DOCSLIB.ORG

Biological Toxins and Their Relative Toxicity

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Biological Toxins and Their Relative Toxicity ORGANISATION FOR THE PROHIBITION OF CHEMICAL WEAPONS Working Together for a World Free of Chemical Weapons Biological Toxins and their Relative Toxicity What are Toxins? Toxins are toxic substances produced by animals, plants or microbes. They are classied by their source and mechanism of action (neurotoxic or cytotoxic). Neurotoxins aect neurons and are further classied based on the Aatoxin B mechanism by which they create their toxic eect; the subclasses are presynaptic 1 neurotoxins, postsynaptic neurotoxins, ion channel-binding toxins and ionophores. Cytotoxins aect all cell types in the body, causing cellular destruction or interfering LD : 2000000 ng/kg 50 Molecular weight: 312.8 g/mol with metabolic processes such as cell respiration and protein synthesis. Source: Aspergillus avus Ricin Examples of toxins from fungus T-2 Toxin LD50: 3000 ng/kg Molecular weight: 64,000 g/mol Examples of toxins from plants Source: Castor Bean LD50: 1210000 ng/kg Ricinus communis Molecular weight: 466 g/mol Source: Fungal Mycotoxin Aconitine Fusarium Taipoxin LD : 100000 ng/kg VX Agent 50 Molecular weight: 1647 g/mol Abrin Source: Monkshood Aconitum LD : 5000 ng/kg Batrachotoxin 50 Molecular weight: 46,000 g/mol αTityustoxin Source: Elapid Snake Tetrodotoxin Oxyuranus scutellatus LD50: 15000 ng/kg Molecular weight: 267.36 g/mol LD50: 40 ng/kg Molecular weight: 65,000 g/mol Source: Rosary Pea Soman (GD) LD : 2000 ng/kg Conotoxin 50 LD Examples of toxins Molecular weight 50: 8000 ng/kg : 539 g/mol LD50: 9000 ng/kg Source: Poison Dart Frog Molecular weight: 319 g/mol Molecular weight: 8,000 g/mol from insects & animals Source: Puer Fish Source: Scorpion Tetraodontidae Tityinae Sarin (GB) LD50: 64000 ng/kg LD50: 5000 ng/kg Molecular weight: 182.18 g/mol Molecular weight: 1,500 g/mol Source: Cone Snail Conus pennaceus LD50: 100000 ng/kg Maitotoxin Palytoxin Ciguatoxin Molecular weight: 140.09 g/mol Microcystin Saxitoxin LD : 100 ng/kg 50 LD : 150 ng/kg LD50: 400 ng/kg Molecular weight 50 Molecular weight : 3,400 g/mol Molecular weight: 2,700 g/mol : 1,000 g/mol LD : 50000 ng/kg Source: Marine Dinoagellate Source: Fish/Marine Dinoagellate 50 Tetanus Toxins Source: Marine Soft Coral Molecular weight: 994 g/mol Gambierdiscus toxicus Gymnothorax javanicus Palythoa toxica LD : 10000 ng/kg Source: Blue-Green Algae 50 Examples of Examples of toxins from cyanobacteria Molecular weight: 299 g/mol Microcystis aeruginosa Source: Marine Dinoagellate Nerve Agents Ceratium furca (For Reference) LD50: 2 ng/kg Botulinum Toxin Molecular weight: 150,000 g/mol Anatoxin-A(s) Source: Bacterium Clostridium tetani Diphtheria Toxin C. perfringens toxins LD50: 50000 ng/kg LD50: 1 ng/kg Shiga Toxin LD : 100 ng/kg Molecular weight Molecular weight: 150,000 g/mol 50 : 252 g/mol Molecular weight: 62,000 g/mol Source: Blue-Green Algae Source: Clostridium botulinum LD : 310 ng/kg Source: Corynebacterium 50 Anabaena flos-aquae diphtheriae Molecular weight: 40,000 g/mol Source: Clostridium perfringens SEB (Rhesus/Aerosol) Examples of other bacterial toxins References 1. David R. Franz, DVM, Defense Against Toxin Weapons, Veterinary Corps, United States Army (1997). LD50: 2 ng/kg Molecular weight: 55,000 g/mol 2. Chastain, James R., A heuristic methodology for locating monitoring stations to detect contamination Source: Shigella dysenteriae events in portable water distribution systems (2004). 3. Maria Taciana Holanda Cavalcanti, Tatiana Porto, Ana Lúcia Figueiredo Porto, Igor Viana Brandi, José Luiz LD : 27000 ng/kg de Lima Filho, Adalberto Pessoa Junior, Large scale purication of Clostridium perfringens toxins: a 50 review, Brazilian Journal of Pharmaceutical Sciences (2004). Molecular weight: 28,494 g/mol Most Toxic Source: Staphylococcus aureus Least Toxic Comparative Toxicity (Median Lethal Dose, LD 50 in ng/kg) of Selected Toxins And Chemical Agents In Laboratory Mice Decreasing toxicity @opcw /opcwonline @opcw_st /opcwonline /company/opcw /opcw.
