The Coliform Kind: E. Coli and Its “Cousins” the Good, the Bad, and the Deadly
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High Dose Antimicrobial Protocols for Canine Urinary Tract Infections
High Dose Antimicrobial Protocols for Canine Urinary Tract Infections Thesis Presented in Partial Fulfillment of the Requirements for the Masters of Science in the Graduate School of The Ohio State University By Sara J. Irom, D.V.M. Graduate Program in Veterinary Clinical Sciences The Ohio State University 2010 Thesis Committee: Joshua Daniels, Advisor Dennis Chew Andrew Hillier Copyright by Sara J. Irom 2010 Abstract Background: Treatment for canine urinary tract infections (UTI) typically consists of 7- 14 days of empirically chosen antimicrobial drugs. Enrofloxacin is a veterinary approved fluoroquinolone (FQ) antimicrobial and is useful for treatment of canine UTI. Ciprofloxacin, the primary metabolite of enrofloxacin, contributes additive antimicrobial activity. Higher doses of FQs may inhibit the emergence of antimicrobial resistance. Objectives: 1) Determine if dogs with naturally occurring uncomplicated UTI have equivalent microbiologic cure with a high dose short duration protocol of enrofloxacin, compared to a standard antimicrobial protocol. 2) Measure urine concentrations of enrofloxacin, and ciprofloxacin, following a 20mg/kg single oral dose in healthy dogs (n=6). Animals: Client-owned dogs with naturally occurring, uncomplicated UTI (n=38), and healthy dogs owned by students and staff of OSU-VMC (n=6). Methods: A multi-center clinical trial was conducted. Dogs were assigned to 1 of 2 groups in a randomized blinded manner. Dogs in group 1 received treatment with 18- 20mg/kg oral enrofloxacin (Baytril®) once daily for 3 consecutive days. Dogs in Group 2 were treated with 13.75-25mg/kg oral amoxicillin-clavulante (Clavamox®) twice daily ii for 14 days. Urine and plasma concentrations of enrofloxacin and ciprofloxacin were measured following a single dose of 20mg/kg oral enrofloxacin in 6 healthy dogs. -
Bacteriological Contamination of Drinking Water Wells
Wisconsin Department of Natural Resources, Bureau of Drinking Water and Groundwater PUB-DG-003-2017 Bacteriological Contamination of Drinking Water Wells ost private wells provide a safe and uncontaminated source of drinking Mwater. Some wells do however become contaminated with bacteria. Fortunately certified labs can easily test water for coliform bacteria, a common indicator of bacterial contamination in wells. To ensure your well is not contaminated, it is a good idea to regularly test your water. You should have your water tested at least annually and whenever you notice a change in the taste, odor or color of the water. Most bacteria entering the ground surface along with rainwater or snowmelt are filtered out as the water seeps through the soil. Several strains of bacteria can survive a long time and find their way into the groundwater by moving through coarse soils, shallow fractured bedrock, quarries, sinkholes, inadequately grouted wells or cracks in the well casing. Insects or small rodents can also carry bacteria into wells with inadequate caps or seals. Coliform bacteria are naturally occurring in soil and are found on vegetation and in surface waters. Water from a well properly located and constructed should be free of coliform bacteria. While coliform bacteria do not cause illness in healthy individuals, their presence in well water indicates the water system is at risk to more serious forms of contamination. The presence of another type of bacteria, Escherichia coli (E. coli), indicates fecal contamination of the water. Fecal coliform bacteria inhabit the intestines of warm-blooded animals and are typically found in their fecal matter. -
Total and Fecal Coliform Bacteria
