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Artykuły w czasopismach na temat „Biotyping of Enterobacter cloacae”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Silva, Francisco, and TM Pabla Martínez O. "Complejo Enterobacter cloacae." Revista chilena de infectología 35, no. 3 (2018): 297–98. http://dx.doi.org/10.4067/s0716-10182018000300297.

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J. Gupta, Pooja, Minal J. Trivedi, and Harsha P. Soni. "Enterobacter cloacae PNE2 As Promising Plant Growth Promoting Bacterium, Isolated From The Kadi Vegetable Market Waste, Gujarat." Biosciences Biotechnology Research Asia 19, no. 3 (2022): 773–86. http://dx.doi.org/10.13005/bbra/3030.

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Chemical fertilizer use in agricultural areas causes a variety of issues, including pollution, health risks, disruption of natural ecological nutrient cycles, and the loss of biological communities. In this case, chemical fertilizers, herbicides, and other supplements are replaced by plant growth promoting bacteria for sustainable agriculture. The present research work focus on the isolation of the plant growth promoting bacteria from the Kadi vegetable market waste. Derived from morphological, biochemical, and 16S rRNA gene sequence analysis the strain was identified as Enterobacter cloacae P

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Sutton, Granger G., Lauren M. Brinkac, Thomas H. Clarke, and Derrick E. Fouts. "Enterobacter hormaechei subsp. hoffmannii subsp. nov., Enterobacter hormaechei subsp. xiangfangensis comb. nov., Enterobacter roggenkampii sp. nov., and Enterobacter muelleri is a later heterotypic synonym of Enterobacter asburiae based on computational analysis of sequenced Enterobacter genomes." F1000Research 7 (May 1, 2018): 521. http://dx.doi.org/10.12688/f1000research.14566.1.

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Background: The predominant species in clinical Enterobacter isolates is E. hormaechei. Many articles, clinicians, and GenBank submissions misname these strains as E. cloacae. The lack of sequenced type strains or named species/subspecies for some clades in the E. cloacae complex complicate the issue. Methods: The genomes of the type strains for Enterobacter hormaechei subsp. oharae, E. hormaechei subsp. steigerwaltii, and E. xiangfangensis, and two strains from Hoffmann clusters III and IV of the E. cloacae complex were sequenced. These genomes, the E. hormaechei subsp. hormaechei type strain

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4

Sutton, Granger G., Lauren M. Brinkac, Thomas H. Clarke, and Derrick E. Fouts. "Enterobacter hormaechei subsp. hoffmannii subsp. nov., Enterobacter hormaechei subsp. xiangfangensis comb. nov., Enterobacter roggenkampii sp. nov., and Enterobacter muelleri is a later heterotypic synonym of Enterobacter asburiae based on computational analysis of sequenced Enterobacter genomes." F1000Research 7 (June 29, 2018): 521. http://dx.doi.org/10.12688/f1000research.14566.2.

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Background: The predominant species in clinical Enterobacter isolates is E. hormaechei. Many articles, clinicians, and GenBank submissions misname these strains as E. cloacae. The lack of sequenced type strains or named species/subspecies for some clades in the E. cloacae complex complicate the issue. Methods: The genomes of the type strains for Enterobacter hormaechei subsp. oharae, E. hormaechei subsp. steigerwaltii, and E. xiangfangensis, and two strains from Hoffmann clusters III and IV of the E. cloacae complex were sequenced. These genomes, the E. hormaechei subsp. hormaechei type strain

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5

Yang, Yuanyuan, Senyuan Hong, Jinzhou Xu, Cong Li, Shaogang Wang, and Yang Xun. "Enterobacter cloacae: a villain in CaOx stone disease?" Urolithiasis 50, no. 2 (2022): 177–88. http://dx.doi.org/10.1007/s00240-022-01311-8.

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AbstractTo explore the roles microbiome of urinary tract played in calcium oxalate stones (CaOx) formation, we collected two sides’ pelvis urine of patients with unilateral CaOx stones to set self-control to diminish the influence of systemic factors. Patients with unilateral CaOx stones were recruited in our study according to strict criteria. 16S rRNA gene sequencing was applied to every pair of pelvis urine. Bacterial genome sequencing of Enterobacter cloacae was conducted and bioinformatic analysis was applied to explore the possible pathways of Enterobacter cloacae inducing CaOx stones fo

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6

Sui, Yewei, Hongsheng Lu, Zhenhua Hu, and Cuijing Zhang. "Adsorption and Reduction of Heavy Metal Cr (VI) by Enterobacter cloacae SKD and Its Kinetics." Journal of Physics: Conference Series 2393, no. 1 (2022): 012001. http://dx.doi.org/10.1088/1742-6596/2393/1/012001.

