ABSTRACT
Aeromonas dhakensis is reported as an emerging pathogenic species within the genus Aeromonas and is widely distributed in tropical coastal areas. This study provided a detailed description and characterization of a strain of A. dhakensis (202108B1) isolated from diseased Ancherythroculter nigrocauda in an inland region of China. Biochemical tests identified the isolate at the genus level, and the further molecular analysis of concatenated housekeeping gene sequences revealed that the strain belonged to the species A. dhakensis. The isolated A. dhakensis strain was resistant to five antibiotics, namely, penicillin, ampicillin, clindamycin, cephalexin, and imipenem, while it was susceptible to or showed intermediate resistance to most of the other 15 tested antibiotics. The isolated strain of A. dhakensis caused acute hemorrhagic septicemia and tissue damage in artificially infected A. nigrocauda, with a median lethal dose of 7.76 × 104 CFU/fish. The genome size of strain 202108B1 was 5 043 286 bp, including 1 chromosome and 4 plasmids. This is the first detailed report of the occurrence of infection caused by an A. dhakensis strain causing infection in an aquaculture system in inland China, providing important epidemiological data on this potential pathogenic species.
Subject(s)
Aeromonas , Anti-Bacterial Agents , Fish Diseases , Gram-Negative Bacterial Infections , China , Aeromonas/genetics , Aeromonas/isolation & purification , Aeromonas/classification , Aeromonas/drug effects , Aeromonas/pathogenicity , Animals , Anti-Bacterial Agents/pharmacology , Fish Diseases/microbiology , Gram-Negative Bacterial Infections/microbiology , Gram-Negative Bacterial Infections/veterinary , Fishes/microbiology , Phylogeny , Microbial Sensitivity Tests , Aquaculture , Genome, Bacterial , RNA, Ribosomal, 16S/genetics , Plasmids/geneticsABSTRACT
Background: Aeromonas dhakensis is associated with soft tissue infection, bacteremia and gastroenteritis. Involvement of respiratory system in adults is extremely rare. We report a case of fulminant pneumonia and bacteremia due to A. dhakensis in a patient without underlying diseases. Case presentation: A 26-year-old man became ill suddenly with pneumonia after swimming in a river. Despite intensive support measures in the intensive care unit, he died 13 hours after admission and 4 days after his first symptoms. Autopsy showed abundant Gram-negative bacteria, massive inflammatory cell infiltration, edema, necrosis and hemorrhage in lung tissue. A. dhakensis was isolated from blood culture taken at admission and bronchoalveolar lavage fluid (BALF) after intubation. Moreover, A. dhakensis was also detected in lung tissue by metagenomic next-generation sequencing (mNGS) assay. The infection may have come from river water. Conclusion: In patients who develop a fulminant pneumonia after contacting an aquatic environment, A. dhakensis should be alerted and mNGS may aid in the detection of aquatic pathogens by being more sensitive and specific versus traditional bacterial culture.
Subject(s)
Aeromonas , Bacteremia , Bronchoalveolar Lavage Fluid , Gram-Negative Bacterial Infections , Humans , Male , Adult , Aeromonas/isolation & purification , Aeromonas/genetics , Aeromonas/pathogenicity , Bacteremia/microbiology , Bacteremia/diagnosis , Gram-Negative Bacterial Infections/microbiology , Gram-Negative Bacterial Infections/diagnosis , Fatal Outcome , Bronchoalveolar Lavage Fluid/microbiology , Lung/pathology , Lung/microbiology , Pneumonia, Bacterial/microbiology , Pneumonia, Bacterial/diagnosis , High-Throughput Nucleotide Sequencing , MetagenomicsABSTRACT
Aeromonas spp. are commonly found in the aquatic environment and have been responsible for motile Aeromonas septicemia (MAS) in striped catfish, resulting in significant economic loss. These organisms also cause a range of opportunistic infections in humans with compromised immune systems. Here, we conducted a genomic investigation of 87 Aeromonas isolates derived from diseased catfish, healthy catfish and environmental water in catfish farms affected by MAS outbreaks in eight provinces in Mekong Delta (years: 2012-2022), together with 25 isolates from humans with bloodstream infections (years: 2010-2020). Genomics-based typing method precisely delineated Aeromonas species while traditional methods such as aerA PCR and MALDI-TOF were unable identify A. dhakensis. A. dhakensis was found to be more prevalent than A. hydrophila in both diseased catfish and human infections. A. dhakensis sequence type (ST) 656 followed by A. hydrophila ST251 were the predominant virulent species-lineages in diseased catfish (43.7 and 20.7â%, respectively), while diverse STs were found in humans with bloodstream infections. There was evidence of widespread transmission of ST656 and ST251 on striped catfish in the Mekong Delta region. ST656 and ST251 isolates carried a significantly higher number of acquired antimicrobial resistance (AMR) genes and virulence factors in comparison to other STs. They, however, exhibited several distinctions in key virulence factors (i.e. lack of type IV pili and enterotoxin ast in A. dhakensis), AMR genes (i.e. presence of imiH carbapenemase in A. dhakensis), and accessory gene content. To uncover potential conserved proteins of Aeromonas spp. for vaccine development, pangenome analysis has unveiled 2202 core genes between ST656 and ST251, of which 78 proteins were in either outer membrane or extracellular proteins. Our study represents one of the first genomic investigations of the species distribution, genetic landscape, and epidemiology of Aeromonas in diseased catfish and human infections in Vietnam. The emergence of antimicrobial resistant and virulent A. dhakensis strains underscores the needs of enhanced genomic surveillance and strengthening vaccine research and development in preventing Aeromonas diseases in catfish and humans, and the search for potential vaccine candidates could focus on Aeromonas core genes encoded for membrane and secreted proteins.
