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<pre class="comment" style="margin-top: 0; margin-bottom: 0;"><u>Megjegyzés</u>: Export Date: 28 February 2024; CODEN: DCIMD</pre>
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Innate immunity plays a crucial role in host defense against pathogen invasion and its strength and duration requires precise control. Long non-coding RNAs (lncRNAs) have become important regulators of innate immunity, yet their roles in Drosophila immune responses remain largely unknown. In this study, we identified that the overexpression of lncRNA-CR11538 inhibits the expression of antimicrobial peptides (AMPs) Dpt and AttA in Drosophila upon Escherichia coli (E. coli) infection, and influences the survival rate of flies after E. cloacae infection. Mechanically, lncRNA-CR11538 decoys Relish away from AMPs promoter region. We further revealed that Relish can promote the transcription of lncRNA-CR11538. After analyzing the dynamic expression profile of lncRNA-CR11538 during Imd immune response, we put forward a hypothesis that in the late stage of Imd immune response, lncRNA-CR11538 can be activated by Relish and further decoy Relish away from the AMPs promoter to suppress excessive immune signal and maintain immune homeostasis. This mechanism we proposed provides insights into the complex regulatory networks controlling immune responses in Drosophila and suggests potential targets for therapeutic intervention in diseases involving dysregulated immune responses.
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<div class="title"><a href="/gui2/?mode=browse¶ms=publication;34597478" target="_blank">Relish-facilitated lncRNA-CR11538 suppresses Drosophila Imd immune response and maintains immune homeostasis via decoying Relish away from antimicrobial peptide promoters</a></div> <div> <span class="journal-title">DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY</span>
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Chickens exhibit a distinct immune architecture characterised by the absence of draining lymph nodes and the presence of a well-developed mucosa-associated lymphoid tissue. The structure and spatiotemporal development of chicken lymphoid tissues in the intestine are poorly documented. The macroscopically indistinct structure of chicken Peyer's patches has impeded studies into their development. The generation of CSF1R-eGFP reporter transgenic chickens enables visualisation of the development, organisation and extent of chicken lymphoid tissues by unique macroscopic views. CSF1R-eGFP reporter transgenic chickens were used to investigate the distribution and spatiotemporal development of PP and caecal tonsils in embryonic day 18 to 8-week-old chickens. Peyer's patch anlagen are present at ED18 with a similar frequency and distribution pattern observed in 2- and 8week-old chickens. These findings can support in ovo and post-hatch mucosal vaccination strategies and the development of vaccine delivery systems targeted to the specialized epithelium overlying the Peyer's patches.
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Leukocyte immune-type receptors (LITRs) represent a polymorphic and polygenic family of immunoregulatory proteins originally discovered in channel catfish (Ictalurus punctatus; IpLITRs). Belonging to the immunoglobulin superfamily (IgSF), IpLITRs are generally classified as stimulatory or inhibitory types based on their utilization of various intracellular tyrosine-based signaling motifs. While research has shown that IpLITRs can activate as well as abrogate different immune cell effector responses including phagocytosis, recent identification of LITRs within the zebrafish genome (Danio rerio; DrLITRs) revealed the existence of fish LITR-types uniquely containing counteracting stimulatory and inhibitory cytoplasmic tail (CYT) region motifs (i.e., an immunoreceptor tyrosinebased activation motif; ITAM, and immunoreceptor tyrosine-based inhibitory motif; ITIM) within the same receptor. This arrangement is unusual as these motifs typically exist on separate stimulatory (i.e., ITAMcontaining) or inhibitory (i.e., ITIM-containing) immunoregulatory receptors that then co-engage to fine-tune cellular signaling and effector responses. Using a flow cytometric-based phagocytosis assay, we show here that engagement of DrLITR 1.2-expressing cells with antibody coated 4.5 mu m beads causes a robust ITAMdependent phagocytic response and reveal that its tandem ITIM motif surprisingly enhances the DrLITR 1.2induced phagocytic activity while simultaneously decreasing the receptors ability to bind the beads. Confocal microscopy studies also revealed that the ITIM-associated inhibitory signaling molecule SHP-2 is localized to the phagocytic synapse during the phagocytic response. Overall, these results provide the first functional characterization of teleost immune receptors containing a tandem ITAM and ITIM and allow for the proposal of an intracytoplasmic tail signaling model for ITIM-mediated enhancement of ITAM-dependent cellular activation.
