scholarly journals RABBIT POX

1934 ◽  
Vol 60 (4) ◽  
pp. 441-455 ◽  
Author(s):  
Harry S. N. Greene
Keyword(s):  
Causative Agent ◽  
Clinical Manifestations ◽  
Intimate Relationship ◽  
Endothelial Damage ◽  
Breeding Colony ◽  
Atypical Form ◽  
Small Nodule ◽  
Small Pox ◽  
Different Types ◽  
Extensive Necrosis

The lesions found in animals with epidemic rabbit pox have been described in this paper. The most distinctive gross lesion in all organs and tissues was the small nodule or papule which was found to consist of mononuclear infiltration and necrosis. Diffuse lesions were also found in which the infiltration was widespread and accompanied by edema, hemorrhage and extensive necrosis of affected tissues and organs. The possibility of the diffuse lesions being due to the action of secondary invaders was considered, but available evidence indicated that the different types, including pneumonia, represented reactions to a single causative agent. Moreover, an intimate relationship was observed to exist between lesions and small blood vessels in which primary endothelial damage was usually apparent. The degree of vascular damage generally corresponded to the extent of the lesion and it is probable that this in turn corresponded to the dose of the causative agent. The close analogy between the clinical manifestations and pathological processes of this disease in the rabbit and small pox in man led to the conclusion that the disease in the rabbit is essentially the same as small pox, and that it is probably produced by a virus closely related to the virus of small pox. Available evidence indicated that the infection originated in the Institute and that it spread in atypical form or masked by some other disease until it reached the breeding colony as a clearly defined epidemic infection.

scholarly journals The Role of JAK/STAT Molecular Pathway in Vascular Remodeling Associated with Pulmonary Hypertension

2021 ◽  
Vol 22 (9) ◽  
pp. 4980
Author(s):  
Inés Roger ◽  
Javier Milara ◽  
Paula Montero ◽  
Julio Cortijo
Keyword(s):  
Pulmonary Hypertension ◽  
Smooth Muscle ◽  
Pulmonary Artery ◽  
Vascular Remodeling ◽  
Pulmonary Arteries ◽  
Clinical Manifestations ◽  
Different Types ◽  
Artery Remodeling ◽  
Stat Pathway ◽  
Pulmonary Artery Remodeling

Pulmonary hypertension is defined as a group of diseases characterized by a progressive increase in pulmonary vascular resistance (PVR), which leads to right ventricular failure and premature death. There are multiple clinical manifestations that can be grouped into five different types. Pulmonary artery remodeling is a common feature in pulmonary hypertension (PH) characterized by endothelial dysfunction and smooth muscle pulmonary artery cell proliferation. The current treatments for PH are limited to vasodilatory agents that do not stop the progression of the disease. Therefore, there is a need for new agents that inhibit pulmonary artery remodeling targeting the main genetic, molecular, and cellular processes involved in PH. Chronic inflammation contributes to pulmonary artery remodeling and PH, among other vascular disorders, and many inflammatory mediators signal through the JAK/STAT pathway. Recent evidence indicates that the JAK/STAT pathway is overactivated in the pulmonary arteries of patients with PH of different types. In addition, different profibrotic cytokines such as IL-6, IL-13, and IL-11 and growth factors such as PDGF, VEGF, and TGFβ1 are activators of the JAK/STAT pathway and inducers of pulmonary remodeling, thus participating in the development of PH. The understanding of the participation and modulation of the JAK/STAT pathway in PH could be an attractive strategy for developing future treatments. There have been no studies to date focused on the JAK/STAT pathway and PH. In this review, we focus on the analysis of the expression and distribution of different JAK/STAT isoforms in the pulmonary arteries of patients with different types of PH. Furthermore, molecular canonical and noncanonical JAK/STAT pathway transactivation will be discussed in the context of vascular remodeling and PH. The consequences of JAK/STAT activation for endothelial cells and pulmonary artery smooth muscle cells’ proliferation, migration, senescence, and transformation into mesenchymal/myofibroblast cells will be described and discussed, together with different promising drugs targeting the JAK/STAT pathway in vitro and in vivo.

scholarly journals Current concepts in the diagnosis and management of antiphospholipid syndrome and ocular manifestations

