scholarly journals Ontogeny of the Hapuka (Polyprion oxygeneios) Immune System

2021 ◽  
Author(s):  
◽  
Simon Parker
Keyword(s):  
Immune System ◽  
Intestinal Tract ◽  
Head Kidney ◽  
Maternal Transfer ◽  
Developmental Sequence ◽  
Rt Pcr ◽  
Immune Genes ◽  
Immune Organs ◽  
Insight Into ◽  
Polyprion Oxygeneios

<p>In this study the ontogeny of the hapuka (Polyprion oxygeneios) immune system was studied during larval development. In teleost fish, the head kidney, thymus, and spleen are generally regarded as important immune organs. The head kidney was observed at 4 days post hatch (dph), the spleen at 16 dph and lastly the thymus at 20 dph and all 3 lymphoid organs were relatively well developed by 45 dph. The immune genes CSF1R, C3, MHCIIα, TCRα, TCRβ, RAG1, IgM and IgZ were examined by RT-PCR to investigate the leucocyte development. Macrophages appear to be present from hatch with both CSF1R and MHCIIα expression from 1 dph, while IgM is expressed at 9 dph. T-cells appear later in hapuka with TCRβ expression first detected at 32 dph whereas TCRα was not expressed until after 63 dph. Immunostaining using a monoclonal antibody against fish IgM detected IgM in the head kidney at 12 dph, the spleen at 32 dph, the intestinal tract at 45 dph and lastly the thymus at 50 dph. Comparison of the leucocyte populations in juveniles and adults indicated that innate cell populations are late to develop, while the adaptive cells mature earlier in hapuka than expected. Finally, the maternal transfer of immunity was examined and while lysozyme and IgM appear to be transferred, complement does not. Overall this study provides insight into the developmental sequence of immune organs and cells and will be useful in understanding the timing of immune competence in juveniles and adult hapuka.</p>

scholarly journals Ontogeny of the Hapuka (Polyprion oxygeneios) Immune System

2021 ◽  
Author(s):  
◽  
Simon Parker
Keyword(s):  
Immune System ◽  
Intestinal Tract ◽  
Head Kidney ◽  
Maternal Transfer ◽  
Developmental Sequence ◽  
Rt Pcr ◽  
Immune Genes ◽  
Immune Organs ◽  
Insight Into ◽  
Polyprion Oxygeneios

<p>In this study the ontogeny of the hapuka (Polyprion oxygeneios) immune system was studied during larval development. In teleost fish, the head kidney, thymus, and spleen are generally regarded as important immune organs. The head kidney was observed at 4 days post hatch (dph), the spleen at 16 dph and lastly the thymus at 20 dph and all 3 lymphoid organs were relatively well developed by 45 dph. The immune genes CSF1R, C3, MHCIIα, TCRα, TCRβ, RAG1, IgM and IgZ were examined by RT-PCR to investigate the leucocyte development. Macrophages appear to be present from hatch with both CSF1R and MHCIIα expression from 1 dph, while IgM is expressed at 9 dph. T-cells appear later in hapuka with TCRβ expression first detected at 32 dph whereas TCRα was not expressed until after 63 dph. Immunostaining using a monoclonal antibody against fish IgM detected IgM in the head kidney at 12 dph, the spleen at 32 dph, the intestinal tract at 45 dph and lastly the thymus at 50 dph. Comparison of the leucocyte populations in juveniles and adults indicated that innate cell populations are late to develop, while the adaptive cells mature earlier in hapuka than expected. Finally, the maternal transfer of immunity was examined and while lysozyme and IgM appear to be transferred, complement does not. Overall this study provides insight into the developmental sequence of immune organs and cells and will be useful in understanding the timing of immune competence in juveniles and adult hapuka.</p>

scholarly journals Transcriptomic signature of rapidly evolving immune genes in a highland fish

