSTRG.15539.1 was associated with SWAP70, HDAC9, CD72 molecule (CD72), and JCHAIN [73] . MSTRG.7747.5 were strongly correlated with CD8B molecule (CD8B), HDAC9, CD72, and Insulin-like growth factor level (IGF-I) [73] .

LncRNA directly regulates MDV gene expression is another approach for chicken host to response to MD. It was evidenced by the upregulation of viral gene-Meq (an essential gene for MDV progression), induced by downregulation of linc-GALMD1 [72] .

LncRNAs act as an upstream regulator to modulate miRNA expression, thus exhibiting specific function during MD viral infection was also an approach for lncRNA to regulate MDV infection. linc-GALMD3, which has a higher expression level in CD4 + T cells after MDV infection, was found to be located on the upstream of the gene transcribes miR-223 [74] . The loss of function of linc-GALMD3 will suppress miR-223 expression and MDV replication. Additionally, DEG analysis of RNA-Seq between the linc-GALMD3 knockdown and control MSB1 (MDCC-MSB1) cells showed that about 27 DEGs were also miR-223 target genes, which implied the cis regulatory mechanism of linc-GALMD3 on miR-223 [74] . The linc-GALMD3-miR-223-target DEGs interaction network could be used for further investigation during MDV infection.

The selected lncRNAs, their targets, and their functions during the MDV infections were shown in Table 3 . 

Numerous researches have been focused on the exploration of miRNA expression profile and their potential role during the infection of MDV. Hundreds of miRNAs were significantly differentially expressed between MDV-infected and noninfected groups [75] [76] [77] [78] [79] [80] . let7 [75] , miR-199a-1 [75, 77] , miR-26a [75, 77] , miR-181a [75, 77] miR-16 [75] miR-223 [76] , miR-150 [76] , miR-155 [76, 79] , miR-221 [77] , miR-199 [77] , miR-15b [78] , miR-456 [78] , let7i [78] , miR-762 [79] , miR-29b [79] , miR-140-3p [81] , miR-199-3p [81] , and miR-221-5p [81] , were verified by qRT-PCR/Northern blot analysis.

The classical functional mechanism of miRNAs in regulating MDV infection is targeting the 3 UTR of their target genes and inhibiting the transcription of the mRNA or interfering their translation [82] . miR-221/miR-222 were significantly upregulated after MDV infection. The cyclin-dependent kinase (cdk) inhibitors 27 Kip1 has direct effect on cell cycle and cell proliferation [82] . Conserved binding site between miR-221/miR-222 and 27 Kip1 was verified in several species and their target relationship has been confirmed in several cancer cells [82] . In avian, miR-221/miR-222 would also target 27 Kip1 to regulate MSB1 cell proliferation [83] . Retinoid Acid Receptor-Related Orphan Receptor Alpha (RORA) is a suppressor for tumor and could be involved in immunity, inflammation metabolism [84] , and tumor initiation [85] . In MBS1 cells, miR-155 could increase the proliferation, invasiveness, and reduce apoptosis by targeting RORA [86] . Target interactions of miR-181a with MYB proto-oncogene like 1 (MYBL1)/ insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3), and miR-26a with eukaryotic translation initiation factor 3 subunit A (EIF3A), were confirmed by luciferase reporter assays [77] . Furthermore, miR-181a was verified to inhibit proliferation of MSB1 by targeting MYBL1 [87] . Never in mitosis gene A (NIMA)-related kinase 6 (NEK6) is another verified target gene of miR-26a and showed opposite expression pattern with miR-26a between MDV-infected spleens and noninfected controls. miR-26a would exhibit suppression to MSB1 cell proliferation through inhibiting NEK6 [88] . miR-103-3p decreases cell migration by targeting transcription factor Dp-2 (E2F dimerization partner 2) (TFDP2) and cyclin E1 (CCNE1) [89] . For miR-130a, it could inhibit MSB1 cell proliferation and migration by targeting homeobox A3 (HOXA3) and MyoD family inhibitor domain containing (MDFIC) [90] . miR-219b could target B-cell chronic lymphocytic /lymphoma 11B (BCL11B) and suppresses the proliferation, migration, and invasion of MSB1 cells [91] .

As a homologous to MDV-encoded miRNA to participate in regulate the process of MDV infection is another miRNA regulatory mechanism in avian. This was discovered for miR-155, miR-29b, and miR-221. miR-155 shared seed sequence with the same target genes with MDV-induced miRNA, MDV-1-miR-M4 [92] . The shared target genes including PU.1, HIVEP2 (HIVEP zinc finger 2), CEBPβ (CCAAT enhancer binding protein beta), PDCD6 (programmed cell death 6), BCL2L13 (BCL2 like 13), RREB1 (ras responsive element binding protein 1), GPM6B (glycoprotein M6B), MAP3K7IP2 (TGF-beta activated kinase 1/MAP3K7 binding protein 2), and c-Myb (MYB proto-oncogene, transcription factor) [93, 94] . Many of these genes are known to have a specific role in regulating tumor cell proliferation/apoptosis and tumor formation. Additionally, MDV-1-miR-M4 is essential for MDV infection due to the deletion of MDV-1-miR-M4 or a 2 nucleotides mutation on its seed region will lead to an inhibition for the induction of lymphomas. This inhibition could be rescued by gga-miR-155, thus in turn implied miR-155 is a crucial regulator for lymphomas. Toll-like receptor 3 (TLR3) is crucial for innate and adaptive immunity. It was abundantly expressed in MDV-infected CEF cells, resulting in replication inhibition of the RB1B strain of MDV. However, such inhibition would alter both MDV1-miR-M4-5p and miR-155 [95] . miR-29b shared a seed sequence with MDV2-miR-M21, and expression of MDV2-miR-M21 may ensure viral proliferation in host cells. miR-221 shared a seed sequence with both hvt-miR-H14-3p and mdv1-miR-M32 [92, 96, 97] . As the homologous miRNAs of virus-encoded miRNAs, some host miRNAs share the same biding site and even same target genes with virus-encoded miRNAs to influence the biological function of virus-encoded miRNAs may be a new strategy to resist virus invasion.

