enterobacter aerogenes in bergey s manual
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enterobacter aerogenes in bergey s manualHowever, the history of some species now placed in the genus Enterobacter can be traced, albeit with some confusion, to the end of the 19th century. “ Bacillus lactis aerogenes ” was isolated by Escherich (1885) from milk and renamed “ Bacillus aerogenes ” by Kruse (1896) and “ Aerobacter aerogenes ” by Beijerinck (1900). Until 1955, differentiation of this organism from Friedlander’s bacillus (now called Klebsiella pneumoniae ) was not clear, and most authors considered “ B. lactis aerogenes ” or “ Aerobacter aerogenes ” to be either nonmotile or to contain both motile and nonmotile strains ( Grimbert and Legros, 1900; Edwards and Fife, 1955 ). This led Edwards and Fife (1955) to state that “ A. aerogenes ” strains were in fact Klebsiella strains. In the first. This process is experimental and the keywords may be updated as the learning algorithm improves.The “Herbicola” group. Report on water supply and sewerage (part II). Reports of the Massachusetts Board of Public Health Google Scholar Judicial Commission. 1963 Opinion 28 Rejection of the bacterial generic name Cloaca Castellani and Chalmers and acceptance of Enterobacter Hormaeche and Edwards as a bacterial generic name with type species Enterobacter cloacae (Jordan) Hormaeche and Edwards. International Bulletin of Bacteriological Nomenclature and Taxonomy 13 38 Google Scholar Judicial Commission. 1973 Opinion 48 Rejection of the name Aerobacter liquefaciens Beijerinck and conservation of the name Aeromonas Stanier with Aeromonas hydrophila as the type species. In: Buchanan, R. E., and Gibbons, N. E. (ed.), Bergey’s manual of determinative bacteriology, 8th ed. Growth of microbiol pathogens in fluids of intravenous infusion.In: Dworkin M., Falkow S., Rosenberg E., Schleifer KH., Stackebrandt E. (eds) The Prokaryotes. Springer, New York, NY. Angela Lacombe-Antoneli, S. Piriz, S.http://www.emilioborsani.it/fckloaded/dishwashers-service-manuals.xml
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Vadillo Acta veterinaria Hungarica 2007 2 Selection of proteolytic bacteria with ability to inhibit Vibrio harveyi during white shrimp (Litopenaeus vannamei) cultivation Pattamarat Rattanachuay, D. Kantachote, P. Suntinanalert 2007 11 Inhibition ofListeria monocytogenes by plantaricin NA, an antibacterial substance fromLactobacillus plantarum N. A. Olasupo Folia Microbiologica 2008 13 503 Citations Fields of Study Fields of Study All Fields Art Biology Business Computer Science Chemistry Economics Engineering Environmental Science Geography Geology History Materials Science Mathematics Medicine Philosophy Physics Political Science Psychology Sociology Citation Type Citation Type All Types Cites Results Cites Methods Cites Background Has PDF More Filters More Filters Filters Sort by Relevance Sort by Most Influenced Papers Sort by Citation Count Sort by Recency In vitro antimicrobial susceptibility of anaerobic bacteria isolated from caprine footrot. Angela Lacombe-Antoneli, S. Piriz, S. Vadillo Biology, Medicine 2007 2 Save Alert Research Feed Selection of proteolytic bacteria with ability to inhibit Vibrio harveyi during white shrimp (Litopenaeus vannamei) cultivation Pattamarat Rattanachuay, D. Kantachote, P. Suntinanalert Biology 2007 11 Save Alert Research Feed Inhibition ofListeria monocytogenes by plantaricin NA, an antibacterial substance fromLactobacillus plantarum N. A. Olasupo Biology 2008 13 Save Alert Research Feed Complete Genome Sequence of Pseudomonas sp. UK4, a Model Organism for Studies of Functional Amyloids in Pseudomonas M. Dueholm, Heidi Nolsoe Danielsen, P. Nielsen Medicine, Biology 2014 7 Save Alert Research Feed Actinomyces naturae sp. nov., the first Actinomyces sp. You may have to register before you can post: click the register link above to proceed. To start viewing messages, select the forum that you want to visit from the selection below.http://www.imagemarte.com.br/arquivos/disk-jockey-pro-it-manual.xml Section, Division of Bacterial and Mycotic Diseases, Atlanta, GA, 30333 USA Search for more papers by this author Section, Division of Bacterial and Mycotic Diseases, Atlanta, GA, 30333 USA Search for more papers by this author I have read and accept the Wiley Online Library Terms and Conditions of Use Shareable Link Use the link below to share a full-text version of this article with your friends and colleagues. Learn more. Copy URL Rahn's original derivation of the name Enterobacteriaceae is not certain. It may have come from his genus Enterobacter, or may have come from the root enterobacterium. I have read and accept the Wiley Online Library Terms and Conditions of Use Shareable Link Use the link below