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Charles University, Faculty of Science, Department of Zoology, Viničná 7, Prague, 128 43, Czech Republic
Wageningen University and Research, Department of Animal Sciences, Animal Breeding and Genomics, Droevendaalsesteeg 1, Wageningen, 6708PB, Netherlands
Federal University of Viçosa, MG, Viçosa, 36570-900, Brazil
Granada University, Science faculty, Department of Parasitology, Granada, Granada, CP:18071, Spain
EMBL, Genomics Core Facility, Meyerhofstraße 1, Heidelberg, 69117, Germany
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Correspondence Address: Vinkler, M.; Charles University, Viničná 7, Czech Republic; email: michal.vinkler@natur.cuni.cz
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<pre class="comment" style="margin-top: 0; margin-bottom: 0;"><u>Megjegyzés</u>: Charles University, Faculty of Science, Department of Zoology, Viničná 7, Prague, 128 43, Czech Republic
Wageningen University and Research, Department of Animal Sciences, Animal Breeding and Genomics, Droevendaalsesteeg 1, Wageningen, 6708PB, Netherlands
Federal University of Viçosa, MG, Viçosa, 36570-900, Brazil
Granada U...</pre>
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Beijing Key Laboratory for Prevention and Control of Infectious Diseases in Livestock and Poultry, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China
Export Date: 1 February 2024
CODEN: DCIMD
Correspondence Address: Li, Y.; Institute of Animal Husbandry and Veterinary Medicine, China; email: chunyudady@sina.com
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<pre class="comment" style="margin-top: 0; margin-bottom: 0;"><u>Megjegyzés</u>: Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China
Animal Science and Technology College, Beijing University of Agriculture, Beijing, China
Beijing Key Laboratory for Prevention and Control of Infectious Diseases in Livestock and Poultry, Beijing Academy of Agriculture and Fo...</pre>
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School of Biotechnology, Jiangsu University of Science and Technology, Jiangsu, Zhenjiang, 212100, China
Key Laboratory of Silkworm and Mulberry Genetic Improvement, Ministry of Agriculture and Rural Affairs, Sericultural Research Institute, Chinese Academy of Agricultural Sciences, Jiangsu, Zhenjiang, 212018, China
State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, 400715, China
Key Laboratory of Sericultural Biology and Genetic Breeding, Ministry of Agriculture, Southwest University, Chongqing, 400715, China
Export Date: 15 January 2024
CODEN: DCIMD
Correspondence Address: Xia, D.; Jiangsu Key Laboratory of Sericultural Biology and Biotechnology, Jiangsu, China; email: xiadingguo@126.com
Chemicals/CAS: guanosine triphosphate, 86-01-1; Antiviral Agents; Guanosine Triphosphate; Insect Proteins
Funding details: National Natural Science Foundation of China, NSFC, 31972616
Funding details: Graduate Research and Innovation Projects of Jiangsu Province, SJCX23_2241
Funding text 1: This work was supported by the Graduate Practice Innovation Program of Jiangsu Province, China ( SJCX23_2241 ) ; the National Natural Science Foundation of China, China (No. 31972616 ).