2019 ◽  
Author(s):  
Chao Tong ◽  
Miao Li ◽  
Kai Zhao
Keyword(s):  
Fish Species ◽  
Complement Activation ◽  
Expression Patterns ◽  
Adaptive Immune System ◽  
Head Kidney ◽  
Immune Gene ◽  
Gene Repertoire ◽  
Immune Genes ◽  
Genome Wide ◽  
Insight Into

AbstractRecent genome-wide studies have begun to elucidate the genomic basis of hypoxia, long-term cold and high saline and alkaline adaptation in highland fish, and a number of key genes contributed to its highland adaptation were identified. An increasing number of studies indicated that immune genes of Tibetan endemic fish species underwent positive selection towards functional shift, while the insight into immune gene repertoire of Tibetan highland fishes from genome-wide studies has largely lagged behind. In this study, we performed one of the first comparative genomics study in particular focusing on the signatures of immune genes in a highland fish, Gymnocypris przewalskii based on immune-relevant tissue transcriptome assemblies. We identified seven putative rapidly evolving immune genes with elevated molecular evolutionary rate (dN/dS) relative to lowland fish species. Using tissue-transcriptome data, we found most of rapidly evolving immune genes were broadly expressed in head-kidney, spleen, gills and skin tissues, which significantly enriched for complement activation and inflammatory response processes. In addition, we found a set of complement activation related genes underwent accelerated evolution and showed consistently repressed expression patterns in response to parasite Ichthyophthirius multifiliis infection. Moreover, we detected a number of immune genes involved in adaptive immune system exhibited distinct signature of upregulated expression patterns after parasite infection. Taken together, this study provided putative transcriptomic signatures of rapidly evolving immune genes, and will gain the insight into Schizothoracine fish adaptation to high-altitude extreme aquatic environments including diversified pathogen challenge.

scholarly journals Transglutaminases Are Active in Perivascular Adipose Tissue

2021 ◽  
Vol 22 (5) ◽  
pp. 2649
Author(s):  
Alexis N. Orr ◽  
Janice M. Thompson ◽  
Janae M. Lyttle ◽  
Stephanie W. Watts
Keyword(s):  
Adipose Tissue ◽  
Vascular Remodeling ◽  
Coagulation Factor ◽  
Sprague Dawley ◽  
Rt Pcr ◽  
Ideal Model ◽  
Perivascular Adipose Tissue ◽  
Tissue Sections ◽  
Insight Into ◽  
Immunohistochemical Analyses

Transglutaminases (TGs) are crosslinking enzymes best known for their vascular remodeling in hypertension. They require calcium to form an isopeptide bond, connecting a glutamine to a protein bound lysine residue or a free amine donor such as norepinephrine (NE) or serotonin (5-HT). We discovered that perivascular adipose tissue (PVAT) contains significant amounts of these amines, making PVAT an ideal model to test interactions of amines and TGs. We hypothesized that transglutaminases are active in PVAT. Real time RT-PCR determined that Sprague Dawley rat aortic, superior mesenteric artery (SMA), and mesenteric resistance vessel (MR) PVATs express TG2 and blood coagulation Factor-XIII (FXIII) mRNA. Consistent with this, immunohistochemical analyses support that these PVATs all express TG2 and FXIII protein. The activity of TG2 and FXIII was investigated in tissue sections using substrate peptides that label active TGs when in a catalyzing calcium solution. Both TG2 and FXIII were active in rat aortic PVAT, SMAPVAT, and MRPVAT. Western blot analysis determined that the known TG inhibitor cystamine reduced incorporation of experimentally added amine donor 5-(biotinamido)pentylamine (BAP) into MRPVAT. Finally, experimentally added NE competitively inhibited incorporation of BAP into MRPVAT adipocytes. Further studies to determine the identity of amidated proteins will give insight into how these enzymes contribute to functions of PVAT and, ultimately, blood pressure.

