scholarly journals Cytoplasmic Inclusions in Corn Snakes, Elaphe guttata, Resembling Inclusion Body Disease of Boid Snakes

2003 ◽  
Vol 13 (2) ◽  
pp. 18-22 ◽  
Author(s):  
Gregory J. Fleming ◽  
Darryl J. Heard ◽  
Elliott R. Jacobson ◽  
Claus Buergelt
2017 ◽  
Vol 91 (15) ◽  
Author(s):  
Mark D. Stenglein ◽  
David Sanchez-Migallon Guzman ◽  
Valentina E. Garcia ◽  
Marylee L. Layton ◽  
Laura L. Hoon-Hanks ◽  
...  

ABSTRACT Inclusion body disease (IBD) is an infectious disease originally described in captive snakes. It has traditionally been diagnosed by the presence of large eosinophilic cytoplasmic inclusions and is associated with neurological, gastrointestinal, and lymphoproliferative disorders. Previously, we identified and established a culture system for a novel lineage of arenaviruses isolated from boa constrictors diagnosed with IBD. Although ample circumstantial evidence suggested that these viruses, now known as reptarenaviruses, cause IBD, there has been no formal demonstration of disease causality since their discovery. We therefore conducted a long-term challenge experiment to test the hypothesis that reptarenaviruses cause IBD. We infected boa constrictors and ball pythons by cardiac injection of purified virus. We monitored the progression of viral growth in tissues, blood, and environmental samples. Infection produced dramatically different disease outcomes in snakes of the two species. Ball pythons infected with Golden Gate virus (GoGV) and with another reptarenavirus displayed severe neurological signs within 2 months, and viral replication was detected only in central nervous system tissues. In contrast, GoGV-infected boa constrictors remained free of clinical signs for 2 years, despite high viral loads and the accumulation of large intracellular inclusions in multiple tissues, including the brain. Inflammation was associated with infection in ball pythons but not in boa constrictors. Thus, reptarenavirus infection produces inclusions and inclusion body disease, although inclusions per se are neither necessarily associated with nor required for disease. Although the natural distribution of reptarenaviruses has yet to be described, the different outcomes of infection may reflect differences in geographical origin. IMPORTANCE New DNA sequencing technologies have made it easier than ever to identify the sequences of microorganisms in diseased tissues, i.e., to identify organisms that appear to cause disease, but to be certain that a candidate pathogen actually causes disease, it is necessary to provide additional evidence of causality. We have done this to demonstrate that reptarenaviruses cause inclusion body disease (IBD), a serious transmissible disease of snakes. We infected boa constrictors and ball pythons with purified reptarenavirus. Ball pythons fell ill within 2 months of infection and displayed signs of neurological disease typical of IBD. In contrast, boa constrictors remained healthy over 2 years, despite high levels of virus throughout their bodies. This difference matches previous reports that pythons are more susceptible to IBD than boas and could reflect the possibility that boas are natural hosts of these viruses in the wild.


mBio ◽  
2012 ◽  
Vol 3 (4) ◽  
Author(s):  
Mark D. Stenglein ◽  
Chris Sanders ◽  
Amy L. Kistler ◽  
J. Graham Ruby ◽  
Jessica Y. Franco ◽  
...  

