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Fecal contamination of the mangrove oyster Crassostrea rhizophorae and the cultivation water at the river pacoti estuary (Eusébio Ceará State): Identification and isolation of Escherichia coli and its susceptibility to different antimicrobians | Contaminação fecal da ostra Crassostrea rhizophorae e da água de cultivo do estuário do Rio Pacoti (Eusébio, Estado do Ceará): Isolamento e identificação de Escherichia coli e sua susceptibilidade a diferentes antimicrobianos
2008
Regine Helena Silva dos Fernandes Vieira | Maylinque Albuquerque Atayde | Edirsana Maria Ribeiro de Carvalho | Fátima Cristiane Teles de Carvalho | Antonio Adauto Fonteles Filho
This study has been designed to assess the microbiological quality of oyster Crassostrea rhizophorae and of the water used in farms located at the Pacoti River estuary, Ceará State, by means of the MPN of total coliforms (Ct) and thermtolerant coliforms (CT). The database consisted of 15 samples collected from June to November, 2006. The water was kept within the limits set up by the current legislation. MPN values were in the ranges of <1.8 18,000 Ct per 100 ml and <1.8 2,000 CT per 100 ml, for the water, and <1.8 3,500 Ct per gram and <1.8 2,800 CT per gram for the oyster itself. Twenty-five strains isolated from the cultivation water and identified as Escherichia coli were tested for susceptibility to a few antimicrobians and proved resistant to ampicillin, nitrofurantoin, tetracycline, sulfazotrin, nalidixic acid, ciprofloxacin and imipenem. From the oysters, four strains were identified as E. coli and proved resistant to tetracycline and imipenem. From the afore-mentioned results, it can be concluded that: Pacoti River waters have received a clean bill of health according to the national legislation; the majority of water-isolated E.coli strains (59.43%) were sensitive to the currently used antimicrobians, except for imipenem to which 80% of the identified E. coli strains proved resistant; sensitivity of the oyster-isolated E. coli strains was found to be high to most of the tested antimicrobians. In all, it is suggested that more clear management measures be made available so as to allow for microbiological quality evaluation of raw-consumed mollusks. | Este estudo objetivou avaliar a qualidade microbiológica da água do cultivo de ostras, do Estuário do Rio Pacoti, assim como a qualidade das ostras, através do Número Mais Provável (NMP) de coliformes totais (Ct) e termotolerantes (CT). Foram realizadas 15 colheitas, entre junho e novembro de 2006. A água do cultivo se manteve dentro dos limites permitidos pela Legislação vingente. O NMP de Ct/100 mL variou de < 1,8 a 18.000 e de CT/100 mL de < 1,8 a 2.000, enquanto as ostras variaram os Ct e CT/g de < 1,8 a 3.500 e < 1,8 a 2.800, respectivamente. Vinte e cinco cepas de Escherichia coli isoladas da água de cultivo testadas quanto a susceptibilidade a alguns antimicrobianos se mostraram resistentes a ampicilina, nitrofurantoína, tetraciclina, sulfazotrin, ácido nalidíxico, ciprofloxacim, e a imipenem. Das ostras, somente quatro cepas, identificadas como E.coli mostraram-se resistentes a tetraciclina e a imipenem. Baseado nos valores obtidos de Ct e CT da amostra de água e ostras, foi possível constatar que: as águas do Rio Pacoti estão em boas condições segundo a legislação nacional; que a maioria das cepas de E. coli (59,43%), isoladas da água do Rio Pacoti foi sensível aos antimicrobianos testados, exceção do imipenem para o qual as cepas de E.coli apresentaram alto percentual de resistência (80%); a sensibilidade das cepas de E.coli isoladas das amostras de ostras apresentou-se alta à maioria dos antibióticos testados.