TOTAL AND FECAL COLIFORM BACTERIA The coliform bacteria group consists of several types of bacteria belonging to the family enterobacteriaceae. These mostly harmless bacteria live in soil, water, and the digestive system of animals. Fecal coliform bacteria, which belong to this group, are present in large numbers in the feces and intestinal tracts of humans and other warm-blooded animals, and can enter water bodies from human and animal waste. If a large number of fecal coliform bacteria (over 200 colonies/100 milliliters or 200 cfu/100 ml) are found in water, it is possible that pathogenic (disease- or illness-causing) organisms are also present in the water. Fecal coliform by themselves are usually not pathogenic; they are indicator organisms, which means they may indicate the presence of other pathogenic bacteria. Pathogens are typically present in such small amounts it is impractical monitor them directly. For more information on E. coli and other pathogenic bacteria, see the U.S. FDA Center for Food Safety & Applied Nutrition's "Bad Bug Book" . Swimming in waters with high levels of fecal coliform bacteria increases the chance of developing illness (fever, nausea or stomach cramps) from pathogens entering the body through the mouth, nose, ears, or cuts in the skin. Diseases and illnesses that can be contracted in water with high fecal coliform counts include typhoid fever, hepatitis, gastroenteritis, dysentery and ear infections. Fecal coliform, like other bacteria, can usually be killed by boiling water or by treating it with chlorine. Washing thoroughly with soap after contact with contaminated water can also help prevent infections. -
Detection and Enumeration of Coliforms in Drinking Water: Current Methods and Emerging Approaches
Journal of Microbiological Methods 49 (2002) 31–54 www.elsevier.com/locate/jmicmeth Detection and enumeration of coliforms in drinking water: current methods and emerging approaches Annie Rompre´ a, Pierre Servais b,*, Julia Baudart a, Marie-Rene´e de-Roubin c, Patrick Laurent a aNSERC Industrial Chair on Drinking Water, Civil, Geological and Mining Engineering, Ecole Polytechnique of Montreal, PO Box 6079, succ. Centre Ville, Montreal, Quebec, Canada H3C 3A7 bEcologie des Syste`mes Aquatiques, Universite´ Libre de Bruxelles, Boulevard du Triomphe, Campus Plaine, CP 221, 1050, Brussels, Belgium cAnjou Recherche, 1 Place de Turenne, 94417 Saint Maurice Cedex, France Accepted 10 September 2001 Abstract The coliform group has been used extensively as an indicator of water quality and has historically led to the public health protection concept. The aim of this review is to examine methods currently in use or which can be proposed for the monitoring of coliforms in drinking water. Actually, the need for more rapid, sensitive and specific tests is essential in the water industry. Routine and widely accepted techniques are discussed, as are methods which have emerged from recent research developments. Approved traditional methods for coliform detection include the multiple-tube fermentation (MTF) technique and the membrane filter (MF) technique using different specific media and incubation conditions. These methods have limitations, however, such as duration of incubation, antagonistic organism interference, lack of specificity and poor detection of slow- growing or viable but non-culturable (VBNC) microorganisms. Nowadays, the simple and inexpensive membrane filter technique is the most widely used method for routine enumeration of coliforms in drinking water. -
Monitoring Antimicrobial Susceptibility in Bacterial Isolates Causing
Nepal Journal of Science and Technology (NJST) (2020), 19(1) : 133-141 DOI: https://doi.org/10.3126/njst.v19i1.29794 Monitoring Antimicrobial Susceptibility in Bacterial Isolates Causing Urinary Tract Infections in a Tertiary NS | Health Original Hospital in Kathmandu Vivek Kumar Singh1*,Mahesh Kumar Chaudhary2, Megha Raj Banjara3, and Reshma Tuladhar3 1Public Health and Infectious Disease Research Center, New Baneshwor, Kathmandu, Nepal, 2 KIST Medical College and Teaching Hospital, Imadole, Lalitpur, Nepal 3Central Department of Microbiology, Tribhuvan University, Kirtipur, Nepal *Corresponding Author [email protected] Abstract Urinary tract infection is the most common infection in females worldwide. One in three women experiences at least one episode of urinary tract infection during their lifetime. The objective of this study was to determine the etiology and antimicrobial profile of urinary tract infection. A cross-sectional study was conducted at a tertiary care hospital in Nepal. Thirteen hundred clean catch mid-stream urine samples were tested through standard microbiological techniques. The isolates from urine samples were identified from biochemical tests. Antibiotic susceptibility testing was performed through the Kirby-Bauer disc diffusion technique following CLSI guidelines. The prevalence of urinary tract infection was found at 24.23%. Escherichia Coli was a predominant etiological agent followed by Staphylococcus aureus. The majority of the infection was found between the age group 21-40, with females mostly infected. Most of the microorganisms were isolated from emtergency, obstetrics-gynecology, and nephrology wards. Most of the isolates were resistant to ampicillin, whereas the majority of the gram-positive isolates were resistant to penicillin.A large number of isolates were found to be sensitive to Gentamycin and nitrofurantoin. -
