Studies On Molecular Epidemiology Of Brucellosis And Tuberculosis In Cattle And Buffaloes
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Abstract
Brucellosis and tuberculosis are neglected zoonoses having worldwide public
newlinehealth concern. The present study was undertaken to elucidate the prevalence of
newlinebrucellosis and tuberculosis in cattle and buffaloes, detect and identify the species by
newlinePCR, understand the genetic diversity among the detected species, investigate the
newlineantimicrobial resistance of pathogens and evaluate the risk factors associated with the
newlineoccurrence of these diseases.
newlineA total of 1070 samples comprising of 330 blood samples, 185 milk samples,
newline310 nasal swabs and 245 vaginal swabs from 300 cattle and 30 buffaloes which were
newlinereared along with cows were collected and examined for detection of brucellosis and
newlinemycobacteriosis in different production systems viz., intensive (110), semi-intensive
newline(110) and extensive system (110). The overall prevalence of brucellosis and
newlinemycobacteriosis was 6.06% (20/330) and 3.33% (11/330), respectively among the
newlineanimals studied. The prevalence of both the diseases was higher in farms with
newlineintensive production system and larger herd size. Sexually active (2-10 years) and
newlineaged animals (5-10 years) were at risk of infection for brucellosis and tuberculosis,
newlinerespectively. Exotic breeds of cattle were more susceptible to mycobacteriosis
newlinecompared to indigenous breeds.
newlineRose bengal plate test (BPT) and indirect enzyme linked immunosorbent
newlineassay (iELISA) tests revealed almost perfect agreement (and#1050;=0.92) with each other.
newlineWhile, SIT and IFN-and#947; ELISA tests revealed substantial agreement (and#1050;=0.50) with each
newlineother. The species of Brucella recognized by Bruce-ladder multiplex PCR in cattle
newlinewere found to be B. melitensis (4) and B. abortus (5) out of 09 samples confirmed by
newlinePCR. Further, all the Mycobacterium spp. detected by PCR were differentiated as non
newlinetuberculous Mycobacterium (NTM) by commercial qPCR kit. Brucella species
newlinedisplayed genetic homogeneity by both PCR-Restriction Fragment Length
newlinePolymorphism (RFLP) and Repetitive Element Palindromic (REP)-PCR techniques.
newlineMultiple Antimicrobial Resistance (MAR) index for B.abortus