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== Historical Perspective == | == Historical Perspective == | ||
* It was first described by [[Edward Holbrook Derrick]]<ref>Derrick EH. ''Q" fever a new fever entity: clinical features. diagnosis, and laboratory investigation. Med J Aust. 1937;11:281-299.''</ref> in [[Slaughterhouse|abattoir]] workers in [[Brisbane]], [[Queensland]], [[Australia]]. | |||
It was first described by [[Edward Holbrook Derrick]]<ref>Derrick EH. ''Q" fever a new fever entity: clinical features. diagnosis, and laboratory investigation. Med J Aust. 1937;11:281-299.</ref> in [[Slaughterhouse|abattoir]] workers in [[Brisbane]], [[Queensland]], [[Australia]]. The "Q" stands for "query" and was applied at a time when the causative agent was unknown; it was chosen over suggestions of "abattoir fever" and "Queensland rickettsial fever", to avoid directing negative connotations at either the cattle industry or the state of Queensland.<ref>{{cite book | author = Joseph E. McDade | chapter = Historical Aspects of Q Fever | title = Q Fever, Volume I: The Disease | editor = Thomas J. Marrie | publisher = CRC Press | year = 1990 | isbn = 0-8493-5984-8 | page = 8}}</ref> | * The "Q" stands for "query" and was applied at a time when the causative agent was unknown; it was chosen over suggestions of "abattoir fever" and "Queensland rickettsial fever", to avoid directing negative connotations at either the cattle industry or the state of Queensland.<ref>{{cite book | author = Joseph E. McDade | chapter = Historical Aspects of Q Fever | title = Q Fever, Volume I: The Disease | editor = Thomas J. Marrie | publisher = CRC Press | year = 1990 | isbn = 0-8493-5984-8 | page = 8}}</ref> | ||
* The [[pathogen]] of Q fever was discovered in 1937, when [[Frank Macfarlane Burnet]] and [[Mavis Freeman]] isolated the bacterium from one of Derrick’s patients.<ref>Burnet FM, Freeman M. Experimental studies on the virus of “Q” fever. Med J Aust 1937; 2: 299-305.</ref> | |||
The [[pathogen]] of Q fever was discovered in 1937, when [[Frank Macfarlane Burnet]] and [[Mavis Freeman]] isolated the bacterium from one of Derrick’s patients.<ref>Burnet FM, Freeman M. Experimental studies on the virus of “Q” fever. Med J Aust 1937; 2: 299-305.</ref> It was originally identified as a species of ''[[Rickettsia]]''. [[H.R. Cox]] and [[Gordon Davis (scientist)|Gordon Davis]] isolated it from [[tick]]s in [[Montana]], [[USA]] in 1938.<ref>Davis, G. E., and H. R. Cox. 1938. [http://www.jstor.org/pss/4582746 A filter-passing infectious agent isolated from ticks. I. Isolation from Dermacentor andersonii, reactions in animals, and filtration.] Public Health Rep. 53:2259-2282.</ref> It is a zoonotic disease whose most common animal reservoirs are cattle, sheep and goats. ''Coxiella burnetii'' is no longer regarded as closely related to [[Rickettsiae]], but as similar to ''[[Legionella]]'' and ''[[Francisella]]'', and is a [[proteobacteria|proteobacterium]]. | * It was originally identified as a species of ''[[Rickettsia conorii|Rickettsia]]''. [[H.R. Cox]] and [[Gordon Davis (scientist)|Gordon Davis]] isolated it from [[tick]]s in [[Montana]], [[USA]] in 1938.<ref>Davis, G. E., and H. R. Cox. 1938. [http://www.jstor.org/pss/4582746 A filter-passing infectious agent isolated from ticks. I. Isolation from Dermacentor andersonii, reactions in animals, and filtration.] Public Health Rep. 53:2259-2282.</ref> It is a zoonotic disease whose most common animal reservoirs are cattle, sheep and goats. ''[[Coxiella burnetii]]'' is no longer regarded as closely related to [[Rickettsiae]], but as similar to ''[[Legionella]]'' and ''[[Francisella]]'', and is a [[proteobacteria|proteobacterium]]. | ||
=== Biological warfare === | === Biological warfare === | ||
* Q fever has been described as a possible biological weapon.<ref name="pmid14592601">{{cite journal |author=Madariaga MG, Rezai K, Trenholme GM, Weinstein RA |title=Q fever: a biological weapon in your backyard |journal=Lancet Infect Dis |volume=3 |issue=11 |pages=709–21 |year=2003 |month=November |pmid=14592601 |doi= 10.1016/S1473-3099(03)00804-1|url=http://linkinghub.elsevier.com/retrieve/pii/S1473309903008041}}</ref> | |||
Q fever has been described as a possible biological weapon.<ref name="pmid14592601">{{cite journal |author=Madariaga MG, Rezai K, Trenholme GM, Weinstein RA |title=Q fever: a biological weapon in your backyard |journal=Lancet Infect Dis |volume=3 |issue=11 |pages=709–21 |year=2003 |month=November |pmid=14592601 |doi= 10.1016/S1473-3099(03)00804-1|url=http://linkinghub.elsevier.com/retrieve/pii/S1473309903008041}}</ref> | * The United States investigated Q fever as a potential [[biological warfare]] agent in the 1950s, with eventual standardization as agent OU. At Fort Detrick and Dugway Proving Ground, human trials were conducted on [[Operation Whitecoat|Whitecoat volunteers]] to determine the median infective dose (18 MICLD<sub>50</sub>/person i.h.) and course of infection. | ||
