scholarly journals Detection of Mycoplasma hyopneumoniae by polymerase chain reaction in swine presenting respiratory problems

2008 ◽  
Vol 39 (3) ◽  
pp. 471-476 ◽  
Author(s):  
M. Yamaguti ◽  
E.E. Muller ◽  
A.I. Piffer ◽  
J.D. Kich ◽  
C.S. Klein ◽  
...  
1991 ◽  
Vol 5 (2) ◽  
pp. 103-109 ◽  
Author(s):  
Ryô Harasawa ◽  
Kaoru Koshimizu ◽  
Osamu Takeda ◽  
Takashi Uemori ◽  
Kiyozo Asada ◽  
...  

2015 ◽  
Vol 65 (1) ◽  
pp. 79-88 ◽  
Author(s):  
SAVIĆ Božidar ◽  
RADANOVIĆ Oliver ◽  
JOVIČIĆ Dubravka ◽  
NEŠIĆ Ksenija ◽  
IVANOVIĆ Snežana ◽  
...  

Abstract A retrospective study on 235 natural cases of Porcine Respiratory Disease Complex in order to determine the etiological agents, their prevalence and interrelationships was performed in Serbia. Lung tissue samples were analyzed by Polymerase Chain Reaction for the presence of Porcine circovirus type 2, Porcine reproductive and respiratory virus, Swine influenza virus, Mycoplasma hyopneumoniae, Pasteurella multocida, Actinobacillus pleuropneumoniae, Haemophilus parasuis, Streptococcus suis and Arcanobacterium pyogenes. A total of 49 different combinations of viral and bacterial pathogens were found. Five different viral and viral/Mhp co-infections were detected. Monobacterial infections were found in 150 cases and polybacterial infection was detected in 85 samples. PCV2 was the main virus detected, and Pm was the most aggressive secondary pathogen detected in PRDC. The reason for PRDC being so prevalent among Serbian pigs is most likely due to the large number of risk factors in the conventional farrow-to-finish system, compared to multi-site production systems. Therefore, measures aimed at a better control of respiratory viruses, particularly Porcine circovirus type 2 and Porcine reproductive and respiratory virus, as well as Mycoplasma hyopneumoniae infections, and adoption of rational decisions on respiratory bacterial pathogens specific therapeutic and preventive strategies at herd level, simultaneously with significant improvements on farm management should reduce the occurrence of PRDC.


2010 ◽  
Vol 144 (1-2) ◽  
pp. 214-218 ◽  
Author(s):  
M. Sibila ◽  
G. Mentaberre ◽  
M. Boadella ◽  
E. Huerta ◽  
E. Casas-Díaz ◽  
...  

Author(s):  
G. W. Hacker ◽  
I. Zehbe ◽  
J. Hainfeld ◽  
A.-H. Graf ◽  
C. Hauser-Kronberger ◽  
...  

In situ hybridization (ISH) with biotin-labeled probes is increasingly used in histology, histopathology and molecular biology, to detect genetic nucleic acid sequences of interest, such as viruses, genetic alterations and peptide-/protein-encoding messenger RNA (mRNA). In situ polymerase chain reaction (PCR) (PCR in situ hybridization = PISH) and the new in situ self-sustained sequence replication-based amplification (3SR) method even allow the detection of single copies of DNA or RNA in cytological and histological material. However, there is a number of considerable problems with the in situ PCR methods available today: False positives due to mis-priming of DNA breakdown products contained in several types of cells causing non-specific incorporation of label in direct methods, and re-diffusion artefacts of amplicons into previously negative cells have been observed. To avoid these problems, super-sensitive ISH procedures can be used, and it is well known that the sensitivity and outcome of these methods partially depend on the detection system used.


2006 ◽  
Vol 175 (4S) ◽  
pp. 485-486
Author(s):  
Sabarinath B. Nair ◽  
Christodoulos Pipinikas ◽  
Roger Kirby ◽  
Nick Carter ◽  
Christiane Fenske

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