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Bombyx mori ras protein3 (BmRas3) is a small molecular protein in the GTPase superfamily, which has the activity of binding guanosine nucleotides and GTP enzymes. It acts as a molecular switch by coupling extracellular signal to different cellular response through the conversion between Ras-GTP conformation and Ras-GDP conformation, thus regulating signal pathways responsible for cell growth, migration, adhesion, survival and differentiation. However, few studies have been done on Ras3 in silkworm, and its function and mechanism are unclear. In this study, we found that the overexpression of BmRas3 inhibited the infection of BmNPV(B. mori nucleopolyhedrovirus), while knockdown of BmRas3 could promote the infection of BmNPV. In addition, after the BmRas3 in silkworm larvae was knockdown, the anti-BmNPV ability of silkworm decreased and the survival rate of silkworm was affected. Additionly in the cells with BmRas3 overexpression, the transcription level of BmMapkk6 、BmP38、BmJNK、BmERK1/2 and BmERK5 were significantly increased after BmNPV infection, and the transcript levels of BmMapkk6、BmP38、BmJNK、BmERK1/2 and BmERK5 were also inhibited to varying degrees This is the first report on the antiviral effect of BmRas3 in silkworm, which provides a new direction for further study on the anti-BmNPV mechanism of silkworm and screening and cultivation of anti-BmNPV silkworm strain. © 2023 Elsevier Ltd
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<div class="JournalArticle Publication short-list"> <div class="authors"> <span class="author-name" > Xia, D. ✉ </span> <span class="author-type"> </span> ; <span class="author-name" > Jiang, D. </span> <span class="author-type"> </span> ; <span class="author-name" > Yu, P. </span> <span class="author-type"> </span> ; <span class="author-name" > Jia, K. </span> <span class="author-type"> </span> ; <span class="author-name" > Wang, J. </span> <span class="author-type"> </span> ; <span class="author-name" > Shen, D. </span> <span class="author-type"> </span> ; <span class="author-name" > Zhao, Q. </span> <span class="author-type"> </span> ; <span class="author-name" > Lu, C. </span> <span class="author-type"> </span> </div ><div class="title"><a href="/gui2/?mode=browse¶ms=publication;34503674" mtid="34503674" target="_blank">Ras3 in Bombyx mori with antiviral function against B. mori nucleopolyhedrovirus</a></div> <div class="pub-info"> <span class="journal-title">DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY</span> <span class="journal-volume">152</span> <span class="page"> Paper: 105114 </span> <span class="year">(2024)</span> </div> <div class="pub-end"><div class="identifier-list"> <span class="identifiers"> <span class="id identifier oa_none" title="none"> <a style="color:blue" title="10.1016/j.dci.2023.105114" target="_blank" href="https://doi.org/10.1016/j.dci.2023.105114"> DOI </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:blue" title="001145228600001" target="_blank" href="https://www.webofscience.com/wos/woscc/full-record/001145228600001"> WoS </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:blue" title="85180577263" target="_blank" href="http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-85180577263"> Scopus </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:blue" title="38101715" target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=38101715&dopt=Abstract"> PubMed </a> </span> </span> </div> <div class="short-pub-prop-list"> <span class="short-pub-mtid"> Közlemény:34503674 </span> <span class="status-holder"><span class="status-data status-VALIDATED"> Egyeztetett </span></span> <span class="pub-core"> Idéző </span> <span class="pub-type">Folyóiratcikk (Szakcikk ) </span> <!-- && !record.category.scientific --> <span class="pub-category">Tudományos</span> </div> </div> </div><div class="JournalArticle Publication long-list">
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<div class="title"><a href="/gui2/?mode=browse¶ms=publication;34503674" target="_blank">Ras3 in Bombyx mori with antiviral function against B. mori nucleopolyhedrovirus</a></div> <div> <span class="journal-title">DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY</span>
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<pre class="comment" style="margin-top: 0; margin-bottom: 0;"><u>Megjegyzés</u>: School of Biotechnology, Jiangsu University of Science and Technology, Jiangsu, Zhenjiang, 212100, China