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Gunay Uludag ◽  
Neil Onghanseng ◽  
Anh N. T. Tran ◽  
Muhammad Hassan ◽  
Muhammad Sohail Halim ◽  
...  
Keyword(s):  
Antiphospholipid Syndrome ◽  
Antiphospholipid Antibodies ◽  
Clinical Manifestations ◽  
Autoimmune Disorder ◽  
Ocular Involvement ◽  
Ocular Manifestations ◽  
Different Types ◽  
Thrombotic Complications ◽  
Specific Factors ◽  
Arteries And Veins

AbstractAntiphospholipid syndrome (APS) is an autoimmune disorder associated with obstetrical complications, thrombotic complications involving both arteries and veins, and non-thrombotic manifestations affecting multiple other systems presenting in various clinical forms. Diagnosis requires the presence of antiphospholipid antibodies. The exact pathogenesis of APS is not fully known. However, it has recently been shown that activation of different types of cells by antiphospholipid antibodies plays an important role in thrombosis formation. Ocular involvement is one of the important clinical manifestations of APS and can vary in presentations. Therefore, as an ophthalmologist, it is crucial to be familiar with the ocular findings of APS to prevent further complications that can develop. Furthermore, the ongoing identification of new and specific factors contributing to the pathogenesis of APS may provide new therapeutic options in the management of the disease in the future.

scholarly journals Highly Reduced Genome of the New Species Mycobacterium uberis, the Causative Agent of Nodular Thelitis and Tuberculoid Scrotitis in Livestock and a Close Relative of the Leprosy Bacilli

mSphere ◽  
2018 ◽  
Vol 3 (5) ◽  
Author(s):  
Andrej Benjak ◽  
Charlotte Avanzi ◽  
Yvonne Benito ◽  
Franck Breysse ◽  
Christophe Chartier ◽  
...  
Keyword(s):  
Causative Agent ◽  
Clinical Manifestations ◽  
Distinct Species ◽  
Close Relative ◽  
Protein Coding ◽  
Content Type ◽  
Mycobacterial Genome ◽  
Mycobacterium Lepromatosis ◽  
Dairy Animals ◽  
Phylogenomic Analyses

ABSTRACT Nodular thelitis is a chronic enzootic infection affecting dairy cows and goats. The causative agent was recently shown to be related to the leprosy-causing bacilli Mycobacterium leprae and Mycobacterium lepromatosis. In this study, the genome of this pathogen was sequenced and analyzed. Phylogenomic analyses confirmed that the pathogen present in nodular thelitis and tuberculoid scrotitis is a distinct species related to the leprosy bacilli and Mycobacterium haemophilum. Because the pathogen was originally isolated from a bovine udder, it was named “Mycobacterium uberis.” The genome of “M. uberis” is only 3.12 Mb in length, which represents the smallest mycobacterial genome identified so far but which is close to that of leprosy bacilli in size. The genome contains 1,759 protein-coding genes and 1,081 pseudogenes, indicative of extensive reductive evolution and likely the reason that M. uberis cannot be grown axenically. The pseudogenization and genome reduction in M. uberis seem to have been to some extent independent from the results determined for the genomes of the leprosy bacilli. IMPORTANCE M. uberis is an emerging skin pathogen in dairy animals. Its genome underwent massive reduction and gene decay, leading to a minimal set of genes required for an obligatory intracellular lifestyle, which highly resembles the evolution of the leprosy agents M. leprae and M. lepromatosis. The genomic similarity between M. uberis and the leprosy bacilli can help in identifying key virulence factors of these closely related species or in identifying genes responsible for the distinct differences between thelitis or scrotitis and leprosy with respect to clinical manifestations. Specific DNA markers can now be developed for quick detection of this pathogen.

scholarly journals Anisakiasis Pada Ikan Laut Di Indonesia: Prevalensi, Sebaran Dan Potensi Patogenitasnya Pada Manusia

2021 ◽  
Vol 14 (1) ◽  
pp. 11
Author(s):  
Forman Erwin Siagian ◽  
Esy Maryanti
Keyword(s):  
Causative Agent ◽  
Health Problem ◽  
Clinical Manifestations ◽  
Review Article ◽  
Marine Fishes ◽  
Predisposing Factor ◽  
Nematode Worm ◽  
Global Data

Nematode worm Anisakis sp is the causative agent of anisakiasis, a zoonosis which continues to be a health problem in humans, globally. Its clinical spectum varies from mild to very severe and always connected with sea fishes, one important source of nutrition for the community that cannot be ignored. In addition, consumer’s behavior and lifestyle in processing and consuming sea fishes also have has the potency as the predisposing factor for its transmission and clinical manifestations. This review article aimed to describes recent global data on anisakiasis and its occurrence in marine fishes of Indonesian waters and the risk of transmission in the community.

