Subject(s)
Humans , Infant, Newborn , Infant , Breast-Milk Substitutes , Health Facility Environment , Hospitals , Enterobacter , CronobacterABSTRACT
OBJETIVOS: Determinar la existencia de contaminación por patógenos en fórmulas infantiles en polvo (FIP) procesadas en los dos hospitales públicos más grandes de Honduras y evaluar las condiciones de procesamiento de sus servicios de fórmulas infantiles (SFI). MÉTODOS: Estudio exploratorio realizado en dos etapas: ') Evaluación presencial de las condiciones de procesamiento de las FIP de los dos SFI; 2) Recolección y análisis de las muestras FIP para el aislamiento de Cronobacter spp. y enterobacterias. RESULTADOS: La evaluación de los SFI mostró debilidades en diferentes aspectos como infraestructura, almacenamiento, capacitación y registros. Cincuenta muestras fueron recolectadas en total de cinco marcas originarias de seis países. El 38% se encontraban en uso durante el muestreo y 62% fueron recolectadas de latas selladas. Se comprobó la presencia de Cronobacter spp. en 4% (2/50) del total de muestras, una proveniente de cada hospital. Se elaboró y entregó un manual de procesamiento de FIP a cada hospital participante. CONCLUSIONES: Existe contaminación de Cronobacter spp., Klebsiella y Acinetobacter en los dos hospitales hondureños; resultado similar a los estimados en Chile (5%) y Cuba (',6%). Es necesaria la implementación del manual de procesamiento FIP y el monitoreo de estos y otros microorganismos patógenos.
OBJECTIVES: Determine the existence of pathogen contamination in powdered infant formulas (PIF) processed in the two largest public hospitals in Honduras and evaluate the processing conditions of their infant formula services (IFS). METHODS: Exploratory study executed in two stages: ') faceto-face evaluation of the processing conditions of the PIF of the two IFS; 2) Collection and analysis of the PIF samples for Cronobacter spp. and Enterobacteriaceae isolation. RESULTS: The evaluation of the IFS showed weaknesses in different aspects such as infrastructure, storage, training and keeping records. In total, fifty samples were collected, representing five brands from six countries. Thirty eight percent of samples were collected from cans in use during sampling and 62% were collected from sealed cans. The presence of Cronobacter spp. was detected in 4% (2/50) of the total samples, one from each hospital. A PIF processing manual was prepared and delivered to each participating hospital. CONCLUSIONS: Contamination of Cronobacter spp., Klebsiella and Acinetobacter existed in two evaluated Honduran hospitals; results similar to others in Chile (5%) and Cuba ('.6%). It is necessary to implement the PIF processing manual and monitor these and other pathogenic microorganisms
Subject(s)
Humans , Food Contamination , Infant Formula/microbiology , Cronobacter/isolation & purification , Food Microbiology , Dried Full-Cream Milk , Honduras , HospitalsABSTRACT
BACKGROUND/AIMS: Cronobacter sakazakii, an emergent pathogen is considered as a major concern to infants and neonates fed on reconstituted powdered infant milk formula. In conjunction with many other factors, biofilm forming capacity adds to its pathogenic potential. In view of the facts that infants are at highest risk to C. sakazakii infections, and emerging antibiotic resistance among pathogens, it is imperative to evaluate probiotic cultures for their efficacy against C. sakazakii. Therefore, pure probiotic strains were isolated from commercial probiotic products and tested for their antimicrobial and anti-biofilm activities against C. sakazakii. METHODS: A total of 6 probiotic strains were tested for their antibiotic susceptibility followed by antimicrobial activity using cell-free supernatant (CFS) against C. sakazakii. The inhibitory activity of CFS against biofilm formation by C. sakazakii was determined using standard crystal violet assay and microscopic observations. RESULTS: All the probiotic strains were sensitive to ampicillin, tetracycline, vancomycin and carbenicillin whereas most of the strains were resistant to erythromycin and novobiocin. Four of the 6 probiotic derived CFS possessed antimicrobial activity against C. sakazakii at a level of 40 μL. A higher biofilm inhibitory activity (>80%) was observed at initial stages of biofilm formation with weaker activity during longer incubation upto 48 hours (50%–60%). CONCLUSIONS: The study indicated the efficacy of isolated commercial probiotics strains as potential inhibitor of biofilm formation by C. sakazakii and could be further explored for novel bioactive molecules to limit the emerging infections of C. sakazakii.
