scholarly journals A retroviral survey of endangered Eurasian lynx (Lynx lynx) from Croatia

2021 ◽  
Vol 91 (1) ◽  
pp. 65-71
Author(s):  
Tomislav Gomerčić ◽  
◽  
Matko Perharić ◽  
Josip Kusak ◽  
Vedran Slijepčević ◽  
...  

The feline immunodeficiency virus (FIV) and feline leukemia virus (FeLV) may cause persistent, lifelong and lethal infections in domestic and wild felids worldwide. FIV has been confirmed in most Felidae species, while FeLV infection is rare among non-domestic cats. The view that retroviruses are pathogenic in domestic cats but not in other free-ranging felid species was disproved by recent findings of retroviral pathology in several wild felids. The epidemiology of retroviral infections in felids in Croatia was only investigated in urban domestic cats, while there are no data for wild cat species. As the reintroduced Dinaric lynx (Lynx lynx) population suffers from low genetic diversity, which reduces their ability to adapt to new viral outbreaks, the health status of this lynx population is of particular concern. Two different commercial immunochromatographic assays were used for qualitative detection of FIV antibodies and FeLV antigens, while PCR was used for amplification of proviral gag and env genes in Eurasian lynx blood samples. All the 17 Eurasian lynx samples collected between 2001 and 2019 tested negative in both immunochromatographic and molecular tests. Even though our sample size was rather small, considering the fact that the population size of lynx in Croatia is estimated at 40 - 60 animals, our results can be considered representative for the population’s health status. Also, data about retroviral prevalence in Eurasian lynxes are scarce, so any new findings are very valuable.

2015 ◽  
Vol 90 (3) ◽  
pp. 1470-1485 ◽  
Author(s):  
Jumpei Ito ◽  
Takuya Baba ◽  
Junna Kawasaki ◽  
Kazuo Nishigaki

ABSTRACTEndogenous retroviruses (ERVs) are remnants of ancestral retroviral infections of germ cells. Retroviral endogenization is an adaptation process for the host genome, and ERVs are gradually attenuated or inactivated by mutation. However, some ERVs that have been “domesticated” by their hosts eventually gain physiological functions, such as placentation or viral resistance. We previously reported the discovery of Refrex-1, a soluble antiretroviral factor in domestic cats that specifically inhibits infection by feline leukemia virus subgroup D (FeLV-D), a chimeric virus of FeLV, and a feline ERV, ERV-DC. Refrex-1 is a truncated envelope protein (Env) encoded by both ERV-DC7 and ERV-DC16 proviral loci. Here, we reconstituted ancestral and functional Env from ERV-DC7 and ERV-DC16 envelope genes (env) by inducing reverse mutations. Unexpectedly, ERV-DC7 and ERV-DC16 full-length Env (ERV-DC7 fl and ERV-DC16 fl), reconstructed by removing stop codons, did not produce infectious viral particles. ERV-DC7 fl and ERV-DC16 fl were highly expressed in cells but were not cleaved into surface subunits (SU) and transmembrane subunits, nor were they incorporated into virions. G407R/N427I-A429T and Y431D substitutions within the SU C-terminal domain of ERV-DC7 fl and ERV-DC16 fl, respectively, caused these dysfunctions. The residues glycine 407 and tyrosine 431 are relatively conserved among infectious gammaretroviruses, and their substitution causes the same dysfunctions as the tested retroviruses. Our results reveal that specific mutations within the SU C-terminal domain suppressed Env cleavage and incorporation into virions and indicate that these mutations contributed to the domestication of Refrex-1 through multistep events that occurred in the postintegration period.IMPORTANCEDomestic cats are colonized with various exogenous retroviruses (exRVs), such as feline leukemia virus (FeLV), and their genomes contain numerous ERVs, some of which are replication-competent proviruses. The feline hosts, exRVs, and ERVs have complicated genetic interactions and provide an interesting field model for triangular relationships: recombination between FeLV and ERV-DC, which is a feline ERV, generated FeLV-D, a chimeric virus, and FeLV-D is restricted by Refrex-1, an antiretroviral factor corresponding to truncated Env of ERV-DC7 and ERV-DC16. Here, we reconstructed ancestral, functional Env from ERV-DC7 and ERV-DC16envby inducing reverse mutations to elucidate how Refrex-1 was generated from its ancestor. Our results reveal that they were repeatedly inactivated by mutations preventing Env maturation. Our results provide insights into how ERVs were “domesticated” by their hosts and identify the mutations that mediated these evolutions. Notably, experiments that restore inactivated ERVs might uncover previously unrecognized features or properties of retroviruses.


2017 ◽  
Vol 29 (6) ◽  
pp. 889-895 ◽  
Author(s):  
Isaac Makundi ◽  
Yushi Koshida ◽  
Kyohei Kuse ◽  
Takahiro Hiratsuka ◽  
Jumpei Ito ◽  
...  