Subject(s)
Aeromonas , Catfishes , Fish Diseases , Gram-Negative Bacterial Infections , Sepsis , Animals , Catfishes/microbiology , Vietnam/epidemiology , Aeromonas/genetics , Aeromonas/isolation & purification , Aeromonas/classification , Aeromonas/pathogenicity , Gram-Negative Bacterial Infections/microbiology , Gram-Negative Bacterial Infections/veterinary , Gram-Negative Bacterial Infections/epidemiology , Humans , Sepsis/microbiology , Sepsis/veterinary , Sepsis/epidemiology , Fish Diseases/microbiology , Phylogeny , Genomics , Genome, Bacterial , Virulence Factors/genetics , Anti-Bacterial Agents/pharmacologyABSTRACT
Aeromonas hydrophila is a cause of infectious disease outbreaks in carp species cultured in South Asian countries including Pakistan. This bacterium has gained resistance to a wide range of antibiotics and robust preventive measures are necessary to control its spread. No prior use of fish vaccines has been reported in Pakistan. The present study aims to develop and evaluate inactivated vaccines against local strain of A. hydrophila in Pakistan with alum-precipitate as adjuvant. The immunogenic potential of vaccine was evaluated in two Indian major carps (Rohu: Labeo rohita, Mori: Cirrhinus mrigala) and a Chinese carp (Grass carp: Ctenopharyngodon idella). Fish were vaccinated intraperitoneally followed by a challenge through immersion. Fish with an average age of 4-5 months were randomly distributed in three vaccinated groups with three vaccine concentrations of 108, 109 and 1010 colony forming unit (CFU)/ml and a control group. Fixed dose of 0.1ml was applied to each fish on 1st day and a booster dose at 15 days post-vaccination (DPV). Blood samples were collected on 14, 28, 35, 48 and 60 DPV to determine antibody titers in blood serum using compliment fixation test (CFT). Fish were challenged at 60 DPV with infectious A. hydrophila with 108 CFU/ml through immersion. Significantly higher levels of antibody titers were observed from 28 DPV in all vaccinated groups as compared to those in the control group. In challenge experiment the average RPS (relative percent survivability) was 71% for groups vaccinated with 109 and 1010 CFU/ml and 86% for 108 CFU/ml. Vaccine with 108 CFU/ml induced highest immune response followed by 109 and 1010 CFU/ml. The immune response of L. rohita and C. idella was better than that of C. mrigala. In general, normal histopathology was [...].
Aeromonas hydrophila é uma causa de surtos de doenças infecciosas em espécies de carpas cultivadas em países do sul da Ásia, incluindo o Paquistão. Essa bactéria ganhou resistência a uma ampla gama de antibióticos, e medidas preventivas robustas são necessárias para controlar sua disseminação. Nenhum uso anterior de vacinas para peixes foi relatado no Paquistão. O presente estudo tem como objetivo desenvolver e avaliar vacinas inativadas contra cepa local de A. hydrophila no Paquistão com precipitado de alúmen como adjuvante. O potencial imunogênico da vacina foi avaliado em duas carpas principais indianas (Rohu: Labeo rohita, Mori: Cirrhinus mrigala) e uma carpa chinesa (Grass Carp: Ctenopharyngodon idella). Os peixes foram vacinados por via intraperitoneal, seguido de um desafio por imersão. Peixes com idade média de 4-5 meses foram distribuídos aleatoriamente em três grupos vacinados com três concentrações de vacina de 108, 109 e 1010 unidades formadoras de colônias (UFC) / ml e um grupo de controle. Foi aplicada dose fixa de 0,1ml em cada peixe no 1º dia e dose de reforço 15 dias pós-vacinação (DPV). Amostras de sangue foram coletadas em 14, 28, 35, 48 e 60 DPV para determinar os títulos de anticorpos no soro sanguíneo usando o teste de fixação de elogio (CFT). Os peixes foram desafiados a 60 DPV com infecciosa A. hydrophila com 108 CFU / ml por imersão. Níveis significativamente mais elevados de títulos de anticorpos foram observados em 28 DPV em todos os grupos vacinados, em comparação com aqueles no grupo de controle. Na experiência de desafio, o RPS médio (sobrevivência percentual relativa) foi de 71% para os grupos vacinados com 109 e 1010 CFU / ml e 86% para 108 CFU / ml. A vacina com 108 UFC / ml induziu a maior resposta imune seguida por 109 e 1010 UFC / ml. A resposta imune de L. rohita e C. idella foi melhor do que a de C. mrigala. Em geral, histopatologia normal foi observada em diferentes [...].
