Virulent

Distribution by Scientific Domains
Distribution within Life Sciences

Kinds of Virulent

  • highly virulent

  • Terms modified by Virulent

  • virulent form
  • virulent parasite
  • virulent pathogen
  • virulent strain

  • Selected Abstracts


    Evidence of pAgK84 transfer from Agrobacterium rhizogenes K84 to natural pathogenic Agrobacterium spp. in an Italian peach nursery

    PLANT PATHOLOGY, Issue 4 2009
    A. Raio
    Nine Italian peach nurseries, which use Agrobacterium rhizogenes strain K84 to protect plants from crown gall, were monitored for three years with the aim of determining whether transconjugant populations may arise following plasmid exchanges between K84 and autochtonous soil agrobacteria. Six hundred and seventy-eight Agrobacterium isolates were obtained from 120 tumours developed on apricot and peach rootstocks that had been treated in pre-planting with the antagonist. Agrobacteria were characterized for pathogenicity, biovar, opine catabolism and agrocin 84 sensitivity. Colony hybridization was used for screening the isolates harbouring plasmids pTi and/or pAgK84. Analysis of plasmid content and Southern blotting were performed on putative transconjugant agrobacteria found in tumours collected from one nursery where a biological control breakdown was observed. The RFLP analysis of 16S + IGS regions showed that pAgK84 was transferred from the antagonist to virulent and avirulent soil agrobacteria belonging to different ribotypes. Pathogenic transconjugants, inoculated on GF677 rootstocks, were not controlled in vivo by K84 and stably maintained pTi and pAgK84 in the bacterial cells for at least one year. At the end of a biocontrol trial, new transconjugant tumorigenic agrobacteria originated by the transfer of pAgK84 to the pathogen. Virulent and avirulent transconjugants may represent a real threat for biological control by K84 strain since all of them produced agrocin and were insensitive to it. Survival in soil of these populations could make the future application of K84 ineffective. [source]


    The ecology of virulence

    ECOLOGY LETTERS, Issue 10 2006
    Curtis M. Lively
    Abstract Theoretical work has shown that parasites should evolve intermediate levels of virulence. Less attention has been given to the ecology of virulence. Here I explore population-dynamic models of infection in an annual host. The infection does not kill the host; but it can decrease the number of offspring produced by the host, and the magnitude of this effect depends on host population size. Hence, ,virulence' is density dependent, and is defined here as the difference in birth rates between uninfected and infected hosts, divided by the birth rate of uninfected hosts. The results suggest that infection can be highly virulent at the host's equilibrium density, even though the parasite has no effect on the host's intrinsic birth rate. The results also suggest that parasites may help to stabilize host population dynamics. In general, the impact of infection may be underestimated in natural populations. [source]


    Keeping the herds healthy and alert: implications of predator control for infectious disease

    ECOLOGY LETTERS, Issue 9 2003
    Craig Packer
    Abstract Predator control programmes are generally implemented in an attempt to increase prey population sizes. However, predator removal could prove harmful to prey populations that are regulated primarily by parasitic infections rather than by predation. We develop models for microparasitic and macroparasitic infection that specify the conditions where predator removal will (a) increase the incidence of parasitic infection, (b) reduce the number of healthy individuals in the prey population and (c) decrease the overall size of the prey population. In general, predator removal is more likely to be harmful when the parasite is highly virulent, macroparasites are highly aggregated in their prey, hosts are long-lived and the predators select infected prey. [source]


    HIGHER DISEASE PREVALENCE CAN INDUCE GREATER SOCIALITY: A GAME THEORETIC COEVOLUTIONARY MODEL

    EVOLUTION, Issue 9 2005
    Matthew H. Bonds
    Abstract There is growing evidence that communicable diseases constitute a strong selective force on the evolution of social systems. It has been suggested that infectious diseases may determine upper limits of host sociality by, for example, inducing territoriality or early juvenile dispersal. Here we use game theory to model the evolution of host sociality in the context of communicable diseases. Our model is then augmented with the evolution of virulence to determine coevolutionarily stable strategies of host sociality and pathogen virulence. In contrast to a controversial hypothesis by Ewald (1994), our analysis indicates that pathogens may become more virulent when contact rates are low, and their prevalence can ultimately induce greater sociality. [source]


    Helicobacter pylori, coccoid forms and biofilm formation

    FEMS IMMUNOLOGY & MEDICAL MICROBIOLOGY, Issue 2 2009
    Leif Percival Andersen
    Abstract Electron microscopic studies have shown that Helicobacter pylori occurs in three stages: spiral forms, coccoid forms and degenerative forms. The spiral forms are viable, culturable, virulent and can colonize experimental animals and induce inflammation. The coccoid forms may also be viable but are nonculturable, less virulent and are less likely to colonize and induce inflammation in experimental animals than the spiral forms. The degenerative forms are pyknotic, nonculturable, coccoid forms of dead H. pylori. These forms cannot be cultured and the cell membrane has disintegrated but gene material can be detected by PCR in water supplies. There is no substantial evidence for viable H. pylori persisting in water supplies. Epidemiological studies suggest that environmental water is a risk factor for H. pylori infection when compared with tap water, and formation of H. pylori biofilm cannot be excluded. Helicobacter pylori does not seem to take part in biofilm formation in the oral cavity even though the bacterium may be detected. [source]


    Leptospira interrogans is recognized through DC-SIGN and induces maturation and cytokine production by human dendritic cells

    FEMS IMMUNOLOGY & MEDICAL MICROBIOLOGY, Issue 3 2008
    Narintorn Gaudart
    Abstract Leptospirosis is a global zoonotic disease, caused by pathogenic Leptospira species including Leptospira interrogans, that causes public health and livestock problems. Pathogenesis, immune response and cellular receptors for Leptospira are not well understood. Interaction of dendritic cells (DCs) with L. interrogans serovar Autumnalis L-643 and BL-6 isolated from leptospirosis patients, and both virulent and avirulent serovar Pyrogenes 2317 strains isolated from animal were investigated. Carbohydrate analysis using lectins showed that all of these leptospires contained high mannose components as a common backbone and DC-SIGN was involved in leptospires' attachment. Interaction of the L. interrogans strains with DCs induced maturation, but had different effects on IL-10, IL-12p70 and tumor necrosis factor (TNF)-, production. Both virulent and avirulent Pyrogenes 2317 and Autumnalis BL-6 but not L-643 strains induced IL-12p70 and TNF-, production, but minimal IL-10 secretion. These data demonstrated that L. interrogans binds DC-SIGN and induces DCs maturation and cytokine production, which should provide new insights into cellular immune processes during leptospirosis. [source]


