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SF Forsyth 《Australian veterinary journal》2003,81(5):274-274
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Summary Insects belonging to 12 genera in the Order Diptera, found at two large waste potato dumps in Scotland. were contaminated
with soft rot coliform bacteria. In 1973, 5.7% and 3.2% and in 1974, 4.8% and 4.1% of the insects caught at each site yielded
these organisms. The bacteria were identified mainly asErwinia carotovora var.carotovora, though some isolates wereErwinia carotovora var.atroseptica. Isolations from potato dump waste showed that at the time when fly activity was greatest the majority of soft rot coliforms
in the waste wereE. carotovora var.carotovora, despite the fact that tubers originally forming the dumps were almost certainly infected mostly withE. carotovora var.atroseptica. Contaminated insects could readily transmit soft rot coliforms to damaged areas on the aerial parts of potato plants. It
is suggested that potato stocks freed from these organisms by the stem cutting procedure could become re-contaminated by insects
that disperse from potato dumps.
Zusammenfassung Zw?lf Arten von Insekten der Gattung Diptera, periodisch gesammelt auf zwei grossen Kartoffelabfallhaufen in Schottland, waren mit koliformen Nassf?ulebakterien kontaminiert (Tab. 2, 3, 5 und 6). Nur zwei der Arten galten vorher als m?gliche Ubertr?ger dieser Organismen. 1973 waren 4,6% der an den beiden Orten w?hrend der Saison gesammelten Insekten mit diesen Organismen behaftet, 1974 waren es 4,5%. Nicht weniger als 9,6% der Insekten waren bei einigen F?ngen im Jahre 1973 und 14,7% im Jahre 1974 Tr?ger von Nassf?uleErwinia sp. Die Fruchtfliegen (Parascaptomyza sp. undDrosophila spp.) waren 1973 die am h?ufigsten kontaminierten Insekten (Tab. 2 und 3). Diese Gruppe von Insekten war auch 1974 meistens kontaminiert, aber am h?ufigsten wurden die Bakterien vonScatophaga spp. undDelia spp. (Tab. 5 und 6) isoliert. Sowohl 1973 als auch 1974 wurdeErwinia carotovora var.carotovora (in der FolgeE. carotovora genannt) h?ufiger von den Insekten isoliert alsErwinia carotovora var.atroseptica (in der FolgeE. atroseptica genannt) (Tab. 1 und 4), obwohl die Knollen. die ursprünglich den Abfallhaufen ausmachten, fast sicher meistens mitE. atroseptica infiziert waren. Das Verh?ltnis vonE. carotovora zuE. atroseptica, isoliert von Insekten beider Haufen, war 1973 9,5∶1 (13,5∶1 und 5,5∶1 je Abfallhaufen) und 1974 3,8∶1 (2,7∶1 und 6,8∶1 für die beiden Orte).E. atroseptica wurde 1973 nur früh in der Vegetationszeit (vor dem 30. Juli) von den Insekten isoliert (Tab. 1), 1974 nur früh (vor dem 30. Juli) oder sp?t in der Vegetationszeit (nach dem 10. Oktober) (Tab. 4).E. carotovora dagegen konnte in beiden Jahren über die ganze Vegatationszeit isoliert werden (Tab. 1 und 4). Die Wiedergewinnung vonE. atroseptica von Insekten war mit dem Vorhandensein von frisch abgelagerten faulen Knollen zur Zeit. wenn die Insekten gesammelt werden. verbunden. EinzigE. carotovora wurde von Insekten isoliert. die zu einer Zeit gesammelt wurden, wenn auf den Abfallhaufen nur?lteres verfaulendes Material vorhanden war. Isolationen von faulenden Ueberresten, die 1975 dem Abfallhaufen entnommen wurden (Tab. 7), zeigten, dass sowohlE. carotovora als auchE. atroseptica in der Regel das ganze Jahr vorhanden waren.E. atroseptica herrschte früh im Jahr (Januar bis Juni) vor und an einem Ort auch sp?t in der Zeit der Musterentnahme (Oktober bis Dezember).E. carotovora war von Juni bis Oktober der am meisten isolierte Organismus. Das Vorherrschen vonErwinia carotovora var.atroseptica war mit dem Vorhandensein von frisch weggeworfenen Kartoffelknollen früh und sp?t in der Zeit der Musterentnahme verbunden.E. carotovora schien in den faulenden Knollen l?nger zu überleben und war der am meisten isolierte Organismus aus ?lterem verwesendem Material. Die Verh?ltniswerte vonE. carotovora zuE. atroseptica. isoliert von Insekten. waren h?her alsjene, die für das verfaulende Material aus den Abfallhaufen gefunden wurden. Es ist anzunehmen, dass die Insekten selbst einen selektiven Einfluss zu Gunsten vonE. carotovora ausüben. Von einem der Abfallhaufen gesammelten Insekten übertrugen im GlashausE. carotovora sogleich auf verletzte Kartoffelstengel. Man nimmt an, dass Kartoffelbest?nde. die mit Hilfe des Stengelschnittes von koliformen Nassf?uleerregern befreit wurden, durch Insekten, die von Kartoffelabfallhaufen kommen, wieder verseucht werden k?nnen.