Citrobacter Braakii
& M cal ed ni ic li a l C G f e Trivedi et al., J Clin Med Genom 2015, 3:1 o n l o a m n r DOI: 10.4172/2472-128X.1000129 i u c s o Journal of Clinical & Medical Genomics J ISSN: 2472-128X ResearchResearch Article Article OpenOpen Access Access Phenotyping and 16S rDNA Analysis after Biofield Treatment on Citrobacter braakii: A Urinary Pathogen Mahendra Kumar Trivedi1, Alice Branton1, Dahryn Trivedi1, Gopal Nayak1, Sambhu Charan Mondal2 and Snehasis Jana2* 1Trivedi Global Inc., Eastern Avenue Suite A-969, Henderson, NV, USA 2Trivedi Science Research Laboratory Pvt. Ltd., Chinar Fortune City, Hoshangabad Rd., Madhya Pradesh, India Abstract Citrobacter braakii (C. braakii) is widespread in nature, mainly found in human urinary tract. The current study was attempted to investigate the effect of Mr. Trivedi’s biofield treatment on C. braakii in lyophilized as well as revived state for antimicrobial susceptibility pattern, biochemical characteristics, and biotype number. Lyophilized vial of ATCC strain of C. braakii was divided into two parts, Group (Gr.) I: control and Gr. II: treated. Gr. II was further subdivided into two parts, Gr. IIA and Gr. IIB. Gr. IIA was analysed on day 10 while Gr. IIB was stored and analysed on day 159 (Study I). After retreatment on day 159, the sample (Study II) was divided into three separate tubes. First, second and third tube was analysed on day 5, 10 and 15, respectively. All experimental parameters were studied using automated MicroScan Walk-Away® system. The 16S rDNA sequencing of lyophilized treated sample was carried out to correlate the phylogenetic relationship of C. -
Phenotyping and 16S Rdna Analysis After Biofield
Phenotyping and 16S rDNA Analysis after Biofield Treatment on Citrobacter braakii: A Urinary Pathogen Mahendra Kumar Trivedi, Alice Branton, Dahryn Trivedi, Gopal Nayak, Sambhu Charan Mondal, Snehasis Jana To cite this version: Mahendra Kumar Trivedi, Alice Branton, Dahryn Trivedi, Gopal Nayak, Sambhu Charan Mondal, et al.. Phenotyping and 16S rDNA Analysis after Biofield Treatment on Citrobacter braakii: A Urinary Pathogen. Journal of Clinical & Medical Genomics, Omics Publishing Group, 2015, 3 (1), pp.1000129. hal-01435926 HAL Id: hal-01435926 https://hal.archives-ouvertes.fr/hal-01435926 Submitted on 16 Jan 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License & M cal ed ni ic li a l C G f e Trivedi et al., J Clin Med Genom 2015, 3:1 o n l o a m n r DOI: 10.4172/2472-128X.1000129 i u c s o Journal of Clinical & Medical Genomics J ISSN: 2472-128X ResearchResearch Article Article OpenOpen Access Access Phenotyping and 16S rDNA Analysis after Biofield Treatment on Citrobacter braakii: A Urinary Pathogen Mahendra Kumar Trivedi1, Alice Branton1, Dahryn Trivedi1, Gopal Nayak1, Sambhu Charan Mondal2 and Snehasis Jana2* 1Trivedi Global Inc., Eastern Avenue Suite A-969, Henderson, NV, USA 2Trivedi Science Research Laboratory Pvt. -
Coliform Bacteria in Drinking Water Supplies
WHAT ARE COLIFORMS? TOTAL COLIFORMS, FECAL ARE COLIFORM BACTERIA Coliforms are bacteria that are always COLIFORMS, AND E. COLI HARMFUL? present in the digestive tracts of animals, The most basic test for bacterial Most coliform bacteria do not cause including humans, and are found in their contamination of a water supply is the test disease. However, some rare strains of E. wastes. They are also found in plant and soil for total coliform bacteria. Total coliform coli, particularly the strain 0157:H7, can material. counts give a general indication of the cause serious illness. Recent outbreaks sanitary condition of a water supply. of disease caused by E. coli 0157:H7 have generated much public concern about this “Indicator” A. Total coliforms include bacteria that organism. E. coli 0157:H7 has been found organisms