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Abstract Chromium contamination is one of the most common heavy metal pollutants. Degradation of highly toxic Cr(VI) by microbial remediation technology can open up a new way for environmentally friendly and efficient chromium pollution control. The adsorption and reduction kinetics of Cr(VI) by Enterobacter cloacae SKD were studied by the adsorption and reduction experiments of Cr(VI) by Enterobacter cloacae SKD. The mechanism of adsorption and reduction of Cr(VI) by Enterobacter cloacae SKD was revealed, and the characteristics of adsorption and reduction were determined. The results showed

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7

Roca Villanueva, Bernardino, M. L. Peris, C. Chumillas, and José Manuel González Darder. "Meningitis por Enterobacter cloacae." Revista de Neurología 29, no. 10 (1999): 992. http://dx.doi.org/10.33588/rn.2910.99452.

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Hoffmann, Harald, and Andreas Roggenkamp. "Population Genetics of the Nomenspecies Enterobacter cloacae." Applied and Environmental Microbiology 69, no. 9 (2003): 5306–18. http://dx.doi.org/10.1128/aem.69.9.5306-5318.2003.

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ABSTRACT The genetic heterogeneity of the nomenspecies Enterobacter cloacae is well known. Enterobacter asburiae, Enterobacter cancerogenus, Enterobacter dissolvens, Enterobacter hormaechei, Enterobacter kobei, and Enterobacter nimipressuralis are closely related to it and are subsumed in the so-called E. cloacae complex. DNA-DNA hybridization studies performed previously identified at least five DNA-relatedness groups of this complex. In order to analyze the genetic structure and the phylogenetic relationships between the clusters of the nomenspecies E. cloacae, 206 strains collected from 22

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9

Anne DAVIN-RÉGLI. "ENTEROBACTER." ACTUALITES PERMANENTES EN MICROBIOLOGIE CLINIQUE 19, no. 01 (2020): 10. http://dx.doi.org/10.54695/apmc.19.01.1528.

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Le genre Enterobacter comprend 20 espèces (tableau I).Enterobacter cloacae (espèce type du genre Enterobacter) et E.aerogenes sont les espèces les plus fréquemment isolées en cliniqueen France. Les études phylogénétiques ont permis de déclassertrois espèces, Enterobacter intermedius reclassé dans le genreKluyvera, Enterobacter dissolvens reclassé en tant que sous-espèced’Enterobacter cloacae et E. sakazakii dans le genre Cronobacteren 2007 (Iversen et al., 2007). Huit nouvelles espèces ont étédécrites sur la base de l’analyse du 16SrRNA ou du gène rpoB etsont issues d’extraits végétaux, de la

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10

SØGAARD, PER. "RESISTANCE TYPES IN ENTEROBACTER CLOACAE." Acta Pathologica Microbiologica Scandinavica Series B: Microbiology 90B, no. 1-6 (2009): 229–33. http://dx.doi.org/10.1111/j.1699-0463.1982.tb00110.x.

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Ganelin, Robert S., and Michael Ellis. "Cellulitis caused by Enterobacter cloacae." Journal of Infection 24, no. 2 (1992): 218–19. http://dx.doi.org/10.1016/0163-4453(92)93214-b.

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El Sayed, Fouad. "Black Tongue and Enterobacter cloacae." Archives of Dermatology 143, no. 6 (2007): 799. http://dx.doi.org/10.1001/archderm.143.6.815-a.

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13

Suliasih, Suliasih, and Sri Widawati. "PHYTASE PRODUCTION BY Enterobacter cloacae." BIOTROPIA 27, no. 3 (2020): 282–91. http://dx.doi.org/10.11598/btb.0.0.0.1233.

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Â This study aims to isolate the phytase producing bacteria (PPB), a plant growth promoting rhizobacteria (PGPR), from 1Cigna sinensis rhizosphere and to optimize its physicochemical conditioning. Phytase is an enzyme that can hydrolyze the phosphoester bond in organic phosphorus (phytic acid) to form ester phosphate and inorganic phosphate, the available forms of phosphorus. To test its ability to hydrolyze organic phosphates (calcium phytate), the phytase was screened in solid and liquid phytase screening medium (PSM). After isolation, a total of 13 bacteria were positive for this enzymeâ€™s

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14

Barrón-González, María Porfiria, Carlos Mireles-Rangel, Fabiola Lizeth Cuéllar-Guevara, Daniel J. Eguiarte-Lara, and Yadira Quiñones-Gutiérrez. "Inhibición de Enterobacter cloacae por Bifidobacterium longum." Investigación y Ciencia de la Universidad Autónoma de Aguascalientes, no. 77 (May 31, 2019): 19–26. http://dx.doi.org/10.33064/iycuaa2019772094.

