RESUMEN
Salmonellosis associated with reptiles is a well-researched topic, particularly in China and the United States, but it occurs less frequently in Europe. The growth of the human population and changes in the environment could potentially increase the interaction between humans and free-living reptiles, which are an unidentified source of Salmonella species. In this study, we sought to explore this issue by comparing the microbiota of free-living European grass snakes, scientifically known as Natrix natrix, with that of captive banded water snakes, or Nerodia fasciata. We were able to isolate 27 strains of Salmonella species from cloacal swabs of 59 N. natrix and 3 strains from 10 N. fasciata. Our findings revealed that free-living snakes can carry strains of Salmonella species that are resistant to normal human serum (NHS). In contrast, all the Salmonella species strains isolated from N. fasciata were sensitive to the action of the NHS, further supporting our findings. We identified two serovars from N. natrix: Salmonella enterica subspecies diarizonae and S. enterica subspecies houtenae. Additionally, we identified three different virulotypes (VT) with invA, sipB, prgH, orgA, tolC, iroN, sitC, sifA, sopB, spiA, cdtB and msgA genes, and ß-galactosidase synthesised by 23 serovars. The identification of Salmonella species in terms of their VT is a relatively unknown aspect of their pathology. This can be specific to the serovar and pathovar and could be a result of adaptation to a new host or environment.
Asunto(s)
Salmonella , Factores de Virulencia , Animales , Factores de Virulencia/genética , Salmonella/aislamiento & purificación , Salmonella/genética , Salmonella/clasificación , Humanos , Salmonelosis Animal/microbiología , Colubridae/microbiología , Salmonella enterica/genética , Salmonella enterica/aislamiento & purificación , Salmonella enterica/clasificación , Salmonella enterica/crecimiento & desarrollo , Salmonella enterica/patogenicidad , Serpientes/microbiología , Cloaca/microbiologíaRESUMEN
The bacterial species Salmonella enterica (S. enterica) is a highly diverse pathogen containing more than 2600 distinct serovars, which can infect a wide range of animal and human hosts. Recent global emergence of multidrug resistant strains, from serovars Infantis and Muenchen is associated with acquisition of the epidemic megaplasmid, pESI that augments antimicrobial resistance and pathogenicity. One of the main pESI's virulence factors is the potent iron uptake system, yersiniabactin encoded by fyuA, irp2-irp1-ybtUTE, ybtA, and ybtPQXS gene cluster. Here we show that yersiniabactin, has an underappreciated distribution among different S. enterica serovars and subspecies, integrated in their chromosome or carried by different conjugative plasmids, including pESI. While the genetic organization and the coding sequence of the yersiniabactin genes are generally conserved, a 201-bp insertion sequence upstream to ybtA, was identified in pESI. Despite this insertion, pESI-encoded yersiniabactin is regulated by YbtA and the ancestral Ferric Uptake Regulator (Fur), which binds directly to the ybtA and irp2 promoters. Furthermore, we show that yersiniabactin genes are specifically induced during the mid-late logarithmic growth phase and in response to iron-starvation or hydrogen peroxide. Concurring, yersiniabactin was found to play a previously unknown role in oxidative stress tolerance and to enhance intestinal colonization of S. Infantis in mice. These results indicate that yersiniabactin contributes to Salmonella fitness and pathogenicity in vivo and is likely to play a role in the rapid dissemination of pESI among globally emerging Salmonella lineages.
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Proteínas Bacterianas , Regulación Bacteriana de la Expresión Génica , Hierro , Estrés Oxidativo , Salmonella enterica , Animales , Hierro/metabolismo , Ratones , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Salmonella enterica/genética , Salmonella enterica/metabolismo , Salmonella enterica/patogenicidad , Virulencia/genética , Fenoles/metabolismo , Tiazoles/metabolismo , Humanos , Infecciones por Salmonella/microbiología , Transferencia de Gen Horizontal , Femenino , Factores de Virulencia/genética , Factores de Virulencia/metabolismo , Plásmidos/genéticaRESUMEN
Salmonella diarizonae (IIIb) is frequently isolated from reptiles and less frequently from birds and mammals. However, its isolation from invasive human infections has not been widely reported. Migratory mallard ducks are excellent bioindicators of pathogen presence and pathogen antibiotic resistance (AMR). We present the first isolation from a mallard duck in central Europe of the antibiotic-resistant Salmonella enterica subsp. diarizonae with the unique antigenic pattern 58:r:z53 and report its whole-genome sequencing, serosequencing, and genotyping, which enabled the prediction of its pathogenicity and comparison with phenotypic AMR. The isolated strain was highly similar to S. diarizonae isolated from humans and food. Twenty-four AMR genes were detected, including those encoding aminoglycoside, fluoroquinolone, macrolide, carbapenem, tetracycline, cephalosporin, nitroimidazole, peptide antibiotic, and disinfecting agent/antiseptic resistance. Six Salmonella pathogenicity islands were found (SPI-1, SPI-2, SPI-3, SPI-5, SPI-9, and SPI-13). An iron transport system was detected in SPI-1 centisome C63PI. Plasmid profile analyses showed three to be present. Sequence mutations in the invA and invF genes were noted, which truncated and elongated the proteins, respectively. The strain also harbored genes encoding type-III secretion-system effector proteins and many virulence factors found in S. diarizonae associated with human infections. This study aims to elucidate the AMR and virulence genes in S. enterica subsp. diarizonae that may most seriously threaten human health.