to share a full-text version of this article with your friends and colleagues. Learn more. Copy URL Conform to the general definition of the family Enterobacteriaceae. Gram negative. Motile by peritrichous flagella or nonmotile. Aerobic and facultatively anaerobic having both a respiratory and a fermentative type of metabolism, but anaerogenic biotypes occur. Oxidase negative. Chemoorganotrophic. Both acid and gas are formed from most fermentable carbohydrates, but i ?inositol is not utilized and D ?adonitol is utilized only by Escherichia fergusonii. Lactose is fermented by most strains of Escherichia coli Do not grow in KCN ( with the exception of E. The Board, with some changes in membership and Dr Bergey as Chairman, published a second edition of the Manual in 1925 and a third edition in 1930. (from About Bergey's Trust ) These copies cannot be checked out. It can be checked out. Biochemical tests such as indole production test, methyl red test, Voges- Proskauer test, citrate utilization etc. By automating the analysis process of biochemical results, sorting (clustering), and identification of particular genera, the difficulties associated with manual sorting could be resolved..http://dev.pb-adcon.de/node/15232 BioCluster: Tool for Identification and Clustering of Enterobacteriaceae Based on Biochemical Data Article Full-text available Jul 2015 Ahmed Abdullah SM Sabbir Alam Mosa Sultana Mohammed Anwar Hossain Presumptive identification of different Enterobacteriaceae species is routinely achieved based on the biochemical properties. Traditional practice includes manual comparison of each biochemical property of the unknown sample with known reference samples and inference of its identity based on the maximum similarity pattern with the known samples. This process is labor-intensive, time-consuming, error-prone, and subjective. Therefore, automation of sorting and similarity calculation would be advantageous. Here we present a MATLAB-based graphical user interface (GUI) tool named BioCluster. This tool was designed for automated clustering and identification of Enterobacteriaceae based on biochemical test results. In this tool, we used two types of algorithms, i.e., traditional hierarchical clustering (HC) and the Improved Hierarchical Clustering (IHC), a modified algorithm that was developed specifically for the clustering and identification of Enterobacterioceae species. IHC takes into account the variability in result of 1-47 biochemical tests within this Enterobacterioceae family. This tool also provides different options to optimize the clustering in a user-friendly way. Using computer-generated synthetic data and some real data, we have demonstrated that BioCluster has high accuracy in clustering and identifying enterobacterial species based on biochemical test data. This tool can be freely downloaded at. View Show abstract. Le traitement des donnees repose sur l'analyse des quantiles des denombrementsdeC-III. Many other strategies appear to have improved bacterial identification accuracy, such as automated cellular fatty acid (CFA) analysis, yet these strategies require expensive system and standardized culture condition...http://gromoga.com/images/compaq-armada-e700-manual.pdf Many other strategies appear to have improved bacterial identification accuracy, such as automated cellular fatty acid (CFA) analysis, yet these strategies require expensive system and standardized culture condition. Therefore, we selected the Lactobacillaceae family as a representative of bacterial population with several industrial and health importance44454647 to be used in developing FN-Identify method and algorithms.. FN-Identify: Novel Restriction Enzymes-Based Method for Bacterial Identification in Absence of Genome Sequencing Article Full-text available Dec 2015 Mohammed Awad Osama Ouda Ali El-Refy Mohamed Helmy Sequencing and restriction analysis of genes like 16S rRNA and HSP60 are intensively used for molecular identification in the microbial communities. With aid of the rapid progress in bioinformatics, genome sequencing became the method of choice for bacterial identification. However, the genome sequencing technology is still out of reach in the developing countries. In this paper, we propose FN-Identify, a sequencing-free method for bacterial identification. FN-Identify exploits the gene sequences data available in GenBank and other databases and the two algorithms that we developed, CreateScheme and GeneIdentify, to create a restriction enzyme-based identification scheme. FN-Identify was tested using three different and diverse bacterial populations (members of. LactobacillusMycobacteriumThe analysis of the restriction maps of the members of three groups using the fragment numbers information only or along with fragments