Mostrar más [+] Menos [-]Molecular characterization of virulence factors in Escherichia coli strains isolated from parrots with colibacilosis | Caracterização molecular dos fatores de virulência de estirpes de Escherichia coli isoladas de papagaios com colibacilose aviária
2008
Terezinha KNÖBL | Silvia Nery Godoy | Eliana Reiko Matushima | Marta Brito Guimarães | Antonio José Piantino Ferreira
A total of eight Escherichia. coli isolates from psittacine birds were serogrouping and investigated for the virulence factors: pili associated with pyelonephritis (pap), S fimbriae (sfa), afimbrial adhesin (afa), capsule K1 (neu), curli fibers (crl, csgA), temperature-sensitive hemagglutinin (tsh), heat labile (LT) and heat stable (STa and STb) enterotoxins, Shiga-like toxins (Stx1 and Stx2), Cytotoxic necrotizing factor (cnf1), haemolysin (hly), aerobactin production (iuc) and serum resistance (iss). The results showed that the isolates belonged to six serogroups: O23; O54; O64; O76; O128 and O152. The found virulence genes were: crl+ in all isolates, pap+, iuc+ and iss+ in three isolates; tsh+ in two isolates. All strains were negative for genes neu, csgA, sfa, afa, hly, cnf and LT, STa, STb, Stx1, Stx2 toxins. Our findings suggested that some E. coli isolated from psittacine birds present some virulence factors of avian pathogenic E. coli (APEC) pathotype. | Oito amostras de Escherichia coli isoladas de papagaios com colibacilose aviária foram sorogrupadas e investigadas para a presença dos fatores de virulência: pili associado a pielonefrite (pap), fímbria S (sfa), adesina afimbrial (afa), cápsula K1 (neu), curli (crl, csgA), hemaglutinina termosensível (tsh), enterotoxinas termo-lábil (LT) e termo-estável (STa e STb), Shiga-like toxinas (Stx1 e Stx2), Fator citotóxico necrotizante (cnf1), hemolisina (hly), aerobactina (iuc) e resistência sérica (iss). Os resultados mostraram que os isolados pertenciam a seis sorogrupos: O23; O54; O64; O76; O128 e O152. Os genes de virulência detectados foram: crl+ em todos os isolados; pap+; iss+ e iuc+ em três isolados, tsh+ em dois isolados. Todas as amostras foram negativas para os genes neu, csgA, sfa, afa, hly, cnf e para as toxinas LT, STa, STb, Stx1 e Stx2. Estes resultados sugerem que amostras de E. coli isoladas de papagaios apresentam alguns fatores de virulência das amostras do patotipo de E. coli patogênica para aves (APEC).
Mostrar más [+] Menos [-]Experimental peritonitis in horses. Hematological and biochemistry aspects | Peritonite experimental em eqüinos. Aspectos hematológicos e bioquímicos
2000
Luiz Cláudio Nogueira Mendes | Luiz Carlos Marques | Ruben Pablo Schocken-Iturrino | Fernando Antônio de Ávila | Euclides Braga Malheiros
Sixteen adult horses were randomly divided into 4 equal groups (GI, GII, GIII and GIV) of 4 animals and each group was injected intraperitoneally with one of the following suspension: Group I, 100 x 10(7) colony-forming units (CFU) of E. coli diluted in 500 ml of 0.9% saline; Group II, 100 x 10(7) CFU of Bacteroides fragilis in 500 ml of 0.9% saline; Group III, 100 x 10(7) CFU of E. coli in combination with 100 x 10(7) CFU of B. fragilis in 500 ml of 0.9% saline; Group IV, 500 ml of 0.9% saline. Leukopenia appeared in all animals inoculated with bacteria within the first six hours of the experiment. After this period, leukocytosis was observed in some inoculated horses. Horses inoculated with pure cultures of either E. coli or B. fragilis demonstrated mild and self-limiting peritonitis, whereas those inoculated with a combination of both bacteria demonstrated laboratory findings of higher intensity and duration. | Dezesseis eqüinos adultos foram distribuídos aleatoriamente em 4 grupos (GI, GII, GIII e GIV) constituídos por quatro animais, recebendo cada grupo o seguinte inóculo por via intraperitoneal: GI (100 X 10(7) unidades formadoras de colônia (UFC) de Escherichia coli diluídos em 500 ml de solução salina 0,9% estéril); GII (100 X 10(7) UFC de Bacteroides fragilis diluídos em 500 ml de solução salina 0,9% estéril); GIII (100 X 10(7) UFC de Escherichia coli associados a 100 X 10(7) UFC de Bacteroides fragilis diluídos em 500 ml de solução salina 0,9% estéril); GIV (testemunho - 500 ml de solução salina 0,9% estéril). Leucopenia ocorreu em todos os animais inoculados com bactérias, nas primeiras seis horas após as inoculações. Posteriormente a este período, verificou-se em alguns eqüinos inoculados leucocitose. Os eqüinos inoculados com culturas puras de E. coli ou B. fragilis apresentaram peritonites brandas e autolimitantes, enquanto os inoculados com a associação destas bactérias, apresentaram alterações laboratoriais de maior intensidade e duração.