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Patos , Animales , Patos/microbiología , Humanos , Salmonella/genética , Salmonella/patogenicidad , Salmonella/aislamiento & purificación , Salmonella/efectos de los fármacos , Secuenciación Completa del Genoma , Islas Genómicas/genética , Salmonelosis Animal/microbiología , Antibacterianos/farmacología , Salmonella enterica/genética , Salmonella enterica/patogenicidad , Salmonella enterica/aislamiento & purificación , Salmonella enterica/efectos de los fármacos , Farmacorresistencia Bacteriana Múltiple/genética , Genoma Bacteriano , Filogenia , Farmacorresistencia Bacteriana/genética , Plásmidos/genéticaRESUMEN
Salmonella enterica serovar Dublin (S. Dublin) is an important enteric pathogen affecting cattle and poses increasing public health risks. Understanding the pathophysiology and host-pathogen interactions of S. Dublin infection are critical for developing effective control strategies, yet studies are hindered by the lack of physiologically relevant in vitro models. This study aimed to generate a robust ileal monolayer derived from adult bovine organoids, validate its feasibility as an in vitro infection model with S. Dublin, and evaluate the epithelial response to infection. A stable, confluent monolayer with a functional epithelial barrier was established under optimized culture conditions. The model's applicability for studying S. Dublin infection was confirmed by documenting intracellular bacterial invasion and replication, impacts on epithelial integrity, and a specific inflammatory response, providing insights into the pathogen-epithelium interactions. The study underscores the utility of organoid-derived monolayers in advancing our understanding of enteric infections in livestock and highlights implications for therapeutic strategy development and preventive measures, with potential applications extending to both veterinary and human medicine. The established bovine ileal monolayer offers a novel and physiologically relevant in vitro platform for investigating enteric pathogen-host interactions, particularly for pathogens like S. Dublin.
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Interacciones Huésped-Patógeno , Íleon , Organoides , Salmonelosis Animal , Animales , Bovinos , Organoides/microbiología , Íleon/microbiología , Íleon/patología , Salmonelosis Animal/microbiología , Salmonella enterica/patogenicidad , Salmonella enterica/fisiología , Inflamación/microbiología , Inflamación/patología , Mucosa Intestinal/microbiología , Enfermedades de los Bovinos/microbiologíaRESUMEN
The aim of this study was to identify virulence and antimicrobial resistance profiles and determine the sequence type (ST) by multilocus sequence typing (MLST) of Salmonella enterica isolates from bovine carcasses from slaughterhouse located in Minas Gerais state, Brazil, and its relationship with bovine isolates obtained on the American continent based on sequence type profile. The MLST results were compared with all Salmonella STs associated with cattle on American continent, and a multi-locus sequence tree (MS tree) was built. Among the 17 S. enterica isolates, five ST profiles identified, and ST10 were the most frequent, grouping seven (41.2%) isolates. The isolates presented 11 different profiles of virulence genes, and six different antibiotics resistance profiles. The survey on Enterobase platform showed 333 Salmonella STs from American continent, grouped into four different clusters. Most of the isolates in the present study (13/17), were concentrated in a single cluster (L4) composed by 74 STs. As a conclusion, five different STs were identified, with ST10 being the most common. The isolates showed great diversity of virulence genes and antibiotics resistance profiles. Most of the isolates of this study were grouped into a single cluster composed by 74 STs formed by bovine isolates obtained on the American continent.