    Evaluation of DNA polymorphisms amplified by arbitrary primers (RAPD) as genetically associated elements to differentiate virulent and non-virulent Paracoccidioides brasiliensis isolates

    FEMS IMMUNOLOGY & MEDICAL MICROBIOLOGY, Issue 3 2002
    Teresa R Motta
    Abstract Randomly amplified polymorphic DNA (RAPD) analysis of 35 Paracoccidioides brasiliensis isolates was carried out to evaluate the correlation of RAPD profiles with the virulence degree or the type of the clinical manifestations of human paracoccidioidomycosis. The dendrogram presented two main groups sharing 64% genetic similarity. Group A included two isolates from patients with chronic paracoccidioidomycosis; group B comprised the following isolates showing 65% similarity: two non-virulent, six attenuated, five virulent, eight from patients with chronic paracoccidioidomycosis and two from patients with acute paracoccidioidomycosis. The virulent Pb18 isolate and six attenuated or non-virulent samples derived from it were genetically indistinguishable (100% of similarity). Thus, in our study, RAPD patterns could not discriminate among 35 P. brasiliensis isolates according to their differences either in the degree of virulence or in the type of the clinical manifestation of this fungal infection. [source]


    Decreased virulence of a strain of Pseudomonas aeruginosa O12 overexpressing a chromosomal type 1 ,-lactamase could be due to reduced expression of cell-to-cell signaling dependent virulence factors

    FEMS IMMUNOLOGY & MEDICAL MICROBIOLOGY, Issue 3 2000
    Françoise Ramisse
    Abstract Pseudomonas aeruginosa produces a large variety of virulence factors and is characterized by its capacity to rapidly develop resistance when exposed to antibiotics. In order to evaluate a possible correlation between acquired resistance to antibiotics and virulence, we examined the virulence of four isogenic variants of P. aeruginosa O12 that differ in their resistance phenotypes to various ,-lactam antibiotics in a mouse model of acute pneumonia. Strains overproducing a chromosomal type 1 ,-lactamase were less virulent in both immunocompetent and immunosuppressed animals. Whereas the production of the exopolysaccharide alginate was similar between the four strains, extracellular virulence factors (elastase, rhamnolipid) that are controlled by the cell-to-cell signaling system circuit were detected in reduced amounts in the supernatant of the two isolates overproducing type 1 ,-lactamase. These results suggest that strains overexpressing the chromosomal type 1 ,-lactamase could be less virulent because of a reduction of cell-to-cell signaling dependent virulence factor production. [source]


    Flavobacterium columnare chemotaxis to channel catfish mucus

    FEMS MICROBIOLOGY LETTERS, Issue 2 2008
    Phillip H. Klesius
    Abstract Flavobacterium columnare is a Gram-negative pathogen of many species of wild and cultured fish. Isolates from diseased channel catfish belong to either genomovar I or II. Genomovar II isolates were found to be more virulent than genomovar I isolates. The objective of the present study was to determine whether differences exist in the chemotactic response of these genomovars to mucus obtained from the skin, gills and intestines of healthy channel catfish using the capillary chemotaxis assay. Mucus from the skin and gill induced a greater chemotactic response by F. columnare than mucus from the intestine. Sixty percent of mucus from the skin of individual catfish yielded a positive chemotactic response from F. columnare. Finally, skin mucus induced a greater chemotactic response in genomovar II F. columnare than in genomovar I F. columnare isolates. The data indicate that mucus from channel catfish results in a chemotactic response by F. columnare. This positive chemotactic response may be an important first step for F. columnare colonization of channel catfish skin or gills. Although the role that chemotaxis plays in the virulence of F. columnare is not fully defined, the chemotactic response of genomovar ll isolates suggests that chemotaxis is associated with virulence. [source]


    Characteristics of the Cryphonectria parasitica isolated from Quercus in Slovakia

    FOREST PATHOLOGY, Issue 5 2010
    K. Adam, íková
    Summary The occurrence of chestnut blight (Cryphonectria parasitica) on oaks in mixed chestnut-oak forests was studied in 2003,2008 in Slovakia. Infections on living Quercus trees were found at four of seven localities. The disease incidence on oaks ranged from 1.3% to 15.8%. The symptoms on infected oaks were similar to those on chestnut, but less conspicuous. Cankers of C. parasitica were found only on Quercus robur and Q. petraea. A total of 22 isolates of C. parasitica, all virulent, were isolated. Each site yielded only a single vc type (EU12 or EU13). Field inoculation experiments on chestnuts with seven strains of C. parasitica from oaks and an isolate from Castanea sativa showed no differences in virulence. On Quercus robur stems, the cankered area was significantly smaller than on C. sativa and the cankers developed very slowly. [source]


    Evaluation of Juglans species for resistance to Phytophthora cinnamomi:,differences in isolate virulence and response to fosetyl-Al

    FOREST PATHOLOGY, Issue 3 2009
    A. Belisario
    Summary Phytophthora is considered as an important pathogen on walnut, and severe losses are reported in European as well as in American walnut stands. Though several Phytophthora spp. are known to attack walnut, P. cinnamomi is considered the most virulent and widespread in southern Europe. Up to now, no walnut species or hybrid is known to have a high resistance level towards P. cinnamomi. Efforts are addressed in finding rootstock material graft compatible with English walnut and resistant/tolerant to P. cinnamomi. The extension of P. cinnamomi lesions on five Juglans species was studied to find out sources of resistance/tolerance to this pathogen. Walnut species clustered into two main groups, J. hindsii, J. nigra, and J. mandshurica were the less susceptible to the colonization of P. cinnamomi, while J. regia and J. sieboldiana were the most susceptible. On this account, J. mandshurica represents the best alternative as rootstock because its employment overcomes the risk of the occurrence of black line disease, it has good level of resistance to Agrobacterium temefaciens and Brenneria nigrifluens, and it is tolerant to Xanthomonas arboricola pv. juglandis. J. mandshurica is also compatible in cross-pollinations with J. regia and J. nigra. Differences in virulence of P. cinnamomi isolates was assessed and a marked interaction between species and isolate emerged. Treatment with fosetyl-Al by dipping was mainly efficient in reducing the length P. cinnamomi lesions, and an interaction between species and treatment was evident with the highest efficacy on J. regia and J. sieboldiana. [source]


    A comparison of heat pulse velocity and lesion lengths for assessing the relative virulence of mountain pine beetle-associated fungi on jack pine