Load more

Recommended publications
  • Family Practice
    THE JOURNAL OF FAMILY ONLINE EXCLUSIVE PRACTICE Paul K. Carlton, Jr, MD, Brown recluse spider bite? FACS The Texas A&M University Consider this uniquely Health Science Center College Station, Tex conservative treatment [email protected] An antihistamine and observation work as well— and often better—than more intensive therapies. Practice recommendations oped it in 4 phases, which I describe in • Be concerned about brown recluse this article. Not only does this conser- envenomation when a patient vative approach consistently heal con- reports intensifying localized firmed brown recluse bite wounds, but pain disproportionate to physical should a bite be mistakenly attributed findings after a “bite” (C). to the brown recluse (or one of its rela- tives in the Loxosceles genus of spider), • Prescribe an oral antihistamine there is no harm to the patient, nor any alone to control symptoms, even big expense. with a necrotic wound, and mark the IN THIS ARTICLE patient’s progress over 24 hours (C). z Spider bite z Is a brown recluse • If the patient improves dramatically, to blame? or MRSA? continue the antihistamine; with little Due to limited experience among the Page E6 or no improvement, consider giving an wider medical community in identifying antibiotic with the antihistamine (C). spider envenomation,1-4 bite recognition and selection of appropriate therapy can Strength of recommendation (SOR) be difficult. A Good-quality patient-oriented evidence Early findings can be confusing. B Inconsistent or limited-quality patient-oriented evidence C Consensus, usual practice, opinion, disease-oriented Brown recluse bites typically feel like a evidence, case series pin prick.
    [Show full text]
  • Detoxification Strategies for Zearalenone Using
    microorganisms Review Detoxification Strategies for Zearalenone Using Microorganisms: A Review 1, 2, 1 1, Nan Wang y, Weiwei Wu y, Jiawen Pan and Miao Long * 1 Key Laboratory of Zoonosis of Liaoning Province, College of Animal Science & Veterinary Medicine, Shenyang Agricultural University, Shenyang 110866, China 2 Institute of Animal Science, Xinjiang Academy of Animal Sciences, Urumqi 830000, China * Correspondence: [email protected] or [email protected] These authors contributed equally to this work. y Received: 21 June 2019; Accepted: 19 July 2019; Published: 21 July 2019 Abstract: Zearalenone (ZEA) is a mycotoxin produced by Fusarium fungi that is commonly found in cereal crops. ZEA has an estrogen-like effect which affects the reproductive function of animals. It also damages the liver and kidneys and reduces immune function which leads to cytotoxicity and immunotoxicity. At present, the detoxification of mycotoxins is mainly accomplished using biological methods. Microbial-based methods involve zearalenone conversion or adsorption, but not all transformation products are nontoxic. In this paper, the non-pathogenic microorganisms which have been found to detoxify ZEA in recent years are summarized. Then, two mechanisms by which ZEA can be detoxified (adsorption and biotransformation) are discussed in more detail. The compounds produced by the subsequent degradation of ZEA and the heterogeneous expression of ZEA-degrading enzymes are also analyzed. The development trends in the use of probiotics as a ZEA detoxification strategy are also evaluated. The overall purpose of this paper is to provide a reliable reference strategy for the biological detoxification of ZEA. Keywords: zearalenone (ZEA); reproductive toxicity; cytotoxicity; immunotoxicity; biological detoxification; probiotics; ZEA biotransformation 1.