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Antibacterianos , Tipificación de Secuencias Multilocus , Salmonelosis Animal , Salmonella enterica , Factores de Virulencia , Animales , Bovinos , Salmonella enterica/genética , Salmonella enterica/efectos de los fármacos , Salmonella enterica/aislamiento & purificación , Salmonella enterica/patogenicidad , Salmonella enterica/clasificación , Brasil , Antibacterianos/farmacología , Salmonelosis Animal/microbiología , Virulencia/genética , Factores de Virulencia/genética , Pruebas de Sensibilidad Microbiana , Farmacorresistencia Bacteriana/genética , Enfermedades de los Bovinos/microbiología , MataderosRESUMEN
AIMS: Our aim is to characterize through whole-genome sequencing (WGS) the antimicrobial resistance (AMR) and heavy metal tolerance (HMT) genes content, plasmid presence, virulence potential and genomic diversity of the rare non-typhoid Salmonella enterica serovar Orion (S. Orion) from 19 countries of the African, American, Eastern Mediterranean, European, Southeastern Asia and Western Pacific regions. METHODS AND RESULTS: Totally 324 S. Orion genomes were screened for AMR, HMT and virulence genes, plasmids and Salmonella Pathogenicity Islands (SPIs). Genomic diversity was investigated using Multi-Locus Sequence Typing (MLST) and core-genome MLST (cgMLST). Efflux pump encoding genes mdsA and mdsB were present in all genomes analysed, while quinolone chromosomal point mutations and aminoglycoside, beta-lactam, colistin, lincosamide, macrolide, phenicol, sulphonamide, trimethoprim, tetracycline and disinfectant resistance genes were found in 0.3%-5.9%. A total of 17 genomes (5.2%) from Canada, the United Kingdom, the USA and Tanzania showed a potential multi-drug resistance profile. Gold tolerance genes golS and golT were detected in all genomes analysed, while arsenic, copper, mercury, silver and tellurium tolerance genes were found in 0.3%-35.5%. Col(MGD2) was the most frequently detected plasmid, in 15.4% of the genomes. Virulence genes related to adherence, macrophage induction, magnesium uptake, regulation, serum resistance, stress adaptation, type III secretion systems and six SPIs (1, 2, 3, 4, 5, 9, 12, 13, 14 and C63PI) were detected. ST639 was assigned to 89.2% of the S. Orion genomes, while cgMLST showed core-genome STs and clusters of strains specific by countries. CONCLUSION: The high virulence factor frequencies, the genomic similarity among some non-clinical and clinical strains circulating worldwide and the presence of a strain carrying a resistance gene against a last resource antimicrobial like colistin, highlight the potential risk of S. Orion strains for public health and food safety and reinforce the importance to not underestimate the potential hazard of rare non-typhoid Salmonella serovars.
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Antibacterianos , Farmacorresistencia Bacteriana , Genoma Bacteriano , Salmonella enterica , Salmonella enterica/genética , Salmonella enterica/efectos de los fármacos , Salmonella enterica/patogenicidad , Virulencia/genética , Antibacterianos/farmacología , Farmacorresistencia Bacteriana/genética , Humanos , Secuenciación Completa del Genoma , Animales , Infecciones por Salmonella/microbiología , Infecciones por Salmonella/epidemiología , Serogrupo , Plásmidos/genéticaRESUMEN
Salmonella enterica is a pathogenic bacterium known for causing severe typhoid fever in humans, making it important to study due to its potential health risks and significant impact on public health. This study provides evolutionary classification of proteins from Salmonella enterica pangenome. We classified 17,238 domains from 13,147 proteins from 79,758 Salmonella enterica strains and studied in detail domains of 272 proteins from 14 characterized Salmonella pathogenicity islands (SPIs). Among SPIs-related proteins, 90 proteins function in the secretion machinery. 41% domains of SPI proteins have no previous sequence annotation. By comparing clinical and environmental isolates, we identified 3682 proteins that are overrepresented in clinical group that we consider as potentially pathogenic. Among domains of potentially pathogenic proteins only 50% domains were annotated by sequence methods previously. Moreover, 36% (1330 out of 3682) of potentially pathogenic proteins cannot be classified into Evolutionary Classification of Protein Domains database (ECOD). Among classified domains of potentially pathogenic proteins the most populated homology groups include helix-turn-helix (HTH), Immunoglobulin-related, and P-loop domains-related. Functional analysis revealed overrepresentation of these protein in biological processes related to viral entry into host cell, antibiotic biosynthesis, DNA metabolism and conformation change, and underrepresentation in translational processes. Analysis of the potentially pathogenic proteins indicates that they form 119 clusters or novel potential pathogenicity islands (NPPIs) within the Salmonella genome, suggesting their potential contribution to the bacterium's virulence. One of the NPPIs revealed significant overrepresentation of potentially pathogenic proteins. Overall, our analysis revealed that identified potentially pathogenic proteins are poorly studied.