The interaction of host miRNAs with virus-encoded gene is also a regulatory mechanism for miRNAs during the virus infection. For instance, the viral oncoprotein Meq could regulate the expression of miR-21 by binding to the promoter region of miR-21. Meanwhile, miR-21 could target chicken programmed death cell 4 (PDCD4) to suppress growth and apoptosis escape of tumor cells [98] . It provided a viral gene-host miRNA-host gene regulation mechanism involved in the MDV infection. Meanwhile, miR-155 was found to target viral env transcripts and could significantly lower the env transcripts abundance in MSB1 and CEF cells [99] .

The selected-verified miRNAs and their target genes and their functions during the MDV infections are presented in Table 4 . 

Infectious bursal disease (IBD) is a virus disease of young chickens which is caused by avian infectious bursal disease virus (IBDV). IBDV has negative effective on T cells proliferation, causing immunologic suppression in chicken [100, 101] . Moreover, IBD has caused death and vaccination failure to other disease in chicks [101] .

Dendritic cells (DCs) have special role in both innate and acquired immune during virus infection [102] . A microarray study on IBDV-stimulated DCs and non-stimulated DCs revealed 114 lncRNAs, 18 miRNAs, and 965 mRNAs were differentially expressed after stimulated with IBDV [103] . Functional annotation of the DElncRNAs, DEmiRNAs, and DE genes showed that there was an association with cellular response to starvation, protein localization, the RNA biosynthetic process, etc. These were involved in JAK-STAT/MAPK/mTOR/neurotrophin/CCR5/Interleukin-17 (IL-17) signaling pathways, as predicted by a pathway analysis [103] .

miRNAs could regulate viral infection through regulating the IBDV genome sequence. IBDV as a double stranded virus has two segments (segment A and B) and encodes five viral proteins, VP1-VP5, which play different roles in the infection process of IBDV to the host. Of them, VP1 is required for both IBDV replication and virulence [104] . As the target of tumor suppressors in human [105, 106] , miR-21 could suppress IBDV replication via inhibiting the expression of VP1 in avian [107] . Similarly, miR-454 targeting IBDV genomic segment B to inhibit IBDV replication [108] . miR-130b could inhibit IBDV replication through targeting IBDV segment A [109] .

Apart from targeting the viral genome sequence, miRNA could also regulate the IBDV infection through targeting regulators of type I interferon (IFN), as IFN is a crucial cellular molecule to combat viral infection and interferon regulatory factor-dependent pathways play important roles during the infection of various disease. SOCSs (Suppressors of Cytokine Signaling) gene family was known as one kind of negative regulators of IFN. Specially, the inhibition of SOCS6 can increase the expression of IFN-β. miR-454 could suppress the IBDV replication through suppression of SOCS6 [108] . Similarly, miR-130b could facilitate IFN-β expression through binding to the host SOCS5 to inhibit IBDV replication [109] . For miR-155, it was found to suppress IBDV replication through targeting not only SOCS1 but also another type I IFN negative regulator, TANK (TNF receptor-associated factor family member-associated NF-κB activator) [110] . On the contrary, miR-9 could inhibit IFN expression by inhibiting IRF2 and then promoting the replication of IBDV [111] . miR-142-5p was founded to decrease the activity of the IFN-β by directly by targeting the MDA5 and then promoting IBDV replication through IRF7 (interferon regulatory factor 7) signaling pathway [112] . Additionally, miR-2127 has been found to promote IBDV replication by suppressing p53 translation and attenuating p53-mediated innate immune response against IBDV infection [113] .

More novelty, IBDV alters the expression of responsible miRNAs through inducing the demethylation of the miRNA promoter is a new strategy for IBDV to protect themselves for survival from the immune responses induced by related-miRNAs. For instance, IBDV infection could induce the promoters of pre-miR-27 and pre-miR-16-2 demethylation, thus upregulating miR-27b-3p and miR-16-5p expression [114, 115] . Furthermore, miR-27b-3p could increase the expression of chicken IFN-β, NF-κB, and IRF3 (interferon regulatory factor 3) by targeting SOCS3 and SOCS6, thus inhibiting IBDV replication [114] . miR-16-5p increased the caspase-9/3 activity through targeting Bcl2, thus promoting the IBDV-induced apoptosis [115] .

Avian infectious bronchitis virus (IBV) belongs to coronavirus. It mainly replicates in chicken epithelial cells and could infect both meat type and commercial type of small or old chickens [116, 117] . The investigation of the host responsible mRNAs and lncRNAs in IBV-infected DCs revealed thousands of mRNAs were differentiated expressed in IBV-infected avian DCs and noninfected cells [118] . With 1093 up-regulated and 845 down-regulated. miRNAs and lncRNAs interaction provided further information for the candidate therapeutic biomarkers in response to IBV infection [118] . miRNA transcriptome analysis in chicken kidneys showed 58 DE miRNAs were found and were shown to be mostly associated with immune response, catalytic activities, metabolic processes, and gene expression [119] . Among them, miR-1723, miR-7b, miR-222b-3p, miR-1782, miR-6516-3p, miR-202-5p, miR-1559-3p, miR-449a, miR-1454, and miR-1563 were verified by qRT-PCR [119] . As a predicted DEmiRNA by sequence analysis, miR-146a-5p was also found to promote IBV replication of by targeting tumor necrosis factor receptor superfamily member 18 (TNFRSF18) and IL-1 receptor associated kinase-2 (IRAK2) [120] . As another DEmiRNA, miR-30d was showed to inhibit IBV replication through suppressing ubiquitin-specific protease 47 (USP47) in HD11 (avian macrophage-like cells) cells [121] .

