Appendix D: 2008 Canadian Integrated Program for Antimicrobial Resistance Surveillance (CIPARS) annual report – Additional information
Canadian Integrated Program for Antimicrobial Resistance Surveillance (CIPARS)
Appendix D - Additional Information
Abbreviations
General Abbreviations
- A2C-AMP
- Resistance to amoxicillin-clavulanic acid, cefoxitin, ceftiofur, and ampicillin
- AARD
-
Alberta Agriculture and Rural
Development - ACSSuT
- Resistance to ampicillin, chloramphenicol, streptomycin, sulfisoxazole, and tetracycline
- ACKSSuT
- Resistance to ampicillin, chloramphenicol, kanamycin, streptomycin, sulfisoxazole, and tetracycline
- AKSSuT
- Resistance to ampicillin, kanamycin, streptomycin, sulfisoxazole, and tetracycline
- AMU
- Antimicrobial use
- ATC
- Anatomical Therapeutic Chemical
- ATCC
- American Type Culture Collection
- BPW
- Buffered peptone water
- CAHI
- Canadian Animal Health Institute
- CCS
- Canadian CompuScript
- CFIA
- Canadian Food Inspection Agency
- CLSI
- Clinical and Laboratory Standards Institute
- CQA®
- Canadian Quality Assurance
- CTM
- Close to market weight
- DANMAP
- Danish Integrated AntimicrobialResistance Monitoring and Research Program
- DDD
- Defined daily dose
- GSS
- Global Salmonella Surveillance
- IMS
- Intercontinental Medical Statistics
- ISO
- International Standards Organization
- LFZ
- Laboratory for Foodborne Zoonoses
- mCCDA
- Modified cefoperazone charcoal deoxycholate agar
- MHB
- Mueller Hinton broth
- MIC
- Minimal inhibitory concentration
- MRSA
- Methicillin-resistant Staphylococcus aureus
- MSRV
- Modified semi-solid Rappaport Vassiliadis
- NA
- Not available
- N/A
- Not applicable
- NC
- Not classified
- NML
- National Microbiology Laboratory
- OIÉ
- Organisation Mondiale de la Santé Animale
- PCVAD
- Porcine circovirus-associated disease
- PHAC
- Public Health Agency of Canada
- PPHL
- Provincial Public Health Laboratory
- PRRS
- Porcine reproductive and respiratory syndrome
- PT
- Phage type
- STL
- Salmonella Typing Laboratory
- USA
- United States of America
- VDD
- Veterinary Drugs Directorate
Antimicrobials
- AMC
- Amoxicillin-clavulanic acid
- AMK
- Amikacin
- AMP
- Ampicillin
- AZM
- Azithromycin
- CHL
- Chloramphenicol
- CIP
- Ciprofloxacin
- CLI
- Clindamycin
- CRO
- Ceftriaxone
- DAP
- Daptomycin
- ERY
- Erythromycin
- FLA
- Flavomycin
- FLR
- Florfenicol
- FOX
- Cefoxitin
- GEN
- Gentamicin
- KAN
- Kanamycin
- LIN
- Lincomycin
- LNZ
- Linezolid
- NAL
- Nalidixic acid
- NIT
- Nitrofurantoin
- PEN
- Penicillin
- QDA
- Quinupristin-dalfopristin
- SSS
- Sulfisoxazole
- STR
- Streptomycin
- SXT
- Trimethoprim-sulfamethoxazole
- TEL
- Telithromycin
- TET
- Tetracycline
- TIG
- Tigecycline
- TIO
- Ceftiofur
- TYL
- Tylosin
- VAN
- Vancomycin
Canadian Provinces and Territories
- AB
- Alberta
- BC
- British Columbia
- MB
- Manitoba
- NB
- New Brunswick
- NL
- Newfoundland and Labrador
- NS
- Nova Scotia
- NT
- Northwest Territories
- NU
- Nunavut
- ON
- Ontario
- PEI
- Prince Edward Island
- QC
- Québec
- SK
- Saskatchewan
- YT
- Yukon Territory
Glossary
Antimicrobial: Substance (including natural and synthetic products) that kills or inhibits the growth of organisms such as bacteria, fungi, viruses, or parasites. Throughout this report, the term "antimicrobial" is used to refer only to drugs effective against bacteria.