    FOREST PATHOLOGY, Issue 4 2008
    A. V. Rice
    Summary The mountain pine beetle (MPB) vectors three blue-stain fungi, Grosmannia clavigera, Ophiostoma montium and Leptographium longiclavatum, which contribute to the success of the beetles and the death of the trees. The utility of two methods, heat pulse velocity (HPV) and lesion length, for assessing the relative virulence of these fungi were compared on jack pine in central Alberta. The HPV monitoring apparatus failed to detect xylem sap flow in any of the trees and, thus, could not be used to assess fungal virulence. In contrast, measurement of lesion lengths was more sensitive and provided further evidence that G. clavigera and L. longiclavatum are more virulent than O. montium. The failure of the HPV apparatus to detect sap flow suggests that the study trees were moisture stressed, a factor likely to increase their susceptibility to MPB. Thus, this method is not appropriate for assessing the response of the most susceptible (i.e. drought stressed) trees to MPB and its associated fungi. [source]


    Seasonal effect on infection and development of lesions caused by Cryphonectria parasitica in Castanea sativa

    FOREST PATHOLOGY, Issue 4 2003
    L. Guérin
    Summary Seasonal variation in the development of chestnut blight, caused by Cryphonectria parasitica, was investigated by inoculating in situ chestnut trees and in vitro excised chestnut segments, at either monthly or 3-monthly intervals throughout 30 months. Inoculations were made with conidia and mycelium of a virulent isolate and with mycelium of a hypovirulent isolate. Conidial inoculations of living sprouts or excised segments between May and July resulted in the greatest incidence of infection whereas inoculations in autumn and winter, in vitro as well as in situ, did not reveal any visible disease. However, from these symptomless inoculated stems, C. parasitica was isolated 3 months after inoculation. Inoculations with the mycelium of the virulent isolate always resulted in lesions, except in January 1999, and the greatest rate of lesion development occurred for inoculations made in the spring and summer. There was a significant seasonal effect on lesion development. Lesions caused by the hypovirulent isolate, smaller than those caused by the virulent isolate, followed a similar seasonal pattern. The same seasonal variations were observed for inoculations in vitro of excised segments. Relative water content (RWC) of chestnut bark significantly varied with bark sampling date. The rate of lesion development in sprouts significantly correlated with average minimum (ATn) and maximum (ATx) temperatures and the sum of rainfall during inoculation period, with the rate of lesion development measured in excised segments 10 days after inoculation (R10d) and with RWC measured on the day of inoculation. In multiple regression models, variables ATx and R10d best explained variation in lesion development. Résumé La variation saisonnière du développement de la maladie du chancre causée par Cryphonectria parasitica a étéétudiée en réalisant, une fois par mois ou par trimestre pendant deux ans et demi, des inoculations de châtaigniers in situ et des inoculations in vitro de branches coupées. Les inoculations ont été réalisées avec des conidies et du mycélium d'un isolat virulent et avec du mycélium d'un isolat hypovirulent. En Mai et Juin, les inoculations conidiennes ont provoqué le taux d'infection le plus élevé, in situ et in vitro. A l'inverse, en automne et en hiver, ces inoculations n'ont pas causé de symptômes. Cependant C. parasitica a été réisolé 3 mois plus tard, sur ces tiges ne présentant aucune lésion. Les inoculations avec du mycélium ont toujours résulté en des lésions, excepté en Janvier 1999, et le développement des lésions (R1m) a été le plus rapide au printemps et en été. La date d'inoculation a eu un effet significatif sur l'extension des lésions. Le même effet saisonnier était observé sur le développement des lésions causées par l'isolat hypovirulent, plus petites que celles causées par l'isolat virulent. Les mêmes variations saisonnières de l'extension des lésions étaient observées in vitro sur tiges excisées. Un effet saisonnier significatif a été mis en évidence sur la teneur en eau relative des écorces de châtaignier (RWC). Le développement des lésions dans les tissus vivants était significativement corrélé avec les températures moyennes minimale (ATn) et maximale (ATx) et la somme des précipitations (SR) calculées sur chaque période d'incubation, avec le développement des lésions in vitro (R10d) et avec RWC. La variation saisonnière du développement des lésions était le mieux expliquée, par un modèle de régression multiple, par ATx et R10d pour l'isolat virulent, et par ATx pour l'isolat hypovirulent. Zusammenfassung Der jahreszeitlich bedingte Einfluß auf die Entstehung von Kastanienrindenkrebs, verursacht von Cryphonectria parasitica, wurde durch Inokulation von Kastanienbäumen in situ und durch Beimpfung von geschnittenen Triebsegmenten in vitro in monatlichen oder drei-monatlichen Intervallen über dreißig Monate untersucht. Zur Inokulation wurden Myzel und Konidien eines virulenten Isolates und Myzel eines hypovirulenten Isolates verwendet. Mit Konidien wurde zwischen Mai und Juni die größte Infektionshäufigkeit auf lebenden Sprossen oder Triebsegmenten erreicht, während Inokulationen im Herbst und Winter keine sichtbaren Symptome hervorriefen. Jedoch konnte C. parastica drei Monate nach Inokulation von lebenden Sprossen isoliert werden, auch wenn keine Läsion sichtbar war. Außer im Januar 1999 führte Inokulation mit Myzel des virulenten Isolates immer zu Läsionen. Am häufigsten traten Läsionen bei Inokulationen im Frühling und im Sommer auf. Der Einfluß des Inokulationszeitpunktes auf die Ausbildung von Läsionen war signifikant. Inokulationen mit dem hypovirulenten Isolat zeigten eine ähnliche jahreszeitliche Schwankung wie jene mit dem virulenten Isolat, führten aber zu kleineren Läsionen. Die gleichen jahreszeitlichen Variationen wurden bei in vitro Inokulation von Kastanientrieben beobachtet. Der relative Wassergehalt (RWC) der Borke variierte signifikant mit dem Beprobungszeitpunkt der Borke. Die Bildung von Läsionen an lebenden Sprossen korrelierte signifikant mit den durchschnittlichen Temperaturminima (ATn) und -maxima (ATx), mit der Gesamtregenmenge (SR) während der Inokulationsperiode, mit der Bildung von Läsionen an Triebsegmenten (R10d) und mit dem am Inokulationstag gemessenen RWC. In einem multiplen Regressionsanalysenmodell zeigte sich, dass die jahreszeitliche Schwankung der Ausbildung von Kastanienrindenkrebs beim virulenten Isolat am besten durch die Variablen ATx und R10d, beim hypovirulenen Isolat durch ATx erklärt wurde. [source]