Subject(s)
Humans , Infant , Infant, Newborn , Ampicillin , Biofilms , Carbenicillin , Cronobacter sakazakii , Cronobacter , Drug Resistance, Microbial , Erythromycin , Gentian Violet , Milk , Novobiocin , Probiotics , Tetracycline , VancomycinABSTRACT
Infections by Cronobacter spp. are hazardous to infants since they can lead to neonatal meningitis, bacteremia, and necrotizing enterocolitis. Cronobacter spp. are frequently resistant to β-lactam derivatives, macrolides, and aminoglycosides. In addition, multi-resistant strains have also been detected. In China, the isolation rate of Cronobacter spp. from commercial powdered infant formula (PIF) or follow-up formula (FUF) is relatively high. Nevertheless, clinical cases of Cronobacter infection have been ignored to date. Here we describe two cases of Cronobacter infection detected at the Wuhan Women and Children Medical Care Center Hospital (Wuhan City, China). We provide the genomic analysis of the isolates and the antibiotic-resistance profiles of the two strains. The Cronobacter strains identified in this study were not susceptible to third-generation cephalosporins, aminoglycoside, and/or trimethoprim-sulfamethoxazole. Whole genome sequencing revealed various genes known to encode antibiotic resistance. Future studies are needed to determine whether the genes predicted in this study are functional. As with Enterobacter spp., the antibiotic resistance of Cronobacter is a serious issue that requires more attention.
Subject(s)
Female , Humans , Infant , Anti-Bacterial Agents , Pharmacology , Cronobacter , Drug Resistance, Multiple, Bacterial , Fatal Outcome , Gram-Negative Bacterial Infections , Microbiology , Meningitis, Bacterial , MicrobiologyABSTRACT
Cronobacter spp. é um patógeno oportunista que pode causar infecções em indivíduos de qualquer idade, cuja incidência é maior em neonatos, pacientes imunocomprometidos e idosos. Neste estudo Cronobacter spp. foi pesquisado em 90 amostras de queijos (30 do tipo Minas Frescal, 30 do tipo Prato e 30 do tipo Prato fatiado). As espécies isoladas foram identificadas, e foi avaliado o perfil de suscetibilidade a antimicrobianos. A pesquisa foi realizada utilizando-se pré-enriquecimento em água peptonada tamponada, enriquecimento seletivo no caldo lauril sulfato triptose contendo vancomicina, isolamento no meio Enterobacter sakazakii Isolation Agar e identificação no Vitek 2.0. As espécies foram identificadas por meio de múltipla PCR com alvo no gene cgcA. O antibiograma foi realizado pela técnica de difusão em ágar (Kirby-Bauer). Cronobacter spp. foi isolada em uma (1,1 %) amostra de queijo tipo Minas Frescal, identificada como C. sakazakii que apresentou sensibilidade a todos os antimicrobianos testados. Cronobacter spp. pode nمo representar risco à saْde dos indivíduos pelo consumo de queijos produzidos com leite pasteurizado. Entretanto, a presença de Cronobacter spp. em uma amostra de queijo demonstra falhas na produção, o que reforça a necessidade de maior adesão às Boas Práticas de Fabricação.
Cronobacter spp. is an opportunistic pathogen that may cause infections in individuals ofany age, and the highest incidence occurs in neonates, immunocompromised patients andelderly persons. This study investigated Cronobacter spp. occurrence in 90 cheese samples(30 Minas Frescal type cheeses, 30 Prato type and 30 sliced Prato type). The isolatedspecies were identified and the antimicrobial susceptibility profile of the isolated strains wasevaluated. The microbiological assay was performed with pre-enrichment in buffered peptonewater, and selective-enrichment in modified lauryl sulphate tryptose broth containingvancomycin. Isolation and identification were done in Enterobacter sakazakii Isolation Agar andin Vitek 2.0, respectively. The species identification was performed by multiple PCR targetingcgaA gene. Antibiogram was done using agar diffusion method (Kirby-Bauer). Cronobacter spp.was isolated from one (1.1 %) sample of Minas Frescal type cheese, identified as C. sakazakii which was sensitive to all of tested antimicrobials. Cronobacter spp. does not represent arisk to the individuals health by consuming cheeses made from pasteurized milk. However,the presence of Cronobacter spp. in one sample of analyzed cheese indicates failures in their production, reinforcing the need for following the Good Manufacturing Practices.