Cases of Q fever detected in residents of the novosibirsk region hospitalized with suspection of infections transmitted by ticks

2021 ◽  
Vol 66 (4) ◽  
pp. 229-236
Author(s):  
E. I. Bondarenko ◽  
E. S. Filimonova ◽  
E. I. Krasnova ◽  
E. V. Krinitsina ◽  
S. E. Tkachev
Keyword(s):  
Causative Agent ◽  
Q Fever ◽  
Clinical Manifestations ◽  
Test Methods ◽  
Pcr Analysis ◽  
Laboratory Diagnostics ◽  
Novosibirsk Region ◽  
Complex Approach ◽  
Wide Range ◽  
The Republic

Coxiella burnetii is the causative agent of Q fever (coxiellosis), which, in addition to acute manifestations, often occurs in a latent form, is prone to chronic course and, in the absence of antibiotic therapy, has a high risk of disability or death. As a result of the presence of a wide range of clinical manifestations specific to other infectious diseases, the use of laboratory test methods (LTM) is required to make a diagnosis. The presence of Q fever anthropurgic foci in the Novosibirsk region was described in the 90s of the last century, but due attention to its laboratory diagnostics is not paid in this region. The aim of the study was to identify genetic and serological markers of the causative agent, C. burnetii, in patients of the Novosibirsk region who were admitted for treatment with fever with suspected tick-borne infections (TBIs). DNA marker of the causative agent of Q fever was detected in blood samples by real time PCR in 9 out of 325 patients. In three patients, the presence of C. burnetii DNA was confirmed by sequencing of the IS1111 and htpB gene fragments. In ELISA tests, antibodies against the causative agent of coxiellosis were detected in the blood sera of 4 patients with positive results of PCR analysis. Contact with tick was registered in 7 out of 9 patients who had C. burnetii DNA and lacked markers of other TBIs. Six people were infected in the Novosibirsk region, two suffered from tick’s bite in Altai, and one case was from the Republic of Kyrgyzstan. Thus, a complex approach using both PCR analysis and ELISA provided the identification of markers of the Q fever causative agent in patients admitted with suspected TBIs, thereby differentiating it from other infections. Contact with ticks in most cases suggests that infection with C. burnetii had a transmissible pathway.

scholarly journals COVID-19: A Thunderstorm for mankind

2020 ◽  
Vol 31 (2) ◽  
pp. 81-93
Author(s):  
Ham Nazmul Ahasan ◽  
Musavvir Samin
Keyword(s):  
Causative Agent ◽  
Clinical Manifestations ◽  
Hubei Province ◽  
Viral Pneumonia ◽  
Medical Professionals ◽  
New Findings

In December 2019 an outbreak of viral pneumonia occurredinWuhan, Hubei Province of People’sRepublic of China (PRC). Later, it was found the responsible virus was SARS-CoV-2 and WHOrecognized it as a Pandemic on 11th March 2020. As of 15th July, in 213 countries, 580,038 deathshave occurred among 13,382,020 cases. Currently, many research are going on throughout theworld and they are coming up with new findings and observations every day. Based on the currentpublished literatures, this review systemically summarizes up to date information regarding structureof the causative agent, epidemiology, pathogenesis, clinical manifestations, diagnosis and treatmentoptions of COVID-19 in the hope that it will add to the knowledge of medical professionals andformulate better plans for future. Bangladesh J Medicine July 2020; 31(2) :81-93

Singularities of haemorrhagic syndrome in children with native and acquired deficiencies of von Willebrand factor