    [Show full text]
  • Interactions of Insecticidal Spider Peptide Neurotoxins with Insect Voltage- and Neurotransmitter-Gated Ion Channels
    Interactions of insecticidal spider peptide neurotoxins with insect voltage- and neurotransmitter-gated ion channels (Molecular representation of - HXTX-Hv1c including key binding residues, adapted from Gunning et al, 2008) PhD Thesis Monique J. Windley UTS 2012 CERTIFICATE OF AUTHORSHIP/ORIGINALITY I certify that the work in this thesis has not previously been submitted for a degree nor has it been submitted as part of requirements for a degree except as fully acknowledged within the text. I also certify that the thesis has been written by me. Any help that I have received in my research work and the preparation of the thesis itself has been acknowledged. In addition, I certify that all information sources and literature used are indicated in the thesis. Monique J. Windley 2012 ii ACKNOWLEDGEMENTS There are many people who I would like to thank for contributions made towards the completion of this thesis. Firstly, I would like to thank my supervisor Prof. Graham Nicholson for his guidance and persistence throughout this project. I would like to acknowledge his invaluable advice, encouragement and his neverending determination to find a solution to any problem. He has been a valuable mentor and has contributed immensely to the success of this project. Next I would like to thank everyone at UTS who assisted in the advancement of this research. Firstly, I would like to acknowledge Phil Laurance for his assistance in the repair and modification of laboratory equipment. To all the laboratory and technical staff, particulary Harry Simpson and Stan Yiu for the restoration and sourcing of equipment - thankyou. I would like to thank Dr Mike Johnson for his continual assistance, advice and cheerful disposition.
    [Show full text]
  • Feed Safety 2016
    Annual Report The surveillance programme for feed materials, complete and complementary feed in Norway 2016 - Mycotoxins, fungi and bacteria NORWEGIAN VETERINARY INSTITUTE The surveillance programme for feed materials, complete and complementary feed in Norway 2016 – Mycotoxins, fungi and bacteria Content Summary ...................................................................................................................... 3 Introduction .................................................................................................................. 4 Aims ........................................................................................................................... 5 Materials and methods ..................................................................................................... 5 Quantitative determination of total mould, Fusarium and storage fungi ........................................ 6 Chemical analysis .......................................................................................................... 6 Bacterial analysis .......................................................................................................... 7 Statistical analysis ......................................................................................................... 7 Results and discussion ...................................................................................................... 7 Cereals .....................................................................................................................
    [Show full text]
  • National Resource Material Green and Black Poison Frog (Dendrobates Auratus)
    Indicative 10 Project National Resource Material Green and Black Poison frog (Dendrobates auratus) Michelle T. Christy and Win Kirkpatrick 2017 Department of Primary Industries and Regional Development 3 Baron-Hay Court, South Perth, WA 6151 An Invasive Animals CRC Project Contents Summary ............................................................................. 2 Key Messages ................................................................... 2 Classification ................................................................... 2 Common names ................................................................ 3 Biology and Ecology ................................................................ 3 Identification ................................................................... 3 Behaviours and Traits ......................................................... 4 Food and Foraging ............................................................. 4 Reproduction and Lifecycle ................................................. 5 Habitat ......................................................................... 5 Global Range ........................................................................ 5 Potential for Introduction ........................................................ 6 Potential for Eradication.......................................................... 7 Impacts ............................................................................... 7 Economic ........................................................................ 7 Environmental
    [Show full text]
  • Biological Toxins Fact Sheet
    Work with FACT SHEET Biological Toxins The University of Utah Institutional Biosafety Committee (IBC) reviews registrations for work with, possession of, use of, and transfer of acute biological toxins (mammalian LD50 <100 µg/kg body weight) or toxins that fall under the Federal Select Agent Guidelines, as well as the organisms, both natural and recombinant, which produce these toxins Toxins Requiring IBC Registration Laboratory Practices Guidelines for working with biological toxins can be found The following toxins require registration with the IBC. The list in Appendix I of the Biosafety in Microbiological and is not comprehensive. Any toxin with an LD50 greater than 100 µg/kg body weight, or on the select agent list requires Biomedical Laboratories registration. Principal investigators should confirm whether or (http://www.cdc.gov/biosafety/publications/bmbl5/i not the toxins they propose to work with require IBC ndex.htm). These are summarized below. registration by contacting the OEHS Biosafety Officer at [email protected] or 801-581-6590. Routine operations with dilute toxin solutions are Abrin conducted using Biosafety Level 2 (BSL2) practices and Aflatoxin these must be detailed in the IBC protocol and will be Bacillus anthracis edema factor verified during the inspection by OEHS staff prior to IBC Bacillus anthracis lethal toxin Botulinum neurotoxins approval. BSL2 Inspection checklists can be found here Brevetoxin (http://oehs.utah.edu/research-safety/biosafety/ Cholera toxin biosafety-laboratory-audits). All personnel working with Clostridium difficile toxin biological toxins or accessing a toxin laboratory must be Clostridium perfringens toxins Conotoxins trained in the theory and practice of the toxins to be used, Dendrotoxin (DTX) with special emphasis on the nature of the hazards Diacetoxyscirpenol (DAS) associated with laboratory operations and should be Diphtheria toxin familiar with the signs and symptoms of toxin exposure.