are found in the soil, in water that has been in cattle, chickens, pigs, and sheep. Most of Water pollution caused by fecal influenced by surface water, and in human the reported human cases have been due contamination is a serious problem or animal waste. to eating under cooked hamburger. Cases due to the potential for contracting of E. coli 0157:H7 caused by contaminated B. Fecal coliforms are the group of the diseases from pathogens (disease- drinking water supplies are rare. causing organisms). Frequently, total coliforms that are considered to be concentrations of pathogens from present specifically in the gut and feces fecal contamination are small, and of warm-blooded animals. Because the the number of different possible origins of fecal coliforms are more specific pathogens is large. -
Microbial Populations of Fresh and Cold Stored Donkey Milk by High-Throughput Sequencing Provide Indication for a Correct Management of This High-Value Product
applied sciences Communication Microbial Populations of Fresh and Cold Stored Donkey Milk by High-Throughput Sequencing Provide Indication for A Correct Management of This High-Value Product Pasquale Russo 1,*, Daniela Fiocco 2 , Marzia Albenzio 1, Giuseppe Spano 1 and Vittorio Capozzi 3 1 Department of Sciences of Agriculture, Food, and Environment, University of Foggia, via Napoli 25, 71122 Foggia, Italy; [email protected] (M.A.); [email protected] (G.S.) 2 Department of Clinical and Experimental Medicine, University of Foggia, Viale Pinto 1, 71122 Foggia, Italy; daniela.fi[email protected] 3 Institute of Sciences of Food Production, National Research Council (CNR), c/o CS-DAT, Via Michele Protano, 71121 Foggia, Italy; [email protected] * Correspondence: [email protected] Received: 12 March 2020; Accepted: 25 March 2020; Published: 28 March 2020 Abstract: Donkey milk is receiving increasing interest due to its attractive nutrient and functional properties (but also cosmetic), which make it a suitable food for sensitive consumers, such as infants with allergies, the immunocompromised, and elderly people. Our study aims to provide further information on the microbial variability of donkey milk under cold storage conditions. Therefore, we analysed by high-throughput sequencing the bacterial communities in unpasteurized donkey milk just milked, and after three days of conservation at 4 ◦C, respectively. Results showed that fresh donkey milk was characterized by a high incidence of spoilage Gram-negative bacteria mainly belonging to Pseudomonas spp. A composition lower than 5% of lactic acid bacteria was found in fresh milk samples, with Lactococcus spp. being the most abundant. -
International Journal of Systematic and Evolutionary Microbiology (2016), 66, 5575–5599 DOI 10.1099/Ijsem.0.001485
International Journal of Systematic and Evolutionary Microbiology (2016), 66, 5575–5599 DOI 10.1099/ijsem.0.001485 Genome-based phylogeny and taxonomy of the ‘Enterobacteriales’: proposal for Enterobacterales ord. nov. divided into the families Enterobacteriaceae, Erwiniaceae fam. nov., Pectobacteriaceae fam. nov., Yersiniaceae fam. nov., Hafniaceae fam. nov., Morganellaceae fam. nov., and Budviciaceae fam. nov. Mobolaji Adeolu,† Seema Alnajar,† Sohail Naushad and Radhey S. Gupta Correspondence Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Radhey S. Gupta L8N 3Z5, Canada [email protected] Understanding of the phylogeny and interrelationships of the genera within the order ‘Enterobacteriales’ has proven difficult using the 16S rRNA gene and other single-gene or limited multi-gene approaches. In this work, we have completed comprehensive comparative genomic analyses of the members of the order ‘Enterobacteriales’ which includes phylogenetic reconstructions based on 1548 core proteins, 53 ribosomal proteins and four multilocus sequence analysis proteins, as well as examining the overall genome similarity amongst the members of this order. The results of these analyses all support the existence of seven distinct monophyletic groups of genera within the order ‘Enterobacteriales’. In parallel, our analyses of protein sequences from the ‘Enterobacteriales’ genomes have identified numerous molecular characteristics in the forms of conserved signature insertions/deletions, which are specifically shared by the members of the identified clades and independently support their monophyly and distinctness. Many of these groupings, either in part or in whole, have been recognized in previous evolutionary studies, but have not been consistently resolved as monophyletic entities in 16S rRNA gene trees. The work presented here represents the first comprehensive, genome- scale taxonomic analysis of the entirety of the order ‘Enterobacteriales’. -