ABSTRACTInclusion body disease (IBD) is an infectious fatal disease of snakes typified by behavioral abnormalities, wasting, and secondary infections. At a histopathological level, the disease is identified by the presence of large eosinophilic cytoplasmic inclusions in multiple tissues. To date, no virus or other pathogen has been definitively characterized or associated with the disease. Using a metagenomic approach to search for candidate etiologic agents in snakes with confirmed IBD, we identified andde novoassembled the complete genomic sequences of two viruses related to arenaviruses, and a third arenavirus-like sequence was discovered by screening an additional set of samples. A continuous boa constrictor cell line was established and used to propagate and isolate one of the viruses in culture. Viral nucleoprotein was localized and concentrated within large cytoplasmic inclusions in infected cells in culture and tissues from diseased snakes. In total, viral RNA was detected in 6/8 confirmed IBD cases and 0/18 controls. These viruses have a typical arenavirus genome organization but are highly divergent, belonging to a lineage separate from that of the Old and New World arenaviruses. Furthermore, these viruses encode envelope glycoproteins that are more similar to those of filoviruses than to those of other arenaviruses. These findings implicate these viruses as candidate etiologic agents of IBD. The presence of arenaviruses outside mammals reveals that these viruses infect an unexpectedly broad range of species and represent a new reservoir of potential human pathogens.IMPORTANCEInclusion body disease (IBD) is a common infectious disease of captive snakes. IBD is fatal and can cause the loss of entire animal collections. The cause of the disease has remained elusive, and no treatment exists. In addition to being important to pet owners, veterinarians, breeders, zoological parks, and aquariums, the study of animal disease is significant since animals are the source of virtually every emerging infectious human disease. We searched for candidate causative agents in snakes diagnosed with IBD and found a group of novel viruses distantly related mainly to arenaviruses but also to filoviruses, both of which can cause fatal hemorrhagic fevers when transmitted from animals to humans. In addition to providing evidence that strongly suggests that these viruses cause snake IBD, this discovery reveals a new and unanticipated domain of virus biology and evolution.


Development ◽  
1963 ◽  
Vol 11 (4) ◽  
pp. 659-665
Author(s):  
Vergil H. Ferm ◽  
Lawrence Kilham

The objective of our present studies has been to follow the course of mumps virus when injected intravenously into pregnant hamsters during early stages of gestation, in order to determine possible relations to fetal disease and/or malformations. Several considerations prompted the selection of mumps virus for these investigations. One was that, while rubella (Gregg, 1941) and cytomegalic inclusion body disease (Weller & Hanshaw, 1962) have been the only two viruses shown to have a definite cause-effect relation in the etiology of human congenital malformations, there has been a continuing suspicion that mumps virus may also act as a teratogenic agent in human pregnancy (Kaye & Reaney, 1962; Blattner & Heys, 1961; Hyatt, 1961). A second reason was that mumps virus has a natural pathogenicity for hamsters (Kilham & Overman, 1953). In addition, this agent is capable of infecting women at term, the strain used in present experiments having been obtained from human milk a few days post-partum (Kilham, 1951).


2012 ◽  
Vol 23 (11) ◽  
pp. 2057-2065 ◽  
Author(s):  
Yang Wang ◽  
Girish C. Melkani ◽  
Jennifer A. Suggs ◽  
Anju Melkani ◽  
William A. Kronert ◽  
...  

Hereditary myosin myopathies are characterized by variable clinical features. Inclusion body myopathy 3 (IBM-3) is an autosomal dominant disease associated with a missense mutation (E706K) in the myosin heavy chain IIa gene. Adult patients experience progressive muscle weakness. Biopsies reveal dystrophic changes, rimmed vacuoles with cytoplasmic inclusions, and focal disorganization of myofilaments. We constructed a transgene encoding E706K myosin and expressed it in Drosophila (E701K) indirect flight and jump muscles to establish a novel homozygous organism with homogeneous populations of fast IBM-3 myosin and muscle fibers. Flight and jump abilities were severely reduced in homozygotes. ATPase and actin sliding velocity of the mutant myosin were depressed >80% compared with wild-type myosin. Light scattering experiments and electron microscopy revealed that mutant myosin heads bear a dramatic propensity to collapse and aggregate. Thus E706K (E701K) myosin appears far more labile than wild-type myosin. Furthermore, mutant fly fibers exhibit ultrastructural hallmarks seen in patients, including cytoplasmic inclusions containing aberrant proteinaceous structures and disorganized muscle filaments. Our Drosophila model reveals the unambiguous consequences of the IBM-3 lesion on fast muscle myosin and fibers. The abnormalities observed in myosin function and muscle ultrastructure likely contribute to muscle weakness observed in our flies and patients.


2009 ◽  
Vol 141 (4) ◽  
pp. 305
Author(s):  
B. Richter ◽  
H. Eblinger ◽  
A. Kübber-Heiss

2008 ◽  
Vol 44 (3) ◽  
pp. 622-628 ◽  
Author(s):  
Marie E. Pinkerton ◽  
James F. X. Wellehan ◽  
April J. Johnson ◽  
April J. Childress ◽  
Scott D. Fitzgerald ◽  
...  

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