Key Laboratory of Silkworm and Mulberry Genetic Improvement, Ministry of Agriculture and Rural Affairs, Sericultural Research Institute, Chinese Academy of Agricultural Sciences, Jiangsu, Zhenjiang, 212018, China
State Key Laboratory of Silkwor...</pre>
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The Stimulator of Interferon Genes (STING, also known as MITA/ERYS/MPYS) is an adaptor molecule that plays a crucial role in the RLR pathway and responds to DNA and RNA viruses. In the present study, we have identified two novel isoforms of STING (the canonical form named as LcSTINGa and its alternative splicing isoform named as LcSTINGb) from teleost Lates calcarifer. LcSTINGa has an ORF of 1230 bp, encoding a 409 amino acid protein, while its alternative splicing variant, LcSTINGb, features an ORF of 987 bp, encoding 328 amino acids. LcSTINGa is predicted to contain four transmembrane helices, whereas LcSTINGb has only two. The Lates STING protein showed about 86.85% identity with Perca flavescens, 86.45% with Seriola and 39.51% with Homo sapiens. The tissue distribution studies revealed that the STING variants were constitutively expressed in all the tissues examined, with the highest expression in blood. In-vivo upregulation of LcSTINGa and LcSTINGb mRNA following immune challenge with poly (I:C), Red-spotted grouper nervous necrosis virus (RGNNV) and zymosan A suggests its significance in the immune response.
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<div class="JournalArticle Publication short-list"> <div class="authors"> <span class="author-name" > Sathyan, Krishnapriya Raji </span> <span class="author-type"> </span> ; <span class="author-name" > Premraj, Avinash </span> <span class="author-type"> </span> ; <span class="author-name" > Chaudhary, Mansi </span> <span class="author-type"> </span> ; <span class="author-name" > Ramachandran, Rajesh </span> <span class="author-type"> </span> ; <span class="author-name" > Puthiyedathu, Sajeevan Thavarool ✉ </span> <span class="author-type"> </span> </div ><div class="title"><a href="/gui2/?mode=browse¶ms=publication;34459443" mtid="34459443" target="_blank">Alternative splicing variants of stimulator of interferon genes (STING) from Asian seabass (Lates calcarifer) and their immune response against red spotted grouper nervous necrosis virus (RGNNV)</a></div> <div class="pub-info"> <span class="journal-title">DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY</span> <span class="journal-volume">149</span> <span class="page"> Paper: 105062 , 13 p. </span> <span class="year">(2023)</span> </div> <div class="pub-end"><div class="identifier-list"> <span class="identifiers"> <span class="id identifier oa_none" title="none"> <a style="color:black" title="10.1016/j.dci.2023.105062" target="_blank" href="https://doi.org/10.1016/j.dci.2023.105062"> DOI </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:blue" title="001084292600001" target="_blank" href="https://www.webofscience.com/wos/woscc/full-record/001084292600001"> WoS </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:black" title="85171452673" target="_blank" href="http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-85171452673"> Scopus </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:black" title="37726038" target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=37726038&dopt=Abstract"> PubMed </a> </span> </span> </div> <div class="short-pub-prop-list"> <span class="short-pub-mtid"> Közlemény:34459443 </span> <span class="status-holder"><span class="status-data status-VALIDATED"> Egyeztetett </span></span> <span class="pub-core"> Idéző </span> <span class="pub-type">Folyóiratcikk (Szakcikk ) </span> <!-- && !record.category.scientific --> <span class="pub-category">Tudományos</span> </div> </div> </div><div class="JournalArticle Publication long-list">
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<div class="title"><a href="/gui2/?mode=browse¶ms=publication;34459443" target="_blank">Alternative splicing variants of stimulator of interferon genes (STING) from Asian seabass (Lates calcarifer) and their immune response against red spotted grouper nervous necrosis virus (RGNNV)</a></div> <div> <span class="journal-title">DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY</span>
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