Subject(s)
Animals , Aeromonas/pathogenicity , Carps , Gram-Negative Bacterial Infections/veterinary , Vaccines/analysis , Vaccines/therapeutic useABSTRACT
Objetivou-se avaliar a ocorrência de Aeromonas spp. em peixes e amostras de água na região semiárida de Pernambuco e avaliar a frequência de aerolissina (aerA), enterotoxina citotóxica (act), enterotoxina citotônica (alt) e serina protease (ahp) nesses isolados. Foram analisados 70 peixes vivos e oito mortos com sinais clínicos de aeromoniose e 16 amostras de água. Aeromonas spp. foram identificadas por análises microbiológicas (provas bioquímicas) e molecular, usando-se primers específicos para a região 16S rRNA, e a distribuição dos quatro fatores de virulência (aerA, alt, act e ahp) foi investigada por ensaio de PCR. Cento e cinquenta e cinco (84,7%) isolados foram confirmados como Aeromonas spp. na análise molecular. Os genes de virulência mais frequentes foram act (53,55%) e aerA (51,61%). De acordo com o tipo de amostra, observou-se maior frequência do gene aerA (87,5% P=0,0474) em isolados de peixes mortos e a menor frequência do gene act (47,73% P=0,0002) em peixes vivos. Este estudo demonstrou a presença de aeromoniose no cultivo de tilápias em tanques-rede, nos municípios de Jatobá e Petrolândia, na região semiárida de Pernambuco. A detecção de aerA, act e alt pode ser utilizada na tipagem de virulência de Aeromonas spp.(AU)
The purpose of this study was to evaluate the occurrence of Aeromonas spp. from fishes and tilapia net-cage farm water in semi-arid regions of Pernambuco and to evaluate the frequency of the aerolysin (aerA), cytotoxic enterotoxin (act), cytotonic enterotoxin (alt) and serine protease (ahp) genes in Aeromonas isolates. 70 live and eight dead fish with aeromoniosis clinical signs and 16 water samples were analyzed. Aeromonas spp. isolated were identified by microbiological (biochemical evidence) and molecular analysis using specific primers for 16SrRNA region, while the distribution of four virulence factors, including aerA, alt, act and ahp, was investigated by PCR assay. One hundred fifty-five (84.7%) isolates were confirmed as Aeromonas spp. by molecular analysis. The most frequent virulence genes in isolates were act (53.55%) and aerA (51,61%). According to the kind of sample, the higher frequency of aerA gene (87.5% P= 0.0474) was observed in isolates from dead fish and the lowest frequency of act gene (47.73% P= 0.0002) from live fish. This study found the presence of aeromoniosis on tilapia farming in net-cages on Jatobá and Petrolândia counties in the semiarid Pernambuco region. The detection of aerA, act and alt can be used for virulence typing of Aeromonas spp. isolates.(AU)
Subject(s)
Animals , Tilapia/microbiology , Aeromonas/pathogenicity , Cichlids/microbiology , Fisheries , VirulenceABSTRACT
Resumen Las especies del género Aeromonas se encuentran ampliamente distribuidas en ecosistemas acuáticos, son bacilos Gram negativas, oxidasa positivas y fermentadoras de glucosa que han sido consideradas patógenas emergentes en humanos. Por otra parte, Aeromonas pertenece a la microbiota normal de los peces, no obstante, estos microorganismos poseen una diversidad de factores de virulencia responsables de una variedad de infecciones en humanos, principalmente de tipo gastrointestinal. La presencia de Aeromonas en productos destinados a consumo de alta demanda comercial como la tilapia genera preocupación sanitaria por el potencial patogénico que posee esta bacteria. En este contexto, identificar genes de virulencia presentes en cepas de Aeromonas aisladas en Oreochromis spp. para consumo humano en Reynosa, Tamaulipas, México; es de importancia ante la escasez de estudios moleculares al respecto en la zona. En el presente estudio se analizó el potencial patogénico de 15 cepas de Aeromonas previamente identificadas molecularmente mediante PCR y secuenciación, procedentes de Oreochromis spp. Mediante PCR se analizaron seis genes de virulencia (alt, ast, aerA, hlyA, gcat y stx1) y las cepas utilizadas como control fueron: Aeromonas hydrophila subsp. hydrophila ATCC 7966, Aeromonas caviae 429865 INP, Escherichia coli O157:H7 y Escherichia coli K12. El 100 % (n = 15) de las cepas presentaron al menos un gen de virulencia, el gen aerA se detectó en 86.66 % de las cepas analizadas, mientras que los genes ast y stx1 no fueron identificados. Se encontró que las cepas de Aeromonas presentaban genes asociados en una misma cepa: aerA/gcat, alt/aerA, alt/ aerA/gcat/hlyA y alt/aerA/gcat, de los cuales aerA/gcat se observó con mayor frecuencia y principalmente en A. veronii, mientras que, A. hydrophila presentó el mayor número de asociaciones de genes de virulencia. Estos hallazgos indican que las cepas de Aeromonas aisladas en Oreochromis spp. tienen el potencial de causar enfermedades en humanos. Por lo tanto, es necesario proporcionar información sobre esta bacteria emergente, para tratar y controlar eficazmente cualquier posible evento epidemiológico causado por la misma.(AU)
