Response to intramammary challenge with putatively host-adapted and non-adapted strains of Streptococcus uberis in cattle
dc.contributor.advisor
Zadoks, Ruth
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dc.contributor.advisor
McNeilly, Tom
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dc.contributor.author
Tassi, Riccardo
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dc.contributor.sponsor
other
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dc.date.accessioned
2016-06-29T15:26:06Z
dc.date.available
2016-06-29T15:26:06Z
dc.date.issued
2015-07-04
dc.description.abstract
Streptococcus uberis is an important cause of intramammary infection in dairy cattle.
Strains of S. uberis appear to differ in their ability to cause disease based on previous
epidemiological studies. We explored the pathogenicity of 2 strains of S. uberis,
where one strain represented a putatively host-adapted type based on its ability to
cause persistent infection and to spread from cow to cow in a lactating herd. This
type was part of a clonal complex that is commonly associated with bovine mastitis.
The other strain, which was isolated from a transient infection in a single animal in
the same herd and did not belong to any known clonal complex, was selected as
putatively non-adapted type. Cows (6 per strain) were experimentally challenged in a
single hind quarter and the adjacent hind quarter was used as mock challenged
control quarter. Both strains showed an equal ability grow in milk of challenge
animals in vitro. All cows that were challenged with the putatively host-adapted
strain developed clinical signs of mastitis, including fever and milk yield depression
as well as elevated somatic cell count due to influx of polymorphonuclear leucocytes
and lymphocytes. The cytokine response followed a specific order, with an increase
in IL-1β, IL-6 and IL-8 levels at the time of first SCC elevation, followed by an
increase in IL-10, IL-12p40 and TNF-α levels approximately 6 h later. In 4 of 6
animals, IL-17A was detected in milk between 57 and 168 h post challenge. The
increase in IL-17A levels coincided with inversion of the pre-challenge CD4+:CD8+
T lymphocyte ratio, and was observed from 96 h post challenge. This was followed
by normalisation of the CD4+:CD8+ ratio due to continued increase of the CD8+
concentration up to 312 h post challenge. Spontaneous resolution of infection was
observed in 5 animals and coincided with a measurable IL-17A response in 4
animals, suggesting that IL-17 may be involved in the resolution of intramammary
infection. To explore the mechanism of action of IL-17A we stimulated bovine PMN
and bovine blood derived macrophages with recombinant IL-17A in vitro. IL-17A
enhanced the killing ability of phagocyte toward the challenge strain. With the
exception of minor elevation of IL-8 levels, no clinical, cytological or immunological
response was detected in quarters challenged with the non-adapted strain. The
observed strain specific pathogenicity was consistent across animals, implying that it
is determined by pathogen factors rather than host factors. We further studied in vitro
possible mechanisms involved in the differences observed between the two strains
such as ability to adhere to the mammary epithelial cells, ability to resist to killing by
phagocytes and ability to form biofilm. The adapted strain FSL Z1-048 showed an
increased ability to adhere to the epithelial cells and an increase ability to resist to
killing of monocyte derived macrophages. These mechanisms thus could potentially
explain the in vivo observations.
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dc.identifier.uri
http://hdl.handle.net/1842/15910
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.relation.hasversion
Tassi, R., T. McNeilly, J. Fitzpatrick, M. Fontaine, D. Reddick, C. Ramage, M. Lutton, Y. Schukken, and R. Zadoks. 2013. Strain-specific pathogenicity of putative host-adapted and non adapted strains of Streptococcus uberis in dairy cattle. Journal of Dairy Science 96(8):5129-5145
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dc.subject
cattle
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dc.subject
mastitis
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dc.subject
interleukin-17A
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dc.subject
Streptococcus uberis
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dc.subject
lymphocyte
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dc.title
Response to intramammary challenge with putatively host-adapted and non-adapted strains of Streptococcus uberis in cattle
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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