Subject(s)
Cronobacter , Cheese , Polymerase Chain Reaction , Microbial Sensitivity TestsABSTRACT
Cronobacter spp. emergiu como perigo microbiológico em fórmulas infantis desidratadas (FID), responsável por infecções graves em neonatos. Contudo, muitos pacientes não ingeriram FID, o que indica que outros alimentos podem atuar como veículo do patógeno. Os objetivos deste estudo foram pesquisar Cronobacter spp. em alimentos infantis, identificar as espécies e avaliar o perfil de suscetibilidade aos antimicrobianos das cepas isoladas. Foram analisadas 47 amostras pré-cozidas de cereais à base de grãos, amidos de milho e farinhas lácteas. A pesquisa foi realizada com pré-enriquecimento em água peptonada tamponada, enriquecimento seletivo no Cronobacter Screening Broth, isolamento por meio de Enterobacter sakazakii Isolation Agar e identificação no Vitek 2.0. A identificação das espécies foi realizada por reação em cadeia pela polimerase com alvo nos genes rpoB e cgcA. O antibiograma foi realizado pelo método de difusão em ágar (Kirby-Bauer). Cronobacter spp. foi identificada em 11 amostras (23,4 %). Oito cepas foram identificadas como C. sakazakii (72,7 %), duas como C. malonaticus (18,2 %) e uma como C. dublinensis (9,1 %). Apenas uma cepa de C. malonaticus apresentou resistência intermediária a ciprofloxacina. Os produtos destinados à alimentação infantil avaliados podem apresentar risco, no caso destes alimentos serem ingeridos por pacientes pertencentes ao grupo de risco, como neonatos e idosos.
Cronobacter spp. emerged as a microbiological hazard in powdered infant formulas (PIF)causing severe infections in newborns. However, among these patients many of them had not ingested PIF indicating that other foods categories might be as the pathogen vehicle. This study aimed at investigating Cronobacter spp. in infant foods, identifying the species and evaluatingthe antimicrobial susceptibility profile of the isolated strains. Forty-seven samples of precooked grain-based cereals, corn starch and milk flours were analyzed. The microbiological analysis was performed with pre-enrichment in buffered peptone water, followed by selective-enrichment in Cronobacter Screening Broth, isolation in Enterobacter sakazakii Isolation Agar and identificationin Vitek 2.0. The identification of species was performed by polymerase chain reaction targetingrpoB and cgaA genes. The antibiogram was carried out using the agar diffusion method(Kirby-Bauer). Cronobacter spp. was identified in 11 samples (23.4 %). Eight strains wereidentified as C. sakazakii (72.7 %), two as C. malonaticus (18.2 %) and one as C. dublinensis (9.1 %). Only one C. malonaticus strain showed an intermediate resistance to ciprofloxacin. The evaluated samples produced for infant feeding might cause hazard when ingested by patients belonging tothe risk group as newborns and elderly.
Subject(s)
Humans , Male , Female , Child , Infant Food , Cronobacter , Polymerase Chain Reaction , Microbial Sensitivity TestsABSTRACT
Cronobacter spp. emergiu como perigo microbiológico em fórmulas infantis desidratadas (FID), responsável por infecções graves em neonatos. Contudo, muitos pacientes não ingeriram FID, o que indica que outros alimentos podem atuar como veículo do patógeno. Os objetivos deste estudo foram pesquisar Cronobacter spp. em alimentos infantis, identificar as espécies e avaliar o perfil de suscetibilidade aos antimicrobianos das cepas isoladas. Foram analisadas 47 amostras pré-cozidas de cereais à base de grãos, amidos de milho e farinhas lácteas. A pesquisa foi realizada com pré-enriquecimento em água peptonada tamponada, enriquecimento seletivo no Cronobacter Screening Broth, isolamento por meio de Enterobacter sakazakii Isolation Agar e identificação no Vitek 2.0. A identificação das espécies foi realizada por reação em cadeia pela polimerase com alvo nos genes rpoB e cgcA. O antibiograma foi realizado pelo método de difusão em ágar (Kirby-Bauer). Cronobacter spp. foi identificada em 11 amostras (23,4 %). Oito cepas foram identificadas como C. sakazakii (72,7 %), duas como C. malonaticus (18,2 %) e uma como C. dublinensis (9,1 %). Apenas uma cepa de C. malonaticus apresentou resistência intermediária a ciprofloxacina. Os produtos destinados à alimentação infantil avaliados podem apresentar risco, no caso destes alimentos serem ingeridos por pacientes pertencentes ao grupo de risco, como neonatos e idosos.