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Enterobacter cloacae forma parte de la microbiota intestinal en humanos, pertenece al phylum de las Proteobacterias, familia Enterobacteriaceae, género Enterobacter, especie E. cloacae; se caracteriza por ser ubicua, oportunista, fármaco-resistente y responsable de bacteriemias e infecciones nosocomiales, por lo que se hace necesaria la búsqueda de alternativas para su tratamiento y control. En este trabajo se muestra evidencia de la inhibición del crecimiento de E. cloacae empleando metabolitos bacterianos o sobrenadantes libres de células (también conocidos como postbióticos) producidos por

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15

Roberts, Daniel P., and Carol J. Sheets. "Carbohydrate nutrition of Enterobacter cloacae ATCC 39978." Canadian Journal of Microbiology 37, no. 2 (1991): 168–70. http://dx.doi.org/10.1139/m91-026.

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Utilization of carbohydrate and production of carbohydrate-degrading enzymes by the plant beneficial bacterium Enterobacter cloacae ATCC 39978 was studied. Enterobacter cloacae did not grow on any of the carbohydrate polymers supplied as carbon and energy sources. However, E. cloacae did grow on all the mono- and oligo-saccharides and β-glucosides tested, with the exceptions of D-arabinose and D-fucose. No carbohydrate depolymerase activities were detected in culture supernatants from E. cloacae. In contrast, a number of glycosidase activities including β-glucosidase, β-N-acetylglucosaminidase

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Amarasiri, Mohan, Hiroki Kawai, Masaaki Kitajima, Satoshi Okabe, and Daisuke Sano. "Specific interactions of rotavirus HAL1166 with Enterobacter cloacae SENG-6 and their contribution on rotavirus HAL1166 removal." Water Science and Technology 79, no. 2 (2019): 342–48. http://dx.doi.org/10.2166/wst.2019.050.

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Abstract Contribution of specific interactions between human enteric viruses and wastewater suspended solids on human enteric virus removal by microfiltration was studied. A cross-flow microfiltration system was used with rotavirus HAL1166 and Enterobacter cloacae SENG-6 as the model virus and wastewater suspended solid. Cleavage of rotavirus HAL1166 protein VP4 by trypsin produces the VP8* subunit, which specifically interacts with histo-blood group antigen (HBGA). In the presence of Enterobacter cloacae SENG-6, the trypsin-treated rotavirus concentration reduced with time (R2 &gt; 0.6) c

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Saleh, Saleema S., and Bernard R. Glick. "Involvement ofgacSandrpoSin enhancement of the plant growth-promoting capabilities ofEnterobacter cloacaeCAL2 and UW4." Canadian Journal of Microbiology 47, no. 8 (2001): 698–705. http://dx.doi.org/10.1139/w01-072.

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The plant growth-promoting bacteria Enterobacter cloacae CAL2 and UW4 were genetically transformed with a multicopy plasmid containing an rpoS or gacS gene from Pseudomonas fluorescens. The transformed strains were compared with the nontransformed strains for growth, indoleacetic acid (IAA) production, antibiotic production, 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase activity, siderophore production, cell morphology, and the ability to promote canola root elongation. All transformed strains had a longer lag phase, were slower in reaching stationary phase, and attained a higher cell

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Hossain, Sanjida, Md Abdullah Yusuf, Shamsun Nahar, Adneen Moureen, Sazzad Bin Shahid, and SM Shamsuzzaman. "Evaluation of Protective Antibody Response following Vaccination with Formaldehyde Inactivated Enterobacter cloacae." Bangladesh Journal of Medical Microbiology 18, no. 1 (2024): 44–49. https://doi.org/10.3329/bjmm.v18i1.77624.

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Background: Multi-drug-resistant (MDR) strains of Enterobacter cloacae are becoming increasingly prevalent worldwide, which is reducing treatment options. Objective: The purpose of the present study was to evaluate protective antibody response following vaccination with formaldehyde inactivated Enterobacter cloacae. Methodology: The study used formaldehyde inactivated MDR Enterobacter cloacae obtained from various clinical samples to immunize 10 Swiss albino mice through intradermal injection. After the third dose of immunization, the mice were challenged with live Enterobacter cloacae through

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Bhadra, Bhaskar, Ashis Kumar Nanda, and Ranadhir Chakraborty. "Enterobacter nickelidurans sp. nov., a novel nickel tolerant enterobacteria isolated from Torsa river water of India." NBU Journal of Plant Sciences 5, no. 1 (2011): 15–23. http://dx.doi.org/10.55734/nbujps.2011.v05i01.003.