Mostrar más [+] Menos [-]Serologic characterization and typing of the toxins produced by strains of Escherichia coli isolated from swines with diarrhoea in the state of São Paulo | Identificação sorológica e caracterização das toxinas de estirpes de Escherichia coli isoladas de suínos com diarréia, criados no Estado de São Paulo
1992
Simone Assis Rosa de Aquino Viegas | Roberto Mitio Yanaguita | Edgar de Aquino Viegas | Luzinete Alves Silva | Silvio Arruda Vasconcellos
<p>Faecal samples were collectcd from 85 piglets with diarrhoea in five pig farms located in the Municipalities of Bragança Paulista and Guarulhos in the State of São Paulo, Brazil. The presence of thermostable entcrotoxin (STa), was achieved by the new-born mouse test; whereas for the (STb) type, it was used the test in tied loops of pig bowel. Among the serogroups investigated, the 0149 was found in 19 (22.35%) isolations, having 16 (18.82%) of them producing STa entcrotoxin, and three (3.52%) the STa and STb types. In the serogroup 0139, e ight (9.41%) strains produced STa enterotoxin. The serogroups 010, 0119, 0148 and 0158 produced only the STa enterotoxin. However, the serogroup 020 presented some more features: one (1.17%) sample had STb enterotoxin and two (2.35%) produced, simultaneously, STa and STb. Two (2.35%) STa entcrotoxin positive samples were observed, in the serogroups 035 and 0157.</p> | <p>Em cinco criações de suínos localizadas nos municípios de Bragança Paulista e Guarulhos, no Estado de São Paulo, Brasil, foram colhidas amostras de fezes de 85 leitões, com um a 30 dias de idade, apresentando quadro clínico de diarréia. A pesquisa de enterotoxina termoestável (STa) foi efetivada através do teste em camundongos recém-nascidos enquanto a demonstração da STb foi realizada em alça ligada de intestino de suíno. O sorogrupo 0149 foi constatado em 19 (22,35%) isolamentos dos quais 16 (18,82%) produziram enterotoxina STa e três (3,53%) produziram enterotoxinas STa e STb. O sorogrupo 0139 foi observado em oito (9,41%) estirpes produtoras da enterotoxina STa. Os sorogrupos 010, 0119, 0148 e 0158 somente foram produtores de enterotoxina STa; entretanto, o sorogrupo 020 apresentou ainda um (1,17%) isolamento com enterotoxina STb e dois (2,35%) produzindo simultaneamente STa e STb. Foram observadas duas (2,35%) estirpes produtoras de enterotoxina STa nos sorogrupos 035 e 0157.</p>
Mostrar más [+] Menos [-]Similaridade genética entre APEC e cepas de Escherichia coli isoladas de Guaruba guarouba em um estudo com psitacídeos hígidos de cativeiro | Genetic similarity between APEC and Escherichia coli strains isolated from Guaruba guarouba in a survey on healthy captive psittacine birds
2013
Fabíola Eloisa Setim Prioste | Marcos Paulo Vieira Cunha | Rodrigo Hidalgo Fricielle Teixeira | Ticiana Zwargg | Rosely Gioia Di-Chiacchio | Priscilla Anne Melville | Nilson Roberto Benites | Juliana Sinhorini | Eliana Reiko Matushima | Terezinha Knöbl