Newcastle disease is caused by a single-stranded RNA virus, Newcastle disease virus (NDV), resulting in a high mortality rate in infected chicken worldwide [122] .

Only few studies have been focused on ncRNA investigation associated with ND. One study performed mRNA-seq and small RNA-seq to identify the interaction pairs of mRNA-miRNA involved in ND. 1069 miRNA-mRNA pairs were found. Among them, the interaction of miR-203a and transglutaminase 2 (TGM2) were confirmed by both qRT-PCR and dual-luciferase reporter assay [123] . Additionally, miR-19b-3p could promote the expression of inflammatory cytokines and suppress NDV replication by targeting ring finger protein 11 (RNF11) and zinc-finger protein, MYND-type containing 11 (ZMYND11), which are two negative moderators of NF-κB signaling [124] . miR-455-5p could suppress NDV replication by directly targeting SOCS3 [125] . miR-375 inhibited NDV growth through targeting the M gene of NDV and host Drosophila-like RNA binding protein 4 (ELAVL4) [126] .

Orthomyxoviridae family [127] . Other viruses in this family include influenza B and influenza C virus, but only influenza A virus has been found in birds [127, 128] . Although avian influenza causes only mild illness, it still can be very dangerous because of its high transmission among birds, and even among human beings [129, 130] .

Several RNA-seq researches had revealed the expression profile and associated pathways in response to AIV infection in different tissues and cells in avian [131] [132] [133] [134] . According to the bioinformatics analysis of the expression and the associated pathways of the DEmiRNAs in those researches, miR-34a, miR-122-2, miR-122-1, miR-206, miR-146a, miR-155, miR-1719, miR-1599, miR-1594, miR-451, miR-146, miR-1576, miR-1636, miR-206, miR-142-5p, miR-17-5p, miR-19b miR-133c, miR-1710, miR-181a/b, miR-30b/c/e, and miR-455 were considered to be strong candidate miRNAs related to the immune response of AIV infection in chickens [131] [132] [133] [134] .

The genome of type A influenza includes eight segments and each segment-encoded protein is crucial for viral replication and pathogenesis [133] . miRNAs interact with virus genes is also one approach for miRNA to control or resist AIV. Many chicken host miRNAs have been analyzed to have target relationship with avian influenza [135] . Specially, the non-structural protein 1 (NS1) is one protein of segment 8 of H5N1 genome that is directly associated with the pathogenicity of the influenza strain. miR-1658 could regulate the AIV infection by targeting the NS1 gene of H5N1 genome [135] . Moreover, PB1 (polymerase PB1), PB1-F2 (PB1-F2 protein), and N40 were three proteins encoded by segment 2 of H5N1 virus. miR-1710, miR-133c, and miR-146c were predicted to target PB1-F2, PB1, and N40 proteins, implying that they potentially regulate H5N1 infecting by interacting with virus genes [133] .

Reticuloendotheliosis, a reticuloendotheliosis virus (REV)-induced disease, is highly prevalent in avian and human [136] . It can cause chronic B cell and T-cell lymphomas [137] , delayed growth, immunodepression, and tumor in birds [138] .

To the best of our knowledge, only few studies related to ncRNAs have been investigated during RE infections. High-throughput sequencing has been conducted in REV-infected and non-infected tissues or cells and the results identified many candidate DEmiRNAs involved in REV infection. These DEmiRNAs could target immune-related genes and participate in immune-related pathways [138] [139] [140] . Among them, miR-2945, miR-106-3p/5p, miR-29b/3p/, miR-7b, miR-16c-5p/, miR-122-5p, miR-155, miR-18a-5p, miR-147, miR-184-3p, miR-222b-5p/3p, miR-145b-5p, miR-20b-5p, and miR-1b-3p expressions were verified by qRT-PCR. GO term analysis showed that these miRNAs are related to apoptotic process, intracellular signal transduction, cell death regulation. Also, many important KEGG pathways were enriched, such as MAPK signaling, endocytosis, focal adhesion, apoptosis, cell cycle pathways, mTOR signaling, cell growth and death, and immune system.

Specially, of so many DEmiRNAs, the underlying regulatory mechanisms of miR-155 and novel-72 were verified and indicated that they play distinct role in response REV infection. For miR-155, it showed a high expression level during REV infection in CEF cells. It has been demonstrated that miR-155 could inhibit apoptosis by targeting caspase-6 and accelerate cell cycle through inhibiting FOXO3a and JARID2 (jumonji, AT rich interactive domain 2) expression during the REV infection [141, 142] . For novel-72, it showed a significantly lower expression in REV-infected cells. Four predicated target genes of novel-72, PDPK1 (phosphoinositide dependent protein kinase-1), mTOR (mammalian target of rapamycin), S6K1 (S6 Kinase 1), and eIF4E (Eukaryotic Initiation Factor 4E) of mTOR signaling pathway were related to cell proliferation and survival, indicating that novel-72 could be involved in mTOR signaling pathway to mediate the cell fate during REV infection [139] .

