Two new species of myxosporeans are described from the gall bladders of hoki, Macruronus magellanicus Lönnberg, 1907, caught in the Southeast Pacific off Chile and in the Southwest Atlantic off the Falkland Islands. Pseudalataspora kovalevae n. sp. is described morphologically and genetically. Of the 12 species of Pseudalataspora previously described from the gall bladders of marine fish, P. kovalevae is most similar in morphology to P. umbraculiformis Gaevskaya and Kovaleva, 1984. The 18S rRNA gene sequence from P. kovalevae is the first for a member of the genus Pseudalataspora. Based on currently available myxosporean 18S rRNA gene sequence data, P. kovalevae shares greatest sequence identity with species of the genus Ceratomyxa (C. anko and C. pantherini). Palliatus magellanicus n. sp. is described morphologically only; it differs considerably in morphology, host species and locality from the five other Palliatus species described from marine fishes. A third species from the gall bladder is also described morphologically and genetically. On the basis of its morphology it is tentatively identified as Myxidium baueri Kovaleva and Gaevskaya, 1982, for which M. magellanicus is a new host record. Molecular analysis indicates that, of those species for which data are available, M. baueri is most closely related to Myxidium coryphaenoideum Noble, 1966 based on 18S rRNA gene sequence data, though support for a phylogenetic grouping is low.
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http://dx.doi.org/10.11646/zootaxa.3647.4.4 | DOI Listing |
Front Public Health
December 2024
Department of Pharmacy, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Background: The incidence of gall bladder cancer (GBC), one of the most prevalent bile duct malignancies, differs with ethnicity and geographic location. To treat unresected GBC in the Chinese setting, this study aimed to assess the financial effectiveness of a combination of modified gemcitabine and oxaliplatin.
Methods: Data from a randomized controlled study in which individuals with metastatic GBC were treated with oxaliplatin and gemcitabine demonstrated improved survival.
Discov Oncol
December 2024
Department of Electrical Engineering, Assam Engineering College, Assam, India.
Radiomics is a method that extracts many features from medical images using various algorithms. Medical nomograms are graphical representations of statistical predictive models that produce a likelihood of a clinical event for a specific individual based on biological and clinical data. The radiomic nomogram was first introduced in 2016 to study the integration of specific radiomic characteristics with clinically significant risk factors for patients with colorectal cancer lymph node metastases.
View Article and Find Full Text PDFMicrob Pathog
December 2024
Universidade Federal de São Paulo, Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Diadema, São Paulo, Brasil, CEP 09972-270; Universidade Estadual de Campinas, Instituto de Biologia, Campinas, Brasil, CEP 13083-862.
Myxosporeans are a diverse group of cnidarian endoparasites of aquatic animals, with more than 2,600 described species. The genus Ceratomyxa includes some 270 species that are mostly coelozoic and infect the gall bladders of mainly marine fish. During our survey in Tapajós River in the Brazilian Amazon, two Ceratomyxa species were discovered in the gallbladders of the anostomid fishes Schyzodon fasciatus and Schyzodon vittatus.
View Article and Find Full Text PDFInt J Radiat Oncol Biol Phys
December 2024
Departments of Surgical Gastroenterology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow.
Purpose: CT is the standard of care for patients presenting with unresectable advanced GBC but their prognosis remains poor. The value of consolidation CTRT after initial CT is uncertain. We therefore conducted a single centre open label randomised trial evaluating consolidation CTRT versus Observation after four cycles of CT in patients whose disease did not progress during CT (partial responders/stable disease).
View Article and Find Full Text PDFNephrol Dial Transplant
December 2024
International Alport Syndrome Alliance and Alport UK, ERKNet ePAG.
Glomerular nephropathy resulting from the genetic defects in COL4A3/4/5 genes including the classical Alport syndrome (AS) is the second commonest hereditary kidney disease characterized by persistent haematuria progressing to the need of kidney replacement therapy, frequently associated with sensorineural deafness, and occasionally with ocular anomalies. Diagnosis and management of COL4A3/4/5 glomerulopathy is a great challenge due to its phenotypic heterogeneity, multiple modes of inheritance, variable expressivity, and disease penetrance of individual variants as well as imperfect prognostic and progression factors and scarce and limited clinical trials, especially in children. As a joint initiative of the European Rare Kidney disease reference Network (ERKNet), European Renal Association (ERA Genes&Kidney) and European Society for Paediatric Nephrology (ESPN) Working Group Hereditary Kidney Disorders, a team of experts including adult and paediatric nephrologists, kidney geneticists, audiologists, ophthalmologists and a kidney pathologist were selected to perform a systematic literature review on 21 clinically relevant PICO (Patient or Population covered, Intervention, Comparator, Outcome) questions.
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