    Incomplete movement of Cryphonectria hypovirus 1 within a vegetative compatibility type of Cryphonectria parasitica in natural cankers on grafted American chestnut trees

    FOREST PATHOLOGY, Issue 6 2002
    E. P. Hogan
    Summary American chestnut trees, grafted in 1980 from large survivors, were inoculated in 1982 and 1983 with four white (European) hypovirulent strains of Cryphonectria parasitica, infected with C. hypovirus 1 (CHV1); this hypovirus has been shown to be capable of moving rapidly within the mycelium of a vegetative compatibility (vc) type of C. parasitica in blight cankers. Using a 49-cell lattice plot, 17.8×17.8 cm, the spatial patterns and frequencies of white and pigmented isolates and white and pigmented vc types were investigated within superficial cankers on the grafts located outside the hypovirulent-strain-inoculated zone. Four of six cankers assayed contained white isolates, and three of the four had random spatial patterns of white isolates, based on join-count statistics. Vc tests, using pigmented isolates and pigmented single-spore colonies of white isolates, indicated that the majority of white and pigmented isolates recovered from each of two cankers assayed were in one vc type. White and pigmented lattice-plot cells of the same vc type were frequently in contact with each other, indicating incomplete movement of CHV1 within a vc type. Nine and 10 vc types were found in the two cankers; it is hypothesized that small, white vc type areas in each canker may be a source of CHV1 transmission to the major vc types. Based on join-count statistics, the spatial pattern of the single, major vc type in one canker was non-random (aggregated), whereas the other canker had a random major vc type pattern. White and pigmented in vitro variants (sectors) of C. parasitica, that resemble white and pigmented in vivo variants in spatial contact and vc compatibility, were intermediate hypovirulent and virulent on forest American chestnuts, and dsRNA positive and negative, respectively. Incomplete movement of CHV1 within a vc type could be a major cause of the prevalence of pigmented isolates in superficial cankers on chestnut trees. Résumé Des châtaigniers américains greffés en 1980 à partir de grands arbres survivants, ont été inoculés en 1982 et 1983 avec quatre souches blanches (européennes) hypovirulentes de Cryphonectria parasitica, infectées par l'hypovirus 1 (CHV 1). Cet hypovirus avait été montré capable de migrer rapidement dans le mycélium végétativement compatible (vc) de C. parasitica dans des chancres. Grâce un dispositif à 49 cellules (17,8×17,8 cm), la répartition spatiale et la fréquence des isolats blancs et pigmentés, et des GCV, ont étéétudiées dans des chancres superficiels chez les greffons, en dehors de la zone inoculée par les souches hypovirulentes. Quatre des six chancres étudiés contenaient des isolats blancs, dont la répartition spatiale était erratique chez trois d'entre eux. Les tests de compatibilité végétative, utilisant des isolats pigmentés et des colonies pigmentées mono-sporées d'isolats blancs, ont montré que la majorité des isolats blancs et des isolats colorés trouvés dans chacun des deux chancres analysés, était d'un seul type végétatif. Les cellules du dispositif, blanches ou pigmentées du même GCV, étaient fréquemment en contact, ce qui indique un mouvement incomplet de CHV1 dans un GCV. Neuf et dix GCV ont été trouvés dans les deux chancres et on avance l'hypothèse que de petites zones à GCV blancs dans chaque chancre peuvent être une source de transmission de CHV1 aux types végétatifs majoritaires. L'unique GCV majoritaire dans un des chancres n'était pas réparti au hasard (agrégé), mais il l'était dans l'autre chancre. Les variants blancs et pigmentés in vitro (secteurs) de C. parasitica, qui ressemblent aux variants blancs et pigmentés in vivo en contact spatial, étaient intermédiaires en hypovirulence et en virulence sur les châtaigniers américains, et respectivement positifs et négatifs pour le dsRNA. Un mouvement incomplet de CHV1 dans un GCV pourrait être la principale cause de la prévalence d'isolats pigmentés dans des chancres superficiels. Zusammenfassung Amerikanische Kastanien (Castanea dentata), die im Jahr 1980 von adulten überlebenden Exemplaren veredelt worden waren, wurden 1982 und 1983 mit vier unpigmentierten, hypovirulenten Stämmen von Cryphonectria parasitica aus Europa inokuliert, die mit dem Cryphonectria parasitica - hypovirus 1 (CHV 1) infiziert waren. Es war nachgewiesen, dass sich dieses Hypovirus rasch innerhalb des Myzels eines vc-Typs von C. parasitica in Krebsen ausbreiten konnte. Bei oberflächlichen Krebsen an veredelten Bäumen ausserhalb der mit dem hypovirulenten Stamm inokulierten Zone wurde auf einer 17,8×17,8 cm grossen Fläche (die in 49 Quadrate unterteilt wurde) die räumliche Verteilung und die Häufigkeit von unpigmentierten und pigmentierten Isolaten sowie der vc-Typen untersucht. Vier von sechs analysierten Krebsen enthielten weisse Isolate und drei davon zeigten zufällige Verteilungsmuster der Isolate (gemäss Joint-Count-Statistik). Vc-Tests mit pigmentierten Isolaten und pigmentierten Einzelsporkulturen von weissen Isolaten zeigten, dass die Mehrheit der weissen und der pigmentierten Isolate von zwei Krebsen zur gleichen vc-Gruppe gehörten. Weisse und pigmentierte Probepunkte mit dem gleichen vc-Typ waren häufig benachbart, was eine unvollständige Ausbreitung des CHV 1 innerhalb eines vc-Typs anzeigt. In den 2 Krebsen wurden 9 bzw. 10 vc-Typen nachgewiesen und es wird vermutet, dass kleine Bereiche mit weissem vc-Typ innerhalb eines Krebses als Reservoir für die Übertragung des Virus zu den dominanten vc-Typen fungieren können. Mit Hilfe der Joint-Count-Statistik wurde nachgewiesen, dass das räumliche Muster des einen, dominanten vc-Typs in einem Krebs nicht zufällig, sondern aggregiert war, während der andere Krebs ein zufälliges Verteilungsmuster der vc-Typen aufwies. Weisse und pigmentierte Varianten von C. parasitica, die in vitro auftraten (Sektoren), und die den weissen und pigmentierten Varianten sehr ähnlich sind, die in der Natur in räumlichem Kontakt zueinander auftreten, und die vegetativ kompatibel sind, zeigten in Feldversuchen auf C. sativa eine mittlere Hypovirulenz bzw. Virulenz. Ausserdem waren sie dsRNA positiv bzw. negativ. Die unvollständige Ausbreitung des CHV 1 innerhalb einer vc-Typs könnte das überwiegen pigmentierter Isolate in oberflächlichen Krebsen erklären. [source]