Abstract 293: Cardiac Arrest and Resuscitation Causes Immunodeficiency That Involves the Hypothalamic-Pituitary-Adrenal Axis

Circulation ◽  
2018 ◽  
Vol 138 (Suppl_2) ◽  
Author(s):  
Yuntian Shen ◽  
Qiang Zhao ◽  
Jiangbo Wu ◽  
Zhuoran Wang ◽  
Wei Yang
Keyword(s):  
Immune Response ◽  
Cardiac Arrest ◽  
Immune System ◽  
Hpa Axis ◽  
Time Course ◽  
Immune Cell ◽  
Infectious Complications ◽  
Hypothalamic Pituitary Adrenal ◽  
Immune Organs ◽  
High Incidence

Introduction: Cardiac arrest (CA) is associated with high mortality and morbidity, which is in part due to infectious complications developed in CA patients. Infection complications, particularly pneumonia, occur in approximately 60% of CA patients. Given this high incidence, we hypothesized that after CA, the immune system is impaired, which increases the susceptibility of CA patients to potential infections. Therefore, in this study, we systematically examined the immune response in the brain and peripheral immune organs after CA. Methods: Mice were subjected to CA and cardiopulmonary resuscitation (CA/CPR). Flow cytometry, ELISA, immunohistochemistry, and quantitative PCR were used to analyze the immune response in various post-CA organs. Results: First, we characterized the time course of the immune response in the spleen after CA/CPR. CA/CPR induced significant changes in all major immune cell populations. Notably, B cell frequencies decreased, while T cell frequencies increased, in various organs on day 3 post-CA. Further, the levels of pro-inflammatory cytokines, eg IL-6, were markedly increased in the blood and brain after CA. Critically, we found that the lymphocyte counts in the spleen and thymus were dramatically lower in CA mice than in sham mice. Interestingly, CA/CPR caused progressive atrophy of the spleen and thymus. Since it has been shown that CA/CPR alters activity of the hypothalamic-pituitary-adrenal (HPA) axis, we speculated that CA-induced atrophy of lymphoid organs is mediated by the HPA axis. Thus, we treated CA mice with RU486, a glucocorticoid receptor antagonist. Indeed, this treatment reversed CA-induced organ atrophy and mitigated immune cell depletion, both in the thymus and spleen. Conclusions: We provided for the first time evidence that CA/CPR rapidly induced a systemic inflammatory response followed by impairment of the immune system, which eventually led to a massive loss of immune cells in the peripheral immune organs. This CA-induced immunodeficiency appears to be mediated by dysregulation of the HPA axis. Our findings here may be of high clinical significance, considering the high incidence of infectious complications in CA patients and their detrimental effects on CA outcome.

scholarly journals Secretome Profiling of Atlantic Salmon Head Kidney Leukocytes Highlights the Role of Phagocytes in the Immune Response to Soluble β-Glucan

2021 ◽  
Vol 12 ◽  
Author(s):  
Dimitar B. Iliev ◽  
Guro Strandskog ◽  
Mehrdad Sobhkhez ◽  
Jack A. Bruun ◽  
Jorunn B. Jørgensen
Keyword(s):  
Immune System ◽  
Atlantic Salmon ◽  
Primary Cultures ◽  
Head Kidney ◽  
Cell Types ◽  
Mononuclear Phagocytes ◽  
Immunostimulatory Activity ◽  
Complement Receptor 3 ◽  
Bacteria And Fungi