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Proteínas Bacterianas , Genoma Bacteriano , Islas Genómicas , Salmonella enterica , Islas Genómicas/genética , Salmonella enterica/genética , Salmonella enterica/patogenicidad , Salmonella enterica/clasificación , Proteínas Bacterianas/genética , Proteínas Bacterianas/química , Proteínas Bacterianas/metabolismo , Humanos , Dominios ProteicosRESUMEN
Antimicrobial resistance (AMR) poses an escalating global public health threat. Canals are essential in Thailand, including the capital city, Bangkok, as agricultural and daily water sources. However, the characteristic and antimicrobial-resistance properties of the bacteria in the urban canals have never been elucidated. This study employed whole genome sequencing to characterize 30 genomes of a causal pathogenic bacteria, Salmonella enterica, isolated from Bangkok canal water between 2016 and 2020. The dominant serotype was Salmonella Agona. In total, 35 AMR genes and 30 chromosomal-mediated gene mutations were identified, in which 21 strains carried both acquired genes and mutations associated with fluoroquinolone resistance. Virulence factors associated with invasion, adhesion, and survival during infection were detected in all study strains. 75.9% of the study stains were multidrug-resistant and all the strains harbored the necessary virulence factors associated with salmonellosis. One strain carried 20 resistance genes, including mcr-3.1, mutations in GyrA, ParC, and ParE, and typhoid toxin-associated genes. Fifteen plasmid replicon types were detected, with Col(pHAD28) being the most common type. Comparative analysis of nine S. Agona from Bangkok and 167 from public databases revealed that specific clonal lineages of S. Agona might have been circulating between canal water and food sources in Thailand and globally. These findings provide insight into potential pathogens in the aquatic ecosystem and support the inclusion of environmental samples into comprehensive AMR surveillance initiatives as part of a One Health approach. This approach aids in comprehending the rise and dissemination of AMR and devising sustainable intervention strategies.IMPORTANCEBangkok is the capital city of Thailand and home to a large canal network that serves the city in various ways. The presence of pathogenic and antimicrobial-resistant Salmonella is alarming and poses a significant public health risk. The present study is the first characterization of the genomic of Salmonella strains from Bangkok canal water. Twenty-two of 29 strains (75.9%) were multidrug-resistant Salmonella and all the strains carried essential virulence factors for pathogenesis. Various plasmid types were identified in these strains, potentially facilitating the horizontal transfer of AMR genes. Additional investigations indicated a potential circulation of S. Agona between canal water and food sources in Thailand. The current study underscores the role of environmental water in an urban city as a reservoir of pathogens and these data obtained can serve as a basis for public health risk assessment and help shape intervention strategies to combat AMR challenges in Thailand.
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Antibacterianos , Farmacorresistencia Bacteriana Múltiple , Genoma Bacteriano , Factores de Virulencia , Secuenciación Completa del Genoma , Tailandia/epidemiología , Factores de Virulencia/genética , Antibacterianos/farmacología , Farmacorresistencia Bacteriana Múltiple/genética , Genoma Bacteriano/genética , Microbiología del Agua , Plásmidos/genética , Salmonella enterica/genética , Salmonella enterica/aislamiento & purificación , Salmonella enterica/efectos de los fármacos , Salmonella enterica/clasificación , Salmonella enterica/patogenicidad , Salmonella/genética , Salmonella/aislamiento & purificación , Salmonella/clasificación , Salmonella/efectos de los fármacos , Pruebas de Sensibilidad Microbiana , Genómica , Humanos , Filogenia , Infecciones por Salmonella/microbiología , SerogrupoRESUMEN
Salmonella enterica is a leading cause of bacterial food-borne illness in humans and is responsible for millions of cases annually. A critical strategy for the survival of this pathogen is the translocation of bacterial virulence factors termed effectors into host cells, which primarily function via protein-protein interactions with host proteins. The Salmonella genome encodes several paralogous effectors believed to have arisen from duplication events throughout the course of evolution. These paralogs can share structural similarities and enzymatic activities but have also demonstrated divergence in host cell targets or interaction partners and contributions to the intracellular lifecycle of Salmonella. The paralog effectors SopD and SopD2 share 63% amino acid sequence similarity and extensive structural homology yet have demonstrated divergence in secretion kinetics, intracellular localization, host targets, and roles in infection. SopD and SopD2 target host Rab GTPases, which represent critical regulators of intracellular trafficking that mediate diverse cellular functions. While SopD and SopD2 both manipulate Rab function, these paralogs display differences in Rab specificity, and the effectors have also evolved multiple mechanisms of action for GTPase manipulation. Here, we highlight this intriguing pair of paralog effectors in the context of host-pathogen interactions and discuss how this research has presented valuable insights into effector evolution.