2013 ◽  
Vol 4 (1) ◽  
pp. 78-85
Author(s):  
Kseniya Ivanovna Pshenichnaya ◽  
Yegor Viktorovich Lyugayev ◽  
Olga Georgiyevna Golovina
Keyword(s):  
Clinical Manifestation ◽  
Von Willebrand Factor ◽  
Clinical Studies ◽  
Clinical Manifestations ◽  
Underlying Disease ◽  
Von Willebrand Disease ◽  
Acquired Von Willebrand Syndrome ◽  
Different Types ◽  
Von Willebrand ◽  
Willebrand Factor

Deficiencies of content in blood and activity of von Willebrand factor can be inborn or acquired with diseases of different nature. Acquired deficiencies of von Willebrand factor or acquired von Willebrand syndrome in children have been described in several clinical studies. This research paper contains data on clinical manifestation and dynamics of haemorrhagic syndrome in 30 children between 13 months and 18 years of age with acquired von Willebrand factor, suffering from different types of pathology. Similarly, clinical manifestations and dynamics of angiostaxis have been studied in 33 children with von Willebrand disease. It has been determined that clinical manifestations of microcirculatory angiostaxis are the same for children from both groups; however, children with acquired von Willebrand syndrome showed dominating limited numbers of haemorrhagical symptoms that were shorter in duration and less intense. Besides, hematomic component of haemorrhagic syndrome was absent. Eventually, accompanied by positive dynamic of the underlying disease, relapses of haemorrhagic syndrome cease, which does not happen in case of the patients with von Willebrand disease.

scholarly journals Clinical Manifestations and Diagnostic Challenges in Acute Porphyrias

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Henry Trier ◽  
Vikram P. Krishnasamy ◽  
Pashtoon Murtaza Kasi
Keyword(s):  
End Stage Renal Disease ◽  
Laboratory Testing ◽  
Biosynthetic Pathway ◽  
Clinical Manifestations ◽  
Definitive Diagnosis ◽  
Enzyme Deficiency ◽  
Different Types ◽  
Acute Porphyrias ◽  
Stage Renal Disease ◽  
End Stage

The porphyrias are a group of disorders characterized by an enzyme deficiency in the heme biosynthetic pathway. These can be classified into either erythropoietic or hepatic forms depending on the site of the major enzyme deficiency. The diagnosis of acute porphyrias, however, can be very challenging due to overlapping features amongst the various types. Initial suspicion is based on a myriad of clinical manifestations, which then are confirmed by laboratory testing where available. Genetic testing is now also available for the different types of porphyrias, aiding in the definitive diagnosis. Here, we present a challenging case of porphyria in a patient with end-stage renal disease and present the diagnostic challenges associated with the case and the ways forward.

scholarly journals Structured RNA Markers for Genotyping of Tick-Borne Encephalitis Virus

2018 ◽  
Vol 13 (1) ◽  
pp. 13-37
Author(s):  
V.D. Gusev ◽  
L.A. Miroshnichenko ◽  
T.N. Titkova ◽  
Yu.P. Dzhioev ◽  
I.V. Kozlova ◽  
...  
Keyword(s):  
Clinical Manifestations ◽  
Encephalitis Virus ◽  
Correct Identification ◽  
Disease Treatment ◽  
Pathogenic Potential ◽  
Tick Borne Encephalitis ◽  
Comprehensive Information ◽  
Different Types ◽  
Rna Fragments ◽  
Tick Borne Encephalitis Virus

Tick-borne encephalitis is one of the most dangerous natural focal infections. The causative agent of the disease is tick-borne encephalitis virus (TBEV ) transmitted by ticks . There are three main subtypes of TBEV with different clinical manifestations of the disease, but existence of other subtypes is also possible. Effectiveness of the disease treatment can largely depend on the correct identification of TBEV genotype. Comprehensive information about the genotype is contained in the full coding sequence of TBEV genome. А limited number of genotyping markers can be extracted from it in the form of relatively short structured RNA fragments. In this paper, a rather general approach to the isolation of structured RNA markers for the genotyping of TBEV is formulated. Three types of structures are considered: periodicity, fractal-like constructs and compactly localized combinations of different types of repetitions. The choice of these structures for the purposes of genotyping and their possible role in the formation of the pathogenic potential of the virus is substantiated. The approach was tested on the full coding sequences of TBEV (161 strains). Examples of the most characteristic markers of each of the three types are given.

Sign in / Sign up

Export Citation Format

Share Document