    Pathogenicity of fungi isolated from Quercus suber in Catalonia (NE Spain)

    FOREST PATHOLOGY, Issue 5 2000
    J. Luque
    Summary Thirty-four fungal species isolated from cork oak (Quercus suber) in Catalonia (NE Spain) during 1992,95 were tested for pathogenicity either in stem, leaf or root inoculations. Eleven species were found to be pathogenic on stem: Biscogniauxia mediterranea, Botryosphaeria stevensii, Diatrype cf. stigma, Endothia gyrosa, Fusarium solani, Graphium sp., Ophiostoma quercus, Phomopsis sp., Phytophthora cinnamomi, Sporendocladia bactrospora and an unidentified Coelomycete. Three fungi showed pathogenic effects on leaves: Dendrophoma myriadea, Lembosia quercina and Phomopsis quercella. No clear pathogenic effects were detected in the root inoculation experiment. Trunk pathogens were differentiated into two groups according to the effects induced in the inoculated plants; B. stevensii, Phomopsis sp. and P. cinnamomi caused the death of the inoculated plants and induced the formation of large cankers and vascular necroses. The other pathogenic species also produced severe cankers and vascular lesions, but no significant mortality was detected. Water stress increased the lesions caused by B. mediterranea and Phomopsis sp., but limited those of P. cinnamomi and the rest of the inoculated fungi. However, water stress did not significantly affect the damage caused by B. stevensii, which was the most virulent of the species tested. Leaf pathogens only showed their effects if the leaf cuticle was previously damaged. Lembosia quercina caused small dark lesions whereas D. myriadea and P. quercella produced large necrotic areas in well-watered plants. The lesions caused by the last two fungi were reduced by water stress. Résumé Le pouvoir pathogène de trente-quatre espèces fongiques isolées de chêne liège en Catalogne (nord-est de l'Espagne) de 1992 à 1995 a été testé par inoculation sur tronc, feuilles et racines. Onze espèces se sont montrées pathogènes sur tronc: Biscogniauxia mediterranea, Botryosphaeria stevensii, Diatrype cf. stigma, Endothia gyrosa, Fusarium solani, Graphium sp., Ophiostoma quercus, Phomopsis sp., Phytophthora cinnamomi, Sporendocladia bactrospora et un Coelomycète non identifié. Trois champignons ont eu un effet pathogène sur feuilles: Dendrophoma myriadae, Lembosia quercina et Phomopsis quercella. Aucun effet clair n'a été détecté chez les inoculations de racines. Les pathogènes de tronc se répartissaient en deux groupes selon leurs effets en inoculation; B. stevensii, Phomopsis sp. et P. cinnamomi provoquaient la mort des plants et induisaient le formation de grands chancres et des nécroses vasculaires. Les autres espèces pathogènes produisaient aussi des chancres graves et des lésions vasculaires, mais pas de mortalité significative. Un stress hydrique augmentait les lésions provoquées par B. mediterranea et Phomopsis sp. mais limitait ceux de P. cinnamomi et des autres champignons inoculés. Cependant, le stress hydrique n'affectait pas significativement les dégâts par B. stevensii qui était la plus agressive des espèces testées. Les pathogènes foliaires n'avaient d'effet que si la cuticule foliaire était préalablement endommagée. Lembosia quercina provoquait de petites lésions sombres et D. myriadea et P. quercella provoquaient de grandes plages nécrotiques chez les plants bien arrosés; les lésions causées par ces deux derniers champignons étaient réduites par le stress hydrique. Zusammenfassung Die Pathogenität von 34 Pilzarten, die im Zeitraum 1992,1995 von Korkeichen (Quercus suber) in Katalonien (NO-Spanien) isoliert wurden, wurden mit Hilfe von Trieb-, Blatt- oder Wurzelinokulationen untersucht. Am Stamm erwiesen sich 11 Arten als pathogen: Biscogniauxia mediterranea, Botryosphaeria stevensii, Diatrype cf. stigma, Endothia gyrosa, Fusarium solani, Graphium sp., Ophiostoma quercus, Phomopsis sp., Phytophthora cinnamomi, Sporendocladia bactrospora und ein nicht identifizierter Coelomycet. Drei Arten verursachten Symptome auf Bla¨ttern: Dendrophoma myriadea, Lembosia quercina und Phomopsis quercella. Bei den Wurzelinokulationen wurden keine pathogenen Effekte beobachtet. Bei den Stammpathogenen wurden nach den von ihnen an den inokulierten Pflanzen verursachten Symptomen zwei Gruppen unterschieden: B. stevensii, Phomopsis sp. und P. cinnamomi verursachten den Tod der Pflanzen und induzierten die Bildung von grossen Rinden- und Xylemnekrosen. Die anderen pathogenen Arten verursachten ebenfalls starke Rindennekrosen und Gefa¨ssla¨sionen, es wurde jedoch keine auffallende Mortalita¨t beobachtet. Unter Wasserstress war die durch B. mediterranea und Phomopsis sp. induzierte Nekrosebildung versta¨rkt, dagegen war sie bei P. cinnamomi und den u¨brigen inokulierten Pilzen reduziert. Wasserstress beeinflusst jedoch das Ausmass der Scha¨digung durch B. stevensii, der virulentesten der untersuchten Arten, nicht. Die Blattpathogene verursachten nur dann Symptome, wenn zuvor die Blattcuticula bescha¨digt worden war. Lembosia quercina verursachte kleine dunkle La¨sionen, wa¨hrend D. myriadea und P. quercella bei gut bewa¨sserten Pflanzen grosse Nekrosen verursachten. Diese Symptome waren unter Wasserstress weniger stark ausgepra¨gt. [source]


    COMPLETE NUCLEOTIDE SEQUENCE OF SPHEROIDIN GENES OF CALLIPTAMUS IT ALICUS ENTOMOPOXVIRUS(CIEPV) AND GOMPHOCERUS SIBIRICUS ENTOMOPOXVIRUS(GSEPV)