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Proteínas Bacterianas , Interacciones Huésped-Patógeno , Infecciones por Salmonella , Proteínas Bacterianas/metabolismo , Proteínas Bacterianas/genética , Humanos , Interacciones Huésped-Patógeno/genética , Infecciones por Salmonella/microbiología , Infecciones por Salmonella/metabolismo , Salmonella enterica/metabolismo , Salmonella enterica/genética , Salmonella enterica/patogenicidad , Factores de Virulencia/metabolismo , Factores de Virulencia/genética , Proteínas de Unión al GTP rab/metabolismo , Proteínas de Unión al GTP rab/genética , Animales , Evolución MolecularRESUMEN
Salmonella enterica é um importante patógeno na indústria de alimentos, relacionado com gastroenterites alimentares. Staphylococcus aureus é causador de infecção intestinal. Neste cenário, a inativação fotodinâmica (IFD) surge como uma alternativa de desinfecção desses patógenos. A IFD consiste na interação de três elementos: um agente fotossensibilizador (FS) , luz e oxigênio molecular. Esta interação promove espécies reativas de oxigênio, causando danos irreparáveis à célula . Estes microrganismos possuem morfologia celular diversa, portanto uma concentração ideal de FS para cada cepa se faz necessária para o sucesso da técnica. O comprimento de onda absorvido pelo FS Protoporfirina IX corresponde ao vermelho do espectro eletromagnético (630 nm). Concentrações de 10 e 20 μM do pró-fármaco ácido aminolevulínico (ALA), observou-se a inativação de S. aureus em 20 μM, S. enterica manteve-se em crescimento. A IFD mostrou-se como uma promissora técnica para controle microbiano.
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Bacterias/patogenicidad , Fotoquimioterapia/métodos , Protoporfirinas , Salmonella enterica/patogenicidad , Staphylococcus aureus/patogenicidadRESUMEN
Abstract INTRODUCTION Salmonella enterica serovar Panama belongs to the D1 serogroup and is frequently associated with nontyphoidal salmonellosis in humans. This study aimed to characterize isolates collected from Northeast Brazil by phenotypic and molecular methods. METHODS Forty four S. Panama strains were examined for antimicrobial susceptibility, virulence genes, and pulsed field gel electrophoresis (PFGE) types. RESULTS All strains were susceptible to antibiotics (except for streptomycin), presented classical virulence factors, and could be clustered into four groups and 18 pulsotypes. CONCLUSIONS This work calls for continuous surveillance for the emergence of antibiotic resistance and new clones in a geographical area.
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Animales , Salmonella enterica/genética , Factores de Virulencia/genética , Variación Genética , Brasil , Pruebas de Sensibilidad Microbiana , Electroforesis en Gel de Campo Pulsado , Salmonella enterica/aislamiento & purificación , Salmonella enterica/efectos de los fármacos , Salmonella enterica/patogenicidad , Farmacorresistencia Bacteriana Múltiple , Antibacterianos/farmacologíaRESUMEN
Abstract Salmonella Gallinarum is a host-restrict pathogen that causes fowl typhoid, a severe systemic disease that is one of the major concerns to the poultry industry worldwide. When infecting the bird, SG makes use of evasion mechanisms to survive and to replicate within macrophages. In this context, phoPQ genes encode a two-component regulatory system (PhoPQ) that regulates virulence genes responsible for adaptation of Salmonella spp. to antimicrobial factors such as low pH, antimicrobial peptides and deprivation of bivalent cations. The role of the mentioned genes to SG remains to be investigated. In the present study a phoPQ-depleted SG strain (SG ΔphoPQ) was constructed and its virulence assessed in twenty-day-old laying hens susceptible to fowl typhoid. SG ΔphoPQ did cause neither clinical signs nor mortality in birds orally challenged, being non-pathogenic. Furthermore, this strain was not recovered from livers or spleens. On the other hand, chickens challenged subcutaneously with the mutant strain had discreet to moderate pathological changes and also low bacterial counts in liver and spleen tissues. These findings show that SG ΔphoPQ is attenuated to susceptible chickens and suggest that these genes are important during chicken infection by SG.
