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   Detection of Leishmania RNA Virus in Leishmania Parasites  
   
نویسنده zangger h. ,ronet c. ,desponds c. ,kuhlmann f.m. ,robinson j. ,hartley m.-a. ,prevel f. ,castiglioni p. ,pratlong f. ,bastien p. ,müller n. ,parmentier l. ,saravia n.g. ,beverley s.m. ,fasel n.
منبع plos neglected tropical diseases - 2013 - دوره : 7 - شماره : 1
چکیده    Background: patients suffering from cutaneous leishmaniasis (cl) caused by new world leishmania (viannia) species are at high risk of developing mucosal (ml) or disseminated cutaneous leishmaniasis (dcl). after the formation of a primary skin lesion at the site of the bite by a leishmania-infected sand fly,the infection can disseminate to form secondary lesions. this metastatic phenotype causes significant morbidity and is often associated with a hyper-inflammatory immune response leading to the destruction of nasopharyngeal tissues in ml,and appearance of nodules or numerous ulcerated skin lesions in dcl. recently,we connected this aggressive phenotype to the presence of leishmania rna virus (lrv) in strains of l. guyanensis,showing that lrv is responsible for elevated parasitaemia,destructive hyper-inflammation and an overall exacerbation of the disease. further studies of this relationship and the distribution of lrvs in other leishmania strains and species would benefit from improved methods of viral detection and quantitation,especially ones not dependent on prior knowledge of the viral sequence as lrvs show significant evolutionary divergence. methodology/principal findings: this study reports various techniques,among which,the use of an anti-dsrna monoclonal antibody (j2) stands out for its specific and quantitative recognition of dsrna in a sequence-independent fashion. applications of j2 include immunofluorescence,elisa and dot blot: techniques complementing an arsenal of other detection tools,such as nucleic acid purification and quantitative real-time-pcr. we evaluate each method as well as demonstrate a successful lrv detection by the j2 antibody in several parasite strains,a freshly isolated patient sample and lesion biopsies of infected mice. conclusions/significance: we propose that refinements of these methods could be transferred to the field for use as a diagnostic tool in detecting the presence of lrv,and potentially assessing the lrv-related risk of complications in cutaneous leishmaniasis. © 2013 zangger et al.
آدرس department of biochemistry,university of lausanne,epalinges,vaud, Switzerland, department of biochemistry,university of lausanne,epalinges,vaud, Switzerland, department of biochemistry,university of lausanne,epalinges,vaud, Switzerland, department of medicine,division of infectious diseases,washington university school of medicine,st. louis,mo, United States, department of molecular microbiology,washington university school of medicine,st. louis,mo, United States, department of biochemistry,university of lausanne,epalinges,vaud, Switzerland, department of biochemistry,university of lausanne,epalinges,vaud, Switzerland, department of biochemistry,university of lausanne,epalinges,vaud, Switzerland, french national reference centre for leishmaniases,département de parasitologie-mycologie,chru de montpellier,montpellier,france,university montpellier 1,faculty of medicine,umr cnrs 5290/ird 224/um1/um2 mivegec,montpellier, France, french national reference centre for leishmaniases,département de parasitologie-mycologie,chru de montpellier,montpellier,france,university montpellier 1,faculty of medicine,umr cnrs 5290/ird 224/um1/um2 mivegec,montpellier, France, institute of parasitology,vetsuisse faculty berne,university of bern,bern, Switzerland, department of dermatology,hôpitaux du valais,sierre,valais, Switzerland, centro internacional de entrenamiento e investigaciones médicas (cideim),cali, Colombia, department of molecular microbiology,washington university school of medicine,st. louis,mo, United States, department of biochemistry,university of lausanne,epalinges,vaud, Switzerland
 
     
   
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