The selected-verified miRNAs and their target genes and their functions during the IBDV, IBD, NDV, AIV, and REV infections were listed below (Table 5 ). FOXO3a, JARID2 inhibit apoptosis and accelerate cell cycle during the REV infection [141, 142] As avian virus disease has been well studied, the mechanisms that miRNAs participate in avian virus diseases are clear now. There are four functional mechanisms have been reported: (1) Direct interaction with the host gene ( Figure 2a ) [82] ; (2) acts as homologous to virus-encoded miRNAs and shares the same target gene with virus-encoded miRNAs (Figure 2b ) [92] [93] [94] [95] [96] [97] 143] ; (3) interacts with virus genomic gene (Figure 2c) [98, 99, [107] [108] [109] ; (4) alters the expression of responsible miRNAs through inducing the demethylation of the miRNA promoter to protect virus themselves to survival from the immune responses induced by related-miRNAs (Figure 2d ) [114, 115] . 

Chicken coccidiosis is an epidemic parasitic disease can be caused by nine Eimeria spices, including Eimeria tenella, necatrix, maxima, acervuline, brunetti, mivati, hagani, praecox, and mitis. They 

Chicken coccidiosis is an epidemic parasitic disease can be caused by nine Eimeria spices, including Eimeria tenella, necatrix, maxima, acervuline, brunetti, mivati, hagani, praecox, and mitis. They are infecting chicken intestinal epithelial cells. Among them, Eimeria tenella, Eimeria maxima, and Eimeria necatrix have the higher pathogenicity. One RNA sequence analysis of differentially expressed lncRNAs, circRNAs, and mRNAs has been performed in chicken small intestines during Eimeria necatrix infection. This RNA sequence analysis obtained 1543 DEmRNAs, 95 DElncRNAs, 13 DEcircRNAs [144] . Functional annotation for lncRNAs, miRNAs, and circRNAs were correlated with chicken host immune defense and pathogenesis during E. necatrix infection [144] . In addition, miRNA expression was compared between naturally or Eimeria maxima and Eimeria acervulina -infected Ross 308 broilers using RNA sequencing. Among DEmiRNAs, miR-122-5p, miR-144-3p, and miR-205b were verified by qRT-PCR [145] , however, their potential roles during avian coccidiosis need further investigations. The regulatory mechanisms of ncRNAs in response to coccidiosis remain largely unknow.

Cryptosporidium baileyi (C. baileyi) belongs to Cryptosporidium species in birds [146] . It can infect in the epithelial cells of bursa or respiratory tract, causing respiratory diseases [146, 147] . In broiler chickens, it can cause high mortality and morbidity [148] . One research focused on the identification of lncRNAs, circRNAs, and mRNAs involved in C. baileyi infection in chickens' tracheal tissues. It found 124 lncRNAs, 104 circRNAs, and 1317 mRNAs were differentially expressed. GO analysis found that the targets and source genes of mRNAs and lncRNAs are all involved in immune response and immune system process, while KEGG analysis showed that they are related to intestinal immune network for IgA production, cell adhesion molecules (CAMs), cell cycle, and the cytokine-cytokine receptor interaction. The circRNAs were significantly enriched in pathways associated with tight junction and glycerolipid metabolism, nucleotide sugar metabolism, and amino sugar [149] . However, the underlying molecular mechanism of ncRNAs in response to C. baileyi infection needs further investigation.

Campylobacter jejuni (C. jejuni) is a foodborne pathogen that causes human diarrhea on consuming chicken products which are contaminated by C. jejuni [150] . Two studies on ncRNAs associated with C. jejuni have been reported [138, 151, 152] . Solexa sequencing for cecal tissue from C. jejuni inoculated and non-inoculated SPF chicken showed 4 miRNAs, miR-155, miR-1416-5p, miR-19b-3p, and miR-19a-3p were significantly differentially expressed [151] . In addition, miR-30b, miR-30c, miR-148a, and miR-1416-5p were able to interact with the SOCS3 in response to C. jejuni inoculation which indicated they may mediate C. jejuni infection through regulating SOCS3 [152] .

Necrotic enteritis is usually caused by Clostridium perfringens with symptoms of weight depression, appetite loss, and even cause death to chickens [153] . Small RNA-seq showed many miRNAs were differently expressed after challenged by NE [154] [155] [156] . miR-215, miR-194, miR-217, miR-200a, miR-216a, miR-200b, miR-216b, miR-34b, miR-429, miR-1684, miR-9-5p, miR-196-5p, miR-20b-5p and let-7d were confirmed by qRT-PCR [154, 156] . Some miRNAs were correlated with immune-related mRNA expression levels, such as miR-216 and TGFβR2 (transforming growth factor beta receptor 2), miR-30b/miR-30c/miR-455-5p and SOCS3, miR-181a/b and CXCL14 (C-X-C motif chemokine ligand 14) , miR-429 and TNFSF11β (TNF superfamily member 11 beta), miR-223 and HSP90β1 (heat shock protein 90 beta family member 1), miR-1329 and NFKBIZ (NFKB inhibitor zeta), miR-1674 and ARHGEF (FERM, ARH/RhoGEF and pleckstrin domain protein 1), miR-30e/ miR-32 and SERPINF1 (serpin family F member 1) [155] . Many immune-related pathways were identified for DEmiRNA targets, such as MAPK, ErbB, Notch, TGF-β, JAK-STAT, Cytosolic etc. Specially, JAK-STAT as the key pathway, 20 genes of this pathway showed marked differential expression, strongly suggesting the crucial role of JAK-STAT pathway in regulating NE [157] . The miR-200a-3p could regulate inflammatory factor and MAPK signaling pathway-related gene in response to NE. For instance, it regulated the expression of IL-1β, IFN-γ, IL-12p40 (interleukin 12B), IL-17A (interleukin 17A), LITAF (lipopolysaccharide induced TNF factor), and ZAK (also known as MAP3K20-mitogen-activated protein kinase kinase kinase 20), MAP2K4 (mitogen-activated protein kinase kinase 4), and TGFβ2 (transforming growth factor beta 2) of MAPK signaling pathway [158] . The miR-10a could inhibit the expression of MyD88-dependent pathway-related genes, including TRAF6 (TNF receptor associated factor 6), TAK1 (TGF-beta activated kinase 1 (MAP3K7) binding protein 1), NF-κB1 (nuclear factor kappa B subunit 1), and downstream genes of the MyD88-dependent pathway related genes, including IL-1β, IFN-γ, IL-12p40, TNFSF15 (TNF superfamily member 15), and LITAF. It strongly indicated that miR-10a regulates the NE through Toll-like receptor pathway [159] .