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Animales , Femenino , Enfermedades de las Aves de Corral/microbiología , Salmonelosis Animal/microbiología , Proteínas Bacterianas/genética , Salmonella enterica/metabolismo , Salmonella enterica/patogenicidad , Silenciador del Gen , Enfermedades de las Aves de Corral/patología , Salmonelosis Animal/patología , Bazo/microbiología , Bazo/patología , Proteínas Bacterianas/metabolismo , Virulencia , Pollos , Salmonella enterica/genéticaRESUMEN
Salmonella detection is a key point in food safety testing, because of the frequent association of this pathogen with food poisoning in humans. The standard bacteriological tests currently used for Salmonella-detection are time-consuming; therefore, there is a need to develop alternative methods to accelerate the detection. In order to accelerate Salmonella diagnosis, we used the immunomagnetic separation assay associated with bacteriophage P22 for the rapid detection of the following Salmonella serovars in chicken rinses of drumsticks, artificially contaminated with 5, 10, and 100 CFU/25mL of bacteria: Salmonella enterica subsp. enterica serovar Heidelberg (S. Heidelberg), Salmonella enterica subsp. enterica serovar Enteritidis (S. Enteritidis) and Salmonella enterica subsp. enterica serovar Typhimurium (S. Typhimurium). The efficiency of the technique, represented by the time required for detection of positive and negative samples, was compared with that of the standard diagnostic tests used for this pathogen, the bacteriological assay and the polymerase chain reaction (PCR)-based test. This study confirmed the ability of the bacteriophage-associated immunomagnetic separation assay to identify 99.6% of Salmonella-positive samples of the three serovars tested. In contrast, the bacteriological assay and PCR-based test detected 95.1% and 98.5% of the Salmonella-positive samples respectively.(AU)
A detecção de Salmonella é um ponto crucial para a segurança alimentar, devido a frequente associação deste patógeno com infecções alimentares em humanos. O método padrão para detecção de Salmonella é o bacteriológico, mas o tempo requerido para o processamento das amostras e o diagnóstico final é longo, por isso existe a necessidade de desenvolvimento de métodos alternativos que visem acelerar esta etapa. Para isto utilizamos a separação imunomagnética associada ao bacteriófago P22 como técnica de detecção rápida para os seguintes sorovares de Salmonella: Salmonella enterica subsp. enterica sorovar Heidelberg (S. Heidelberg), Salmonella enterica subsp. enterica sorovar Enteritidis (S. Enteritidis) e Salmonella enterica subsp. enterica sorovar Typhimurium (S. Typhimurium), os quais foram inoculados artificialmente em lavados de sobre-coxas de frango nas seguintes concentrações: 5, 10 e 100 UFC/25mL. A eficiência da técnica, representada pelo tempo requerido para detecção de amostras positivas ou negativas, foi comparado com os testes rotineiramente utilizados para detecção de Salmonella, o exame bacteriológico e a reação em cadeia da polimerase (PCR). Este estudo confirmou a capacidade do teste de separação imunomagnética associado a bacteriófago, o qual identificou 99,6% das amostras positivas para Salmonella, dos três sorovares testados. Já o bacteriológico e PCR identificaram respectivamente 95,1% e 98,5% das amostras positivas.(AU)
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Animales , Aves de Corral/microbiología , Salmonella enterica/patogenicidad , Técnicas y Procedimientos Diagnósticos/veterinariaRESUMEN
Os pombos domésticos e silvestres estão distribuídos por todo o mundo e carreiam micro-organismos patogênicos ao homem e a outros animais, podendo ser um dos responsáveis pela disseminação de Salmonella spp. Este patógeno gera grande preocupação para a economia mundial, uma vez que cria transtornos para a indústria avícola quando ocorre contaminação dos plantéis e ônus para a saúde pública devido a surtos de infecção alimentar causados por esta bactéria. Dessa forma, objetivou-se realizar um levantamento acerca da participação do pombo doméstico na possível disseminação de Salmonella spp.(AU)
Domestic and wild pigeons are distributed throughout the world and carrie micro-organisms that are pathogenic to humans and other animals. They can be one of the animals in charge of the dissemination of Salmonella spp., pathogen of great concern for the world economy as it creates inconvenience to the poultry industry when there is contamination of herds and impacts on public health due to outbreaks of foodborne infection caused by this bacterium. Therefore, the objective was to conduct a survey about the participation of the domestic pigeon in the possible dissemination of Salmonella spp.(AU)
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Columbidae/microbiología , Salmonella enterica/patogenicidad , Contaminación de Alimentos , Salud PúblicaRESUMEN
Salmonellaenterica serovar Heidelberg es uno de los principales agentes causantes de salmonelosis en humanos en Estados Unidos y Canadá, sin embargo, resulta infrecuente en los países de Sudamérica y Europa. En este trabajo se caracterizó un aislamiento de S. Heidelberg resistente a oximino-cefalosporinas recuperado de un paciente internaen un hospital de la Ciudad de Buenos Aires. Se evidenció la presencia de un plásmido de 97 kbperteneciente al grupo de incompatibilidad IncN, portador del gen blaCMY-2. ISEcp1 fue localizado corriente arriba de blaCMY-2, promoviendo su expresión y movilización.El aislamiento de S. Heidelberg correspondió al secuenciotipo 15 y en la virotipifi cación se detectó el gen sopE. En este trabajo describimos por primera vez la producción de CMY-2 en una cepa de S. Heidelberg en nuestro país y América Latina
