TY - JOUR
T1 - Prevalence of tuberculous lymphadenitis in slaughtered cattle in Eastern Cape, South Africa
AU - Bhembe, Nolwazi L.
AU - Jaja, Ishmael F.
AU - Nwodo, Uchechukwu U.
AU - Okoh, Anthony I.
AU - Green, Ezekiel
N1 - Publisher Copyright:
© 2017 The Author(s)
PY - 2017/8
Y1 - 2017/8
N2 - Objective To detect the prevalence of Mycobacterium tuberculosis complex (MTBC) in the lymph nodes of slaughtered cattle collected from selected abattoirs in Eastern Cape Province of South Africa. Methods A total of 376 lymph nodes were collected from slaughtered cattle over a period of 12 months. Certain characteristics (sex, age, body condition score, and breed) were observed to be associated with MTBC among slaughtered cattle. Collected samples were cultured and tested for acid-fast bacilli (AFB). DNA was isolated, purified, and quantified using a spectrophotometer. Quantified DNA was confirmed to be MTBC by multiplex PCR targeting two genes (IS6110 and mpb64). Results Of the 376 collected lymph nodes, 182 were positive when tested by Ziehl–Neelsen stain and 162 were confirmed positive for MTBC by PCR. MTBC was isolated from lymph nodes with nodular lesions (72.8%, 118/162) and inflamed lymph nodes (27.1%, 44/162). All detected MTBC isolates were positive for region of deletion 1 (RD1). No isolate was detected to have Mycobacterium bovis bacille Calmette–Guérin (BCG). However, 3.1% had M. bovis and 96.9% had M. tuberculosis. Conclusions The presence of live Mycobacterium strains in slaughtered cattle poses a health risk to beef consumers and abattoir workers.
AB - Objective To detect the prevalence of Mycobacterium tuberculosis complex (MTBC) in the lymph nodes of slaughtered cattle collected from selected abattoirs in Eastern Cape Province of South Africa. Methods A total of 376 lymph nodes were collected from slaughtered cattle over a period of 12 months. Certain characteristics (sex, age, body condition score, and breed) were observed to be associated with MTBC among slaughtered cattle. Collected samples were cultured and tested for acid-fast bacilli (AFB). DNA was isolated, purified, and quantified using a spectrophotometer. Quantified DNA was confirmed to be MTBC by multiplex PCR targeting two genes (IS6110 and mpb64). Results Of the 376 collected lymph nodes, 182 were positive when tested by Ziehl–Neelsen stain and 162 were confirmed positive for MTBC by PCR. MTBC was isolated from lymph nodes with nodular lesions (72.8%, 118/162) and inflamed lymph nodes (27.1%, 44/162). All detected MTBC isolates were positive for region of deletion 1 (RD1). No isolate was detected to have Mycobacterium bovis bacille Calmette–Guérin (BCG). However, 3.1% had M. bovis and 96.9% had M. tuberculosis. Conclusions The presence of live Mycobacterium strains in slaughtered cattle poses a health risk to beef consumers and abattoir workers.
KW - Amplification
KW - Bovine tuberculosis
KW - Fingerprinting
KW - Multiplex PCR
UR - http://www.scopus.com/inward/record.url?scp=85021146554&partnerID=8YFLogxK
U2 - 10.1016/j.ijid.2017.05.005
DO - 10.1016/j.ijid.2017.05.005
M3 - Article
C2 - 28552545
AN - SCOPUS:85021146554
SN - 1201-9712
VL - 61
SP - 27
EP - 37
JO - International Journal of Infectious Diseases
JF - International Journal of Infectious Diseases
ER -