Résumé 12 genres d'insectes appartenant à l'ordre des Diptères, capturés périodiquement en Ecosse. sur deux grands tas de déchets de pommes de terre se sont révélés être contaminés par des bactéries coliformes. agents de la pourriture molle (tableaux 2, 3, 5 et 6). Auparavant, seuls 2 genres avaient été cités comme vecteurs possibles de ces microorganismes. En 1973, 4.6% des insectes capturés aux 2 endroits, et en cours de saison. portaient ces parasites de la pomme de terre. En 1974. 4,5% étaient également contaminés. Pour l'ensemble de ces captures. il y a eu 9.6% des insectes en 1973. et 14.7% en 1974 qui portaientErwinia sp. Les mouches des fruits (Parascaptomyza etDrosophila spp.) ont été le plus fréquemment contaminés en 1973 (tableaux 2 et 3). Ce groupe d'insectes était également atteint en 1974. mais les bactéries on été plus fréquemment isolées à partir deScatophaga spp. etDélia spp. (tableaux 5 et 6). En 1973 et 1974.Erwinia carotovora var.carotovora (dans la suiteE. carotovora) a été plus fréquemment isolé de ces insectes qu'Erwinia carotovora var.atroseptica (dans la suiteE. atroseptica) (tableaux 1 et 4) bien que les tubercules constituant à l'origine les tas de déchets étaient certainement plus infestés parE. atroseptica. Le rapport entreE. carotovora etE. atroseptica pour les isolements sur insectes provenant des deux endroits a été 9,5/1 (respectivement 13.5/1 et 5.5/1 pour chacun des tas de déchets) en 1973 et 3,8/1 (2,7/1 et 6,8/1) en 1974.E. atroseptica n'a été isolé que t?t dans l'année (avant le 30 juillet) en 1973 (tableau 1) et 1974 (tableau 4) elle l'a été précocement (avant le 30 juillet) ou tardivement (après le 10 octobre).E. carotovora, par contre, l'a été durant toute la saison pendant les deux années (tableuaux 1 et 4) l'isolement d'E. atroseptica est lié au moment de la capture des insectes, à la présence de tubercules nouvellement pourris lors de la mise en tas. Par contreE. carotovora a été isolé à partir des insectes capturés sur les tas où il n'y avait que du matériel présentant des pourritures plus agées. En 1975, des isolements effectués sur les tas de déchets ont montré qu'E. carotovora etE. atroseptica étaient habituellement présents toute l'année (tableau 7).E. atroseptica était prédominante en début de saison (de janvier à juin). II n'y a eu qu'un seul cas où on l'a observé plus tardivement durant la période d'échantillonage (octobre à décembre).E. carotovora a été le principal organisme isolé de juin à octobre. La prédominance d'E. atroseptica était associée à la présence de tubercules nouvellement entreposés précocement et tardivement durant la période d'échantillonage.E. carotovora semblait subsister plus longuement dans les tubercules pourris et était le principal organisme isolé à partir de matériel altéré le plus agé. Les rapportsE. carotovora surE. atroseptica obtenus à partir des isolements effectués sur insectes ont été plus élévés que ceux trouvés à partir du matériel pourri en provenance des tas. Les auteurs suggèrent que les insectes euxmêmes peuvent exercer une action sélective en faveur d'E. carotovora. Les insectes collectés à partir d'un des tas peuvent transmettre facilementE. carotovora aux pommes de terre se trouvant en serre et dont les tiges sont endommagées. Les auteurs suggèrent que les lots de pommes de terre indemnes de bactéries coliformes grace au procédé de bouturage peuvent être à nouveau recontaminé à partir des tas de déchets de pommes de terre et par l'intermédiaire des insectes.相似文献
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Christensen BW Roberts JF Pozor MA Giguere S Sells SF Donahue JM 《Journal of the American Veterinary Medical Association》2006,228(8):1234-1239
CASE DESCRIPTION: A 4-year-old Thoroughbred mare was evaluated because of placental abnormalities and a retained placental remnant. CLINICAL FINDINGS: Microbial culture of the placenta yielded pure growth of Amycolatopsis spp. Histologic examination of the placenta revealed a focally expanding chorionitis with intralesional gram-positive filamentous bacilli and multifocal allantoic adenomatous hyperplasia on the apposing allantoic surface. TREATMENT AND OUTCOME: Treatment with lavage and oxytocin resulted in expulsion of the placental remnant within hours of parturition. The mare did not become pregnant again despite multiple breedings. The foal appeared healthy but died of complications during an elective surgical procedure at 7 weeks of age. CONCLUSIONS AND CLINICAL RELEVANCE: To the author's knowledge, all previously confirmed cases of nocardioform placentitis have been in mares bred in the central Kentucky region. Indications that the pathogen in the mare reported here is a different species than that isolated in Kentucky suggest that this is an emerging disease. Mares with nocardioform placentitis usually do not have the same clinical signs as mares with placentitis resulting from an ascending pathogen. 相似文献
