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The purpose of this study was to analyze the correlation of the rate of Mycoplasma hyopneumoniae (M. hyo) in slaughter pigs with season, climate change and enzootic pneumonia (EP) lesions. We collected 530 slaughter pig lungs with suspected lesions from two slaughterhouses in different seasons and weather conditions from November 2014 to March 2017 in Changsha Hunan Province, China. The EP lesions of these lungs were quantified, and a PCR analysis was used to detect M. hyo in samples of bronchoalveolar lavage fluid (BALF). Twenty percent, 10%, and 9% of the lung specimens were scored 1-5, 6-10, and ≥ 11, respectively. Additionally, we found that 36% of all BALF samples tested positive for M. hyo. Among the lung specimens collected in winter, 41% scored 1 or more, and 53% tested positive for M. hyo. With respect to seasons, the lung specimens collected in summer showed the least number of EP lesions and the lowest positive testing rate for M. hyo. Of these specimens, 27% scored 1 or more, and 22% tested positive for M. hyo. Additionally, low temperature and fast temperature change (during 10 days before sampling) were associated with a higher rate of M. hyo detection in BALF. There was a positive correlation between the lung EP lesion score and the detection rate of M. hyo in the BALF of slaughter pigs. In conclusion, lung EP lesion scoring in slaughter pigs is of referential value to the evaluation of the dynamics of M. hyo infection in a swine population. It is essential to control the spread of M. hyo by careful management of swine populations, and the prevention and control of M. hyo in fattening pigs is of great significance to the eradication of the disease.
Pasteurella multocida (P. multocida), an opportunistic zoonotic pathogen associated with high morbidity and mortality in livestock, shows significant temporal and geographical variation in its serotype distributions and phenotypic characteristics. The aim of this study was To investigate capsular types, lipopolysaccharide (LPS) genotypes, and virulence-associated genes of P. multocida strains isolated from pigs. A total of 801 samples (lungs, tonsils, nasal swabs) were collected from slaughterhouses and various regions of the Hunan province. P. multocida strains were isolated from various samples, classified, and virulence-associated genes were detected by polymerase chain reaction (PCR). 124 P. multocida strains were assigned to six groups based on both capsular type and LPS genotype, namely A: L3 (capsular type A and LPS genotype 3, 64/124); A: L6 (16/124); D: L6 (38/124); F: L3 (4/124); L3 (1/124) and 1 untypable strain. Of the 23 virulence-associated genes investigated in this study, 14 were highly expressed in 98% to 100% of the 124 strains. While tbpA was undetectable in any of the isolated strains, hsf-1, pfhA, tadD, toxA, pmHAS, hgbA, hgbB, and nanB showed differential distribution among the strain groups. Interestingly, pfhA (Mutation or inactivation of pfhA was reported to decrease the virulence of P. multocida) was found in 46% of group A: L3 strains and in 100% of group F: L3 strains, but not found in other groups. Further investigation is needed to determine whether strains in group A: L3show greater virulence than the A: L6 P. multocida strains.
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