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A Gram-negative, rod-shaped, nickel-resistant bacterium, designated as strain NiVas 114', was isolated from waters of Torsa River in Hasimara, West Bengal, India. The strain NiVasl 14 possessing inducible nickel resistance can tolerate maximally 10mM nickel chloride. Southern blot assays of genomic DNA of NiVas 114 using probe(s) generated from known nickel resistance determinants (cnr/ ncc/ nrel nerí nir). under conditions of low stringency, produced no detectable signal except for cnrA gene of Ralstonia metallidurans CH34 (formerly Alcaligenes eutropha CH34) in which weak hybridization signa

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Yunita, Vivi Alfi, Hasnah Natsir, Ahyar Ahmad, and Maswati Baharuddin. "Chitinase Enzyme-Producing Endophytic Bacterias From the Roots of the Plant Gembolo (Dioscorea bulbifera): Isolation, Characterization and its Potential as an Antifungal Agent." Molekul 19, no. 1 (2024): 117. http://dx.doi.org/10.20884/1.jm.2024.19.1.9422.

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Chitinase is an enzyme of the chitinolytic group that has many roles in agriculture, especially as an antifungal, because chitin is one of the constituent components of the fungal cell wall. This study aimed to isolate and identify endophytic bacteria from gembolo (Dioscorea bulbifera) roots and to characterize the chitinase enzyme from these endophytic bacteria to be used as an antifungal. Isolation and identification of gembolo plant root endophytic bacteria using PCR method of 16S rRNA gene amplification and sequencing. Characterization of the chitinase enzyme produced includes determining

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Bennett, William, Katrin Mende, Wesley R. Campbell, et al. "Enterobacter cloacae infection characteristics and outcomes in battlefield trauma patients." PLOS ONE 18, no. 8 (2023): e0290735. http://dx.doi.org/10.1371/journal.pone.0290735.

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Enterobacter cloacae is a Gram-negative rod with multidrug-resistant potential due to chromosomally-induced AmpC β-lactamase. We evaluated characteristics, antibiotic utilization, and outcomes associated with battlefield-related E. cloacae infections (2009–2014). Single initial and serial E. cloacae isolates (≥24 hours from initial isolate from any site) associated with a clinical infection were examined. Susceptibility profiles of initial isolates in the serial isolation group were contrasted against last isolate recovered. Characteristics of 112 patients with E. cloacae infections (63 [56%]

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Grichko, Varvara P., and Bernard R. Glick. "Identification of DNA sequences that regulate the expression of the Enterobacter cloacae UW4 1-aminocyclopropane-1-carboxylic acid deaminase gene." Canadian Journal of Microbiology 46, no. 12 (2000): 1159–65. http://dx.doi.org/10.1139/w00-113.

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Analysis of the DNA sequence upstream of the previously isolated Enterobacter cloacae UW4 ACC deaminase gene (Shah et al. 1998) suggests that this segment contains several features that are thought to be involved in the transcriptional regulation of this gene. These features include half of a CRP (cAMP receptor protein) binding site, an FNR (fumarate-nitrate reduction) regulatory protein binding site, an LRP (leucine responsive regulatory protein) binding site, and an LRP-like protein coding region. ACC deaminase activity was measured following growth of either various Escherichia coli strains

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Pontes, Daniela Santos, Cláudia Iracema Lima-Bittencourt, Marcela Santiago Pacheco Azevedo, Edmar Chartone-Souza, and Andréa Maria Amaral Nascimento. "Phenotypic and genetic analysis of Enterobacter spp. from a Brazilian oligotrophic freshwater lake." Canadian Journal of Microbiology 53, no. 8 (2007): 983–91. http://dx.doi.org/10.1139/w07-060.

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We characterized a population of Enterobacter spp. of the Enterobacter cloacae complex isolated from an oligotrophic lake; most isolates were identified as E. cloacae. Fingerprinting polymerase chain reaction (PCR), along with morphological, biochemical, physiological, and plasmid profiles analyses, including antimicrobial susceptibility testing, were performed on 22 environmental isolates. Misidentification occurred when using the API 20E identification system. Analysis of 16S rDNA sequences confirmed the close relatedness between species of the E. cloacae complex. The tDNA PCR allowed the di

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Irawati, Wahyu, Vania Austine Callista Timotius, Ruben Patrick Adhiwijaya, Bellen Mouretta, Steven Anggawinata, and Eunike Bunga Marvella. "12 TEXTILE DYES DECOLORIZATION BY COPPER-RESISTANT-BACTERIA KLEBSIELLA GRIMONTII, SHIGELLA FLEXNERI, ENTEROBACTER CLOACAE ISOLATED FROM CISADANE RIVER TANGERANG." BIOLINK (Jurnal Biologi Lingkungan Industri Kesehatan) 9, no. 2 (2023): 151–62. http://dx.doi.org/10.31289/biolink.v9i2.7731.

