Literature DB >> 15327797

Impact of sawdust and wood shavings in bedding on pig tuberculous lesions in lymph nodes, and IS1245 RFLP analysis of Mycobacterium avium subsp. hominissuis of serotypes 6 and 8 isolated from pigs and environment.

L Matlova1, L Dvorska, K Palecek, L Maurenc, M Bartos, I Pavlik.   

Abstract

Among 25,027 slaughter pigs raised in two farms, tuberculous lesions were detected in the lymph nodes of 898 (3.6%) of them. Tuberculous lesions were most commonly found in the mesenteric (601; 2.4%) and head (451; 1.8%) lymph nodes. Mycobacteria were isolated from 49 of 120 randomly selected mesenteric, head and bronchial lymph nodes with diagnosed tuberculosis originating from both farms. Forty six Mycobacterium avium subsp. hominissuis, one M. chelonae and two M. fortuitum isolates were found in the lymph nodes of pigs. No statistically significant difference was detected between farms A and B for isolation rates of mycobacteria from the lymph nodes of pigs and their species composition. To investigate the source of the pigs' infections, culture examinations of 117 samples from the external environment were performed. Mycobacteria were isolated from 25 samples from the external environment (21.4%). Mycobacterial isolates were also detected in eleven (91.7%) and two (16.7%) of 12 used sawdust and 12 of non-used (fresh) sawdust samples, respectively. None of 12 wood shavings was culture-positive. Twelve of 13 sawdust isolates were classified as M. a. hominissuis of serotypes 6 and 8 and genotype IS901- and IS1245+; the remaining isolate was classified as species M. fortuitum. Other conditionally pathogenic mycobacteria were only isolated from 12 of the remaining 81 samples from the external environment (excluding bedding). A total of eight isolates (two pig and six sawdust samples originating from farms A and B) were examined by IS1245 restriction fragment length polymorphism (IS1245 RFLP) analysis. These isolates produced five distinct IS1245 RFLP types with more than 20 bands. Based on identical IS1245 RFLP types of one pig isolate and two isolates of used sawdust from farm A, we have concluded that contaminated sawdust was the source of mycobacterial infection for pigs in our study.

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Year:  2004        PMID: 15327797     DOI: 10.1016/j.vetmic.2004.06.003

Source DB:  PubMed          Journal:  Vet Microbiol        ISSN: 0378-1135            Impact factor:   3.293


  23 in total

1.  Risk factors of non-tuberculous mycobacterial lymphadenitis in children: a case-control study.

Authors:  Patricia W Garcia-Marcos; Mercedes Plaza-Fornieles; Ana Menasalvas-Ruiz; Ramon Ruiz-Pruneda; Pedro Paredes-Reyes; Santiago Alfayate Miguelez
Journal:  Eur J Pediatr       Date:  2017-03-06       Impact factor: 3.183

2.  Microbiomes of unreactive and pathologically altered ileocecal lymph nodes of slaughter pigs.

Authors:  Evelyne Mann; Monika Dzieciol; Barbara U Metzler-Zebeli; Martin Wagner; Stephan Schmitz-Esser
Journal:  Appl Environ Microbiol       Date:  2013-10-18       Impact factor: 4.792

3.  Efficient differentiation of Mycobacterium avium complex species and subspecies by use of five-target multiplex PCR.

Authors:  Sung Jae Shin; Byung Soo Lee; Won-Jung Koh; Elizabeth J B Manning; Kelly Anklam; Srinand Sreevatsan; Randall S Lambrecht; Michael T Collins
Journal:  J Clin Microbiol       Date:  2010-09-01       Impact factor: 5.948

4.  Pathogenesis of systemic Mycobacterium avium infection in pigs through histological analysis of hepatic lesions.

Authors:  Kenji Hibiya; Kimiko Utsunomiya; Takashi Yoshida; Satoshi Toma; Futoshi Higa; Masao Tateyama; Jiro Fujita
Journal:  Can J Vet Res       Date:  2010-10       Impact factor: 1.310

5.  Sequencing of hsp65 distinguishes among subsets of the Mycobacterium avium complex.

Authors:  Christine Y Turenne; Makeda Semret; Debby V Cousins; Desmond M Collins; Marcel A Behr
Journal:  J Clin Microbiol       Date:  2006-02       Impact factor: 5.948

6.  "Mycobacterium avium subsp. hominissuis" in neck lymph nodes of children and their environment examined by culture and triplex quantitative real-time PCR.

Authors:  Marija Kaevska; Iva Slana; Petr Kralik; Udo Reischl; Jaroslava Orosova; Alena Holcikova; Ivo Pavlik
Journal:  J Clin Microbiol       Date:  2010-11-17       Impact factor: 5.948

7.  Persistence of Mycobacterium avium subsp. paratuberculosis at a farm-scale biogas plant supplied with manure from paratuberculosis-affected dairy cattle.

Authors:  I Slana; R Pribylova; A Kralova; I Pavlik
Journal:  Appl Environ Microbiol       Date:  2011-03-11       Impact factor: 4.792

8.  Comparison of variable-number tandem-repeat markers typing and IS1245 restriction fragment length polymorphism fingerprinting of Mycobacterium avium subsp. hominissuis from human and porcine origins.

Authors:  Taneli Tirkkonen; Jaakko Pakarinen; Elina Rintala; Terhi Ali-Vehmas; Harri Marttila; Olli At Peltoniemi; Johanna Mäkinen
Journal:  Acta Vet Scand       Date:  2010-03-10       Impact factor: 1.695

Review 9.  Mycobacterium avium in the postgenomic era.

Authors:  Christine Y Turenne; Richard Wallace; Marcel A Behr
Journal:  Clin Microbiol Rev       Date:  2007-04       Impact factor: 26.132

10.  Mycobacterium avium subsp. paratuberculosis and M. avium subsp. avium are independently evolved pathogenic clones of a much broader group of M. avium organisms.

Authors:  Christine Y Turenne; Desmond M Collins; David C Alexander; Marcel A Behr
Journal:  J Bacteriol       Date:  2008-02-01       Impact factor: 3.490

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