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ãáÎÕ ÇáÈÍË ÝííííÐååÇííííÓÉåÇÓÊÎÇãííííÇåÇãííííÛÉÊÈØåìííííÎÇ åÈ íííí Çå Î ííííÇå íííí -åäáãíííí íå Ê äííííÒØåÈíííííåÇÓíííí ÎØåÇÓ æÛ ííííÎ åÓáÈÛ ííííÎ åå ÇÓ íííí å ÇÓÈÎÖíííÐåÇÓäãííí ÖÐå ÕíííÎæåÛ íííÐå Öííí ÊåÇÓãííí åÇÓ íííÎÑåÝíííãåäÈíííÒÓäåÈííííåÇÝíííÒØåÛÊÎä ííí åÛííí åÖÈ íííÒåÈííííåÈãíííÒÓ åÝíííãå Ûííí åÇÓ Î ííí å íííÎå 9>%(åÈííííåÖÈáíííÇå 79:2 å ííí ÇíåÛííí åÝ ííí ãåÛííí åÖÈííí å 4:7 å > 4å ííí Çíå 7 > ÇÓÕííí Ç ÙåÇ íííÎåÇÓ ííí åÇÓ íííÒÇÎ å Öííí ÊåÇÝíííÒØå È íííÇåÝíííãå 9 Ê äííííÇå : 98 =>%(åÈíííííåÈãííííá åÇÓãíííí á ÑÇå ííííÇåÇÓ Î íííí (å 97 åÊ äííííÇå <;ã 74 %(åÈíííííåÈÊ äííííÇå Ç å ííííÇå ííííÎåÇÓÕíííí Ç ( åÇÓ íííí å 4åÛíííí åÛÖ ÇííííÒåÈíííííååÇÓ äííííÒØåÇÓ È ííííÇåÇ ííííÎØå Öíííí Êå æÛ Î ííííÒå ííííÒÈÊ åÓá Èííííæãå > ÇÓÈÖ ííííÎ åÓÛãíííí íåìííííÎ Çå ; 9;98 %(åÈíííííå 9 Mycobacterium ÊìíííÎ íå 77977 %(åÈííííå 2<åÇ íííÎØåÇìíííæÒ åÉ íííÇåÈÛ ÎÊíííÇå Ûííí åÛ Î íííÒåÈ íííÊ Òå æÛÎ íííÒåÇÓÈÛ íííÎ åÝÒÎãííí ä Ö ä ãåÛííííí å ÎØåÈÒ íííííÇå (M.bovis ãå ÇÈíííííÒåÇÓãííííí íåÇÓÈÛ íííííÇå => 9>>%(åÛííííí åÛ Î íííííÒåÈ íííííÊ Òå æÛÎ íííííÒåÇÓÈÛ íííííÎ åÇÓ íííííÎ )farcinogenes) å(ãåÊìíííÎ íåÊ äíííÇå < 4499 %(å L J) ÇÎ íííÇå ãííí íåÈííííåÇÓ äíííÒØåÇÓÛíííÐåÓííí åÛ íííÎåÇìíííæÒ åÉ íííÇåÈÛ ÎÊíííÇåÝíííÐåÈãíííÛä ØåÓ äãíííÛ í-åÖäãííííå Ç íííÎØåäÈííí å ÒÇÎ íííÒåÊäíííÊÈÒåÛííí å Öíííä ÒåÊáíííÐåÊÎÖíííÇå íííÎÇÎ å> 8åÊÎÖíííÇåÈ íííÇåÓÈíííÊ å 9-=åÇãíííÒ ãåÇãíííÛÉÊ åÇÓ ííí åÇÓÈÎÖíííÐåÇÓäãííí ÖÐå Ó ííí å 97 åÊ äíííÇåÈííííå íííÇå íííÎåÇÓÕííí Ç å ÇÓíííÓ åÇ íííÎå Öííí ÊåÇÓÛ íííÒ å ííí ÈÐåÈííí ÈíãåäãíííÛäÑåÈííííåÇíííÓÉåÇÓÊÎÇãíííÇåÇíåÇãíííÛÉÊÇ åÛ ÒäíííÒØå ÇÓ ííí åÇÓÈÖ íííÎÑå Ç íííÒÇåÇÓÈÖ Î íííÇå ÇÓ ííí åÇÓÈÎÖííííÐåÇÓäãííí ÖÐå ÈæííííåÇãíííÛÉÊÇÈ ÒåÝíííÐåÝ íííí å ÛÒæ íííÊå Öííí Êå æÛÎ íííÒåÇÓÈÛ íííÎ åÈíííííå å Û ííííÎåÇÖííííÒÝÇåÓá ííííÎ å )PCR) ÇÓ äííííÒØåÇÓÈìÛ ãÇÓ ííííÒØåÇÓÛÒæ Ê ííííÇå ÒãííííÛÉÊÇ åÇÓÛ ÒäííííÒØåÇÓ Ê ãííííÇåÈãíííí åÇÉÛ ííííÒÎåÇÓ Ó Èíííí ÎÇ åÇÓÛãáãííííáÐ ÇÓÛ á Ê ÇåÇÓÈÛ Çå ÒÓ ÒåÝÐåÛÒæ Êå Û Î ÝåÇÓÈ ØåÈíå ÒæÛ Î ÒåÇÓÈÛ Î å Summary Ziehl-Neelsen stained smear, mycobacterial culture and histopathological examination were used to investigate bovine tuberculosis in tuberculosis suspect lesions collected from Omdurman and Wau slaughterhouse. A total of 194 (7.92%) out of 2450 animals examined, displayed granulomatous lesions. One hundred and fifty two (78.35%), specimens were collected from Omdurman Central abattoir, Khartoum State, and the rest, 42 (21.65%), from wau, Bahr El-Ghazal State. Ninty (46.36%) out of 194 smears prepared from granulomatous lesions revealed presence 0f acid-fast bacteria. Twenty (22.22%) out of 90 showed branching filaments organisms identified as Mycobacterium farcinogenes (M. farcinogenes) the remaining 70 (77.78 %) were bacilli and tentatively identified as M. bovis. Of the 174 specimens, that showed no branching filaments, only 20 (11.49%), showed visible growth when plated out onto Lowenstein- Jensen medium (LJ) and incubated aerobically at 37ºC for 4-8 weeks. Histopathologically the 42 specimens from Wau showed chronic granulomatous inflammation. In conclusion, microscopical, bacteriological and Histopathological examinations, are useful techniques in detecting mycobacteria in suspected specimens. Confirmatory molecular biology techniques such as PCR are highly recommended to augment the conventional techniques for thorough identification and characterization of the isolated mycobacteria.

 
 
   
 
 

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