Abstract The genus Aeromonas are widely distributed in aquatic ecosystems are Gram-negative rods, oxidase-positive, and glucose-fermenting, considered emerging pathogens in humans. Aeromonas belongs to the fish microbiota, these microorganisms have a diversity of virulence factors responsible for a variety of infections in humans mainly gastrointestinal diseases. The presence of Aeromonas in products intended for consumption with high commercial demand such as tilapia generates sanitary concern due to the pathogenic potential of this bacteria. In this context, identification of virulence genes in strains of Aeromonas isolated in Oreochromis spp. intended for human consumption in Reynosa, Tamaulipas, Mexico is important due to the lack of molecular studies in this geographical area. In the present study the pathogenic potential of 15 strains of Aeromonas (A. veronii, A. hydrophila and A. schubertii) from Oreochromis spp. for human consumption were analyzed. Through PCR six virulence genes were analyzed (alt, ast, aerA, hlyA, gcat and stx1) and the strains used as control were: Aeromonas hydrophila subsp. hydrophila ATCC 7966, Aeromonas caviae 429865 INP, Escherichia coli O157: H7 and Escherichia coli K12. El 100 % (n = 15) of the strains harbored at least one virulence gene, aerA gene was detected in 86.66 % of the analyzed strains, while ast and stx1 genes were not identified. Moreover, Aeromonas strains had associated genes in the same strain: aerA / gcat, alt / aerA, alt / aerA / gcat / hlyA and alt / aerA / gcat, of which aerA / gcat were observed mostly in A. veronii, while A. hydrophila had the highest associations. These findings indicate that the strains of Aeromonas isolated in Oreochromis spp. have the potential to cause human diseases, and therefore, this species used as food, could be a vehicle for infections caused by Aeromonas. It also allows to provide information on this emerging microorganism to effectively treat and control any epidemiological event caused by Aeromonas spp. in the future.(AU)
Subject(s)
Ecosystem , Aeromonas/pathogenicity , Cichlids , Virulence , MexicoABSTRACT
INTRODUCCIÓN: en la actualidad las especies del género Aeromonas han emergido como un problema de salud pública, son ellas los agentes etiológicos de las enfermedades diarreicas con el aumento de la atención médica por años. Los procedimientos convencionales para su diagnóstico son muy engorrosos, laboriosos y duraderos. Una nueva metodología que emplea medios de cultivo cromogénicos ha permitido la simplificación y aceleración de su diagnóstico, que ofrece resultados altamente específicos. OBJETIVO: estudiar el efecto de la combinación de diferentes agentes selectivos de los microorganismos grampositivos sobre el aumento de la capacidad de recuperación, cuantificación y diferenciación de las especies de Aeromonas. MÉTODOS: se estudió el efecto inhibidor de la combinación de agentes selectivos (desoxicolato de sodio (0,05-0,2 g·L-1), sales biliares (0,65 g·L-1), verde brillante (0,025-0,03 g·L-1), cristal violeta (0,001-0,01 g·L-1) y sulfito de sodio (0,8 g·L-1) sobre los microorganismos grampositivos, así como la capacidad de recuperación, cuantificación y diferenciación de las especies de Aeromonas. Como base se utilizó la formulación de CromoCen AGN, sin el desoxicolato de sodio. RESULTADOS: los valores de las productividades de los medios CromoCen AE y CromoCen AGN a partir del inóculo 1,5 × 102 UFC·mL-1 resultaron, para: A. hydrophila 116,8 % y 23,9 %, A. caviae 100,8 % y 3,95 %, A. bestiarium 93,6 % y 28,8 %, A. culicicola 85,1 % y 66,12 %, A. veronii 116,7 % y 59,2 %, A. popoffi 86,56 % y 13,2 %, A. trota 94,8 % y 11,25 % y para A. eucrinophila 103,9 % y 2,80 %. La nueva composición cromogénica logró la diferenciación de los microorganismos por sus características culturales: color, forma, superficie, bordes en las colonias y proteólisis del medio circundante. CONCLUSIONES: la combinación de diferentes agentes selectivos para la inhibición de los microorganismos grampositivos coadyuvo el aumento de la capacidad de recuperación, cuantificación y diferenciación de las especies de Aeromonas.
INTRODUCTION: Species of the genus Aeromonas are a current public health problem, for they are the etiological agents responsible for the growing incidence of diarrheal diseases requiring medical care. Conventional procedures for their diagnosis are very complicated, laborious and time-consuming. A new methodology based on the use of chromogenic culture media allows diagnostic simplification and acceleration, yielding highly specific results. OBJECTIVE: Study the effect of combining several selective agents for gram-positive microorganisms upon an increased capacity for recovery, quantification and differentiation of Aeromonas species. METHODS: Assessment was conducted of the inhibiting effect of combined selective agents (sodium deoxycholate (0.05-0.2 g·L-1), bile salts (0.65 g·L-1), brilliant green (0.025-0.03 g·L-1), crystal violet (0.001-0.01 g·L-1) and sodium sulfite (0.8 g·L-1)) on gram-positive microorganisms, as well as their capacity for recovery, quantification and differentiation of Aeromonas species. The base used was the CromoGen AGN formulation without sodium deoxycholate. RESULTS: Productivity values for the media CromoCen AE and CromoCen AGN based on inoculation of 1.5 × 102 CFU·mL-1 were 116.8 % and 23.9 % for A. hydrophila, 100.8 % and 3.95 % for A. caviae, 93.6 % and 28.8 % for A. bestiarium, 85.1 % and 66.12 % for A. culicicola, 116.7 % and 59.2 % for A. veronii, 86.56 % and 13.2 % for A. popoffi, 94.8 % and 11.25 % for A. trota, and 103.9 % and 2.8 0% for A. eucrinophila. The new chromogenic composition enabled differentiation of microorganisms based on their cultural characteristics: color, shape, surface, colony borders and environmental proteolysis. CONCLUSIONS: Combination of various selective agents for the inhibition of grampositive microorganisms led to an increased capacity for recovery, quantification and differentiation of Aeromonas species.