2010 ◽  
Vol 134 (1-2) ◽  
pp. 61-67 ◽  
Author(s):  
Marina L. Meli ◽  
Valentino Cattori ◽  
Fernando Martínez ◽  
Guillermo López ◽  
Astrid Vargas ◽  
...  

2017 ◽  
Vol 29 (5) ◽  
pp. 660-668 ◽  
Author(s):  
Mariana M. Furtado ◽  
Sueli A. Taniwaki ◽  
Iracema N. de Barros ◽  
Paulo E. Brandão ◽  
José L. Catão-Dias ◽  
...  

We describe molecular testing for felid alphaherpesvirus 1 (FHV-1), carnivore protoparvovirus 1 (CPPV-1), feline calicivirus (FCV), alphacoronavirus 1 (feline coronavirus [FCoV]), feline leukemia virus (FeLV), feline immunodeficiency virus (FIV), and canine distemper virus (CDV) in whole blood samples of 109 free-ranging and 68 captive neotropical felids from Brazil. Samples from 2 jaguars ( Panthera onca) and 1 oncilla ( Leopardus tigrinus) were positive for FHV-1; 2 jaguars, 1 puma ( Puma concolor), and 1 jaguarundi ( Herpairulus yagouaroundi) tested positive for CPPV-1; and 1 puma was positive for FIV. Based on comparison of 103 nucleotides of the UL24-UL25 gene, the FHV-1 sequences were 99–100% similar to the FHV-1 strain of domestic cats. Nucleotide sequences of CPPV-1 were closely related to sequences detected in other wild carnivores, comparing 294 nucleotides of the VP1 gene. The FIV nucleotide sequence detected in the free-ranging puma, based on comparison of 444 nucleotides of the pol gene, grouped with other lentiviruses described in pumas, and had 82.4% identity with a free-ranging puma from Yellowstone Park and 79.5% with a captive puma from Brazil. Our data document the circulation of FHV-1, CPPV-1, and FIV in neotropical felids in Brazil.


2020 ◽  
Vol 94 (21) ◽  
Author(s):  
Elliott S. Chiu ◽  
Sue VandeWoude

ABSTRACT While feline leukemia virus (FeLV) has been shown to infect felid species other than the endemic domestic cat host, differences in FeLV susceptibility among species has not been evaluated. Previous reports have noted a negative correlation between endogenous FeLV (enFeLV) copy number and exogenous FeLV (exFeLV) infection outcomes in domestic cats. Since felids outside the genus Felis do not harbor enFeLV genomes, we hypothesized absence of enFeLV results in more severe disease consequences in felid species lacking these genomic elements. We infected primary fibroblasts isolated from domestic cats (Felis catus) and pumas (Puma concolor) with FeLV and quantitated proviral and viral antigen loads. Domestic cat enFeLV env and long terminal repeat (LTR) copy numbers were determined for each individual and compared to FeLV viral outcomes. FeLV proviral and antigen levels were also measured in 6 naturally infected domestic cats and 11 naturally infected Florida panthers (P. concolor coryi). We demonstrated that puma fibroblasts are more permissive to FeLV than domestic cat cells, and domestic cat FeLV restriction was highly related to enFeLV-LTR copy number. Terminal tissues from FeLV-infected Florida panthers and domestic cats had similar exFeLV proviral copy numbers, but Florida panther tissues have higher FeLV antigen loads. Our work indicates that enFeLV-LTR elements negatively correlate with exogenous FeLV replication. Further, Puma concolor samples lacking enFeLV are more permissive to FeLV infection than domestic cat samples, suggesting that endogenization can play a beneficial role in mitigating exogenous retroviral infections. Conversely, presence of endogenous retroelements may relate to new host susceptibility during viral spillover events. IMPORTANCE Feline leukemia virus (FeLV) can infect a variety of felid species. Only the primary domestic cat host and related small cat species harbor a related endogenous virus in their genomes. Previous studies noted a negative association between the endogenous virus copy number and exogenous virus infection in domestic cats. This report shows that puma cells, which lack endogenous FeLV, produce more virus more rapidly than domestic cat fibroblasts following cell culture challenge. We document a strong association between domestic cat cell susceptibility and FeLV long terminal repeat (LTR) copy number, similar to observations in natural FeLV infections. Viral replication does not, however, correlate with FeLV env copy number, suggesting that this effect is specific to FeLV-LTR elements. This discovery indicates a protective capacity of the endogenous virus against the exogenous form, either via direct interference or indirectly via gene regulation, and may suggest evolutionary outcomes of retroviral endogenization.


2018 ◽  
Vol 96 (8) ◽  
pp. 839-846 ◽  
Author(s):  
S.V. Naidenko ◽  
J.A. Hernandez-Blanco ◽  
E.V. Pavlova ◽  
M.N. Erofeeva ◽  
P.A. Sorokin ◽  
...  