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OBJECTIVE: To identify Actinobacillus spp isolates recovered from fetuses and pericardial fluid from horses affected with mare reproductive loss syndrome (MRLS) and determine whether these bacterial species are the same as those isolated from clinically normal horses. SAMPLE POPULATION: Isolates of actinobacilli recovered from 18 horses with pericarditis and 109 fetuses aborted by mares affected by MRLS. Procedures-Actinobacillus spp isolates were identified to the level of species or subspecies by use of conventional phenotypic tests and biochemical and enzyme test kits. The 16S rRNA gene from selected isolates was amplified, purified, and sequenced. Sequence data were compared with sequence data for actinobacilli in GenBank. RESULTS: Of the 109 isolates obtained from fetuses, 14 were Actinobacillus equuli subsp equuli, 65 were A equuli subsp haemolyticus, 28 were Bisgaard taxon 10-like bacterium, and 2 were Actinobacillus genomospecies 1. Of the 18 isolates from horses with pericarditis, 4 were A equuli subsp equuli, 13 were A equuli subsp haemolyticus, and 1 was Bisgaard taxon 10-like bacterium. Comparisons with published data and GenBank data revealed that the isolates recovered from horses with MRLS were the same as those isolated from the oral cavity or alimentary tract of healthy horses. CONCLUSIONS AND CLINICAL RELEVANCE: Actinobacillus spp isolates recovered from fetuses and pericardial fluid samples of horses affected by MRLS in 2001 to 2003 were identical to Actinobacillus spp found in the oral cavity and alimentary tracts of healthy horses. 相似文献
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Soulen Jr RJ JM Byers MS Osofsky B Nadgorny T Ambrose SF Cheng Broussard C T Tanaka PR J Nowak JS Moodera A Barry JMD Coey 《Science (New York, N.Y.)》1998,282(5386):85-88
A superconducting point contact is used to determine the spin polarization at the Fermi energy of several metals. Because the process of supercurrent conversion at a superconductor-metal interface (Andreev reflection) is limited by the minority spin population near the Fermi surface, the differential conductance of the point contact can reveal the spin polarization of the metal. This technique has been applied to a variety of metals where the spin polarization ranges from 35 to 90 percent: Ni0.8Fe0.2, Ni, Co, Fe, NiMnSb, La0.7Sr0.3MnO3, and CrO2. 相似文献
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R H Kessler M Ristic D M Sells C A Carson 《American journal of veterinary research》1979,40(12):1767-1773
Anaplasma marginale propagated in vitro showed an increasing rate of replication in a sequence of three experiments. The changes in the percentage of parasitized erythrocytes and identification of the organism in culture were monitored by the Giemsa-staining and the direct fluorescent antibody techniques. The ultrastructure of the organism in culture also was determined. The percentage of parasitized erythrocytes increased more than three times in the first experiment during a period of 8 days, and about ten times in the second experiment during a period of 14 days. After 8 days of observation of the primary culture in the third experiment, the trend of growth was more rapid than in the first and second experiment. The viability of the organism was verified by inoculation of susceptible calves, using 13- and 33-day cultures of the first and the second experiments, respectively. The primary cultures were subcultured twice by dilution with normal bovine erythrocytes. 相似文献
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AM See KL Swindells MJ Sharman KL Haack D Goodman A Delaporta I Robertson SF Foster 《Australian veterinary journal》2009,87(7):292-295
Objective To establish reference values for activated coagulation time (ACT) in normal cats and dogs, by visual assessment of clot formation using the MAX-ACTTM tube.