Subject(s)
Humans , Chromogenic Compounds , Aeromonas/pathogenicity , Dysentery/ethnology , Sodium Sulfite/methodsABSTRACT
Aeromonas spp. são bactérias Gram negativas, oportunistas, de natureza ubíqua, isoladas principalmente de amostras de água. Até o presente momento foram reconhecidas 31 espécies, sendo as de maior importância médica Aeromonas hydrophila, Aeromonas caviae e Aeromonas veronii. A patogenicidade do gênero é considerada multifatorial, sendo este produtor de diversos tipos de toxinas e com envolvimento de outros fatores capazes de facilitar a penetração e o estabelecimento do agente no hospedeiro, causando doença. O objetivo desta revisão é elucidar o papel dos alimentos de origem animal como fontes de contaminação de bactérias do gênero Aeromonas para o ser humano. Isolamentos de aeromonas de diversos produtos de origem animal têm sido relatados, como carne, leite e seus derivados, além de frutos do mar, e em ambientes de processamento, como abatedouros, frigorífcos e laticínios. Tem-se buscado determinar fontes de contaminação dos alimentos, e a água foi definida como o principal disseminador. Aeromonas já foi definida como sendo a causadora de diversas enfermidades, desde afecções gastrointestinais até casos de meningite e morte. Considerando os alimentos de origem animal como importantes veículos de transmissão para o ser humano e o reconhecimento da água como fonte de disseminação do agente, torna-se imprescindível o tratamento adequado da água utilizada nos estabelecimentos processadores de alimentos para a segurança alimentar.(AU)
Aeromonas spp. are opportunistic, ubiquitous Gram negative bacteria, mostly isolated from water samples. Until the present time, 31 species have been recognized, and the most medically important are Aeromonas hydrophila, Aeromonas caviae and Aeromonas veronii. The pathogenicity of the genus is considered to be multifactorial, and it can produce several types of toxins, with the involvement of other factors that facilitate the penetration and the establishment of the agent in the host, thus causing the disease. Te objective of this review is to elucidate the role of foods of animal origin as sources of contamination of aeromonas to humans. Aeromonas have been reported in various animal products such as meat, milk, dairy products, and seafood, and also in processing environments such as slaughterhouses, meat and dairy plants. There has been the attempt to determine sources of food contamination, being the water defined as the main disseminator. Aeromonas has been defined as the cause of many diseases, from gastrointestinal affections to cases of meningitis and even death. Considering that animal foods are an important source of contamination for humans and because of the recognition of water as a source of dissemination, it is essential for food security to provide the proper treatment of water used in food processing establishments.(AU)
Subject(s)
Virulence , Food Contamination , Aeromonas/pathogenicity , Foods of Animal Origin , Gram-Negative Bacteria , Diarrhea , Food Microbiology , NoxaeABSTRACT
273 bacterial strains were isolated from 20 Chinese longsnout catfish samples. The biochemical characteristics of all strains conformed to the species description of Aeromonas veronii bv. veronii on the basis of Vitek GNI+ card. Furthermore, 16S rDNA, gyrB and rpoD sequences of the representative strain PY50 were sequenced and showed high similarity with A. veronii bv. veronii in Genbank. Antibiotic-resistance of the representative strain PY50 was assessed by the Kirby-Bauer disk diffusion method, and the results showed it was susceptible and moderately susceptible to 13 and 4 of the 21 antimicrobial agents tested. Extracellular products of strain PY50 contained gelatinase, lecithinase, elastase, most of lipase and lipopolysaccharide. Virulence of strain PY50 and extracellular products to Chinese longsnout catfish were also tested, and LD50 were about 3.47~10(4) CFU per fish and 11.22 Êg per fish in intraperitoneal injection respectively. This is the first report that A. veronii bv. veronii was the pathogenic agent of ulcerative syndrome in Chinese longsnout catfish.
Subject(s)
Animals , Aeromonas/isolation & purification , Aeromonas/pathogenicity , Anti-Bacterial Agents/analysis , Enzyme Activators/analysis , Catfishes/genetics , Catfishes/microbiology , Food SamplesABSTRACT
This work aimed to assess pathogenic potential and clonal relatedness of Aeromonas sp. and Vibrio cholerae isolates recovered during a diarrhea outbreak in Brazil. Clinical and environmental isolates were investigated for the presence of known pathogenic genes and clonal relatedness was assessed by intergenic spacer region (ISR) 16S-23S amplification. Four Aeromonas genes (lip, exu, gcat, flaA/B) were found at high overall frequency in both clinical and environmental isolates although the lip gene was specifically absent from selected species. A fifth gene, aerA, was rarely found in A. caviae, the most abundant species. The ISR profile revealed high heterogeneity among the Aeromonas isolates and no correlation with species identification. In contrast, in all the V. cholerae isolates the four genes investigated (ctxA, tcpA, zot and ace) were amplified and revealed homogeneous ISR and RAPD profiles. Although Aeromonas isolates were the major enteric pathogen recovered, their ISR profiles are not compatible with a unique cause for the diarrhea events, while the clonal relationship clearly implicates V. cholerae in those cases from which it was isolated. These results reinforce the need for a better definition of the role of aeromonads in diarrhea and whether they benefit from co-infection with V. cholerae.
O objetivo deste trabalho foi estabelecer o potencial patogênico e a relação clonal de isolados de Aeromonas sp. e Vibrio cholerae obtidos durante um surto de diarréia. Isolados clínicos e ambientais foram investigados quanto à presença de genes de virulência e sua relação clonal foi obtida através de amplificação da Região Espaçadora Intergênica (REI) 16S-23S. Quatro genes de Aeromonas (lip, exu, gcat, flaA/B) foram encontrados em alta frequência embora o gene lip tenha se mostrado ausente em algumas espécies. Um quinto gene, aerA, foi raramente encontrado em A. caviae, a espécie mais abundante. O perfil da REI revelou alta heterogeneidade entre os isolados de Aeromonas e nenhuma correlação com espécie. Em contraste, todas as amostras de V. cholerae amplificaram os genes investigados (ctxA, tcpA, zot e ace) e revelaram perfil clonal através de REI e RAPD. Embora Aeromonas tenha sido o principal patógeno isolado, o perfil da REI não é compatível como única causa para os eventos de diarréia, enquanto a relação clonal de V. cholerae aponta esse microrganismo como o provável agente do surto. Estes resultados reforçam a necessidade de definir melhor o papel de Aeromonas em diarréias e de que forma essas bactérias se beneficiam quando em co-infecção com V. cholerae.