Salmonella enterica serovar enteritidis (SE) is the most common serotype of the Salmonella bacteria. Chicken SE infection is mainly caused by ingesting water or consuming food contaminated with Salmonella bacteria. CircRNAs have been identified through next-generation sequencing during SE infection [160] . Total of 62 circRNAs were significantly differentially expressed (30 upregulated and 32 downregulated) between the control and treated groups. The immune-related pathway associated with the DE circRNAs including, adrenergic signaling in cardiomyocytes, herpes simplex infection, and signaling pathway of MAPK/ p53/VEGF/Notch. Three immune-related genes, TXNDC9 (thioredoxin domain containing 9), JAG2 (jagged canonical Notch ligand 2), and NFATC2 (nuclear factor of activated T cells 2), generated 11 DE circRNAs involved in the B cell receptor signaling pathway, B cell proliferation, drug biological process, and cytokine production [160] . In addition, miR-1306-5p regulated the immune response to SE by inhibiting the Toll-interacting protein (Tollip), which is an up-regulator for inflammatory cytokines-NF-κB, IL-6 (interleukin 6), TNF-α, and IL-1β (interleukin 1-beta) [161] . miR-101-3p and miR-155 could alter the expression of their target genes, LRRC59 (leucine rich repeat containing 59) and IRF4 (interferon regulatory factor 4), and decrease the expression of pro-inflammatory cytokines during SE infection [162] . In addition, miR-1662, miR-1416-5p, and miR-34a-5p showed opposite expression pattern with the immune-related target genes of BCL10 (B-cell CLL/lymphoma 10), TLR21 (Toll-like receptor 21), NOTCH2 (notch 2), TLR1LA (toll-like receptor 1 family member A), and THBS1 (thrombospondin 1), indicating their important roles in SE infection [163] .

Salmonella typhimurium (S. typhimurium) commonly occurred in avian and humans [164] . It is a major food-borne pathogen and has an impact on the microbiological safety of eggs which is also a risk factor to humans [165] . A previous study revealed 14 miRNAs that were significantly altered by the infection of S. typhimurium [166] . Among them, miR-3525, miR-215-5p, miR-193a-5p, miR-122-5p, and miR-375 were verified by qRT-PCR. The predicted DEmiRNAs target genes were enriched in immune system development, stress-activated MAPK cascade, the regulation of cAMP-dependent protein kinase activity, and the regulation of immune system process (such as, MAPK and Wnt signaling pathways) [166] .

The selected-verified miRNAs and their target genes and their functions during the bacterial infections were listed below (Table 6 ). 

ncRNAs are recognized as powerful regulatory molecules and have been largely investigated in various disease process of different species, including avians. The unique functional mechanisms of miRNA, lncRNA, and circRNA were revealed.

Although the underlying functional mechanism of ncRNAs has been revealed in many species, it is still beginning to emerge in response to avian disease, except for miRNAs. Researches on circRNAs and lncRNAs are basically performed on the analysis of their expression profile and associated pathways. ncRNAs have been found to play roles during the infection of various avian diseases through different approaches. For lncRNAs and circRNAs, they mainly exhibit their function through lncRNA/circRNA-miRNA-mRNA axis, however, in some cases they could also regulate the immune process by directly interacting with RNA binding proteins or virus gene sequence. miRNAs can regulate various aspects of immune response process. In avian, some specific miRNAs were identified to be differentially expressed in many different types of chicken diseases from virus, parasite, and bacteria, such as miR-155 [68, 110, 141, 142] , miR-221/222 [60, 83, 119, 138] , miR-130 [59, 90, 109] , miR-30 [121, 152, 155] , miR-34 [59, 63, 132, 154, 163] , let-7 [57, 81, 155] , miR-181 [77, 134, 155] , miR-16 [80, 115] , miR-455 [125, 134, 155] , etc. It indicated their extensive roles in regulating avian immunity. Especially, miR-155 has been reported to play important roles in response to different kinds of avian diseases, such as ALV [68] , MD [76] , IBD [110] , Avian influenza [132] , Reticuloendotheliosis [141, 142] , Campylobacter jejuni [151] , and also Salmonella enterica serovar Enteritidis [162] .

The functional mechanisms of ncRNAs in regulating avian immune system can be categorized into three mechanisms: First, ncRNAs interact with pathogenic gene of virus/parasite/bacterium; second, ncRNAs act as a homologous to the product of pathogen; third, ncRNAs directly interact with host resistant and susceptible genes.