    [Show full text]
  • What Is Staphylococcus Aureus (Staph)?
    What is Staphylococcus aureus (staph)? Staphylococcus aureus, often referred to simply as "staph," are bacteria commonly carried on the skin or in the nose of healthy people. Approximately 25% to 30% of the population is colonized (when bacteria are present, but not causing an infection) in the nose with staph bacteria. Sometimes, staph can cause an infection. Staph bacteria are one of the most common causes of skin infections in the United States. Most of these skin infections are minor (such as pimples and boils) and can be treated without antibiotics (also known as antimicrobials or antibacterials). However, staph bacteria also can cause serious infections (such as surgical wound infections, bloodstream infections, and pneumonia). What is MRSA (methicillin-resistant Staphylococcus aureus)? Some staph bacteria are resistant to antibiotics. MRSA is a type of staph that is resistant to antibiotics called beta-lactams. Beta-lactam antibiotics include methicillin and other more common antibiotics such as oxacillin, penicillin and amoxicillin. While 25% to 30% of the population is colonized with staph, approximately 1% is colonized with MRSA. Who gets staph or MRSA infections? Staph infections, including MRSA, occur most frequently among persons in hospitals and healthcare facilities (such as nursing homes and dialysis centers) who have weakened immune systems. These healthcare-associated staph infections include surgical wound infections, urinary tract infections, bloodstream infections, and pneumonia. Are people who are positive for the human immune deficiency virus (HIV) at increased risk for MRSA? Should they be taking special precautions? People with weakened immune systems, which include some patients with HIV infection, may be at risk for more severe illness if they get infected with MRSA.
    [Show full text]
  • Clostridium Perfringens
    CLOSTRIDIUM PERFRINGENS: SPORES & CELLS MEDIA & MODELING Promotor: prof. dr. ir. Frans M. Rombouts Hoogleraar in de levensmiddelenhygiëne en –microbiologie Co-promotor: dr. Rijkelt R. Beumer Universitair docent Leerstoelgroep levensmiddelenmicrobiologie Promotiecommissie: prof. dr. ir. Johan M. Debevere (Universiteit Gent, België) dr. ir. Servé H.W. Notermans (TNO Voeding, Zeist) prof. dr. Michael W. Peck (Institute of Food Research, Norwich, UK) prof. dr. ir. Marcel H. Zwietering (Wageningen Universiteit) CLOSTRIDIUM PERFRINGENS: SPORES & CELLS MEDIA & MODELING Aarieke Eva Irene de Jong Proefschrift ter verkrijging van de graad van doctor op gezag van de rector magnificus van Wageningen Universiteit, prof. dr. ir. L. Speelman, in het openbaar te verdedigen op dinsdag 21 oktober 2003 des namiddags te vier uur in de Aula A.E.I. de Jong – Clostridium perfringens: spores & cells, media & modeling – 2003 Thesis Wageningen University, Wageningen, The Netherlands – With summary in Dutch ISBN 90-5808-931-2 ABSTRACT Clostridium perfringens is one of the five major food borne pathogens in the western world (expressed in cases per year). Symptoms are caused by an enterotoxin, for which 6% of type A strains carry the structural gene. This enterotoxin is released when ingested cells sporulate in the small intestine. Research on C. perfringens has been limited to a couple of strains that sporulate well in Duncan and Strong (DS) medium. These abundantly sporulating strains in vitro are not necessarily a representation of the most dangerous strains in vivo. Therefore, sporulation was optimized for C. perfringens strains in general. None of the tested media and methods performed well for all strains, but Peptone-Bile- Theophylline medium (with and without starch) yielded highest spore numbers.
