Vascular permeability and coagulation during Rickettsia riekettsii infection in dogs

M. G. Davidson From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by M. G. Davidson in
Current site
Google Scholar
PubMed
Close
 DVM
,
E. B. Breitschwerdt From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by E. B. Breitschwerdt in
Current site
Google Scholar
PubMed
Close
 DVM
,
D. H. Walker From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by D. H. Walker in
Current site
Google Scholar
PubMed
Close
 MD
,
M. G. Levy From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by M. G. Levy in
Current site
Google Scholar
PubMed
Close
 PhD
,
C. S. Carlson From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by C. S. Carlson in
Current site
Google Scholar
PubMed
Close
 DVM
,
E. M. Hardie From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by E. M. Hardie in
Current site
Google Scholar
PubMed
Close
 DVM, PhD
,
C. A. Grindem From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by C. A. Grindem in
Current site
Google Scholar
PubMed
Close
 DVM, PhD
, and
M. P. Nasisse From the Departments of Companion Animal and Special Species Medicine (Davidson, Brietschwerdt, Carlson, Hardie, Nasisse) and Microbiology, Pathology, and Parasitology (Levy, Grindem), College of Veterinary Medicine, North Carolina State Unviersity, 4700 Hillsborough St at William Moore Dr, Raleigh, NC 27606, and the Department of Pathology, University of North Carolina, School of Medicine, Chapel Hill, NC 27514 (Walker).

Search for other papers by M. P. Nasisse in
Current site
Google Scholar
PubMed
Close
 DVM

SUMMARY

The vascular permeability of the ocular fundus, alterations in the coagulation system, and plasma concentrations of thromboxane B2 (txb2) and 6-keto-prostaglandin F, (6-keto-pgf) were studied in dogs following intradermal inoculation with 5 × 105 tcid50 of Rickettsia rickettsii. Twenty-four to 48 hours after the onset of fever and rickettsemia, multifocal areas of retinal vasculitis were evident, which corresponded to areas of altered vascular permeability demonstrated by fluorescein angiography. The number and intensity of retinal vessels with sodium fluorescein leakage peaked during the second week after inoculation, and retinal vascular permeability remained altered during the third week of infection, well past the phase of clinical and clinicopathologic recovery.

Development of retinal vasculitic foci was associated with thrombocytopenia, increased concentrations of circulating fibrinogen, and slight prolongation of activated partial thromboplastin time. Increased concentrations of fibrin/fibrinogen degradation products were detected in 4 of 9 dogs. Despite the degree of vascular endothelial damage evident on fluorescein angiographic and histologic studies in these dogs, plasma txb2 and 6-keto-pgf concentrations were not increased.

SUMMARY

The vascular permeability of the ocular fundus, alterations in the coagulation system, and plasma concentrations of thromboxane B2 (txb2) and 6-keto-prostaglandin F, (6-keto-pgf) were studied in dogs following intradermal inoculation with 5 × 105 tcid50 of Rickettsia rickettsii. Twenty-four to 48 hours after the onset of fever and rickettsemia, multifocal areas of retinal vasculitis were evident, which corresponded to areas of altered vascular permeability demonstrated by fluorescein angiography. The number and intensity of retinal vessels with sodium fluorescein leakage peaked during the second week after inoculation, and retinal vascular permeability remained altered during the third week of infection, well past the phase of clinical and clinicopathologic recovery.

Development of retinal vasculitic foci was associated with thrombocytopenia, increased concentrations of circulating fibrinogen, and slight prolongation of activated partial thromboplastin time. Increased concentrations of fibrin/fibrinogen degradation products were detected in 4 of 9 dogs. Despite the degree of vascular endothelial damage evident on fluorescein angiographic and histologic studies in these dogs, plasma txb2 and 6-keto-pgf concentrations were not increased.

All Time Past Year Past 30 Days
Abstract Views 0 0 0
Full Text Views 9914 9884 1743
PDF Downloads 57 49 7
Advertisement