sizes successfully identified all of the members of the three groups using a minimum of four and maximum of eight restriction enzymes. Our results demonstrate the utility and accuracy of FN-Identify method and its two algorithms as an alternative method that uses the standard microbiology laboratories techniques when the genome sequencing is not available. They may be alone or forming pairs, usually have no capsule and feature motile with 5 polar flagella in one pole. In hospitals, S. marcescens bacteria has been involved in necrotic fasciitis in patients treated with steroids in bullous cellulitis after animal bite and in hemodialysis patients or skin ulcers... Negative reaction in methyl red test, as well as for indole production.Previously known only as commensal micro-organisms are known today to be responsible for serious health problems worldwide mainly in immunocompromised patients, being reported many outbreaks associated with these bacteria. Micro-organisms belonging to the CESP group are related to infections in many sites such as respiratory tract, urinary tract, gastrointestinal, colonizing wounds and devices, especially in hospitalized patients. Are producers of beta-lactamase chromosome inducible, such as the AMPc enzyme type that during use of antimicrobials can express an increase in the production of beta-lactam resistance. Also noteworthy is the production of beta-lactamases of extended spectrum and carbapenemase. It is believed that the transmission of bacteria from CESP group among patients in the hospital environment is amplified due to the lower adherence to hand hygiene by healthcare professionals. Due to its multidrug resistance, its therapeutic option is limited and the best choice is the fourth generation of cephalosporins such as cefepime and tigecycline (glycylcycline). As a member of the Enterobacteriaceae family, E. coli in general contain between 48.5 and 52.1 percent guaninecytosine in their DNA ( Brenner et al., 2005 ). E. coli can be isolated from humans and numerous animal hosts, and occur throughout most of the gastrointestinal tract.. Shiga Toxin-Producing Escherichia coli in Food: Incidence, Ecology, and Detection Strategies Article Jan 2016 FOOD CONTROL Adam Baker Peter Rubinelli Si Hong Park Steve Ricke Commensal Escherichia coli are commonly utilized for investigating the genetic and biochemical requirements of microorganisms, and have served in a wide variety of applications. Pathogenic E. coli known as Shiga toxin (Stx)-producing E. coli (STEC) are associated with various food products including ground beef. These pathogens are present in a wide range of environments, and have caused numerous foodborne outbreaks and recalls. These outbreaks and the increased awareness of STEC have led to certain STEC serotypes to be declared adulterants in non-intact raw meat. Various STEC detection methods have been investigated, and numerous cultural and molecular-based detection methods continue to be modified to meet regulatory requirements. However, STEC serotypes may possess certain characteristics that lead to bias in the likelihood of a certain serotype being detected in an assay. Understanding the characteristics of these STEC serotypes will provide means for optimizing the detection platforms, and as a result limit foodborne illness and recalls caused by STEC due to enhanced cultural and molecular detection capabilities. The time of colonies' appearance, their size, and morphology were recorded. Getting proper raw material of sugar beets (roots) is a problem for agriculture. Some disease symptoms observed on sugar beet roots are atypical tumor-like deformations. The causative agent of these deformations is known in the old literature as Xanthomonas beticola. The disease’s name in Poland is “tuberkuloza” and in the USA it refers to a description of a pocket disease—therefore we may consider those diseases to be the same. The clear description of X. beticola disease can be found in many phytopathological manuals printed in the past and nowadays. Symptoms of the disease were noted in Poland last year, and the preliminary data of the yield quality show that the quality of diseased roots is worse (less sugar content) than of healthy roots. For the proper disease diagnoses, the literature was searched and this searching lead us to conclusion that there is no simple way to recognize the causal organism in the field conditions, and we suppose that X. beticola does not exist. Selected isolate STJP (on the basis of phosphate solubilization ability) was identified by phenotypic (flagellated or non-flagellated, shape and size) and biochemical features such as oxidase, urease, catalase, gelatinase, indole, H 2 S, citrate, and nitrate production as per Bergey's Manual of Systematic Bacteriology (Garrity 2005). The cell shape of the bacterium was confirmed by scanning electron microscopy (SEM) performed according to the method of Golding et al. (2016)... Isolate STJP was found positive for oxidase, urease, catalase, and gelatinase, but negative for indole, H 2 S, citrate, and nitrate production. On the basis of phenotypic and biochemical traits, isolate STJP was found to be a member of genus Bacillus sp.The comparison of the whole 16S rRNA gene sequence of a neighbour isolate of STJP showed 99 similarities with Bacillus safensis strain NBRC 100820.. Phosphate-solubilizing Bacillus sp.In addition to phosphate solubilization ability, isolate Bacillus sp. Amongst all the treatments, highest oil yield and menthol content were observed when treated with Bacillus sp. STJP along with TCP can be used to increase the production of menthol and oil yield of M. arvensis. This approach of using fertilizer along with phosphate solubilizing Bacillus sp.A combined use of efficient phosphate solubilising bacteria loaded with plant growth promoting characters along with TCP can thus be far effective way for enhancing the yield of crops in a sustainable manner. View Show abstract.Relatively little is known about the species composition and ecology of these biofilms due to challenges associated with sample acquisition from actual DWDS. We report the analysis of biofilms from five pipe samples collected from the same region of a DWDS in Florida, USA, over an 18 month period between February 2011 and August 2012. The bacterial abundance and composition of biofilm communities within the pipes were analyzed by heterotrophic plate counts and tag pyrosequencing of 16S rRNA genes, respectively. Bacterial numbers varied significantly based on sampling date and were positively correlated with water temperature and the concentration of nitrate. However, there was no significant relationship between the concentration of disinfectant in the drinking water (monochloramine) and the abundance of bacteria within the biofilms. Pyrosequencing analysis identified a total of 677 operational taxonomic units (OTUs) (3 distance) within the biofilms but indicated that community diversity was low and varied between sampling dates. Biofilms were dominated by a few taxa, specifically Methylomonas, Acinetobacter, Mycobacterium, and Xanthomonadaceae, and the dominant taxa within the biofilms varied dramatically between sampling times. The drinking water characteristics most strongly correlated with bacterial community composition were concentrations of nitrate, ammonium, total chlorine and monochloramine, as well as alkalinity and hardness. Biofilms from the sampling date with the highest nitrate concentration were the most abundant and diverse and were dominated by Acinetobacter. The supply of Fe(II) in the form of FeSO 4 might be attributed to this microbial succession.. Chemolithotrophic denitrification by nitrate-dependent anaerobic iron oxidizing (NAIO) process: Insights into the evaluation of seeding sludge Article Mar 2018 CHEM ENG J Meng Zhang Zhugucheng Zhang Shuxian Wen Ping Zheng Nitrate-dependent anaerobic iron oxidation (NAIO) is a chemolithotrophic bioprocess that converts nitrate to. Seeding sludge is vital for the application of NAIO process, but scarce information is available about the capability of active sludge. In this work, activated sludge (AS) and anaerobic granular sludge (AGS) were investigated for their NAIO performance, and AGS was preferred as inocula after systematic evaluation on three aspects. The present work clarifies about the choice of seeding sludge for the application of the chemolithotrophic NAIO process and for the development of biotechnology. Among all, isolate PF23 was selected as it produced highest amount of EPS on exposure to salt stress... Isolate PF23 was selected from the collection of pseudomonads, as it displayed maximum stress tolerance capacity and high EPS production. The comparison of complete 16S rRNA gene sequence (Fig. 1) of the isolate PF23 with the sequence of the other strains of the genus Pseudomonas showed 99 relatedness to Pseudomonas aeruginosa (Gen Bank accession number AB691548.1 and KC417305.1).. Screening for MCL-PHA-Producing Fluorescent Pseudomonads and Comparison of MCL-PHA Production Under Iso-osmotic Conditions Induced by PEG and NaCl Article Full-text available Dec 2013 Curr Microbiol Ekta Khare Jyotsana Chopra Naveen Arora The medium chain length polyhydroxyalkanoates (MCL-PHA) have attracted much attention from academic and industrial communities for their interesting applications in medical field. The aim of this study was to screen high MCL-PHA-producing fluorescent pseudomonads, and to compare the effect of osmotic stress generated by NaCl (ionic) and polyethylene glycol (PEG, non-ionic inert polymer) on PHA production. A total of 50 fluorescent pseudomonads isolated from rhizospheric soil were screened for PHA production by Sudan Black staining. Out of all the PHA-producing isolates only five were MCL-PHA producers as detected by MCL-PCR. Isolate Bar1 identified as Pseudomonas fluorescens by 16S rRNA gene sequencing was selected for further analysis due to its high MCL-PHA production ability. The iso-osmotic stress generated by NaCl and PEG-6000 showed 5.75- and 3.19-fold enhanced production of PHA at -2 bar osmotic potential, over control (0 bar), respectively. There was 1.8-fold enhanced production of PHA at -2 bar osmotic stress induced by NaCl over PEG. PEG reduces availability of water to microorganisms without reducing exogenously provided nutrients which appear to be responsible for its down performance over NaCl. The FTIR analysis of PHA sample purified from cells showed strong marker bands near 1742, 2870, 1170, 1099, and 2926 cm(-1), corresponding to MCL-PHA. The study reported that supplementation of NaCl (electrolyte) in growth media enhances the production of MCL-PHA which can be very useful for its industrial production. Finally, this methodology will permit selection of the best pentose isomerase to be studied and allow preliminary comparisons between different L-arabinose isomerases through evaluation of the enzymatic activity of cell-free extracts.Table 1 shows the group of 29 bacterial strains used in this study. All of them were species or subspecies previously identified employing the taxonomic keys given by the 2 nd Edition of Bergey's Manual of Systematic Bacteriology Volume 2 Part B ( Brenner et al., 2005 ) and Volume 3 (De Vos et al., 2009) except for Enterococcus faecium DBFIQ ID: E36, which was also PCR-identified by partial sequencing of 16S rDNA. In the case of E. faecium DBFIQ ID: E36, vancomycin resistance and ?-hemolysis tests were also performed.. Screening and selection of wild strains for L-arabinose isomerase production Article Full-text available Dec 2013 BRAZ J CHEM ENG Ricardo M. Manzo Arturo Carlos Simonetta Amelia C Rubiolo Enrique Mammarella The majority of L-arabinose isomerases have been isolated by recombinant techniques, but this methodology implies a reduced technological application. From all evaluated bacterial strains, Enterococcus faecium DBFIQ ID: E36, Enterococcus faecium DBFIQ ID: ETW4 and Pediococcus acidilactici ATCC ID: 8042 were, in this order, the best L-arabinose fermenting strains. Afterwards, to assay L-arabinose metabolization and L-arabinose isomerase activity, cell-free extract and saline precipitated cell-free extract of the three bacterial cultures were obtained and the production of ketoses was determined by the cysteine carbazole sulfuric acid method. Results showed that the greater the L-arabinose metabolization ability, the higher the enzymatic activity achieved, so Enterococcus faecium DBFIQ ID: E36 was selected to continue with production, purification and characterization studies. This work thus describes a simple microbiological method for the selection of L-arabinose fermenting bacteria for the potential production of the enzyme L-arabinose isomerase. Stenotrophomonas and Achromobacter were also common in the Cluster 1 samples, and members of both of these bacterial genera are known opportunistic pathogens involved in nosocomial infections of immunocompromised patients. These characteristics have not been previously described in Porites and do not match common Caribbean coral diseases. The lesions were observed only in warmer months and at shallow depths on the fore reef in Belize. Analysis of the microbial community composition based on the V4 hypervariable region of 16S ribosomal RNA genes revealed that the surface microbiomes associated with nonsymptomatic corals were dominated by the members of the genus Endozoicomonas, consistent with other studies. Comparison of the microbiomes of nonsymptomatic and lesioned coral colonies sampled in July and September revealed two distinct groups, inconsistently related to the disease state of the coral, but showing some temporal signal. The loss of Endozoicomonas was characteristic of lesioned corals, which also harbored potential opportunistic pathogens such as Alternaria, Stenotrophomonas, and Achromobacter. The presence of lesions in P. astreoides coincided with a decrease in the relative abundance of Endozoicomonas, rather than the appearance of specific pathogenic taxa. View Show abstract. P. aeruginosa is a well-recorded cause of nosocomial infections among infants in neonatal intensive care units (Foca et al., 2000). Particularly vulnerable targets are the individuals with fatal burns, or those who have been subjected to surgical procedures, catheterization, and