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1.
J Invertebr Pathol ; 200: 107970, 2023 09.
Artículo en Inglés | MEDLINE | ID: mdl-37422088

RESUMEN

Biological invasions may act as conduits for pathogen introduction. To determine which invasive non-native species pose the biggest threat, we must first determine the symbionts (pathogens, parasites, commensals, mutualists) they carry, via pathological surveys that can be conducted in multiple ways (i.e., molecular, pathological, and histological). Whole animal histopathology allows for the observation of pathogenic agents (virus to Metazoa), based on their pathological effect upon host tissue. Where the technique cannot accurately predict pathogen taxonomy, it does highlight pathogen groups of importance. This study provides a histopathological survey of Pontogammarus robustoides (invasive amphipod in Europe) as a baseline for symbiont groups that may translocate to other areas/hosts in future invasions. Pontogammarus robustoides (n = 1,141) collected throughout Poland (seven sites), were noted to include a total of 13 symbiotic groups: a putative gut epithelia virus (overall prevalence = 0.6%), a putative hepatopancreatic cytoplasmic virus (1.4%), a hepatopancreatic bacilliform virus (15.7%), systemic bacteria (0.7%), fouling ciliates (62.0%), gut gregarines (39.5%), hepatopancreatic gregarines (0.4%), haplosporidians (0.4%), muscle infecting microsporidians (6.4%), digeneans (3.5%), external rotifers (3.0%), an endoparasitic arthropod (putatively: Isopoda) (0.1%), and Gregarines with putative microsporidian infections (1.4%). Parasite assemblages partially differed across collection sites. Co-infection patterns revealed strong positive and negative associations between five parasites. Microsporidians were common across sites and could easily spread to other areas following the invasion of P. robustoides. By providing this initial histopathological survey, we hope to provide a concise list of symbiont groups for risk-assessment in the case of a novel invasion by this highly invasive amphipod.


Asunto(s)
Anfípodos , Apicomplexa , Microsporidios , Parásitos , Animales , Anfípodos/microbiología , Interacciones Huésped-Parásitos , Reino Unido , Especies Introducidas , Apicomplexa/fisiología
2.
Dis Aquat Organ ; 136(1): 51-62, 2019 Oct 02.
Artículo en Inglés | MEDLINE | ID: mdl-31575834

RESUMEN

The Trematoda are a group of phylogenetically diverse metazoan parasites that exhibit complex life cycles that often pass through invertebrate and vertebrate hosts. Some trematodes influence their host's behaviour to benefit transmission. Their parasitic influence may impact host population size by inhibiting an individual's reproductive capacity. We assessed the impact of infection by Podocotyle atomon on the reproductive behaviour and fecundity of its amphipod intermediate host, Gammarus zaddachi, using laboratory and field studies. Parasite prevalence was high in the field, with males more likely to be infected (prevalence in males 64%, in females 39%). Males also suffered a higher parasite burden than females. Infected females were less active, but we found no evidence for a reduction in female reproductive success. Infected females also had comparable pairing success to uninfected females. In males, infection reduced survival and fecundity, with mortality being highest, and sperm numbers lowest, in heavily infected individuals. Trematode parasites are sometimes associated with altered host fecundity, but studies often lack the relevant experimental data to explore the evolution of the trait. We discuss this among information specific to the effect of P. atomon infection in G. zaddachi.


Asunto(s)
Anfípodos/fisiología , Anfípodos/parasitología , Interacciones Huésped-Parásitos , Trematodos/patogenicidad , Animales , Femenino , Fertilidad , Masculino , Reproducción
3.
Trends Parasitol ; 38(8): 642-659, 2022 08.
Artículo en Inglés | MEDLINE | ID: mdl-35667993

RESUMEN

Microsporidian diversity is vast. There is a renewed drive to understand how microsporidian pathological, genomic, and ecological traits relate to their phylogeny. We comprehensively sample and phylogenetically analyse 125 microsporidian genera for which sequence data are available. Comparing these results with existing phylogenomic analyses, we suggest an updated taxonomic framework to replace the inconsistent clade numbering system, using informal taxonomic names: Glugeida (previously clades 5/3), Nosematida (4a), Enterocytozoonida (4b), Amblyosporida (3/5), Neopereziida (1), and Ovavesiculida (2). Cellular, parasitological, and ecological traits for 281 well-defined species are compared with identify clade-specific patterns across long-branch Microsporidia. We suggest that future taxonomic circumscriptions of Microsporidia should involve additional markers (SSU/ITS/LSU), and that a comprehensive suite of phenotypic and ecological traits help to predict broad microsporidian functional and lineage diversity.