Subject(s)
Humans , Aeromonas/genetics , Coinfection/microbiology , Disease Outbreaks , Diarrhea/microbiology , Gram-Negative Bacterial Infections/microbiology , Vibrio cholerae O1/genetics , Aeromonas/pathogenicity , Brazil/epidemiology , Coinfection/epidemiology , DNA, Bacterial/genetics , Diarrhea/epidemiology , Genotype , Gram-Negative Bacterial Infections/epidemiology , Polymerase Chain Reaction , Random Amplified Polymorphic DNA Technique , Vibrio cholerae O1/pathogenicity , Virulence/geneticsABSTRACT
Fifty four strains of Aeromonas spp were isolated from patients with acute diarrheic episodes by using Aerokey II and Aeroesquema methods. In vitro antimicrobial susceptibility and virulence factors were analyzed. The most frequently isolated specie was Aeromonas caviae. Over 75 percent of strains exhibited resistance to penicillins and ce-phalosporins; for the other antibiotic groups resistance was under 20 percent. Twenty six strains (48.1 percent) were multiresist-ant. At least one virulence factor among those evaluated in the study was present in 53 (98.1 percent) of the 54 strains.
Se identificaron 54 cepas de Aeromonas aisladas de pacientes con enfermedad diarreica aguda mediante los métodos Aerokey II y Aeroesquema. Se determinó la susceptibilidad antimicrobiana y algunos factores de virulencia. La especie encontrada en mayor frecuencia fue Aeromonas caviae. Se observaron valores de resistencia por sobre 75 por ciento para penicilinas y cefalotina; para el resto de los antimicrobianos estos valores se encontraron bajo 20 por ciento>; 26 cepas (48,1 por ciento) presentaron multi-resistencia. Al menos un factor de virulencia de los investigados estuvo presente en 53 (98,1 por ciento) de las 54 cepas analizadas.
Subject(s)
Child, Preschool , Humans , Aeromonas/pathogenicity , Diarrhea/microbiology , Gram-Negative Bacterial Infections/microbiology , Virulence Factors/analysis , Acute Disease , Aeromonas/classification , Aeromonas/drug effects , Anti-Bacterial Agents/pharmacology , Cuba , Gram-Negative Bacterial Infections/complications , Microbial Sensitivity Tests , Phenotype , VirulenceABSTRACT
Entre los nuevos agentes capaces de producir diarrea aguda se ha descrito la participación de Aeromonas hydrophila. Con objeto de conocer la incidencia e importancia relativa de este potencial enteropatógeno en nuestro medio, estudiamos 285 niños menores de 2 años con síndrome diarreico agudo y 140 niños controles pareados en edad y sexo en 2 ciudades (Santiago y Valparaíso) durante los veranos 1983-84 y 85-86. El aislamiento de Aeromonas hydrophila en pacientes de Valparaíso fue de 5,5% (4/73) en niños con diarrea y 2,3% (1/44) en controles, diferencia estadísticamente no significativa. No hubo aislamiento de este agente en Santiago (0/212). Se efectuó estudio de enterotoxicidad de las cepas aisladas que resultó negativo tanto para enterotoxinas termoestable (ST) mediante modelo de ratón y para enterotoxina termolábil (LT) mediante ELISA. Las variaciones geográficas observadas en el aislamiento de aeromonas en diarrea aguda, puede correlacionarse tal vez con existencia de reservorios acuáticos naturales
Subject(s)
Infant , Humans , Male , Female , Aeromonas/isolation & purification , Diarrhea, Infantile/microbiology , Drug Resistance, Microbial , Aeromonas/pathogenicity , Anti-Bacterial Agents/pharmacology , Enterotoxins/analysisABSTRACT
Aeromas has been described as an emergent foodborne pathogen of increasing importance. In this study, we report that 48(per cent) of 50 Pintado fish samples collected at the retail market of São Paulo city were positive for Aeromas sp, as detected by the direct plating method. When the presence/absence method was used, the positivity was 42(per cent). A caviae was the most frequent species, followed by A. hydrophila and A. sobria. Production of cytotoxic enterotoxin, observed in suckling mouse assay, was detected in 67(per cent) of A sobria strains, in 60(per cent) of A. hydrophila strains and in 40(per cent) of A. caviae strains. In vitro tests, performed with HEp-2 cells, showed that 88(per cent) of A. hydrophila, 27(per cent) of A. sobria and 13(per cent) of A. caviae strains were positive for this toxin. The in vivo production of cytotonic enterotoxin, tested after heating the filtrates at 56degreeC for 20 minutes, was detected in 17(per cent) of A. sobria, in 10(per cent) of A. caviae and in none of A. hydrophila strains in vivo. All analyzed strains did not alter HEp-2 cells. 20(per cent) and 16(per cent) of A. sobria and A. caviae isolates, respectively, presented capacity to adhere to HEp-2 cells. In counterpart, invasion of HEp-2 cells was not observed in any isolate. The Aeromonas isolates were sensitive to the majority of the antimicrobiol agents tested.