Cronobacter spp. emerged as a microbiological hazard in powdered infant formulas (PIF) causing severe infections in newborns. However, among these patients many of them had not ingested PIF indicating that other foods categories might be as the pathogen vehicle. This study aimed at investigating Cronobacter spp. in infant foods, identifying the species and evaluating the antimicrobial susceptibility profile of the isolated strains. Forty-seven samples of precooked grain-based cereals, corn starch and milk flours were analyzed. The microbiological analysis was performed with pre-enrichment in buffered peptone water, followed by selective-enrichment in Cronobacter Screening Broth, isolation in Enterobacter sakazakii Isolation Agar and identification in Vitek 2.0. The identification of species was performed by polymerase chain reaction targeting rpoB and cgaA genes. The antibiogram was carried out using the agar diffusion method (Kirby-Bauer). Cronobacter spp. was identified in 11 samples (23.4 %). Eight strains were identified as C. sakazakii (72.7 %), two as C. malonaticus (18.2 %) and one as C. dublinensis (9.1 %). Only one C. malonaticus strain showed an intermediate resistance to ciprofloxacin. The evaluated samples produced for infant feeding might cause hazard when ingested by patients belonging to the risk group as newborns and elderly.
Subject(s)
Cronobacter , Polymerase Chain Reaction , Microbial Sensitivity TestsABSTRACT
Cronobacter spp. é um patógeno oportunista que pode causar infecções em indivíduos de qualquer idade, cuja incidência é maior em neonatos, pacientes imunocomprometidos e idosos. Neste estudo Cronobacter spp. foi pesquisado em 90 amostras de queijos (30 do tipo Minas Frescal, 30 do tipo Prato e 30 do tipo Prato fatiado). As espécies isoladas foram identificadas, e foi avaliado o perfil de suscetibilidade a antimicrobianos. A pesquisa foi realizada utilizando-se pré-enriquecimento em água peptonada tamponada, enriquecimento seletivo no caldo lauril sulfato triptose contendo vancomicina, isolamento no meio Enterobacter sakazakii Isolation Agar e identificação no Vitek 2.0. As espécies foram identificadas por meio de múltipla PCR com alvo no gene cgcA. O antibiograma foi realizado pela técnica de difusão em ágar (KirbyBauer). Cronobacter spp. foi isolada em uma (1,1 %) amostra de queijo tipo Minas Frescal, identificada como C. sakazakii que apresentou sensibilidade a todos os antimicrobianos testados. Cronobacter spp. pode não representar risco à saúde dos indivíduos pelo consumo de queijos produzidos com leite pasteurizado. Entretanto, a presença de Cronobacter spp. em uma amostra de queijo demonstra falhas na produção, o que reforça a necessidade de maior adesão às Boas Práticas de Fabricação.
Cronobacter spp. is an opportunistic pathogen that may cause infections in individuals of any age, and the highest incidence occurs in neonates, immunocompromised patients and elderly persons. This study investigated Cronobacter spp. occurrence in 90 cheese samples (30 Minas Frescal type cheeses, 30 Prato type and 30 sliced Prato type). The isolated species were identified and the antimicrobial susceptibility profile of the isolated strains was evaluated. The microbiological assay was performed with pre-enrichment in buffered peptone water, and selective-enrichment in modified lauryl sulphate tryptose broth containing vancomycin. Isolation and identification were done in Enterobacter sakazakii Isolation Agar and in Vitek 2.0, respectively. The species identification was performed by multiple PCR targeting cgaA gene. Antibiogram was done using agar diffusion method (Kirby-Bauer). Cronobacter spp. was isolated from one (1.1 %) sample of Minas Frescal type cheese, identified as C. sakazakii which was sensitive to all of tested antimicrobials. Cronobacter spp. does not represent a risk to the individuals health by consuming cheeses made from pasteurized milk. However, the presence of Cronobacter spp. in one sample of analyzed cheese indicates failures in their production, reinforcing the need for following the Good Manufacturing Practices.