Asunto(s)
Microsporidios , Microsporidios/genética , Filogenia
4.
Drug Metab Dispos ; 39(9): 1747-54, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21646438

RESUMEN

After oral administration to humans, eltrombopag undergoes extensive cleavage of its hydrazine linkage to metabolites, which are exclusively eliminated in urine. In vitro, the cleavage pathway was not detected in systems using cytochrome P450 enzymes, renal or hepatic microsomes, or hepatocytes but was readily evident after anaerobic incubation with rodent cecal contents or human fecal homogenate. Antibiotic treatment in vitro and in vivo inhibited eltrombopag cleavage, further indicating that cleavage is via gut microbes. Antibiotic treatment did not alter the systemic exposure of eltrombopag in mice. Oral and intravenous pharmacokinetic characterization in the mice with one of the cleavage products indicated that it was readily absorbed, conjugated, and eliminated in urine, consistent with its fate after oral administration of eltrombopag. Variation in this microbial pathway, for example by antibiotic cotherapy, is unlikely to be clinically significant.


Asunto(s)
Benzoatos/metabolismo , Hidrazinas/metabolismo , Pirazoles/metabolismo , Administración Oral , Animales , Antibacterianos/farmacología , Benzoatos/farmacocinética , Ciego/efectos de los fármacos , Ciego/microbiología , Sistema Enzimático del Citocromo P-450/metabolismo , Heces/química , Femenino , Hepatocitos/metabolismo , Humanos , Hidrazinas/farmacocinética , Riñón/metabolismo , Hígado/metabolismo , Masculino , Ratones , Microsomas/enzimología , Microsomas/metabolismo , Pirazoles/farmacocinética , Ratas Sprague-Dawley
5.
Artículo en Inglés | MEDLINE | ID: mdl-12075212

RESUMEN

OBJECTIVES: The factors that influence postoperative pain after root canal treatment are not completely understood. The purpose of this prospective clinical study was to evaluate postoperative pain after root canal therapy performed in 1 appointment versus 2 appointments. STUDY DESIGN: Seventy-two patients requiring root canal therapy on permanent molars were included in this study. Patients were randomly assigned to either the 1-appointment or the 2-appointment group. Both vital and nonvital teeth were included. The standardized protocol for all teeth involved local anesthesia, isolation and access, engine-driven rotary nickel-titanium canal instrumentation to a minimum size #5 (.028 mm).04 taper Profile with step-back flaring, and irrigation with 2.5% NaOCl. Teeth in group 1 (n = 39) were obturated at the first appointment by using laterally condensed gutta-percha and Roth 811 sealer. Teeth in group 2 (n = 33) were closed with a sterile dry cotton pellet and Cavit restoration and were obturated at a second appointment 7 to 14 days later. A modified Visual Analogue Scale was used to measure preoperative pain and pain at 6, 12, 24, and 48 hours after the first appointment. Statistical analysis was performed to compare groups at each interval by using an independent-samples t test with Bonferroni adjustment. RESULTS: There was no statistically significant difference between groups at preoperative intervals or at any of the 4 postoperative intervals (P <.01). CONCLUSIONS: There was no difference in postoperative pain between patients treated in 1 appointment and patients treated in 2 appointments. The majority of patients in both groups reported no pain or only minimal pain within 24 to 48 hours of treatment.


Asunto(s)
Dolor Postoperatorio/etiología , Tratamiento del Conducto Radicular/métodos , Citas y Horarios , Sulfato de Calcio/uso terapéutico , Aleaciones Dentales , Cementos Dentales , Desinfectantes/uso terapéutico , Combinación de Medicamentos , Estudios de Seguimiento , Gutapercha/uso terapéutico , Humanos , Diente Molar , Níquel , Dimensión del Dolor , Polivinilos/uso terapéutico , Estudios Prospectivos , Materiales de Obturación del Conducto Radicular/uso terapéutico , Irrigantes del Conducto Radicular/uso terapéutico , Obturación del Conducto Radicular , Preparación del Conducto Radicular/instrumentación , Preparación del Conducto Radicular/métodos , Tratamiento del Conducto Radicular/efectos adversos , Rotación , Hipoclorito de Sodio/uso terapéutico , Estadística como Asunto , Titanio , Diente no Vital/terapia , Óxido de Zinc/uso terapéutico , Cemento de Óxido de Zinc-Eugenol/uso terapéutico
6.
Bioorg Med Chem Lett ; 17(6): 1713-7, 2007 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-17236763

RESUMEN

N,N'-diarylsquaramides were prepared and evaluated as antagonists of CXCR2. The compounds were found to be potent and selective antagonists of CXCR2. Significant differences in SAR was observed relative to the previously described N,N'-diarylurea series. As was the case in the N,N'-diarylurea series, placing sulfonamide substituent adjacent to the acidic phenol significantly reduced the clearance in rat pharmacokinetic studies.


Asunto(s)
Ciclobutanos/síntesis química , Ciclobutanos/farmacología , Ciclobutanos/farmacocinética , Receptores de Interleucina-8B/antagonistas & inhibidores , Urea/análogos & derivados , Urea/síntesis química , Urea/farmacología , Urea/farmacocinética , Animales , Células CHO , Fenómenos Químicos , Química Física , Cricetinae , Cricetulus , Indicadores y Reactivos , Espectrometría de Masas , Fenoles/química , Ratas , Ratas Sprague-Dawley , Relación Estructura-Actividad , Sulfonamidas/química
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