    INSECT SCIENCE, Issue 3 2004
    Yong-dan Li
    Abstract, The spheroidin genes of Calliptamus italicus entomopoxvirus (CiEPV) and Gomphocerus sibiricus entomopoxvirus (GsEPV) were obtained by PCR, and the fragments were cloned, se-quenced and analyzed. The CiEPV and GsEPV spheroidin genes respectively harbored ORFs of 2 922 bps and 2 967 bps that were capable of coding polypeptides of 109.2 and 111.1 kDa. Computer analysis indicated that CiEPV and GsEPV spheroidins shared less than 20% amino acid identities with lepidopteran AmEPV and coleopteran AcEPV spheroidins, but more than 80% amino acid identities with orthopteran OaEPV, MsEPV and AaEPV spheroidins. The CiEPV and GsEPV spheroidins respectively contained 19 and 21 cysteine residues that were particularly abundant at the C-termini, as is the case with those of the other orthopteran EPV spheroidins. The numbers and locations of the cysteine residues of the spheroidins were most similar to those of the spheroidins of EPVs that are virulent on the same insect orders. The promoter regions of the two spheroidin genes were highly conserved (99%) among the orthopteran EPVs and also contained the typical very A+T rich and TAAATG signal mediating transcription of poxvirus late genes. We also sequenced an incomplete ORF downstream of the pheroidin gene of CiEPV and GsEPV. The ORF was in the opposite direction to the spheroidin gene and was homologous to MSV072 putative protein of MsEPV. [source]


    Where will pathogen inactivation have the greatest impact?

    ISBT SCIENCE SERIES: THE INTERNATIONAL JOURNAL OF INTRACELLULAR TRANSPORT, Issue 1 2007
    T. Hervig
    Blood safety has always been a major task in transfusion medicine. A strategy to obtain this aim should include donor education, donor selection, and testing of blood donations. Pathogen inactivation adds another level of safety. In the fractionation industry, pathogen inactivation methods are mandatory. Several countries also use pathogen-inactivated plasma , from pools or single donors. Concerning the cellular blood components, there is still no method available for red cell concentrates, whereas methods for platelet concentrates are available in some countries and others are in the pipeline for commercialization. The efficiency of the ,old' methods to increase blood safety and the costs of the methods seem to be major obstacles for the introduction of the systems. There are also concerns on product quality and loss of volume during the inactivation process. As the importance of pathogen inactivation is largest in countries with blood donors who carry infections it is impossible to protect against, either due to high incidence of the infection or due to shortage of tests, cost will be a major question when pathogen inactivation is considered. Pathogen inactivation of red cell concentrates will also be a necessity. When pathogen inactivation methods are available for all blood components, they will have great impact to protect the patients in countries where a high percentage of the population is infected by agents transmissible through blood transfusion, and in all situations to protect against new pathogens and ,old' pathogens that become more virulent. The total risk of contracting infectious diseases through blood transfusion will probably be important when implementation of new methods for pathogen inactivation is considered. [source]


    Phage-selected lipopolysaccharide mutants of Pectobacterium atrosepticum exhibit different impacts on virulence

    JOURNAL OF APPLIED MICROBIOLOGY, Issue 2 2010
    T.J. Evans
    Abstract Aims:, To positively select Pectobacterium atrosepticum (Pa) mutants with cell surface defects and to assess the impact of these mutations on phytopathogenesis. Methods and Results:, Several phages were isolated from treated sewage effluent and were found to require bacterial lipopolysaccharide (LPS) for infection. Two strains with distinct mutations in LPS were obtained by transposon mutagenesis. Along with a third LPS mutant, these strains were characterized with respect to various virulence-associated phenotypes, including growth rate, motility and exoenzyme production, demonstrating that LPS mutations are pleiotropic. Two of the strains were deficient in the synthesis of the O-antigen portion of LPS, and both were less virulent than the wild type. A waaJ mutant, which has severe defects in LPS biosynthesis, was dramatically impaired in potato tuber rot assays. The infectivity of these novel phages on 32 additional strains of Pa was tested, showing that most Pa isolates were sensitive to the LPS-dependent phages. Conclusions:, Native LPS is crucial for optimal growth, survival and virulence of Pa in vivo, but simultaneously renders such strains susceptible to phage infection. Significance and Impact of the Study:, This work demonstrates the power of phages to select and identify the virulence determinants on the bacterial surface, and as potential biocontrol agents for Pa infections. [source]


    Virulent spores of Bacillus anthracis and other Bacillus species deposited on solid surfaces have similar sensitivity to chemical decontaminants

    JOURNAL OF APPLIED MICROBIOLOGY, Issue 1 2007
    J-L. Sagripanti
    Abstract Aims:, To compare the relative sensitivity of Bacillus anthracis and spores of other Bacillus spp. deposited on different solid surfaces to inactivation by liquid chemical disinfecting agents. Methods and Results:, We prepared under similar conditions spores from five different virulent and three attenuated strains of B. anthracis, as well as spores of Bacillus subtilis, Bacillus atrophaeus (previously known as Bacillus globigii), Bacillus cereus, Bacillus thuringiensis and Bacillus megaterium. As spore-surface interactions may bias inactivation experiments, we evaluated the relative binding of different spores to carrier materials. The survival of spores deposited on glass, metallic or polymeric surfaces were quantitatively measured by ASTM standard method E-2414-05 which recovers spores from surfaces by increasing stringency. The number of spores inactivated by each decontaminant was similar and generally within 1 log among the 12 different Bacillus strains tested. This similarity among Bacillus strains and species was observed through a range of sporicidal efficacy on spores deposited on painted metal, polymeric rubber or glass. Conclusions:, The data obtained indicate that the sensitivity of common simulants (B. atrophaeus and B. subtilis), as well as spores of B. cereus, B. thuringiensis, and B. megaterium, to inactivation by products that contain either: peroxide, chlorine or oxidants is similar to that shown by spores from all eight B. anthracis strains studied. Significance and Impact of the Study:, The comparative results of the present study suggest that decontamination and sterilization data obtained with simulants can be safely extrapolated to virulent spores of B. anthracis. Thus, valid conclusions on sporicidal efficacy could be drawn from safer and less costly experiments employing non-pathogenic spore simulants. [source]


    The newly isolated lytic bacteriophages st104a and st104b are highly virulent against Salmonella enterica