    [Show full text]
  • Occurrence, Impact on Agriculture, Human Health, and Management Strategies of Zearalenone in Food and Feed: a Review
    toxins Review Occurrence, Impact on Agriculture, Human Health, and Management Strategies of Zearalenone in Food and Feed: A Review Dipendra Kumar Mahato 1 , Sheetal Devi 2, Shikha Pandhi 3, Bharti Sharma 3 , Kamlesh Kumar Maurya 3, Sadhna Mishra 3, Kajal Dhawan 4, Raman Selvakumar 5 , Madhu Kamle 6 , Awdhesh Kumar Mishra 7,* and Pradeep Kumar 6,* 1 CASS Food Research Centre, School of Exercise and Nutrition Sciences, Deakin University, Burwood, VIC 3125, Australia; [email protected] 2 National Institute of Food Technology Entrepreneurship and Management (NIFTEM), Sonipat, Haryana 131028, India; [email protected] 3 Department of Dairy Science and Food Technology, Institute of Agricultural Sciences, Banaras Hindu University, Varanasi 221005, India; [email protected] (S.P.); [email protected] (B.S.); [email protected] (K.K.M.); [email protected] (S.M.) 4 Department of Food Technology and Nutrition, School of Agriculture Lovely Professional University, Phagwara 144411, India; [email protected] 5 Centre for Protected Cultivation Technology, ICAR-Indian Agricultural Research Institute, Pusa Campus, New Delhi 110012, India; [email protected] 6 Applied Microbiology Lab., Department of Forestry, North Eastern Regional Institute of Science and Technology, Nirjuli 791109, India; [email protected] 7 Department of Biotechnology, Yeungnam University, Gyeongsan 38541, Gyeongbuk, Korea * Correspondence: [email protected] (A.K.M.); [email protected] (P.K.) Citation: Mahato, D.K.; Devi, S.; Abstract: Mycotoxins represent an assorted range of secondary fungal metabolites that extensively Pandhi, S.; Sharma, B.; Maurya, K.K.; occur in numerous food and feed ingredients at any stage during pre- and post-harvest conditions. Mishra, S.; Dhawan, K.; Selvakumar, Zearalenone (ZEN), a mycotoxin categorized as a xenoestrogen poses structural similarity with R.; Kamle, M.; Mishra, A.K.; et al.
    [Show full text]
  • Aflatoxins and Dairy Cattle
    Texas Dairy Matters Higher Education Supporting the Industry AFLATOXINS AND DAIRY CATTLE Ellen R. Jordan, Ph.D. Extension Dairy Specialist Department of Animal Science Texas A&M AgriLife Extension Service The Texas A&M University System Whenever crops are under stress, the potential for aflatoxins increases. Aflatoxins are poisonous by-products of the growth of some species of the mold fungus Aspergillus. Some crops may be contaminated with aflatoxins, particularly whenever drought stress occurs. When lactating animals are fed aflatoxin contaminated feed, they excrete aflatoxin metabolites into the milk. The aflatoxins are capable of causing aflatoxicosis in consumers of milk. This is why government regulations specify that milk must be free of aflatoxin. However, action is not taken until the aflatoxin level exceeds 0.5 ppb in market milk, the level below which there is no hazard for the consuming public. "Action levels" for livestock represent the level of contamination at which the feed may be injurious to their health or result in contamination of milk, meat or eggs. Action levels by class of livestock are in table 1. Aflatoxicosis is a disease caused by the consumption of aflatoxins, the mold metabolites produced by some strains of Aspergillus flavus and Aspergillus parasitisus. The four most common aflatoxins are B1, B2, G1 and G2. Contaminated grains and grain by- products are the most common sources of aflatoxins in Texas. Corn silage may also be a source of aflatoxins, because the ensiling process does not destroy the toxins already present in silage. Aspergillus flavus growth on corn. Table 1: The FDA Center for Veterinary Medicine "Action" levels for aflatoxin in feed grain in interstate commerce.