treatment with broad -spectrum antibiotics ( Garrity et al., 2005 ). This organism's ability to persist and multiply in moist environments, and on moist equipments (e.g.. In Vitro Antibacterial Activity of Emblica officinalis and Tamarindus indica Seed Extracts against Multidrug Resistant Acinetobacter baumannii. Article Full-text available Jan 2014 Vijay Kothari Abstract - Seed extracts of Emblica officinalis, Tamarindus indica, Sygyzium cumini, and Manilkara zapota, prepared in View Show abstract. These results were confirmed using API 20NE system and the numerical profile is presented inTable 3. Our results show the biodiversity of the activated sludge samples obtained from wastewater plants of Khenchela. Three of these strains which are Acinetobacter junii, Pseudomonas aeruginosa, Moraxella lacunata belong to the.We also show that Proteobacteria are the most abundant with a rate of 87.5.. Screening of Bacteria Isolated from Activated Sludges for Phosphate Removal from Wastewater Article Full-text available Jan 2015 Oumaima Naili Messaoud Benounis Leyla Benammar The objective of the current study is to isolate phosphate removing microbes from activated sludge for wastewater remediation in the area of Khenchela (Eastern Algeria). Phosphate rate was determined using colorimetric method and batch tests were developed to evaluate the biomass composition of the sludge. Four efficient pure strains isolated from activated sludge samples and identified as Acinetobacter junii, Pseudomonas aeruginosa, Moraxella lacunata, Alcaligenes denitrificans. Our results show that applying of mixed bacterial culture containing mostly isolated strains for bioremediation purpose can be used successfully for the elimination of phosphate from activated sludge of wastewater treatment plants. From the identified strains, six were confirmed as P. syringae using 16S rRNA, with identities of 99 with P. syringae pv glycinea, P. syringae pv tabaci and P. syringae pv syringae. This species is a fluorescent pseudomonad clustering within rRNA similarity Group I of the genus Pseudomonas ( Brenner et al. 2005 ). The steps followed in this work to isolate and identify phytopathogenic pseudomonads re-affirm the need to combine biochemical and molecular methods to obtain the definitive identity of a microorganism.. Antimicrobial activity of essential oils of Thymus vulgaris and Oreganum vulgare on phytopathogenic strains isolated from soybean Article Full-text available Oct 2014 Maria de las Mercedes Oliva Maria Evangelina Carezzano Milena Giuliano Mirta Susana Demo The aim of this work was to study the antimicrobial activity of essential oils obtained from Thymus vulgaris (thyme) and Oreganum vulgare (oregano) on phytopathogenic Pseudomonas species isolated from soybean. Strains with characteristics of P. syringae were isolated from leaves of soybean plants with blight symptoms. Ten of these could be identified in Group Ia of LOPAT as P. syringae. Six of these were confirmed as P. syringae using 16S rRNA, indicating the presence of these phytopathogenic bacteria in east and central Argentina. All the phytopathogenic bacteria were re-isolated and identified from the infected plants. MIC values for thyme were 11.5 mg ml?1 and 5.7 mg ml?1 on P. syringae strains, while oregano showed variability in the inhibitory activity. Both essential oils inhibited all P. syringae strains, with better inhibitory activity than the antibiotic streptomycin. The oils were not bactericidal for all pseudomonads. Both oils contained high carvacrol (29.5 and 19.7, respectively) and low thymol (1.5). Natural products obtained from aromatic plants represent potential sources of molecules with biological activity that could be used as new alternatives for the treatment of phytopathogenic bacteria infections.This article is protected by copyright. All rights reserved. Esterase activity was observed when A. faecalis MOR02 used Tween 80 as a substrate and fatty acids were released. Swarming motility was observed in TSA (Trypticase Soy Agar) plates inoculated with the bacteria, where zones of consolidation or terraces, commonly known as bull's eye, were observed.. Identification of a New Alcaligenes faecalis Strain MOR02 and Assessment of Its Toxicity and Pathogenicity to Insects Article Full-text available Dec 2014 J Biomed Biotechnol Rosa ESTELA Quiroz Castaneda Ared Mendoza Veronica Obregon-Barboza Edgar Dantan We report the isolation of a bacterium from Galleria mellonella larva and its identification using genome sequencing and phylogenomic analysis. This bacterium was named Alcaligenes faecalis strain MOR02. Microscopic analyses revealed that the bacteria are located in the esophagus and intestine of the nematodes Steinernema feltiae, S. carpocapsae, and H. bacteriophora. Using G.