Antimicrobial resistance: Observed when the minimal inhibitory concentration of an antimicrobial is equal to or greater than the defined resistance breakpoint. Resistant bacteria are able to withstand the effects of an antimicrobial principally through 1 of these 4 mechanisms: 1) drug inactivation or modification by enzyme production, 2) adaptation of bacterial metabolism, 3) structural modification of antimicrobial targets and, 4) mechanisms to decrease drug permeability or increase drug elimination. Moreover, some bacteria have natural (or intrinsic) resistance to certain antimicrobials.
Co-resistance: Coexistence of 2 or more genes or mutations in the same bacterial strain, each of which confers resistance to a different class of drug. Also designated "associated resistance"
(Aarestrup, 2006).
Cross-resistance: Situation in which resistance to 1 drug is associated with resistance to another drug, and that resistance is attributable to a single biochemical mechanism (Aarestrup, 2006). For more details, see Appendix C.3 in the 2005 CIPARS Annual Report.
Defined daily dose (DDD): Statistical measure of drug consumption developed by the World Health Organization to standardize comparisons of drug usage at international and other levels, independently of cost or drug formulation.
Minimal inhibitory concentration (MIC): Lowest antimicrobial concentration required to inhibit bacterial growth after an overnight in vitro incubation. The MIC is used to confirm or monitor antimicrobial resistance in bacteria. Resistance is said to exist when the MIC is higher than the defined breakpoint of resistance for a given bacterial isolate.
Multidrug resistance: Used in this report to describe resistance to more than 1 structurally-unrelated class of antimicrobials in a given bacteria isolate, regardless of the resistance mechanisms involved. Multidrug resistance (also referred to as multiple drug resistance or multiresistance) can result from bacterial mechanisms of cross-resistance and/or co-resistance. For more details, see the 2005 CIPARS Annual Report, Appendix C.3.
References
Aarestrup FM. Antimicrobial resistance in bacteria of animal origin. 1st ed. Washington DC: ASM Press, 2006.
Anderson E, Williams R. Bacteriophage typing of enteric pathogens and staphylococci and its use in epidemiology. J Clin Pathol 1956;9:94-127.
Anderson E. The phagetyping of Salmonella other than S. Typhi. In: Van Oye E, ed. The world problem of salmonellosis. The Hague, The Netherlands: Dr W. Junk Publishers, 1964;89-100.
Anderson E, Ward L, de Saxe M, et al. Bacteriophage-typing designations of Salmonella Typhimurium. J Hyg (Lond) 1977;78:297-300.
Callow B. A new phage typing scheme for Salmonella Typhimurium. J Hyg (Lond) 1959;57:346-359.
Demczuk W, Soule G, Clark C, et al. Phage-based typing scheme for Salmonella enterica serovar Heidelberg, a causative agent of food poisonings in Canada. J Clin Microbiol 2003;41:4279-4284.
Ewing WH. Edwards and Ewing's identification of Enterobacteriaceae. 4th ed. New York: Elsevier Science Publishing Co, 1986.
Farmer J, Hickman F, Sikes J. Automation of Salmonella typhi phage-typing. Lancet 1975;2(7939):787-790.
Grimont, PAD. Antigenic Formulae of the Salmonella Serovars. 9th ed. Cedex, France: Collaborating Center for Reference and Research on Salmonella, Institut Pasteur, 2007.
Kauffman F. The bacteriology of Enterobacteriaceae. Baltimore: Williams and Wilkins Co, 1966.
Le Minor L. Guidelines for the preparation of Salmonella antisera. Paris, France: WHO Collaborating Centre for Reference and Research on Salmonella, Pasteur Institute, 2001.
Le Minor L, Popoff M. Antigenic formulas of the Salmonella serovars. 8th revision. Paris, France: WHO Collaborating Centre for Reference and Research on Salmonella, Pasteur Institute, 2001.
Murray PR, Baron EJ, Pfaller MA, Jorgensen JH, Yolken RH, eds. Manual of clinical microbiology. 8th ed. Washington DC, ASM Press, 2005.
Ravel A. Development of the Canadian antimicrobial resistance surveillance system (agri-food sector) - sampling design options. Presented to the National Steering Committee on Antimicrobial Resistance in Enterics, Canada, 2001. 79 pp.
Ravel A. AMR Surveillance in food at retail - Proposal for a pilot project - DRAFT #2. 2002. 13 pp.
Shipp C, Rowe B. A mechanised microtechnique for Salmonella serotyping. J Clin Pathol 1980;33:595-597.
Ward L, de Sa J, Rowe B. A phage-typing scheme for Salmonella Enteritidis. Epidemiol Infect 1987;99:291-294.
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