Epigenetic Regulation by Long Noncoding RNAs

Ribosome profiling provides evidence that large noncoding RNAs do not encode proteins

Classification and function of small open reading frames

The Translation of Non-Canonical Open Reading Frames Controls Mucosal Immunity

Peptides/Proteins Encoded by Non-coding RNA: A Novel Resource Bank for Drug Targets and Biomarkers

Origins and Mechanisms of miRNAs and siRNAs

Small RNAs as Guardians of the Genome

Subtractive hybridization identifies novel differentially expressed ncRNA species in EBV-infected human B cells

Non-coding RNAs in Development and Disease: Background, Mechanisms, and Therapeutic Approaches

Long noncoding intronic RNAs are differentially expressed in primary and metastatic pancreatic cancer

Molecular Mechanisms of Long Noncoding RNAs

A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced

H19 Imprinting Control Region Methylation Requires an Imprinted Environment Only in the Male Germ Line

The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

Transcription of Two Long Noncoding RNAs Mediates Mating-Type Control of Gametogenesis in Budding Yeast

The non-coding RNA TERRA is a natural ligand and direct inhibitor of human telomerase

Intergenic transcription is required to repress the Saccharomyces cerevisiae SER3 gene

Methylation of adenine residues in DNA of eukaryotes

The p53-induced lincRNA-p21 derails somatic cell reprogramming by sustaining H3K9me3 and CpG methylation at pluripotency gene promoters

PARTICLE, a Triplex-Forming Long ncRNA, Regulates Locus-Specific Methylation in Response to Low-Dose Irradiation

Long noncoding RNAs: Functional surprises from the RNA world

Control of myogenesis by rodent SINE-containing lncRNAs

A natural antisense transcript regulates Zeb2/Sip1 gene expression during Snail1-induced epithelial-mesenchymal transition

But Not Its lncRNA Products, Induces Imprinted Igf2r Silencing

Circular RNAs are a large class of animal RNAs with regulatory potency

Identification of mecciRNAs and their roles in the mitochondrial entry of proteins

Circular RNAs in the Mammalian Brain Are Highly Abundant, Conserved, and Dynamically Expressed

Kinetic expression analysis of the cluster mdv1-mir-M9-M4, genes meq and vIL-8 differs between the lytic and latent phases of Marek's disease virus infection

Translation of yes-associated protein (YAP) was antagonized by its circular RNA via suppressing the assembly of the translation initiation machinery

Endoribonucleolytic Cleavage of m6A-Containing RNAs by RNase P/MRP Complex

Circ-ZNF609 Is a Circular RNA that Can Be Translated and Functions in Myogenesis

Novel Role of FBXW7 Circular RNA in Repressing Glioma Tumorigenesis

Natural RNA circles function as efficient microRNA sponges

Exon-intron circular RNAs regulate transcription in the nucleus

The RNA Binding Protein Quaking Regulates Formation of circRNAs

Extensive translation of circular RNAs driven by N6-methyladenosine

IRES-mediated cap-independent translation, a path leading to hidden proteome

How are circRNAs translated by non-canonical initiation mechanisms?

Conserved Seed Pairing, Often Flanked by Adenosines, Indicates that Thousands of Human Genes are MicroRNA Targets

miRNA-dependent gene silencing involving Ago2-mediated cleavage of a circular antisense RNA

MicroRNA-1224 Splicing CircularRNA-Filip1l in an Ago2-Dependent Manner Regulates Chronic Inflammatory Pain via Targeting Ubr5

METTL1 Promotes let-7 MicroRNA Processing via m7G Methylation

Primary transcripts of microRNAs encode regulatory peptides

Translational dynamics revealed by genome-wide profiling of ribosome footprints in Arabidopsis

Small RNA sequences derived from pre-microRNAs in the supraspliceosome

Myotropic Avian Leukosis Virus subgroup J Infection in a Chicken

A novel subgroup of exogenous avian leukosis virus in chickens

The long view: 40 years of Marek's disease research andAvian Pathology

Circular RNA alterations are involved in resistance to avian leukosis virus subgroup-J-induced tumor formation in chickens

Circular RNA and mRNA profiling reveal competing endogenous RNA networks during avian leukosis virus, subgroup J-induced tumorigenesis in chickens

Circular RNA Vav3 sponges gga-miR-375 to promote epithelial-mesenchymal transition

Expression patterns of novel circular RNAs in chicken cells after avian leukosis virus subgroup J infection

Integrated host and viral transcriptome analyses reveal pathology and inflammatory response mechanisms to ALV-J injection in SPF chickens

Comprehensive Transcriptome Analysis Reveals Competing Endogenous RNA Networks During Avian Leukosis Virus, Subgroup J-Induced Tumorigenesis in Chickens

Gene expression profile and long non-coding RNA analysis, using RNA-Seq, in chicken embryonic fibroblast cells infected by avian leukosis virus

Long non-coding RNA and MicroRNA profiling provides comprehensive insight into non-coding RNA involved host immune responses in ALV-J-infected chicken primary macrophage

Aberrant expression of liver microRNA in chickens infected with subgroup J avian leukosis virus

Differential expression of microRNAs in avian leukosis virus subgroup J-induced tumors

Subgroup J avian leukosis virus infection of chicken dendritic cells induces apoptosis via the aberrant expression of microRNAs

Expression of dysregulated miRNA in vivo in DF-1 cells during the course of subgroup J avian leukosis virus infection

Temporal changes of microRNA gga-let-7b and gga-let-7i expression in chickens challenged with subgroup J avian leukosis virus

MicroRNA-23b Promotes Avian Leukosis Virus Subgroup J (ALV-J) Replication by Targeting IRF1

MiR-34b-5p Suppresses Melanoma Differentiation-Associated Gene 5 (MDA5) Signaling Pathway to Promote Avian Leukosis Virus Subgroup J (ALV-J)-Infected Cells Proliferaction and ALV-J Replication