Salmonellaenterica serovar Heidelberg ranks among the most prevalent causes of human salmonellosis in the United States and Canada, although it has been infrequently reported in South American and European countries.Most Salmonella infections are self-limiting; however, some invasive infections require antimicrobial therapy. In this work we characterized an oxyimino-cephalosporin resistant S. Heidelberg isolate recovered from an inpatient in a Buenos Aires hospital. CMY-2 was responsible for the ß-lactam resistance profi le. S. Heidelberg contained a 97 kb plasmid belonging to the Inc N groupharboring blaCMY-2. ISEcp1 was located upstream blaCMY-2 driving its expression and mobilization.The isolate belonged to sequence type 15 and virotyping revealed the presence of sopE gene. In this study we identifi ed the fi rst CMY-2 producing isolate of S. Heidelberg in Argentina and even in South Americ
Asunto(s)
Humanos , Masculino , América del Sur/epidemiología , beta-Lactamasas/análisis , Salmonella enterica/aislamiento & purificación , Plásmidos/análisis , Salmonella enterica/patogenicidadRESUMEN
O objetivo deste experimento foi produzir uma infecção experimental de Salmonella enterica subespécie. enterica sorotipo Panama e verificar a importância da via nasonasal na transmissão entre leitões desmamados. Foram utilizados seis leitões recém-desmamados, adquiridos de granja livre de Salmonella spp. Utilizaram-se baias isoladoras, que proporcionavam o contato nasonasal e eliminavam a possibilidade de outras vias de transmissão e de contaminação externa. Três grupos foram formados: controle, sentinela e infectado. Não foram encontradas amostras positivas para Salmonella spp. em leitões do grupo-controle e sentinelas, e nos animais infectados foi isolada Salmonella Panama em suabes retais e tecidos necropsiados. Os resultados revelaram não haver a transmissão pela via nasonasal entre leitões desmamados, pois, em nenhum momento, o agente foi isolado dos animais sentinelas.
Experimental infection of Salmonella enterica ssp. enterica serovars Panama was proceeded to establish the importance of nose-to-nose contact in the transmission among weaned pigs. Six recently-weaned pigs were acquired from a farm previously selected, free from Salmonella spp. Isolation stalls allowing nose-to-nose contact and eliminating other transmission routes as well outside contamination were used. Three groups were formed: control, sentinel, and infected. Piglets of control and sentinel groups were not positive for Salmonella spp., however, Salmonella Panama was isolated in infected animals in rectal swabs and necropsied tissues. It was concluded that there was not transmission by nose-to-nose contact among weaned pigs, since Samonella Panama was not isolated in the sentinel group at any moment.
Asunto(s)
Animales , Salmonella enterica/patogenicidad , Porcinos/clasificación , Infecciones/microbiología , InvestigaciónRESUMEN
Para la comprensión de las bases genéticas de los mecanismos de patogenicidad de Salmonella se han descrito diversas metodologías para manipular el ADN genómico y generar mutantes con características particulares. En este estudio se reporta la construcción de mutantes a partir de varios serotipos de S. enterica, por sustitución e inactivación de los genes invG/invE en SPI-1 y de los genes ssaJ/ssaK en SPI-2 mediante la técnica de recombinasa Red del fago λ descrita por Datsenko y Wanner (2000). Los genes delecionados en las SPI-1 y SPI-2 codifican para las proteínas que participan en la formación de los sistemas de secreción tipo III, responsables de la invasión y supervivencia intracelular de S. enterica en las células hospedadoras. Los resultados de este trabajo permitirán realizar estudios futuros in vivo para evaluar la posible atenuación de la virulencia de las cepas mutantes, así como aportar nuevos conocimientos sobre los mecanismos genéticos involucrados en la fisiopatogenia de las enfermedades producidas por los serovares estudiados. Además, esta técnica se recomienda para generar de manera eficiente mutantes de diferentes serotipos de S. enterica con la finalidad de estudiar los genes cromosómicos y sus productos.
To understand the genetic basis of Salmonella pathogenicity mechanisms, various methods have been described to manipulate and generate mutant genomic DNA with specific characteristics. In this study we report the construction of mutants from several serotypes of S. enterica, substitution and inactivation of genes invG/invE in SPI-1 gene and ssaJ/ssaK in SPI-2 by the technique of phage λ Red recombinase, as described by Datsenko and Wanner (2000). The gene deletion in SPI-1 and SPI-2 encodes proteins involved in the formation of type III secretion systems responsible for the invasion and intracellular survival of S. enterica in the host cells. The results of this work will allow in vivo studies to evaluate the possible attenuation of virulence of the mutant strains, as well as to provide new insights into the genetic mechanisms involved in the pathogenesis of diseases caused by these bacteria. Moreover, this technique is recommended to efficiently generate mutants of different serotypes of S. enterica in order to study the chromosomal genes and their products.