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Dyes and copper are dangerous contaminants because they are toxic. Bioremediation using indigenous bacteria is the best solution to overcome water pollution. Copper resistant bacteria usually have resistance to dyes thereby helping the bioremediation of dye and copper wastes. This study aims to examine the ability of indigenous bacteria isolated from the Cisadane River, namely Klebsiella grimontii IrCis3, Shigella flexneri IrCis5, Enterobacter cloacae IrCis6, and Enterobacter cloacae IrCis9 in terms of resistance and ability to decolorize 12 textile dyes namely methylene blue, malachite green,

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Ren, Yan, Yi Ren, Zhemin Zhou, et al. "Complete Genome Sequence of Enterobacter cloacae subsp. cloacae Type Strain ATCC 13047." Journal of Bacteriology 192, no. 9 (2010): 2463–64. http://dx.doi.org/10.1128/jb.00067-10.

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ABSTRACT Enterobacter cloacae is an important nosocomial pathogen. Here, we report the completion of the genome sequence of E. cloacae ATCC 13047, the type strain of E. cloacae subsp. cloacae. Multiple sets of virulence determinant and heavy-metal resistance genes have been found in the genome. To the best of our knowledge, this is the first complete genome sequence of the E. cloacae species.

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GONÇALVES, Célia R., Tania M. I. VAZ, Daniela LEITE, et al. "Molecular epidemiology of a nosocomial outbreak due to Enterobacter cloacae and Enterobacter agglomerans in Campinas, São Paulo, Brazil." Revista do Instituto de Medicina Tropical de São Paulo 42, no. 1 (2000): 1–7. http://dx.doi.org/10.1590/s0036-46652000000100001.

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A total of 73 isolates (57 Enterobacter cloacae and 16 Enterobacter agglomerans), recovered during an outbreak of bacteremia in the Campinas area, São Paulo, Brazil, were studied. Of these isolates, 61 were from parenteral nutrition solutions, 9 from blood cultures, 2 from a sealed bottle of parenteral nutrition solution, and one was of unknown origin. Of the 57 E. cloacae isolates, 54 were biotype 26, two were biotype 66 and one was non-typable. Of 39 E. cloacae isolates submitted to ribotyping, 87.2% showed the same banding pattern after cleavage with EcoRI and BamHI. No important difference

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Martinez, Dianny, Hectorina E. Rodulfo, Lucy Rodriguez та ін. "FIRST REPORT OF METALLO-β-LACTAMASES PRODUCING Enterobacter spp. STRAINS FROM VENEZUELA". Revista do Instituto de Medicina Tropical de São Paulo 56, № 1 (2014): 67–69. http://dx.doi.org/10.1590/s0036-46652014000100010.

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Clinical strains of Enterobacter were isolated from Cumana's Central Hospital in Venezuela, and classified as E. cloacae (21), E. aerogenes (7), E. intermedium (1), E. sakazakii (1) and three unclassified. The strains showed high levels of resistance, especially to SXT (58.1%), CRO (48.8%), CAZ (46.6%), PIP (46.4%), CIP (45.2%) and ATM (43.3%). This is the first report for South America of blaVIM-2 in two E. cloacae and one Enterobacter sp., which also showed multiple mechanisms of resistance. Both E. cloacae showed blaTEM-1, but only one showed blaCTX-M-15 gene, while no blaSHV was detected.

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Naveed, Muhammad, Khizra Jabeen, Rubina Naz, et al. "Regulation of Host Immune Response against Enterobacter cloacae Proteins via Computational mRNA Vaccine Design through Transcriptional Modification." Microorganisms 10, no. 8 (2022): 1621. http://dx.doi.org/10.3390/microorganisms10081621.

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Enterobacter cloacae is mainly responsible for sepsis, urethritis, and respiratory tract infections. These bacteria may affect the transcription of the host and particularly their immune system by producing changes in their epigenetics. In the present study, four proteins of Enterobacter cloacae were used to predict the epitopes for the construction of an mRNA vaccine against Enterobacter cloacae infections. In order to generate cellular and humoral responses, various immunoinformatic-based approaches were used for developing the vaccine. The molecular docking analysis was performed for predic

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Sofatin, Septyani, Ania Citraresmini, and Dirga Sapta Sara. "Increasing the Effectivity of Liquid Organic Fertilizer Enriched with Enterobacter cloacae to increase Phosphate Availability and Yield of Maize in Inceptisols." E3S Web of Conferences 444 (2023): 04019. http://dx.doi.org/10.1051/e3sconf/202344404019.