Seroprevalence to nine different virus pathogens was estimated for Russian big cats (Amur tiger (Panthera tigris altaica Temminck, 1844) and far-eastern leopard (Panthera pardus orientalis (Schiegel, 1857))) in Southern Primorie, Russia (n = 25), in 2008–2016. Serum samples from smaller cats (Eurasian lynx (Lynx lynx (Linnaeus, 1758)) and far-eastern wildcat (leopard cat) (Prionailurus bengalensis euptilurus (Elliot, 1871))) were also tested for these pathogens (n = 19) during the same period. Felids of Russian Southern Primorie showed seroprevalence to eight out of nine tested pathogens, including highly dangerous feline immunodeficiency virus, feline leukemia virus, and canine distemper virus. Antibodies to feline panleukopenia virus were found to be much more widespread in cats (45%) than antibodies to any other virus. They were detected in samples taken from tigers, leopards, and far-eastern wildcats but not lynxes. Antibodies to pseudorabies virus were detected only in Amur tiger (29%), whose main prey is the most common carrier of the virus (wild boar), unlike for the other studied cats’ species.


1997 ◽  
Vol 75 (12) ◽  
pp. 1994-2002 ◽  
Author(s):  
Emmanuelle Fromont ◽  
Franck Courchamp ◽  
Dominique Pontier ◽  
Marc Artois

It is thought that parasites may exert selective pressure on the social structure of host populations. We compared the impact of feline immunodeficiency virus (FIV) and feline leukemia virus (FeLV), two retroviruses commonly found in domestic cats (Felis catus). Because of low transmissibility and virulence, both infections have a worldwide distribution and low prevalence. Transmission modes differ: FIV is transmitted only through biting, while FeLV transmission occurs by biting, licking, grooming, and sharing food and from mother to fetus. FeLV is also more pathogenic than FIV. We compared FIV and FeLV prevalence and risk factors within five populations of cats. FIV infection occurred almost exclusively among adult male cats fighting to acquire and maintain dominant status. Classes at risk for FeLV infection included sexually intact cats allowed to roam freely. The impact of FeLV on host population growth was greater than that of FIV but varied among populations. Our results show that FIV is favoured by individual aggressiveness and a hierarchical social system, while FeLV is more prevalent among socially active cats. FeLV may constitute a source of selective pressure against numerous amicable contacts, particularly in urban cat populations, where aggression among individuals is reduced.


2012 ◽  
Vol 14 (8) ◽  
pp. 583-586 ◽  
Author(s):  
Nadia R de Almeida ◽  
Maria G M Danelli ◽  
Lucia H P da Silva ◽  
Mitika K Hagiwara ◽  
Carlos Mazur

2020 ◽  
Author(s):  
Elliott S. Chiu ◽  
Sue VandeWoude

AbstractWhile feline leukemia virus (FeLV) has been shown to infect felid species other than the endemic domestic cat host, differences in FeLV susceptibility among species has not been evaluated. Previous reports have noted a negative correlation between enFeLV copy number and exogenous FeLV infection outcomes in domestic cats. Since felids outside the genus Felis do not harbor enFeLV genomes, we hypothesized absence of enFeLV results in more severe disease consequences in felid species lacking these genomic elements. We infected primary fibroblasts isolated from domestic cats (Felis catus) and pumas (Puma concolor) with FeLV and quantitated proviral and viral antigen loads. Domestic cat enFeLV env and LTR copy numbers were determined for each individual and compared to FeLV viral outcomes. FeLV proviral and antigen levels were also measured in 6 naturally infected domestic cats and 11 naturally infected Florida panthers (P. concolor coryi). We demonstrated that puma fibroblasts are more permissive to FeLV than domestic cat cells, and domestic cat FeLV restriction was highly related to enFeLV LTR copy number. Terminal tissues from FeLV-infected Florida panthers and domestic cats had similar exFeLV proviral copy numbers, but Florida panther tissues have higher FeLV antigen loads. Our work indicates enFeLV LTR elements negatively regulate exogenous FeLV replication. Further, Puma concolor lacking enFeLV are more permissive to FeLV infection than domestic cats, suggesting endogenization can play a beneficial role in mitigating exogenous retroviral infections. Conversely, presence of endogenous retroelements may relate to new host susceptibility during viral spillover events.ImportanceFeline leukemia virus (FeLV) can infect a variety of felid species. Only the primary domestic cat host and related small cat species harbor a related endogenous virus in their genomes. Previous studies noted a negative association between the endogenous virus copy number and exogenous virus infection in domestic cats. This report shows that puma cells, which lack endogenous FeLV, produce more virus more rapidly than domestic cat fibroblasts following cell culture challenge. We document a strong association between domestic cat cell susceptibility and FeLV long terminal repeat (LTR) copy number, similar to observations in natural FeLV infections. Viral replication does not, however, correlate with FeLV env copy number, suggesting this effect is specific to FeLV LTR elements. This discovery indicates a protective capacity of the endogenous virus against the exogenous form, either via direct interference or indirectly via gene regulation, and may suggest evolutionary outcomes of retroviral endogenization.


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