Subject(s)
Animals , Aeromonas/drug effects , Aeromonas/pathogenicity , Fishes/microbiology , Anti-Bacterial Agents/pharmacology , Virulence , Microbial Sensitivity Tests , Aeromonas/isolation & purificationABSTRACT
Foram analisadas 163 amostras de fezes de crianças com idade abaixo de 5 anos no período de 1995 a 1996, sendo 91 de fezes diarréicas e 72 de fezes não diarréicas. O material foi coletado em meio para transporte e submetido ao processo de enriquecimento a 4oC por 7 dias. Para o isolamento primário foi utilizado ágar amido ampicilina e incubado a 35oC por 18 a 24 horas. Foram isoladas 20 (21,9%) das seguintes espécies: Aeromonas A. caviae (7,7%), A. salmonicida salmonicida (6,6%), A. sobria (4,3%), A. hydrophila (2,2%) e Salmonicida achromogenes (1,1%). Nenhuma Aeromonas spp foi isolada dos 72 pacientes-controles. A susceptibilidade das amostras de Aeromonas spp aos antimicrobianos foi maior com a ciprofloxacina, diminuindo gradativamente com cloranfenicol, gentamicina, ampicilina e eritromicina.
From 1995 through 1996, 163 fecal specimens of children aged under 5 years were analysed, 91 being from diarrhea feces and 72 without diarrhea. The material was collected in transport medium and submitted to the enrichment procedure at 4 degrees C for 7 days. For the primary isolation starch ampicillin agar was used and incubated at 35 degrees C for 18 to 24 hours. Twenty (20.9%) from the following specimens were isolated: Aeromonas (A.) caviae (7.7%), A. salmonicida salmonicida (6.6%), A. sobria (4.3%), A. hydrophila (2.2%) and Salmonicida achromogenes (1.1%). No Aeromonas spp. was isolated from the 72 control subjects. The Aeromonas spp. susceptibility to antimicrobial was greater with ciprofloxacin, being this susceptibility gradually diminished with chloranphenicol, gentamicin, ampicillin and erythromycin.
Subject(s)
Child, Preschool , Humans , Aeromonas/isolation & purification , Diarrhea/microbiology , Feces/microbiology , Gram-Negative Bacterial Infections/microbiology , Urban Population , Aeromonas/drug effects , Aeromonas/pathogenicity , Anti-Bacterial Agents/pharmacology , Brazil/epidemiology , Diarrhea/epidemiology , Hemolysis , Gram-Negative Bacterial Infections/epidemiology , Prevalence , Urban Population/statistics & numerical data , Microbial Sensitivity Tests/statistics & numerical dataABSTRACT
Práticas nutricionais saudáveis e a globalização cultural popularizaram o consumo de pratos à base de peixe cru, anteriormente restritos aos países orientais. Estimativas mostram que as doenças de origem alimentar causam aproximadamente 76 milhões de casos, 325 mil hospitalizações e 5 mil mortes a cada ano, somente nos Estados Unidos. Casos com etiologia desconhecida somam 62 milhões, com 265 mil hospitalizações e 3.200 mortes. O objetivo deste estudo foi investigar a presença de Escherichia coli, Salmonella spp. e Staphylococcus aureus e cepas potencialmente patogênicas de Aeromonas spp. e Vibrio spp. em peixes comercializados em feiras livres da cidade de São Paulo, Brasil. Vinte amostras de peixes, de diferentes espécies, foram adquiridas em feiras livres e analisadas utilizando metodologia convencional para investigação de patógenos em alimentos. Altos níveis de contaminação fecal foram detectados em 25 por cento das amostras. Staphylococcus aureus foi isolado em 10 por cento das amostras, entretanto em valores abaixo do permitido pela legislação brasileira. Todas as amostras estavam negativas para salmonella spp. V. parahaemolyticus não foi isolada, 30 por cento das amostras foram positivas para outras espécies de Vibrio, inclusive Vibrio cholerae não-O1/não-O139. Aeromonas spp., incluindo A. hydrophilia foi isolada em 50 por cento das amostras de peixe. O isolamento de Vibrio cholerae não-O1/não-O139 e Aeromonas hydrophilia, assim como Staphylococcus aureus e Escherichia coli, sugere que peixes comercializados em feiras livres de São Paulo podem representar um risco para os consumidores e ser um importante veículo de transmissão de espécies enteropatogênicas.