* As a standardized biological, it was manufactured in large quantities at [[Pine Bluff Arsenal]], with 5,098 gallons in the arsenal in bulk at the time of demilitarization in 1970. | |||
The United States investigated Q fever as a potential [[biological warfare]] agent in the 1950s, with eventual standardization as agent OU. At Fort Detrick and Dugway Proving Ground, human trials were conducted on [[Operation Whitecoat|Whitecoat volunteers]] to determine the median infective dose (18 MICLD<sub>50</sub>/person i.h.) and course of infection. As a standardized biological, it was manufactured in large quantities at [[Pine Bluff Arsenal]], with 5,098 gallons in the arsenal in bulk at the time of demilitarization in 1970. | * Q fever is a category "B" agent.<ref name="pmid12704232">{{cite journal |author=Seshadri R, Paulsen IT, Eisen JA, ''et al.'' |title=Complete genome sequence of the Q-fever pathogen Coxiella burnetii |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=100 |issue=9 |pages=5455–60 |year=2003 |month=April |pmid=12704232 |pmc=154366 |doi=10.1073/pnas.0931379100 |url=http://www.pnas.org/cgi/pmidlookup?view=long&pmid=12704232}}</ref> It can be contagious, and is very stable in aerosols in a wide range of temperatures. Q fever [[microorganisms]] may survive on surfaces up to 60 days. | ||
Q fever is a category "B" agent.<ref name="pmid12704232">{{cite journal |author=Seshadri R, Paulsen IT, Eisen JA, ''et al.'' |title=Complete genome sequence of the Q-fever pathogen Coxiella burnetii |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=100 |issue=9 |pages=5455–60 |year=2003 |month=April |pmid=12704232 |pmc=154366 |doi=10.1073/pnas.0931379100 |url=http://www.pnas.org/cgi/pmidlookup?view=long&pmid=12704232}}</ref> It can be contagious, and is very stable in aerosols in a wide range of temperatures. Q fever microorganisms may survive on surfaces up to 60 days. | |||
==References== | ==References== | ||
Revision as of 23:11, 3 June 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Historical Perspective
- It was first described by Edward Holbrook Derrick[1] in abattoir workers in Brisbane, Queensland, Australia.
- The "Q" stands for "query" and was applied at a time when the causative agent was unknown; it was chosen over suggestions of "abattoir fever" and "Queensland rickettsial fever", to avoid directing negative connotations at either the cattle industry or the state of Queensland.[2]
- The pathogen of Q fever was discovered in 1937, when Frank Macfarlane Burnet and Mavis Freeman isolated the bacterium from one of Derrick’s patients.[3]
- It was originally identified as a species of Rickettsia. H.R. Cox and Gordon Davis isolated it from ticks in Montana, USA in 1938.[4] It is a zoonotic disease whose most common animal reservoirs are cattle, sheep and goats. Coxiella burnetii is no longer regarded as closely related to Rickettsiae, but as similar to Legionella and Francisella, and is a proteobacterium.
Biological warfare
- Q fever has been described as a possible biological weapon.[5]
- The United States investigated Q fever as a potential biological warfare agent in the 1950s, with eventual standardization as agent OU. At Fort Detrick and Dugway Proving Ground, human trials were conducted on Whitecoat volunteers to determine the median infective dose (18 MICLD50/person i.h.) and course of infection.
- As a standardized biological, it was manufactured in large quantities at Pine Bluff Arsenal, with 5,098 gallons in the arsenal in bulk at the time of demilitarization in 1970.
- Q fever is a category "B" agent.[6] It can be contagious, and is very stable in aerosols in a wide range of temperatures. Q fever microorganisms may survive on surfaces up to 60 days.
References
- ↑ Derrick EH. Q" fever a new fever entity: clinical features. diagnosis, and laboratory investigation. Med J Aust. 1937;11:281-299.
- ↑ Joseph E. McDade (1990). "Historical Aspects of Q Fever". In Thomas J. Marrie. Q Fever, Volume I: The Disease. CRC Press. p. 8. ISBN 0-8493-5984-8.
- ↑ Burnet FM, Freeman M. Experimental studies on the virus of “Q” fever. Med J Aust 1937; 2: 299-305.
- ↑ Davis, G. E., and H. R. Cox. 1938. A filter-passing infectious agent isolated from ticks. I. Isolation from Dermacentor andersonii, reactions in animals, and filtration. Public Health Rep. 53:2259-2282.
- ↑ Madariaga MG, Rezai K, Trenholme GM, Weinstein RA (2003). "Q fever: a biological weapon in your backyard". Lancet Infect Dis. 3 (11): 709–21. doi:10.1016/S1473-3099(03)00804-1. PMID 14592601. Unknown parameter
|month=ignored (help) - ↑ Seshadri R, Paulsen IT, Eisen JA; et al. (2003). "Complete genome sequence of the Q-fever pathogen Coxiella burnetii". Proc. Natl. Acad. Sci. U.S.A. 100 (9): 5455–60. doi:10.1073/pnas.0931379100. PMC 154366. PMID 12704232. Unknown parameter
|month=ignored (help)