    JOURNAL OF APPLIED MICROBIOLOGY, Issue 1 2006
    G. O'Flynn
    Abstract Aims:, To screen Irish faecal samples from a variety of sources with a view to isolating novel anti- Salmonella phages and to subsequently evaluate their lytic capability. Methods and Results:, Two novel anti- Salmonella phages st104a and st104b were isolated from a screening programme based on their lytic capability. The phages produced significantly larger plaques (2 mm) on the chosen indicator Salmonella enterica strain, DPC6046, when compared with the well-known control phage, Felix 01 (0·5 mm). Both phages st104a and st104b were found to have a broad host range within the Salm. enterica species. During in vitro trials, both phages (st104a and st104b) reduced Salm. enterica numbers more than 99% within 1 h. In vivo studies, involving the addition of the phage to porcine gastric juice (pH 2·5) demonstrated that phage st104a and phage Felix 01 were capable of surviving (10 and 30% survival respectively) the acidic conditions, unlike st104b, which was undetectable after 2 h exposure. Conclusions:, Two novel lytic anti- Salmonella phages were isolated and characterized. Significance and Impact of the Study:, With the exception of phage Felix 01, there has been relatively little phage therapy work performed using lytic Salmonella phage. In this study, the lytic phages st104a and st104b were isolated as a result of a faecal screening programme. Subsequently, phage st104a was found to have potential for biocontrol of Salm. enterica numbers if administered orally to pigs given their survival in porcine gastric juice, whereas, phage st104b may have potential in reducing cell numbers if applied by alternative approaches. [source]


    Comparative study of nine Lactobacillus fermentum bacteriophages

    JOURNAL OF APPLIED MICROBIOLOGY, Issue 3 2001
    R. Foschino
    Aims:,To investigate the basic properties of six temperate and three virulent phages, active on Lactobacillus fermentum, on the basis of morphology, host ranges, protein composition and genome characterization. Methods and Results:,All phages belonged to the Siphoviridae family; two of them showed prolate heads. The host ranges of seven phages contained a common group of strains. SDS-PAGE protein profiles, restriction analysis of DNA and Southern blot hybridization revealed a high degree of homology between four temperate phages; partial homologies were also detected among virulent and temperate phages. Clustering derived from host range analysis was not related to the results of the DNA hybridizations. Conclusions:,The phages investigated have common characteristics with other known phages active on the genus Lactobacillus. Sensitivity to viral infection is apparently enhanced by the presence of a resident prophage. Significance and Impact of the Study:,These relationships contribute to the explanation for the origin of phage infection in food processes where Lact. fermentum is involved, such as sourdough fermentation. [source]


    The maintenance of sex: host,parasite coevolution with density-dependent virulence

    JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 10 2009
    C. M. LIVELY
    Abstract Why don't asexual females replace sexual females in most natural populations of eukaryotes? One promising explanation is that parasites could counter the reproductive advantages of asexual reproduction by exerting frequency-dependent selection against common clones (the Red Queen hypothesis). One apparent limitation of the Red Queen theory, however, is that parasites would seem to be required by theory to be highly virulent. In the present study, I present a population-dynamic view of competition between sexual females and asexual females that interact with co-evolving parasites. The results show that asexual populations have higher carrying capacities, and more unstable population dynamics, than sexual populations. The results also suggest that the spread of a clone into a sexual population could increase the effective parasite virulence as population density increases. This combination of parasite-mediated frequency-dependent selection, and density-dependent virulence, could lead to the coexistence of sexual and asexual reproductive strategies and the long-term persistence of sex. [source]


    Mechanisms of pathogenesis and the evolution of parasite virulence

    JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 2 2008
    S. A. FRANK
    Abstract When studying how much a parasite harms its host, evolutionary biologists turn to the evolutionary theory of virulence. That theory has been successful in predicting how parasite virulence evolves in response to changes in epidemiological conditions of parasite transmission or to perturbations induced by drug treatments. The evolutionary theory of virulence is, however, nearly silent about the expected differences in virulence between different species of parasite. Why, for example, is anthrax so virulent, whereas closely related bacterial species cause little harm? The evolutionary theory might address such comparisons by analysing differences in tradeoffs between parasite fitness components: transmission as a measure of parasite fecundity, clearance as a measure of parasite lifespan and virulence as another measure that delimits parasite survival within a host. However, even crude quantitative estimates of such tradeoffs remain beyond reach in all but the most controlled of experimental conditions. Here, we argue that the great recent advances in the molecular study of pathogenesis provide a way forward. In light of those mechanistic studies, we analyse the relative sensitivity of tradeoffs between components of parasite fitness. We argue that pathogenic mechanisms that manipulate host immunity or escape from host defences have particularly high sensitivity to parasite fitness and thus dominate as causes of parasite virulence. The high sensitivity of immunomodulation and immune escape arise because those mechanisms affect parasite survival within the host, the most sensitive of fitness components. In our view, relating the sensitivity of pathogenic mechanisms to fitness components will provide a way to build a much richer and more general theory of parasite virulence. [source]


    Relatedness affects competitive performance of a parasitic plant (Cuscuta europaea) in multiple infections

    JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2004
    S. Puustinen
    Abstract Theoretical models predict that parasite relatedness affects the outcome of competition between parasites, and the evolution of parasite virulence. We examined whether parasite relatedness affects competition between parasitic plants (Cuscuta europaea) that share common host plants (Urtica dioica). We infected hosts with two parasitic plants that were either half-siblings or nonrelated. Relative size asymmetry between the competing parasites was significantly higher in the nonrelated infections compared to infections with siblings. This higher asymmetry was caused by the fact that the performance of some parasite genotypes decreased and that of others increased when grown in multiple infections with nonrelated parasites. This result agrees with the predictions of theories on the evolution of parasite virulence: to enhance parasite transmission, selection may favour reduced competition with genetically related parasites in hosts infected by several genotypes. However, in contrast to the most common predictions, nonrelated infections were not more virulent than the sibling infections. [source]


    In vitro markers for virulence in Yersinia ruckeri

    JOURNAL OF FISH DISEASES, Issue 3 2010
    E Tobback
    Abstract In this study, different traits that have been associated with bacterial virulence were studied in Yersinia ruckeri. Two isolates that had been shown to cause disease and mortality in experimentally infected rainbow trout were compared with five avirulent isolates. Both virulent isolates showed high adhesion to gill and intestinal mucus of rainbow trout, whereas the majority of non-virulent strains demonstrated significantly lower adhesion. A decrease in adherence capability following bacterial treatment with sodium metaperiodate and proteolytic enzymes suggested the involvement of carbohydrates and proteins. All strains were able to adhere to and invade chinook salmon embryo cell line (CHSE-214), fathead minnow epithelial cell line (FHM) and rainbow trout liver cell line (R1). One non-virulent strain was highly adhesive and invasive in the three cell lines, whereas the virulent strains showed moderate adhesive and invasive capacity. The internalization of several isolates was inhibited by colchicine and cytochalasin-D, suggesting that microtubules and microfilaments play a role. For all strains, intracellular survival assays showed a decrease of viable bacteria in the cells 6 h after inoculation, suggesting that Y. ruckeri is not able to multiply or survive inside cultured cells. Analysis of the susceptibility to the bactericidal effect of rainbow trout serum demonstrated that virulent Y. ruckeri strains were serum resistant, whereas non-virulent strains were generally serum sensitive. [source]