Subject(s)
Cronobacter/isolation & purification , Cheese/microbiology , Polymerase Chain Reaction , Microbial Sensitivity TestsABSTRACT
<p><b>OBJECTIVE</b>To determine Cronobacter spp. contamination in infant and follow-up powdered formula in China.</p><p><b>METHODS</b>All of 2282 samples were collected from the retail markets in China from January 2012 to December 2012, and analyzed for Cronobacter spp. by the Chinese National Food Safety Standard. Characterization of the isolates was analyzed by pulsed-field gel electrophoresis (PFGE) with XbaI and SpeI restriction enzymes.</p><p><b>RESULTS</b>Cronobacter spp. strains were isolated from 25 samples, and the positive rates in infant powdered formulas and follow-up powdered formulas were 0.90% (10/1011) and 1.18% (15/1271), respectively. Analysis of variable data regarding different purchasing store formats, seasonality, and production locations as well as comparison of infant versus follow-up formulas did not reveal statistically significant factors. During the sampling period, one of six surveillance zones did exhibit a statistically significant trend towards higher positive rate. PFGE characterization of Cronobacter spp. to elucidate genetic diversity revealed only three pairs of Cronobacter spp. out of 25 having the same PFGE patterns.</p><p><b>CONCLUSION</b>The current investigation indicated a lower positive rate of Cronobacter spp. in the powdered formula in China. This evidence suggested contamination originating from multiple different sources during the manufacturing process.</p>
Subject(s)
China , Cronobacter , Electrophoresis, Gel, Pulsed-Field , Infant Formula , MicrobiologyABSTRACT
PURPOSE: We aim to fabricate a thermoplastic poly(methylmethacrylate) (PMMA) Lab-on-a-Chip device to perform continuous- flow polymerase chain reactions (PCRs) for rapid molecular detection of foodborne pathogen bacteria. METHODS: A miniaturized plastic device was fabricated by utilizing PMMA substrates mediated by poly(dimethylsiloxane) interfacial coating, enabling bonding under mild conditions, and thus avoiding the deformation or collapse of microchannels. Surface characterizations were carried out and bond strength was measured. The feasibility of the Lab-on-a-Chip device for performing on-chip PCR utilizing a lab-made, portable dual heater was evaluated. The results were compared with those obtained using a commercially available thermal cycler. RESULTS: A PMMA Lab-on-a-Chip device was designed and fabricated for conducting PCR using foodborne pathogens as sample targets. A robust bond was established between the PMMA substrates, which is essential for performing miniaturized PCR on plastic. The feasibility of on-chip PCR was evaluated using Escherichia coli O157:H7 and Cronobacter condimenti, two worldwide foodborne pathogens, and the target amplicons were successfully amplified within 25 minutes. CONCLUSIONS: In this study, we present a novel design of a low-cost and high-throughput thermoplastic PMMA Lab-on-a-Chip device for conducting microscale PCR, and we enable rapid molecular diagnoses of two important foodborne pathogens in minute resolution using this device. In this regard, the introduced highly portable system design has the potential to enable PCR investigations of many diseases quickly and accurately.
Subject(s)
Bacteria , Cronobacter , Diagnosis , Escherichia coli , Lab-On-A-Chip Devices , Plastics , Polymerase Chain Reaction , Polymethyl MethacrylateABSTRACT
<p><b>OBJECTIVE</b>To investigate the inhibitory effect of Lactobacillus rhamnosus GG ( LGG) against Cronobacter-induced meningitis in neonatal rats.</p><p><b>METHODS</b>The cell adhesion and invasion capacities of Cronobacter were assayed in Caco-2 cells, and the optimal time length and concentration of the bacterium for infection were determined. The suppressive effects of LGG on the adhesion and invasion of Cronobacter in caco-2 cells were tested by competitive and exclusion experiments, and its inhibitory effect against Cronobacter-induced meningitis was evaluated in neonatal rats.</p><p><b>RESULTS</b>Cronobacter showed aggressive adhesion to caco-2 cells with an optimal infection time of 3 h. LGG produced a concentration-dependent inhibition of Cronobacter adhesion and invasion by competing with and excluding the latter for cell adhesion. In neonatal rats, LGG showed an obvious preventive effect and also a moderate therapeutic effect against Cronobacter-induced meningitis.</p><p><b>CONCLUSION</b>LGG can inhibit Cronobacter entry across the intestinal barrier to achieve preventive and therapeutic effects against Cronobacter-induced meningitis.</p>
Subject(s)
Animals , Humans , Rats , Animals, Newborn , Bacterial Adhesion , Caco-2 Cells , Cronobacter , Virulence , Enterobacteriaceae Infections , Therapeutics , Intestines , Microbiology , Lacticaseibacillus rhamnosus , Meningitis, Bacterial , Therapeutics , ProbioticsABSTRACT
Cronobacter spp. é uma bactéria oportunista associada a surtos de infecção em neonatos e criançasem virtude de consumo de fórmulas infantis desidratadas (FID). Neste contexto, o setor reguladortem criado normas específicas para o controle destes agentes patogênicos nas fórmulas infantis. Nesteestudo foi pesquisada a ocorrência de Cronobacter spp. em 60 amostras de FID comercializadas no Riode Janeiro, Brasil. Foram analisadas 30 amostras de fórmulas infantis para lactantes (0-6 meses) e 30 defórmulas infantis de seguimento para lactantes (> 6 meses) seguindo-se a metodologia de cultivo descritano Bacteriological Analytical Manual OnlineFDA (2012). A identificação das colônias característicasfoi realizada com uso de kits ID32E, API20E e do sistema Vitek 2.0; e pela reação da polimerase emcadeia (PCR) com alvo no gene gluA. Nenhuma amostra apresentou contaminação por Cronobacterspp. Concluiu-se que a ocorrência de Cronobacter spp. em FID parece ser baixa, o que indica que osprodutores estão cumprindo o disposto nas normas brasileiras vigentes de forma a evitar a contaminaçãodos produtos por este micro-organismo...