    [Show full text]
  • Medical Management of Biological Casualties Handbook
    USAMRIID’s MEDICAL MANAGEMENT OF BIOLOGICAL CASUALTIES HANDBOOK Sixth Edition April 2005 U.S. ARMY MEDICAL RESEARCH INSTITUTE OF INFECTIOUS DISEASES FORT DETRICK FREDERICK, MARYLAND Emergency Response Numbers National Response Center: 1-800-424-8802 or (for chem/bio hazards & terrorist events) 1-202-267-2675 National Domestic Preparedness Office: 1-202-324-9025 (for civilian use) Domestic Preparedness Chem/Bio Helpline: 1-410-436-4484 or (Edgewood Ops Center – for military use) DSN 584-4484 USAMRIID’s Emergency Response Line: 1-888-872-7443 CDC'S Emergency Response Line: 1-770-488-7100 Handbook Download Site An Adobe Acrobat Reader (pdf file) version of this handbook can be downloaded from the internet at the following url: http://www.usamriid.army.mil USAMRIID’s MEDICAL MANAGEMENT OF BIOLOGICAL CASUALTIES HANDBOOK Sixth Edition April 2005 Lead Editor Lt Col Jon B. Woods, MC, USAF Contributing Editors CAPT Robert G. Darling, MC, USN LTC Zygmunt F. Dembek, MS, USAR Lt Col Bridget K. Carr, MSC, USAF COL Ted J. Cieslak, MC, USA LCDR James V. Lawler, MC, USN MAJ Anthony C. Littrell, MC, USA LTC Mark G. Kortepeter, MC, USA LTC Nelson W. Rebert, MS, USA LTC Scott A. Stanek, MC, USA COL James W. Martin, MC, USA Comments and suggestions are appreciated and should be addressed to: Operational Medicine Department Attn: MCMR-UIM-O U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) Fort Detrick, Maryland 21702-5011 PREFACE TO THE SIXTH EDITION The Medical Management of Biological Casualties Handbook, which has become affectionately known as the "Blue Book," has been enormously successful - far beyond our expectations.
    [Show full text]
  • Targeted Neuronal Cell Ablation in the Drosophila Embryo: Pathfinding by Follower Growth Cones in the Absence of Pioneers
    Neuron, Vol. 14, 707-715, April, 1995, Copyright© 1995 by Cell Press Targeted Neuronal Cell Ablation in the Drosophila Embryo: Pathfinding by Follower Growth Cones in the Absence of Pioneers David M. Lin,* Vanessa J. Auld,*t reach their targets in the CNS (Wigglesworth, 1953). The and Corey S. Goodman ability of the initial axons to guide later growth cones has Howard Hughes Medical Institute led to the suggestion that pioneering growth cones might Division of Neurobiology be endowed with special pathfinding abilities. Do subse- Department of Molecular and Cell Biology quent growth cones possess the same pathfinding abili- Life Science Addition, Room 519 ties, or are they different from the pioneers? University of California, Berkeley Ablation experiments in a variety of organisms thus far Berkeley, California 94720 have provided a range of conflicting answers to this ques- tion. In the grasshopper embryo CNS, the G growth cone turns anteriorly along the P axons in the NP fascicle, a Summary pathway formed by the three descending P and the two ascending A axons. Although the A and P axons normally We developed a rapid method that uses diphtheria fasciculate and follow one another, either can pioneer the toxin, the flp recognition target sequences, and the complete pathway on its own. Furthermore, any one of GAL4-UAS activation system, to ablate specific neu- the P axons will suffice, since when any two of them are rons in the Drosophila embryo and to examine the con- ablated the remaining P pioneers the pathway. When the sequences in large numbers of embryos at many time three P axons are ablated, the G growth cone stalls, and points.
    [Show full text]