    The macrophage chemotactic activity of Edwardsiella tarda extracellular products

    JOURNAL OF FISH DISEASES, Issue 5 2008
    A A Wiedenmayer
    Abstract The chemoattractant capabilities of Edwardsiella tarda extracellular products (ECP) were investigated from two isolates, the virulent FL6-60 parent and less virulent RET-04 mutant. Chemotaxis and chemokinesis were assayed in vitro using blind well chambers with peritoneal macrophages obtained from Nile tilapia, Oreochromis niloticus, 5 days following squalene injection. Non-purified ECP derived from both isolates stimulated predominantly chemokinetic migration of macrophages. Additionally, the ECP were semi-purified by high pressure liquid chromatography. The FL6-60 parent ECP yielded higher molecular weight components than did the ECP from the RET-04 mutant. The chemotactic activity of the macrophages for both the FL6-60 parent and RET-04 mutant semi-purified ECP was increased over the non-purified ECP and overall migration was primarily chemotactic. Exposure to ECP derived from virulent and less virulent E. tarda isolates promoted chemokinetic movement of macrophages that may be involved in inflammatory responses of Nile tilapia to E. tarda infection. [source]


    First description of non-motile Yersinia ruckeri serovar I strains causing disease in rainbow trout, Oncorhynchus mykiss (Walbaum), cultured in Spain

    JOURNAL OF FISH DISEASES, Issue 6 2006
    B Fouz
    Abstract Yersinia ruckeri, the causal agent of enteric redmouth (ERM) disease, was isolated from epizootics that occurred in different Spanish rainbow trout, Oncorhynchus mykiss (Walbaum), farms in which vaccination against ERM had been performed. In all episodes, the most pronounced clinical signs exhibited by affected fish were severe haemorrhages in the mouth, eyes and around the vent. The isolates were identified as Y. ruckeri serovar I by 16S rRNA sequencing together with serological tests. They lacked motility and lipase activity and thus belonged to biotype 2, and were highly virulent for juvenile rainbow trout, both by intraperitoneal injection (from 3.1 × 102 to 6.3 × 103 cfu per fish) and bath challenge (5.1,7.3 × 106 cfu mL,1). This is the first description of Y. ruckeri serovar I biotype 2 causing disease in cultured trout in Spain vaccinated with commercial ERM vaccines. The occurrence of this emergent pathogen in Spanish continental aquaculture from its first isolation in 2001 to date is also documented. [source]


    Acute columnaris infection in channel catfish, Ictalurus punctatus (Rafinesque): efficacy of practical treatments for warmwater aquaculture ponds

    JOURNAL OF FISH DISEASES, Issue 1 2004
    S Thomas-Jinu
    Abstract Columnaris disease was induced in channel catfish, Ictalurus punctatus (Rafinesque), by bath exposure to four highly virulent isolates of Flavobacterium columnare. In untreated controls, mortality began 20 h after exposure and reached 100% by 48 h. Mortality in channel catfish given antibiotic treatments with oxytetracycline or a combination of sulphadimethoxine and ormetoprim in feed prior to bacterial challenge was zero with all four strains of F. columnare. Diquat® (Zeneca Agricultural Products, Wilmington, DE, USA) was the most effective bath treatment; mortality with all four strains was zero. With potassium permanganate, chloramine-T, hydrogen peroxide and copper sulphate, bath treatment efficacy varied significantly among strains (P = 0.0346) and among treatments (P = 0.0033). Bath treatments with chloramine-T and potassium permanganate significantly reduced (P < 0.05) mortality from 100 to 75 and 69%, respectively, but copper sulphate and hydrogen peroxide treatments were not effective. Based on our results, oral antibiotics prevented columnaris disease but, of the bath treatments, only Diquat® produced a dramatic reduction in the mortality of acutely infected fish. Diquat® is labelled for aquatic use as an herbicide in the USA but in large ponds it is prohibitively expensive. [source]


    Inhibitory effects of a monoclonal antibody (MAb-001) on in vitro oxygen consumption and multiplication of the pathogenic haemoflagellate, Cryptobia salmositica Katz

    JOURNAL OF FISH DISEASES, Issue 7 2001
    N Hontzeas
    A monoclonal antibody (MAb-001), against a surface glycoprotein on Cryptobia salmositica inhibited the multiplication and oxygen consumption of both virulent and avirulent strains of the parasite. The classical cysteine proteinase inhibitor (E-64) and a cysteine proteinase activator (EDTA) affected the in vitro multiplication of C. salmositica. Concentrations of E-64 higher than 10 ,M reduced the multiplication of C. salmositica while 5 mM of EDTA enhanced its multiplication. We propose that the cysteine proteinase is an important metabolic enzyme in C. salmositica and that binding of MAb-001 to the enzyme inhibited parasite multiplication and reduced oxygen consumption. [source]


    Identification of a new genotype H wild-type mumps virus strain and its molecular relatedness to other virulent and attenuated strains

    JOURNAL OF MEDICAL VIROLOGY, Issue 2 2003
    Georgios Amexis
    Abstract A single clinical isolate of mumps virus designated 88-1961 was obtained from a patient hospitalized with a clinical history of upper respiratory tract infection, parotitis, severe headache, fever and lymphadenopathy. We have sequenced the full-length genome of 88-1961 and compared it against all available full-length sequences of mumps virus. Based upon its nucleotide sequence of the SH gene 88-1961 was identified as a genotype H mumps strain. The overall extent of nucleotide and amino acid differences between each individual gene and protein of 88-1961 and the full-length mumps samples showed that the missense to silent ratios were unevenly distributed. Upon evaluation of the consensus sequence of 88-1961, four positions were found to be clearly heterogeneous at the nucleotide level (NP 315C/T, NP 318C/T, F 271A/C, and HN 855C/T). Sequence analysis revealed that the amino acid sequences for the NP, M, and the L protein were the most conserved, whereas the SH protein exhibited the highest variability among the compared mumps genotypes A, B, and G. No identifying molecular patterns in the non-coding (intergenic) or coding regions of 88-1961 were found when we compared it against relatively virulent (Urabe AM9 B, Glouc1/UK96, 87-1004 and 87-1005) and non-virulent mumps strains (Jeryl Lynn and all Urabe Am9 A substrains). J. Med. Virol. 70: 284,286, 2003. © 2003 Wiley-Liss, Inc. [source]