Subject(s)
Aeromonas/isolation & purification , Aeromonas/pathogenicity , Fishes , Food Microbiology , Escherichia coli , Food Contamination , Food Hygiene , Health Surveillance , Foodborne Diseases , Molecular Diagnostic Techniques , Salmonella , Staphylococcus aureus , VibrioABSTRACT
La patogenicidad intestinal de Aeromonas para el humano ha sido bien establecida y se conoce que producen enteroxinas, citotoxinas y tienen capacidad de adherencia a las células del epitelio intestinal. En nuestro medio constituyen un importante patógeno intestinal, aislándoseles en 185 (15%) de 1264 coprocultivos positivos, constituyéndose en el quinto patógeno intestinal en frecuencia. Se estudian 185 cepas de Aeromonas, aisladas en el C.R.B. del H.U.M., durante los años 1983-1986. Para la especiación se usa el esquema Popoff y Veron, se sigue a Dean, mediante la utilización de las pruebas de ratones lactantes, para detectar enterotoxina y a Burke y cols. para la hemolisina. De las 185 cepas estudiadas, 84 (45.41%) son A. hydrophila, 21 (11.35%) A. sobria y 80 (43.24%) A. caviae. Este estudio ratifica que en A. hydrophila el patrón VP + L + A- y está presente en cepas que producen enterotoxina capaces, con este mecanismo conocido, de producir infección diarréica. En A. Sobria el patrón VP + L + A- presente en 66.67% no concuerda con la producción de hemolisina y enterotoxina. Esta especie que se reporta también frecuente como enteropatógeno, pudiera no siempre serlo a poseer otros mecanismos distintos de patogenicidad a los estudiados. El estudio es coincidente con otros en que ese patrón no está presente con frecuencia en A. caviae, no obstante, es interesante que 2 son hemolisina+ y 3 enterotoxina+, ello pudiera explicar la enteropatogenicidad que esporádicamente se le reporta
Subject(s)
Infant , Mice , Animals , Aeromonas/classification , Aeromonas/analysis , Aeromonas/pathogenicityABSTRACT
Fourteen strains of Aeromonas veronii were isolated from salt and fresh water in Rio de Janeiro and investigated for the presence of birulence factors. Eleven (79%) A. veronii strains were positive for enterotoxin by the suckling-mouse test and thirteen (93%) produced hemolysin. Of the 13 A. veronii strains that produced hemolysin, seven were investigated for cytotoxin production using Vero cells as indicator cells and all of them were positive
Subject(s)
Animals , Mice , Aeromonas/metabolism , Cytotoxins/biosynthesis , Enterotoxins/biosynthesis , Aeromonas/pathogenicity , Cytotoxins/isolation & purification , Enterotoxins/isolation & purification , Hemolysin Proteins/biosynthesis , Hemolysin Proteins/isolation & purification , Vero Cells/ultrastructure , Virulence , Water MicrobiologyABSTRACT
Se estudiaron los microorganismos de identificacion dificil referidos al laboratorio de bacteriologia del Instituto Nacional de Salud por 5 Instituciones. En 70 casos fue posible obtener una identificacion completa y responsabilizar al microorganismo aislado como agente etiologico de un cuadro clinico. Se trataba de 28 cuadros de septicemia, 26 de meningitis, 4 respiratorios, 7 genitourinarios y 6 varios que incluyeron heridas, abcesos, y conjuntivitis. Los identificados fueron: Serratia en el 38%, Acinetobacter en el 21.4%, Moraxella en el 10%, Alcaligenes en el 8.7%, Aeromonas en el 7.2%, Listeria en el 5.7%, Estreptobacilos en el 4.3% Corynebacterium en el 4.3%, Achromabacter, Cardiobacterium y los grupos M3 y M4 aparece cada uno con el 1.4% constituyendose en verdaderas curiosidades biologicas
Subject(s)
Humans , Acinetobacter/isolation & purification , Acinetobacter/pathogenicity , Aeromonas/isolation & purification , Aeromonas/pathogenicity , Alcaligenes/isolation & purification , Alcaligenes/pathogenicity , Bacterial Infections , Corynebacterium/isolation & purification , Corynebacterium/pathogenicity , Gram-Negative Aerobic Bacteria/isolation & purification , Gram-Negative Aerobic Bacteria/pathogenicity , Listeria monocytogenes/isolation & purification , Listeria monocytogenes/pathogenicity , Moraxella/isolation & purification , Moraxella/pathogenicity , Serratia/isolation & purification , Serratia/pathogenicity , ColombiaABSTRACT
Säo abordados os principais agentes etiológicos da gastroenterite humana, assim como o diagnóstico microbiológico de cada agente
Subject(s)
Humans , Aeromonas/pathogenicity , Bacillus cereus/pathogenicity , Clostridium/pathogenicity , Diarrhea/complications , Escherichia coli/pathogenicity , Gastroenteritis/etiology , Bacterial Infections/diagnosis , Rotavirus Infections/virology , Salmonella/pathogenicity , Vibrio cholerae/pathogenicity , Vibrio parahaemolyticus/pathogenicity , Yersinia/pathogenicity , Aeromonas/isolation & purification , Campylobacter/isolation & purification , Clostridium/isolation & purification , Culture Media , Escherichia coli/isolation & purification , Vibrio cholerae/isolation & purificationABSTRACT
Introdução: Organismos pertencentes ao gênero Aeromonas estão amplamente distribuídos no ambiente aquático sendo atualmente considerados como patógenos emergentes. Estudos demonstraram que, estes podem produzir uma série de fatores de virulência, e ainda um maior número de casos clínicos vêm sendo confirmados e atribuídos às diferentes espécies de Aeromonas. Objetivo: Estudar a ocorrência do gênero Aeromonas em efluentes de um sistema de lagoas de estabilização e discutir o significado da presença destes para a saúde pública. Métodos: A determinação de Aeromonas spp foi realizada pela técnica de tubos múltiplos (NMP/100 mL). Para a verificação da presença e ausência (PA) as colônias foram isoladas em ágar sangue ampicilina, ágar amido ampicilina e ágar MacConkey. As colônias que apresentaram resultados presuntivos para o grupo Aeromonas foram submetidas ao reisolamento em Ágar Amido, e a provas bioquímicas para identificação das espécies. O perfil plasmidialfoi realizado de acordo com a metodologia escrita por BIRNBOIN & DOLLY 1979. Resultados: Aeromonas spp foram isoladas em 72,4 por cento e 55,1 por cento das amostras provenientes da entrada e saídsa da lagoa anaeróbia respectivamente , e em 48,3 por cento da saída facultativa variando as contagens entre <3 e 3,0 x 109 NMP/100 mL. Na unidade de desinfecção por cloro entre <3 e 9,0 x 105 NMP/mL Conclusões: Observou-se que embora haja uma tendência de dacaimento nas contagens de Aeromonas, não é possível eliminá-las do sistema estudado, mesmo após cloração. Esses organismos podem representar um risco à saúde devido à seleção de cepas resistentes que são lançadas no meio ambiente.