Scientific Opinion
SCIENTIFIC OPINION ADOPTED: 29 April 2021 doi: 10.2903/j.efsa.2021.6651 Role played by the environment in the emergence and spread of antimicrobial resistance (AMR) through the food chain EFSA Panel on Biological Hazards (BIOHAZ), Konstantinos Koutsoumanis, Ana Allende, Avelino Alvarez-Ord onez,~ Declan Bolton, Sara Bover-Cid, Marianne Chemaly, Robert Davies, Alessandra De Cesare, Lieve Herman, Friederike Hilbert, Roland Lindqvist, Maarten Nauta, Giuseppe Ru, Marion Simmons, Panagiotis Skandamis, Elisabetta Suffredini, Hector Arguello,€ Thomas Berendonk, Lina Maria Cavaco, William Gaze, Heike Schmitt, Ed Topp, Beatriz Guerra, Ernesto Liebana, Pietro Stella and Luisa Peixe Abstract The role of food-producing environments in the emergence and spread of antimicrobial resistance (AMR) in EU plant-based food production, terrestrial animals (poultry, cattle and pigs) and aquaculture was assessed. Among the various sources and transmission routes identified, fertilisers of faecal origin, irrigation and surface water for plant-based food and water for aquaculture were considered of major importance. For terrestrial animal production, potential sources consist of feed, humans, water, air/dust, soil, wildlife, rodents, arthropods and equipment. Among those, evidence was found for introduction with feed and humans, for the other sources, the importance could not be assessed. Several ARB of highest priority for public health, such as carbapenem or extended-spectrum cephalosporin and/or fluoroquinolone-resistant Enterobacterales (including Salmonella enterica), fluoroquinolone-resistant Campylobacter spp., methicillin-resistant Staphylococcus aureus and glycopeptide-resistant Enterococcus faecium and E. faecalis were identified. Among highest priority ARGs blaCTX-M, blaVIM, blaNDM, blaOXA-48- like, blaOXA-23, mcr, armA, vanA, cfr and optrA were reported. These highest priority bacteria and genes were identified in different sources, at primary and post-harvest level, particularly faeces/manure, soil and water. -
Cultivation-Based Quantification and Identification of Bacteria at Two
microorganisms Communication Cultivation-Based Quantification and Identification of Bacteria at Two Hygienic Key Sides of Domestic Washing Machines Susanne Jacksch 1,2 , Huzefa Zohra 1, Mirko Weide 3, Sylvia Schnell 2 and Markus Egert 1,* 1 Faculty of Medical and Life Sciences, Institute of Precision Medicine, Microbiology and Hygiene Group, Furtwangen University, 78054 Villingen-Schwenningen, Germany; [email protected] (S.J.); [email protected] (H.Z.) 2 Research Centre for BioSystems, Land Use, and Nutrition (IFZ), Institute of Applied Microbiology, Justus-Liebig-University Giessen, 35392 Giessen, Germany; [email protected] 3 International Research & Development–Laundry & Home Care, Henkel AG & Co. KGaA, 40191 Düsseldorf, Germany; [email protected] * Correspondence: [email protected]; Tel.: +49-(7720)-307-4554; Fax: +49-(7720)-307-4207 Abstract: Detergent drawer and door seal represent important sites for microbial life in domes- tic washing machines. Interestingly, quantitative data on the microbial contamination of these sites is scarce. Here, 10 domestic washing machines were swab-sampled for subsequent bacte- rial cultivation at four different sampling sites: detergent drawer and detergent drawer chamber, as well as the top and bottom part of the rubber door seal. The average bacterial load over all washing machines and sites was 2.1 ± 1.0 × 104 CFU cm−2 (average number of colony forming units ± standard error of the mean (SEM)). The top part of the door seal showed the lowest contami- 1 −2 nation (11.1 ± 9.2 × 10 CFU cm ), probably due to less humidity. Out of 212 isolates, 178 (84%) were identified on the genus level, and 118 (56%) on the species level using matrix-assisted laser Citation: Jacksch, S.; Zohra, H.; desorption/ionization (MALDI) Biotyping, resulting in 29 genera and 40 identified species across all Weide, M.; Schnell, S.; Egert, M.