Subjects We recruited 43 cats and 50 dogs for the study; 11 cats and 4 dogs were excluded from the statistical analysis because of abnormalities on clinical examination or laboratory testing including anaemia, prolonged prothrombin time (PT) or activated partial thromboplastin time (APTT), or insufficient plasma volume for comprehensive laboratory coagulation testing.
Procedure Blood samples were collected via direct venipuncture for MAX-ACT, packed cell volume/total solids, manual platelet estimation and PT/APTT measurement. Blood (0.5 mL) was mixed gently in the MAX-ACT tube at 37°C for 30 s, then assessed for clot formation every 5 to 10 s by tipping the tube gently on its side and monitoring for magnet movement. The endpoint was defined as the magnet lodging in the clot. The technique was tested with 10 dogs by collecting two blood samples from the same needle insertion and running a MAX-ACT on each simultaneously.
Results In normal cats the mean MAX-ACT was 66 s (range 55–85 s). In normal dogs the mean was 71 s (range 55–80 s). There was no statistical difference between the first and second samples collected from the same needle insertion.
Conclusions and Clinical Relevance In both cats and dogs, a MAX-ACT result >85 s should be considered abnormal and further coagulation testing should be performed. Additionally, failure to discard the first few drops of the sample does not appear to significantly affect results. 相似文献
Subjects We recruited 43 cats and 50 dogs for the study; 11 cats and 4 dogs were excluded from the statistical analysis because of abnormalities on clinical examination or laboratory testing including anaemia, prolonged prothrombin time (PT) or activated partial thromboplastin time (APTT), or insufficient plasma volume for comprehensive laboratory coagulation testing.
Procedure Blood samples were collected via direct venipuncture for MAX-ACT, packed cell volume/total solids, manual platelet estimation and PT/APTT measurement. Blood (0.5 mL) was mixed gently in the MAX-ACT tube at 37°C for 30 s, then assessed for clot formation every 5 to 10 s by tipping the tube gently on its side and monitoring for magnet movement. The endpoint was defined as the magnet lodging in the clot. The technique was tested with 10 dogs by collecting two blood samples from the same needle insertion and running a MAX-ACT on each simultaneously.
Results In normal cats the mean MAX-ACT was 66 s (range 55–85 s). In normal dogs the mean was 71 s (range 55–80 s). There was no statistical difference between the first and second samples collected from the same needle insertion.
Conclusions and Clinical Relevance In both cats and dogs, a MAX-ACT result >85 s should be considered abnormal and further coagulation testing should be performed. Additionally, failure to discard the first few drops of the sample does not appear to significantly affect results. 相似文献
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Assemblage of structural proteins into 50S subunits was examined in Escherichia coli recovering fromt chloramphenicol treatment. Cells previously labeled with H3-leucine for three generations were incuibated for 30 minutes with chloramnlphenicol. Proteins synthesized during the initial 5 minuites of recovery from chlorarmphenicol treatmnent were labeled with C(14)-leucine. Marked variation in the ratios of C(14)- to H(3)-leucine in ribosomal protein occurred in cells that had been treated with chloramphenicol; luntreated cells displayed little variation. Thle resuilts sliggest that ribosomal proteins are assenmbled into 50S subunits in a nonrandom manner. 相似文献