<!--[if gte mso 9]><xml> <o:OfficeDocumentSettings> <o:AllowPNG/> </o:OfficeDocumentSettings> </xml><![endif]--><p class="MsoNormal">O papel dos psitacídeos como reservatório de Escherichia coli patogênicas para aves (APEC) não é conhecido, mas será útil para a compreensão da interface humano-animal, uma vez que a microbiota entérica destas aves é composta por bactérias Gram-positivas. O objetivo deste estudo foi identificar a presença de APEC em fezes de Guaruba guarouba clinicamente saudáveis. Para isso, foram isoladas e analisadas E. coli presentes em fezes cloacais coletadas de 87 psitacídeos, alojados em seis zoológicos, três criatórios comerciais e um criatório conservacionista. Das 87 aves examinadas, 46 (52,87%) apresentaram E. coli nas fezes. A presença de oito genes de virulência foi determinada pela reação em cadeia pela polimerase (PCR): irp2, iucD, iss, vat, cvi/cva, tsh, astA, e papC, e 29 (63,04%) dos 46 isolados foram positivos para pelo menos um dos oito genes estudados. A frequência dos genes de virulência observada nos isolados de E. coli foi 32.6% (15/46) irp2, 26% (12/46) iucD, 19.5% iss (9/46), 17.4% vat (8/46), 17.4% cvi/cva (8/46), 8.7% tsh (4/46), 4.4% astA (2/46) e 0% papC (0/46). Os isolados foram agrupados em 13 perfis genotípicos de acordo com combinações de genes de virulência, mas apenas duas amostras foram classificadas como APEC, com o perfil iuc, iss, cvi/cva, irp + e iuc, iss, cvi/cva, irp, tsh, iuc, iss, +. Este estudo revela a presença de APEC em aves de cativeiro (G. guarouba) clinicamente saudáveis, sugerindo que estes psitacídeos possam atuar como reservatórios de micro-organismos patogênicos. 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Name="TOC Heading"/> </w:LatentStyles> </xml><![endif]--><!--[if gte mso 10]> <style> /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Tabela normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin-top:0cm; mso-para-margin-right:0cm; mso-para-margin-bottom:10.0pt; mso-para-margin-left:0cm; line-height:115%; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-fareast-language:EN-US;} </style> <![endif]--></p><p class="MsoNormal"><span style="mso-ansi-language: EN-US;" lang="EN-US">The role of psittacine birds as a reservoir of avian pathogenic Escherichia coli (APEC) is not known but would be helpful in understanding the human – animal interface, since the enteric microbiota of these birds consists of Gram positive bacteria. The aim of this study was to identify the presence of APEC in feces of clinically healthy Guaruba guarouba. To do this, we isolated and analyzed E. coli from cloacal fecal samples taken from 87 psittacine birds from six zoologic parks, three commercial breeders and one conservation breeder. Of the 87 birds examined, 46 (52.87%) presented E. coli in feces. The presence of the following eight virulence genes was determined by the polymerase chain reaction (PCR): irp2, iucD, iss, vat, cvi/cva, tsh, astA, and papC, and 29 (63.04%) of 46 E. coli isolates tested were positive at least one of the eight genes studied. The frequency of virulence genes observed in isolates of E. coli were 32.6% (15/46) irp2, 26% (12/46) iucD, 19.5% iss (9/46), 17.4% vat (8/46), 17.4% cvi/cva (8/46), 8.7% tsh (4/46), 4.4% astA (2/46) and 0% papC (0/46). The isolates were grouped in 13 genotypic profiles according to virulence gene combinations, but only 2 isolates were classified as APEC, with the pattern iuc, iss, cvi/cva, irp + and iuc, iss, cvi/cva, irp, tsh, vat +. This study reveals the presence of APEC in clinically healthy captive G. guarouba, suggesting that these psittacine birds may act as reservoir for pathogenic microorganisms. Epidemiological studies are needed to determine the relevance of this species as a reservoir and the implications for conservation of endangered species G. guarouba.</span></p>