Role of gga-miR-221 and gga-miR-222 during Tumour Formation in Chickens Infected by Subgroup J Avian Leukosis Virus

Avian leukosis virus subgroup J promotes cell proliferation and cell cycle progression through miR-221 by targeting CDKN1B

Immunological tolerance in chickens hatching from eggs injected with cell-associated herpesvirus of Turkey (HVT)

Marek's disease virus: Lytic replication, oncogenesis and control

Genome-wide analysis of circular RNAs involved in Marek's disease tumourigenesis in chickens

The National Registry of Genetically Unique Animal Populations: USDA-ADOL Chicken Genetic Lines

The conservation and signatures of lincRNAs in Marek's disease of chicken

Linc-GALMD1 Regulates Viral Gene Expression in the Chicken

Integrated analysis of lncRNA and mRNA repertoires in Marek's disease infected spleens identifies genes relevant to resistance

Long intergenic non-coding RNA GALMD3 in chicken Marek's disease

Differential expression of microRNAs in Marek's disease virus-transformed T-lymphoma cell lines

A Systematic Analysis of miRNA Transcriptome in Marek's Disease Virus-Induced Lymphoma Reveals Novel and Differentially Expressed miRNAs

MiRNA expression signatures induced by Marek's disease virus infection in chickens

Distinct expression pattern of miRNAs in Marek's disease virus infected-chicken splenic tumors and non-tumorous spleen tissues

MicroRNA Profile of Marek's Disease Virus-Transformed T-Cell Line MSB-1: Predominance of Virus-Encoded MicroRNAs

The inhibitory effects of gga-miR-199-3p, gga-miR-140-3p, and gga-miR-221-5p in Marek's disease tumorigenesis

The Cdk inhibitor p27 in human cancer: Prognostic potential and relevance to anticancer therapy

MicroRNAs 221 and 222 target p27Kip1 in Marek's disease virus-transformed tumour cell line MSB-1

Retinoic Acid-Related Orphan Receptors (RORs): Regulatory Functions in Immunity, Development, Circadian Rhythm, and Metabolism

RORα, a Potential Tumor Suppressor and Therapeutic Target of Breast Cancer

Effect of gga-miR-155 on cell proliferation, apoptosis and invasion of Marek's disease virus (MDV) transformed cell line MSB1 by targeting RORA

Chicken gga-miR-181a targets MYBL1 and shows an inhibitory effect on proliferation of Marek's disease virus-transformed lymphoid cell line

gga-miR-26a targets NEK6 and suppresses Marek's disease lymphoma cell proliferation

Chicken gga-miR-103-3p Targets CCNE1 and TFDP2 and Inhibits MDCC-MSB1 Cell Migration

Chicken gga-miR-130a targets HOXA3 and MDFIC and inhibits Marek's disease lymphoma cell proliferation and migration

Gga-miR-219b targeting BCL11B suppresses proliferation, migration and invasion of Marek's disease tumor cell MSB1

Sequence Conservation and Differential Expression of Marek's Disease Virus MicroRNAs

Ortholog Encoded by the Oncogenic Marek's Disease Virus

Marek's disease virus microRNA designated Mdv1-pre-miR-M4 targets both cellular and viral genes

Activation of Toll-like receptor 3 inhibits Marek's disease virus infection in chicken embryo fibroblast cells

Roles of avian herpesvirus microRNAs in infection, latency, and oncogenesis

MicroRNAs of Gallid and Meleagrid herpesviruses show generally conserved genomic locations and are virus-specific

The Oncogenic MicroRNA OncomiR-21 Overexpressed during Marek's Disease Lymphomagenesis Is Transactivated by the Viral Oncoprotein Meq

Expression of the env gene from the avian endogenous retrovirus ALVE and regulation by miR-155

Infectious Bursal Disease: A complex host-pathogen interaction

Infectious bursal disease virus of chickens: Pathogenesis and immunosuppression

Dendritic cells and the control of immunity

Genome-wide profiling of chicken dendritic cell response to infectious bursal disease

The enhanced virulence of very virulent infectious bursal disease virus is partly determined by its B-segment

MicroRNA-21 Targets the Tumor Suppressor Gene Tropomyosin 1 (TPM1)

MicroRNA-21 targets tumor suppressor genes in invasion and metastasis

Overexpression of microRNA gga-miR-21 in chicken fibroblasts suppresses replication of infectious bursal disease virus through inhibiting VP1 translation

gga-miR-454 suppresses infectious bursal disease virus (IBDV) replication via directly targeting IBDV genomic segment B and cellular Suppressors of Cytokine Signaling 6 (SOCS6)

MicroRNA gga-miR-130b Suppresses Infectious Bursal Disease Virus Replication via Targeting of the Viral Genome and Cellular Suppressors of Cytokine Signaling 5

gga-miR-155 Enhances Type I Interferon Expression and Suppresses Infectious Burse Disease Virus Replication via Targeting SOCS1 and TANK

gga-miR-9* inhibits IFN production in antiviral innate immunity by targeting interferon regulatory factor 2 to promote IBDV replication

gga-miR-142-5p attenuates IRF7 signaling and promotes replication of IBDV by directly targeting the chMDA5 s 3 untranslated region

gga-miR-2127 downregulates the translation of chicken p53 and attenuates chp53-mediated innate immune response against IBDV infection

gga-miR-27b-3p enhances type I interferon expression and suppresses infectious bursal disease virus replication via targeting cellular suppressors of cytokine signaling 3 and 6 (SOCS3 and 6)

Epigenetic Upregulation of Chicken MicroRNA-16-5p Expression in DF-1 Cells following Infection with Infectious Bursal Disease Virus (IBDV) Enhances IBDV-Induced Apoptosis and Viral Replication