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Inceptisols have problems of low availability of phosphorus. To improve soil phosphate and P fertilizer efficiency, it is necessary to develop fertilizer enriched with phosphate solubilizing bacteria (PSB). Liquid organic fertilizer enriched with PSB is expected to increase the efficiency in fertilization and improve the yield of sweet corn plants. This study was aimed to determine the effectiveness of liquid organic fertilizer enriched with Enterobacter cloacae on phosphate availability and increase the yield of maize (Zea mays L.) in Jatinangor Inceptisols. This experiment has been carried o

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Hoffmann, Harald, Sibylle Stindl, Wolfgang Ludwig, et al. "Reassignment of Enterobacter dissolvens to Enterobacter cloacae as E. cloacae subspecies dissolvens comb. nov. and emended description of Enterobacter asburiae and Enterobacter kobei." Systematic and Applied Microbiology 28, no. 3 (2005): 196–205. http://dx.doi.org/10.1016/j.syapm.2004.12.010.

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Darmawati, Sri, Langkah Sembiring, Widya Asmara, Wayan T. Artama, and Masashi Kawaichi. "Phylogenetic relationship of Gram Negative Bacteria of Enterobacteriaceae Family in the Positive Widal Blood Cultures based on 16S rRNA Gene Sequences." Indonesian Journal of Biotechnology 19, no. 1 (2015): 64. http://dx.doi.org/10.22146/ijbiotech.8635.

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The purpose of this study was to analyze the phylogenetic relationship of Gram negative bacteria (3strains of Salmonella typhi, 1 strain of Escherichia coli, 1 strain of Serratia marcescens, and 3 strains of Enterobactercloacae) of Enterobacteriaceae family in positive Widal blood cultures based on 16S rRNA gene sequences. Theresults respectively showed that each two 16S rRNA gene clones of Serratia marcescens KD 08.4 had a closerelationship with 16S rRNA gene of Serrratia marcescens ATCC 13880 (similarity: 99.53-99.8%), Eschericia coliBA 30.1 with Eschericia coli ATCC 11775T (similarity: 99.3

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Maaliki, Naji, Jorge Verdecia, and Malleswari Ravi. "Elusive Enterobacter cloacae causing pacemaker endocarditis." IDCases 24 (2021): e01149. http://dx.doi.org/10.1016/j.idcr.2021.e01149.

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Liu, Wing-Yee, Chi-Fat Wong, Karl Ming-Kar Chung, Jing-Wei Jiang, and Frederick Chi-Ching Leung. "Comparative Genome Analysis of Enterobacter cloacae." PLoS ONE 8, no. 9 (2013): e74487. http://dx.doi.org/10.1371/journal.pone.0074487.

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Bannon, M. J., P. R. Stutchfield, A. M. Weindling, and V. Damjanovic. "Ciprofloxacin in neonatal Enterobacter cloacae septicaemia." Archives of Disease in Childhood 64, no. 10 Spec No (1989): 1388–91. http://dx.doi.org/10.1136/adc.64.10_spec_no.1388.

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Solans, R., P. Simeon, R. Cuenca, V. Fonollosa, J. Bago, and M. Vilardell. "Infectious discitis caused by Enterobacter cloacae." Annals of the Rheumatic Diseases 51, no. 7 (1992): 906–7. http://dx.doi.org/10.1136/ard.51.7.906.

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Yap, Ann-Chee, Wuen-Yew Teoh, Kok-Gan Chan, Kae-Shin Sim, and Yeun-Mun Choo. "A new oxathiolane from Enterobacter cloacae." Natural Product Research 29, no. 8 (2014): 722–26. http://dx.doi.org/10.1080/14786419.2014.983507.

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Dedania, Bhavtosh, and Shounak Majumder. "Spontaneous Enterobacter Cloacae Pyogenic Liver Abscess." American Journal of Gastroenterology 109 (October 2014): S377. http://dx.doi.org/10.14309/00000434-201410002-01276.

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Sanyal, D., and G. Dolan. "Enterobacter cloacae in a leukaemic patient." Journal of Hospital Infection 16, no. 2 (1990): 177–78. http://dx.doi.org/10.1016/0195-6701(90)90064-u.

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Riain, U. Ni, M. G. Cormican, J. Flynn, T. Smith, and M. Glennon. "PCR based fingerprinting of Enterobacter cloacae." Journal of Hospital Infection 27, no. 3 (1994): 237–40. http://dx.doi.org/10.1016/0195-6701(94)90131-7.

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Garza-González, Elvira, Sandra Iveth Mendoza Ibarra, Jorge M. Llaca-Díaz та Gloria M. Gonzalez. "Molecular characterization and antimicrobial susceptibility of extended-spectrum β-lactamase-producing Enterobacteriaceae isolates at a tertiary-care centre in Monterrey, Mexico". Journal of Medical Microbiology 60, № 1 (2011): 84–90. http://dx.doi.org/10.1099/jmm.0.022970-0.