Mostrar más [+] Menos [-]Efeito do tempo de conservação de polimorfonucleares do sangue de bezerros sobre o metabolismo oxidativo e a atividade de fagocitose de Escherichia coli | Effect of conservation time on bovine polymorphonuclear leukocytes in calves blood on oxidative burst and Escherichia coli phagocytosis activity
2008
Elizabeth Bohland | Vanessa de Moura Sá-Rocha | Fernanda Cavallini Cyrillo | Fernando José Benesi
Foram avaliados os efeitos do tempo sobre o metabolismo oxidativo e a fagocitose de Escherichia coli, em amostras de polimorfonucleares (PMN) do sangue, de cinco bezerros hígidos, conservadas em banho de gelo por duas (t2), quatro (t4), seis (t6), 12 (t12) e 24 (t24) horas. O metabolismo oxidativo foi avaliado utilizando o Diacetato 2' 7' Diclorofluoresceína (DCFH-DA) e a E. coli, como estímulo. Para a fagocitose a mesma bactéria foi utilizada. As amostras foram analisadas por citometria de fluxo. O metabolismo oxidativo basal dos PMN do sangue de bezerros foi maior nos tempos t4, t6 e t12, do que em t2 (p<0,05). A intensidade de fluorescência do metabolismo oxidativo induzido pela bactéria foi maior nos tempos t4 e t6 do que em t2 (p<0,05). A comparação entre o metabolismo basal e induzido pela bactéria, em cada um dos tempos, mostrou que a maior diferença ocorreu em t2, com valores da média geométrica e desvios padrão respectivos de 18,3 ± 4,4 e 26,7 ± 1,8 (p< 0,05). A atividade de fagocitose, medida pela intensidade de fluorescência, foi maior para as amostras mantidas em gelo por 6 horas do que para t2, t4 e t12 (p<0,05). O percentual de fagocitose não diferiu entre os tempos. O tempo ideal para análise do metabolismo oxidativo foi o de duas horas. Maiores estudos são necessários para se verificar a influência do tempo de conservação na fagocitose de E. coli por PMN do sangue de bovinos. | The time effect on oxidative burst and phagocytosis of Escherichia coli by polymorphonuclear leukocytes of 5 healthy calve blood samples were evaluated. Samples were kept on ice bath for two (t2), four (t4), six (t6), twelve (t12) and 24 hours (t24) before the tests. The oxidative burst was measured using the 2',7'-dichlorfluorescein-diacetate (DCFH-DA) and E.coli as stimulus, also the same bacteria was used to phagocytosis process. The PMN basal oxidative burst of calves blood samples were analyzed by flow cytometry and were higher at times t4, t6 and t12 (p<0,05) than at t2. The oxidative burst fluorescence intensity induced by bacteria was higher at the times t4 and t6 than at t2 (p<0,05). The comparison between the basal oxidative burst and the one induced by bacteria on each time, showed t2 time as the one with the highest difference, with geometric media and standard deviation of 18,3 ± 4,4 and 26,7 ± 1,8 (p< 0,05), respectively. Phagocytosis activity was measured by fluorescence intensity and was higher on samples kept on ice bath for 6 hours than those at t2, t4 and t12 (p<0,05). The phagocytosis percentage did not differ between the different times. The ideal time to test the oxidative burst was 2 hours (t2). Further researches are necessary to verify the conservation time influence on E.coli phagocytosis by PMN of bovine blood.
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