Global distributions and strain diversity of avian infectious bronchitis virus: A review

Whole-genome characterization of Uruguayan strains of avian infectious bronchitis virus reveals extensive recombination between the two major South American lineages

Microarray analysis of infectious bronchitis virus infection of chicken primary dendritic cells

MicroRNA transcriptome analysis in chicken kidneys in response to differing virulent infectious bronchitis virus infections

miR-146a-5p promotes replication of infectious bronchitis virus by targeting IRAK2 and TNFRSF18

Gga-miR-30d regulates infectious bronchitis virus infection by targeting USP47 in HD11 cells

Delayed Newcastle disease virus replication using RNA interference to target the nucleoprotein

Common microRNA-mRNA Interactions in Different Newcastle Disease Virus-Infected Chicken Embryonic Visceral Tissues

Gga-miR-19b-3p Inhibits Newcastle Disease Virus Replication by Suppressing Inflammatory Response via Targeting RNF11 and ZMYND11

MicroRNA gga-miR-455-5p suppresses Newcastle disease virus replication via targeting cellular suppressors of cytokine signaling 3

MiR-375 Has Contrasting Effects on Newcastle Disease Virus Growth Depending on the Target Gene

Evolution and ecology of influenza A viruses

Overview of Influenza Viruses

A review of avian influenza in different bird species

The translation into Spanish of the OIE Manual of diagnostic tests and vaccines for terrestrial animals (mammals, birds and bees): Problems, solutions and conclusions

Identification of differentially expressed miRNAs in chicken lung and trachea with avian influenza virus infection by a deep sequencing approach

Integrated analysis of microRNA expression and mRNA transcriptome in lungs of avian influenza virus infected broilers

Identification of Chicken Pulmonary miRNAs Targeting PB1, PB1-F2, and N40 Genes of Highly Pathogenic Avian Influenza Virus H5N1 in Silico

Xiang, M. microRNAs in avian influenza virus H9N2-infected and non-infected chicken embryo fibroblasts

In-silico search of virus-specific host microRNAs regulating avian influenza virus NS1 expression

Poultry oncogenic retroviruses and humans

Retrovirus-induced disease in poultry

Analysis of microRNA expression profile in specific pathogen-free chickens in response to reticuloendotheliosis virus infection

Integrative Analyses of Transcriptome Sequencing Identify Functional miRNAs in the Chicken Embryo Fibroblasts Cells Infected with Reticuloendotheliosis Virus

Integrated Analysis of miRNA and mRNA Expression Profiles in Spleen of Specific Pathogen-Free Chicken Infected with Avian Reticuloendotheliosis Virus Strain SNV

Reticuloendotheliosis Virus Strain T Induces miR-155, Which Targets JARID2 and Promotes Cell Survival

Regulatory mechanism of microRNA-155 in chicken embryo fibroblasts in response to reticuloendotheliosis virus infection

MicroRNA 29b functions in acute myeloid leukemia

Genome-wide analysis of differentially expressed profiles of mRNAs, lncRNAs and circRNAs in chickens during Eimeria necatrix infection. Parasites Vectors

Diagnosis of sub-clinical coccidiosis in fast growing broiler chickens by MicroRNA profiling

The Life Cycle of Cryptosporidium baileyin. sp. (Apicomplexa, Cryptosporidiidae) Infecting Chickens

Cryptosporidium baileyiinfection associated with an outbreak of ocular and respiratory disease in otus owls (Otus scops) in a rehabilitation centre

Pathobiology of cryptosporidiosis (C. baileyi) in broiler chickens

Genome-wide analysis of differentially expressed profiles of mRNAs, lncRNAs and circRNAs during Cryptosporidium baileyi infection

Campylobacter jejuni-An Emerging Foodborne Pathogen

Chicken cecal microRNAs in the response to Campylobacter jejuni inoculation by Solexa sequencing

Correlation between miRNAs and target genes in response to Campylobacter jejuni inoculation in chicken

Identification and cloning of two immunogenic Clostridium perfringens proteins, elongation factor Tu (EF-Tu) and pyruvate:ferredoxin oxidoreductase (PFO) of C. perfringens

Modulation of microRNAs in two genetically disparate chicken lines showing different necrotic enteritis disease susceptibility

Differential regulation of microRNA transcriptome in chicken lines resistant and susceptible to necrotic enteritis disease

Distribution and differential expression of microRNAs in the intestinal mucosal layer of necrotic enteritis induced Fayoumi chickens

Differentially expressed JAK-STAT signaling pathway genes and target microRNAs in the spleen of necrotic enteritis-afflicted chicken lines

MicroRNA gga-miR-200a-3p modulates immune response via MAPK signaling pathway in chicken afflicted with necrotic enteritis

MicroRNA gga-miR-10a-mediated transcriptional regulation of the immune genes in necrotic enteritis afflicted chickens

Cecal CircRNAs Are Associated With the Response to Salmonella Enterica Serovar Enteritidis Inoculation in the Chicken

Chicken gga-miR-1306-5p targets Tollip and plays an important role in host response against Salmonella enteritidis infection

Splenic microRNA Expression Profiles and Integration Analyses Involved in Host Responses to Salmonella enteritidis Infection in Chickens

Cecal MicroRNAome response to Salmonella enterica serovar Enteritidis infection in White Leghorn Layer

Salmonella typhimurium DT104: A virulent and drug-resistant pathogen

A critical review ofSalmonellaTyphimurium infection in laying hens

Involvement of MicroRNAs in Probiotics-Induced Reduction of the Cecal Inflammation by Salmonella Typhimurium