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Our objective was to analyse phenotypic and genetic data of extended-spectrum β-lactamase (ESBL)-producing Klebsiella pneumoniae, Enterobacter cloacae, Escherichia coli and Serratia marcescens that cause infections in our hospital. Over a 3 year period, 342 randomly selected clinical Enterobacteriaceae isolates were tested for ESBL production and evaluated for the presence of the β-lactamase genes bla SHV, bla TEM, bla CTX-M and bla TLA-1. The antibiotic susceptibilities of these isolates were also determined, and the clonality of the isolates was assessed by PFGE. Based on our analyses, 33/92

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ROIG-SAGUÉS, ARTUR X., MANUELA HERNÁNDEZ-HERRERO, JOSE J. RODRÍGUEZ-JEREZ, EMILIO I. LÓPEZ-SABATER, and MARIA T. MORA-VENTURA. "Histidine Decarboxylase Activity of Enterobacter cloacae S15/19 during the Production of Ripened Sausages and Its Influence on the Formation of Cadaverine." Journal of Food Protection 60, no. 4 (1997): 430–32. http://dx.doi.org/10.4315/0362-028x-60.4.430.

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The histidine decarboxylase activity of Enterobacter cloacae S15/19 was studied during the production process of salchichón, a Spanish ripened sausage. Counts of fecal coliform and histidine decarboxylase bacteria decreased during the production process, showing a good correlation in both inoculated and control samples. In the samples inoculated with Enterobacter cloacae S15/19, fecal coliforms were undetectable the last day of the survey, while the population of histidine decarboxylase bacteria was over 2 log MPN/g. Despite the fact that inoculation with Enterobacter cloacae S15/19 increased

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Rahayu, Widyaningsih, Esti Handayani Hardi, and Gina Saptiani. "PATHOGENICITY OF BACTERIA ENTEROBACTERIACEAE ON ZEBRAFISH AS ANIMAL MODEL." Jurnal Veteriner 21, no. 4 (2020): 512–18. http://dx.doi.org/10.19087/jveteriner.2020.21.4.512.

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Enterobacteriaceae are Gram negative bacteria contain endotoxin and exotoxins which are requirements for pathogenic bacteria and act as opportunistic pathogens. The purpose of this research was to determine the ability of Enterobacteriaceae bacteria to infect zebrafish (Danio rerio) by observing anatomical pathology, mortality, time death and cumulative time of death. The method used in this research is a completely randomized design method (CRD). This research was conducted in three stages, first preparation of zebrasfish as animal model by average size 3-5cm and reach three months old. Secon

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Duponnois, Robin, Amadou M. BÂ, and Thierry Mateille. "Beneficial effects of Enterobacter cloacae and Pseudomonas mendocina for biocontrol of Meloidogyne incognita with the endospore-forming bacterium Pasteuria penetrans." Nematology 1, no. 1 (1999): 95–101. http://dx.doi.org/10.1163/156854199507901.

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Abstract Two rhizosphere bacteria, Enterobacter cloacae and Pseudomonas mendocina, were isolated from the rhizosphere of tomato plants growing in a soil heavily infested with both root-knot nematodes and the parasitoid endospore-forming bacterium Pasteuria penetrans. Bacteria E. cloacae and P. mendocina stimulated plant growth, inhibited the reproduction of the root knot nematode Meloidogyne incognita, and increased the attachment of the endospores of P. penetrans on the nematodes in vitro. E. cloacae significantly increased the reproduction of P. penetrans in plant roots. Consequently, the in

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Zhu, Bo, Miao-Miao Lou, Guan-Lin Xie, et al. "Enterobacter mori sp. nov., associated with bacterial wilt on Morus alba L." International Journal of Systematic and Evolutionary Microbiology 61, no. 11 (2011): 2769–74. http://dx.doi.org/10.1099/ijs.0.028613-0.

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Two isolates of mulberry-pathogenic bacteria isolated from diseased mulberry roots were investigated in a polyphasic taxonomic study. Comparative 16S rRNA gene sequence analysis combined with rpoB gene sequence analysis allocated strains R18-2T and R3-3 to the genus Enterobacter, with Enterobacter asburiae, E. amnigenus, E. cancerogenus, E. cloacae subsp. cloacae, E. cloacae subsp. dissolvens and E. nimipressuralis as their closest relatives. Cells of the isolates were Gram-negative, facultatively anaerobic rods, 0.3–1.0 µm wide and 0.8–2.0 µm long, with peritrichous flagella, showing a DNA G+

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Simi, S., G. V. Carbonell, R. M. Falcón, et al. "A low molecular weight enterotoxic hemolysin from clinical Enterobacter cloacae." Canadian Journal of Microbiology 49, no. 7 (2003): 479–82. http://dx.doi.org/10.1139/w03-060.

