Mr. Alley et al., Chronic non-progressive pneumonia of sheep in New Zealand - a review of the role of Mycoplasma ovipneumoniae, NZ VET J, 47(5), 1999, pp. 155-160
Chronic non-progressive pneumonia (CNP) is a common disease which affects l
ambs in New Zealand during late summer and autumn. Mycoplasma ovipneumoniae
can be recovered from a high proportion of lesions but it is also present
in some normal lungs. Bacteria, especially Pasteurella haemolytica, can als
o be recovered from more than half the lungs of affected animals.
Isolates of M. ovipneumoniae are genetically heterogeneous, as demonstrated
by examination of their DNA or total cellular proteins, and are serologica
lly heterogeneous as shown by metabolic inhibition tests. The number of str
ains present in New Zealand is large and several distinguishable strains ca
n be recovered from each affected lung. Mycoplasma ovipneumoniae has pathog
enic potential as indicated by its ability to produce hydrogen peroxide, ca
use ciliostasis and by its possession of a capsule.
Chronic non-progressive pneumonia can be transmitted consistently to over 5
0% of lambs by inoculation of pooled pneumonic lung homogenate and transmis
sion can be suppressed by broad spectrum antibiotics. In contrast, penicill
in does not prevent the development of lesions but diminishes their severit
y. Pooled lung homogenate treated with digitonin, which inactivates mycopla
smas, has failed to transmit CNP. Pure cultures of M. ovipneumoniae produce
only mild lesions in some animals, whereas inoculation with pooled lung ho
mogenate (from which no viruses were isolated) containing mixed strains of
M. ovipneumoniae and free from bacteria, is more effective in producing les
ions.
Research work to date suggests that CNP may be initiated by colonisation of
the lung by M. ovipneumoniae which causes ciliostasis and elicits an exuda
te allowing colonisation of the lungs by bacteria especially P. haemolytica
and by other strains of M. ovipneumoniae. The immune response to the initi
al strain of M. ovipneumoniae may inhibit its replication but would be less
effective in inhibiting heterologous strains of the organism allowing thei
r sequential replication. Eventually production of a broad immune response
to M. ovipneumoniae would lead to its elimination which in turn would facil
itate the elimination of other microorganisms and the resolution of lesions
. As natural immunity to CNP occurs within the first year, it may be possib
le to develop an effective and useful vaccine. Such a vaccine may need to i
nclude multiple strains of M. ovipneumoniae.