Asunto(s)
Salmonella enterica/fisiología , Salmonella enterica/genética , Salmonella enterica/inmunología , Salmonella enterica/patogenicidad , Salmonella enterica/química , Salmonella enterica/ultraestructura , Mutación/genética , Mutación/inmunologíaRESUMEN
Salmonella enterica es uno de los principales causantes de gastroenteritis infecciosa en el mundo, debido al consumo de alimentos y aguas contaminadas con esta bacteria. Este grupo de bacterias Gram negativas se caracteriza por tener la capacidad de invadir células eucariontes y sobrevivir en el interior de ellas, evento fundamental para que la bacteria cause una enfermedad tanto localizada como sistémica. Las proteínas de virulencia que este agente utiliza para invadir y sobrevivir en células eucariontes son codificadas por genes presentes en islas de patogenicidad, que corresponden a grandes bloques de material genético integrados en el cromosoma bacteriano y que fueron posiblemente adquiridos a través de transferencia lateral de genes desde otros microorganismos. Estudios recientes han permitido identificar el rol que poseen estas proteínas de virulencia en el proceso infectivo de Salmonella y su impacto en el funcionamiento de la célula eucarionte. De este modo, ha sido posible entender de mejor manera los mecanismos moleculares utilizados para infectar a su hospedero y se han identificado posibles blancos terapéuticos para el tratamiento de los cuadros infecciosos causados por este patógeno.
Salmonella enterica is one of the main ethiological agents of infectious gastroenteritis in the world, due the consumption of food and water contaminated with these bacteria. This group of Gram negative bacterials characterized by its capacity to invade eukaryotic cells and survive inside them, an event that is fundamental for the bacteria to cause a localized as well as a systemic disease. The virulence proteins that this bacterium uses to invade and survive within eukaryotic cells are encoded by genes found in pathogenicity islands, big blocks of genetic material integrated in the bacterial chromosome, that were probably acquired through lateral gene transfer from other microorganisms. Recent studies have identified the role that these virulence proteins play in the infective process of Salmonella, and their impact in the function of the eukaryotic cell. This way, it has been possible to better understand the molecular mechanisms used by Salmonella to infect their hosts, and potential therapeutic targets have been identified to improve the treatment of the infection caused by this pathogen.
Asunto(s)
Humanos , Gastroenteritis/microbiología , Salmonella enterica/genética , Salmonella enterica/patogenicidad , Factores de Virulencia/genética , Infecciones por Salmonella/genética , Islas Genómicas , Proteínas Bacterianas , Salmonella/genética , Salmonella/patogenicidad , Virulencia/genéticaRESUMEN
The ability of Lactobacillus acidophilus UFV-H2B20 to antagonize Salmonella enterica subsp. enterica ser. Typhimurium and to reduce the pathological consequences for the host was determining using conventional and gnotobiotic animals. Conventional NIH mice received daily by gavage a 0.1 ml suspension containing about 10(8) cfu L. acidophilus UFV-H2B20 and germfree animals received a single 0.1 ml dose. The gnotobiotic and conventional groups were infected orally with 10(2) and 10(5) cfu of S. Typhimurium, respectively, 7 days after the beginning of treatment. Control groups were treated with sterile saline instead of Lactobacillus. Survival data showed a protective effect against the pathogenic bacteria in both conventional and gnotobiotic Lactobacillus-treated mice. L. acidophilus UFV-H2B20 colonized the digestive tract of gnotobiotic mice and the number of viable cells ranged from 10(9) to 10(10) cfu/g of faeces. In both experimental and control gnotobiotic animals, S. Typhimurium became rapidly established at a level ranging from 108 to 1010 cfu/g of faeces and remained at high levels until the animals died or were sacrificed. In conclusion, the previous treatment of mice with L. acidophilus UFV-H2B20 protects the animals against the experimental infection with S. Typhimurium but this protection was not due to the reduction of the pathogenic populations in the intestines.(au)
Asunto(s)
Animales , Lactobacillus acidophilus/patogenicidad , Probióticos , Salmonella enterica/patogenicidad , Administración Oral , Vida Libre de Gérmenes , RatonesRESUMEN
El género Salmonella es un grupo de microorganismos ubicuos en humanos y animales. En los primeros puede ocasionar cuadros clínicos del tipo de la gastroenteritis, aunque ocasionalmente es causa de infecciones sistémicas que ponen en peligro la vida del paciente. La participación de Salmonella se ha incrementado a nivel mundial, ocasionando brotes epidémicos en unidades de atención pediátrica, en las que se han aislando cepas resistentes a más de un antimicrobiano. El objetivo de este trabajo fue determinar la sensibilidad a un grupo de antimicrobianos y el perfil plasmídico de cepas de Salmonella aisladas de pacientes pediátricos. Los resultados obtenidos mostraron alta resistencia a estreptomicina, ampicilina, cefalotina y tetraciclina. Se observó un plásmido de 20.5 Md en cepas de Salmonella enterica, subespecie typhimurium, heidelberg y derby, en cuyas transconjugantes se logró la transferencia fenotípica de resistencia a ampicilina.