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Seven of 50 Enterobacter cloacae strains from clinical isolates produced small turbid zones of hemolysis in horse and sheep blood agar plates, and the culture supernatants were also positive for hemolytic activity. The hem o l y sin was partially purified from the culture supernatant of E. cloacae by ultrafiltration (PM-10 membrane) and extraction with acetone. Semipurified hemolysin was stable to heating (100 °C, 30 min) and was soluble in organic solvents (acetone, ethanol, and methanol). The toxin showed no loss of biological activity after treatment with trypsin and was stable to acid trea

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Ehrhardt, A. F., C. C. Sanders, J. R. Romero, and J. S. Leser. "Sequencing and analysis of four new Enterobacter ampD Alleles." Antimicrobial Agents and Chemotherapy 40, no. 8 (1996): 1953–56. http://dx.doi.org/10.1128/aac.40.8.1953.

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Sequences of ampD genes from wild-type, temperature-sensitive, and stably derepressed mutants of the wild-type strain of Enterobacter cloacae 029 and the hyperinducible strain E. cloacae 1194E were determined and compared with the ampD gene of the wild-type strain E. cloacae 14. Seventy nucleotide differences were found between the wild-type sequences, resulting in 13 amino acid changes. The deduced amino acid changes do not correspond to published AmpC regulation mutations and expand the number of known mutations leading to altered AmpC beta-lactamase expression in members of the family Enter

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Sowbaranika, U., K. Ashokkumar, G. Abirami, Samson S. Miller, and Balu Prakash. "Characterization and Application of Biosurfactant producing Bacteria and Nanoparticle Synthesis for Bioremediation and Plant Growth Promotion." Research Journal of Biotechnology 20, no. 7 (2025): 19–24. https://doi.org/10.25303/207rjbt019024.

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Biosurfactants are surface-active biomolecules with significant applications in bioremediation, particularly for the breakdown of hydrocarbon pollutants. This study investigates the isolation and characterization of biosurfactant-producing bacterial strains from oil-contaminated soils in Chennai, India, with a focus on Enterobacter cloacae. Screening assays including hemolysis, oil spreading and emulsification, identified Enterobacter cloacae as a promising candidate. Optimal production conditions: 37°C, pH 7, glucose and casein as carbon and nitrogen sources, yielded a high-performance biosur

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Zaid, A. M., J. M. Bonasera, and S. V. Beer. "First Report of Enterobacter Bulb Decay of Onions Caused by Enterobacter cloacae in New York." Plant Disease 95, no. 12 (2011): 1581. http://dx.doi.org/10.1094/pdis-05-11-0375.

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During the summer of 2010, onions (Allium cepa L.) of several cultivars growing in muck-land soils in Orange, Genesee, Orleans, and Oswego counties of New York exhibited leaf dieback and bulb decay consistent with disease symptoms caused by Enterobacter cloacae as described previously (1,3,4). Isolations of bacteria from symptomatic tissues and muck soil were made using onion extract medium (OEM), which contains extracts of autoclaved onions, salts, and inhibitors of fungi and gram-positive bacteria. Some presumptive strains of E. cloacae were isolated; 5 from symptomatic onions growing in Gen

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Roberts, D. P., A. M. Marty, P. D. Dery, and J. S. Hartung. "Isolation and modulation of growth of a colonization-impaired strain of Enterobacter cloacae in cucumber spermosphere." Canadian Journal of Microbiology 42, no. 2 (1996): 196–201. http://dx.doi.org/10.1139/m96-030.

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Enterobacter cloacae A-46 was isolated for use in an environmental containment strategy for genetically modified derivative strains with enhanced biocontrol activity. The population of E. cloacae A-46, a transposon mutant of the plant-beneficial bacterium E. cloacae 501R3, increased 10-fold (significant increase at P ≤ 0.05) in cucumber spermosphere when applied to cucumber seeds along with casamino acids. In contrast, strain A-46 was incapable of proliferation in cucumber spermosphere in the absence of casamino acids. Populations of strain A-46 also failed to increase in corn, cowpea, sunflow

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Haider Salih Abbas, Dhay, and Nabil Salim Saaid Tuwaij. "Screening of Tetracycline’s Resistance Genes among Enterobacter cloacae and Citrobacter spp. isolates." BIO Web of Conferences 139 (2024): 06035. http://dx.doi.org/10.1051/bioconf/202413906035.

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There has been a growing prevalence of tetracycline-resistant bacteria across many species and genera. As a consequence, the efficacy of tetracycline treatment has diminished with time. So this work aimed to study of tetracycline-resistant genes among Enterobacter cloacae and Citrobacter spp. Out of a total of 364 clinical specimens, 135 (37.08%) exhibited bacterial growth. Out of the total, 22 (6.04%) were classified as gram-positive bacteria, 102 (28.02%) as gram-negative bacteria, and 11 (3.02%) as mixed growth (including both gram-negative and gram-positive bacteria). The Vitek-2 system fi

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