Subject(s)
Food Preservation , Cronobacter , Infant Formula , Food Microbiology , Polymerase Chain ReactionABSTRACT
A total of 7 Cronobacter strains were isolated from 703 fecal samples collected in Jinan from June 13 to December 30, 2011, with the positive rate of Cronobacter spp. being 1.0% (95% confidence interval 0.6%-1.4%). Three Cronobacter sakazakii stains were isolated from 157 fecal samples of healthy neonates (95% confidence interval 0.4%-5.5%). This number was slightly higher than that isolated from 273 fecal samples of healthy adults, in which 1 strain of C. sakazakii and 1 strain of Cronobacter malonaticus were isolated, and that from 173 fecal samples of adults with acute diarrhea, in which 1 strain of C. sakazakii and 1 strain of C. malonaticus were isolated, but the differences were not statistically significant (P>0.05). The Cronobacter isolates were all from different genetic sources. It should be noted that Cronobacter carriage may cause infection under certain conditions, especially in neonates.
Subject(s)
Humans , Infant, Newborn , Bacterial Typing Techniques , Cronobacter , Cronobacter sakazakii , Food MicrobiologyABSTRACT
Cronobater spp. (E. sakazakii) é considerada um micro-organismo oportunista que vem ganhando atenção de autoridades de Saúde Pública, pelo crescente número de surtos de infecção em recémnascidos e lactentes. A bactéria está associada a casos raros, com alta taxa de mortalidade, podendo causar meningites, enterocolite necrosante e septicemia. Cronobacter spp. tem ampla disseminação, porém apenas as fórmulas lácteas infantis em pó foram, epidemiologicamente, associadas às doenças causadas por esse agente. No presente estudo foi avaliada a ocorrência de Cronobacter spp. em alimentos destinados às crianças de 0-36 meses de idade, adquiridos em lactário de um hospital público do município de São Paulo. Vinte e seis amostras de fórmulas reconstituídas e 24 produtos em pó foram analisados segundo a metodologia da ISO. Cronobacter spp. foi detectada em uma amostra (3,8 por cento) reconstituída de alimento infantil à base de farinha de milho e em quatro desse produto em pó (16,7 por cento). A bactéria não foi detectada nas fórmulas infantis destinadas às crianças de 0-6 meses, contudo sua presença em outros alimentos infantis pode contribuir para a contaminação do ambiente e dos utensílios dos lactários por meio da contaminação cruzada.
Subject(s)
Humans , Male , Female , Infant, Newborn , Cronobacter , Infant Formula , Hospitals, PublicABSTRACT
Cronobacter sakazakii (C. sakazakii), formerly Enterobacter sakazakii, is an emerging pathogen associated with the ingestion of contaminated reconstituted formula that causes serious illnesses such as bacteremia, septicemia, necrotizing enterocolitis, meningitis and death in low-birth-weight preterm neonatal infants. The objective of this study was to develop an animal model for human neonatal C. sakazakii infections. We acquired timed-pregnant ICR mice and allowed them to give birth naturally. On postnatal day 3.5, each pup was administered orally a total dose of approximately 107 CFU C. sakazakii strain 3439. Mice were observed twice daily for morbidity and mortality. At postnatal day 10.5, the remaining pups were euthanized, and brain, liver, and cecum were excised and analyzed for the presence of C. sakazakii. C. sakazakii was isolated from cecum and other tissues in inoculated mice. In the tissues of C. sakazakii infected mice, meningitis and gliosis were detected in brain. In this study, we confirmed the neonatal ICR mice may be used a very effective animal model for human neonatal C. sakazakii infections.