β‐Glucans (BG) are glucose polymers which are produced in bacteria and fungi but not in vertebrate organisms. Being recognized by phagocytic leukocytes including macrophages and neutrophils through receptors such as dectin-1 and Complement receptor 3 (CR3), the BG are perceived by the innate immune system of vertebrates as foreign substances known as Pathogen Associated Molecular Patterns (PAMPs). The yeast-derived BG has been recognized for its potent biological activity and it is used as an immunomodulator in human and veterinary medicine. The goal of the current study was to characterize the immunostimulatory activity of soluble yeast BG in primary cultures of Atlantic salmon (Salmo salar) head kidney leukocytes (HKLs) in which phagocytic cell types including neutrophils and mononuclear phagocytes predominate. The effect of BG on the secretome of HKL cultures, including secretion of extracellular vesicles (EVs) and soluble protein55s was characterized through western blotting and mass spectrometry. The results demonstrate that, along with upregulation of proinflammatory genes, BG induces secretion of ubiquitinated proteins (UbP), MHCII-containing EVs from professional antigen presenting cells as well as proteins derived from granules of polymorphonuclear granulocytes (PMN). Among the most abundant proteins identified in BG-induced EVs were beta-2 integrin subunits, including CD18 and CD11 homologs, which highlights the role of salmon granulocytes and mononuclear phagocytes in the response to soluble BG. Overall, the current work advances the knowledge about the immunostimulatory activity of yeast BG on the salmon immune system by shedding light on the effect of this PAMP on the secretome of salmon leukocytes.

scholarly journals Bichir external gills arise via heterochronic shift that accelerates hyoid arch development

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Jan Stundl ◽  
Anna Pospisilova ◽  
David Jandzik ◽  
Peter Fabian ◽  
Barbora Dobiasova ◽  
...  
Keyword(s):  
Pharyngeal Arch ◽  
Developmental Sequence ◽  
Free Living ◽  
Pharyngeal Arches ◽  
Hyoid Arch ◽  
Early Appearance ◽  
Evolutionary Changes ◽  
Insight Into ◽  
Living Group ◽  
Early Larvae

In most vertebrates, pharyngeal arches form in a stereotypic anterior-to-posterior progression. To gain insight into the mechanisms underlying evolutionary changes in pharyngeal arch development, here we investigate embryos and larvae of bichirs. Bichirs represent the earliest diverged living group of ray-finned fishes, and possess intriguing traits otherwise typical for lobe-finned fishes such as ventral paired lungs and larval external gills. In bichir embryos, we find that the anteroposterior way of formation of cranial segments is modified by the unique acceleration of the entire hyoid arch segment, with earlier and orchestrated development of the endodermal, mesodermal, and neural crest tissues. This major heterochronic shift in the anteroposterior developmental sequence enables early appearance of the external gills that represent key breathing organs of bichir free-living embryos and early larvae. Bichirs thus stay as unique models for understanding developmental mechanisms facilitating increased breathing capacity.

scholarly journals The neuropeptide receptor NMUR-1 regulates the specificity of C. elegans innate immunity against pathogen infection

2021 ◽  
Author(s):  
Phillip Wibisono ◽  
Shawndra Wibisono ◽  
Jan Watteyne ◽  
Chia-Hui Chen ◽  
Durai Sellegounder ◽  
...  
Keyword(s):  
Innate Immunity ◽  
Immune System ◽  
Immune Responses ◽  
Adaptive Immune System ◽  
Innate Immune ◽  
Innate Immune Responses ◽  
Immune Genes ◽  
C Elegans ◽  
Adaptive Immune ◽  
Functional Assays

A key question in current immunology is how the innate immune system generates high levels of specificity. Like most invertebrates, Caenorhabditis elegans does not have an adaptive immune system and relies solely on innate immunity to defend itself against pathogen attacks, yet it can still differentiate different pathogens and launch distinct innate immune responses. Here, we have found that functional loss of NMUR-1, a neuronal GPCR homologous to mammalian receptors for the neuropeptide neuromedin U, has diverse effects on C. elegans survival against various bacterial pathogens. Transcriptomic analyses and functional assays revealed that NMUR-1 modulates C. elegans transcription activity by regulating the expression of transcription factors, which, in turn, controls the expression of distinct immune genes in response to different pathogens. Our study has uncovered a molecular basis for the specificity of C. elegans innate immunity that could provide mechanistic insights into understanding the specificity of vertebrate innate immunity.

scholarly journals Maternal transfer and sublethal immune system effects of brevetoxin exposure in nesting loggerhead sea turtles (Caretta caretta) from western Florida

2016 ◽  
Vol 180 ◽  
pp. 131-140 ◽  
Author(s):  
Justin R. Perrault ◽  
Katherine D. Bauman ◽  
Taylor M. Greenan ◽  
Patricia C. Blum ◽  
Michael S. Henry ◽  
...  
Keyword(s):  
Immune System ◽  
Sea Turtles ◽  
Caretta Caretta ◽  
Maternal Transfer ◽  
Loggerhead Sea Turtles

scholarly journals Descriptive epidemiology of coronavirus disease 2019 in Nigeria, 27 February–6 June 2020

2020 ◽  
Vol 148 ◽  
Author(s):  
K. O. Elimian ◽  
C. L. Ochu ◽  
E. Ilori ◽  
J. Oladejo ◽  
E. Igumbor ◽  
...  
Keyword(s):  
Health Planning ◽  
Case Fatality ◽  
National Surveillance ◽  
Descriptive Epidemiology ◽  
Rt Pcr ◽  
Chain Reaction ◽  
Response Strategies ◽  
Polymerase Chain ◽  
Insight Into ◽  
Pcr Test

Abstract The objective of this study was to describe the epidemiology of COVID-19 in Nigeria with a view of generating evidence to enhance planning and response strategies. A national surveillance dataset between 27 February and 6 June 2020 was retrospectively analysed, with confirmatory testing for COVID-19 done by real-time polymerase chain reaction (RT-PCR). The primary outcomes were cumulative incidence (CI) and case fatality (CF). A total of 40 926 persons (67% of total 60 839) had complete records of RT-PCR test across 35 states and the Federal Capital Territory, 12 289 (30.0%) of whom were confirmed COVID-19 cases. Of those confirmed cases, 3467 (28.2%) had complete records of clinical outcome (alive or dead), 342 (9.9%) of which died. The overall CI and CF were 5.6 per 100 000 population and 2.8%, respectively. The highest proportion of COVID-19 cases and deaths were recorded in persons aged 31–40 years (25.5%) and 61–70 years (26.6%), respectively; and males accounted for a higher proportion of confirmed cases (65.8%) and deaths (79.0%). Sixty-six per cent of confirmed COVID-19 cases were asymptomatic at diagnosis. In conclusion, this paper has provided an insight into the early epidemiology of COVID-19 in Nigeria, which could be useful for contextualising public health planning.

scholarly journals From microbiota toward gastro-enteropancreatic neuroendocrine neoplasms: Are we on the highway to hell?

2020 ◽  
Author(s):  
Giovanni Vitale ◽  
◽  
Alessandra Dicitore ◽  
Luigi Barrea ◽  
Emilia Sbardella ◽  
...  
Keyword(s):  
Immune System ◽  
Gut Microbiota ◽  
Intestinal Tract ◽  
Potential Role ◽  
Neuroendocrine Neoplasms ◽  
Complex Interplay ◽  
Barrier Integrity ◽  
Tumorigenesis And Progression ◽  
Intestinal Pathogens ◽  
Immune System Modulation

Abstract Gut microbiota is represented by different microorganisms that colonize the intestinal tract, mostly the large intestine, such as bacteria, fungi, archaea and viruses. The gut microbial balance has a key role in several functions. It modulates the host’s metabolism, maintains the gut barrier integrity, participates in the xenobiotics and drug metabolism, and acts as protection against gastro-intestinal pathogens through the host’s immune system modulation. The impaired gut microbiota, called dysbiosis, may be the result of an imbalance in this equilibrium and is linked with different diseases, including cancer. While most of the studies have focused on the association between microbiota and gastrointestinal adenocarcinomas, very little is known about gastroenteropancreatic (GEP) neuroendocrine neoplasms (NENs). In this review, we provide an overview concerning the complex interplay between gut microbiota and GEP NENs, focusing on the potential role in tumorigenesis and progression in these tumors.

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