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an epidemiological study of listeriosis in dairy cattle

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In the second part <strong>of</strong> the <strong>study</strong> a longitud<strong>in</strong>al survey <strong>of</strong> five <strong>dairy</strong> farms was<br />

carried out to determ<strong>in</strong>e the <strong>in</strong>fection rate with Listeria monocytogenes <strong>an</strong>d its<br />

behaviour <strong>in</strong> the environment, <strong>in</strong>dividual cows, pastures, soil, water sources, forage <strong>an</strong>d<br />

bulk milk t<strong>an</strong>ks on the five farms monitored bacteriologically <strong>an</strong>d serologically between<br />

August 96 <strong>an</strong>d May 97. The <strong>in</strong>fection rate varied between farms <strong>an</strong>d months. Two<br />

patterns <strong>of</strong> <strong>in</strong>fection rate were observed. On 3 farms the highest prevalence <strong>of</strong> <strong>in</strong>fection<br />

rates were obta<strong>in</strong>ed between November <strong>an</strong>d April, around 90% <strong>of</strong> <strong>an</strong>imals excreted L.<br />

monocytogenes <strong>in</strong> their faeces dur<strong>in</strong>g this period whereas on the other 2 farms the<br />

<strong>in</strong>fection rate was lower, around 30% <strong>of</strong> <strong>an</strong>imals excreted L. monocytogenes (that was<br />

only <strong>in</strong> March). An ELISA assay employ<strong>in</strong>g Listeriolys<strong>in</strong> O (LLO) was used to<br />

determ<strong>in</strong>e seroconversion before, dur<strong>in</strong>g <strong>an</strong>d after silage feed<strong>in</strong>g <strong>an</strong>d w<strong>in</strong>ter hous<strong>in</strong>g.<br />

Almost all <strong>an</strong>imals exam<strong>in</strong>ed on each farm had <strong>an</strong>ti-LLO <strong>an</strong>tibodies to L.<br />

monocytogenes before silage feed<strong>in</strong>g <strong>an</strong>d hous<strong>in</strong>g. The <strong>an</strong>tibody level rema<strong>in</strong>ed<br />

unch<strong>an</strong>ged throughout the <strong>study</strong> with only a small number <strong>of</strong> <strong>an</strong>imals exhibit<strong>in</strong>g<br />

ch<strong>an</strong>ges on only one farm.<br />

Three species <strong>of</strong> Listeria were isolated from the environmental samples (soil,<br />

grass, silage, water, bedd<strong>in</strong>g). The commonest isolate was L. monocytogenes. L.<br />

<strong>in</strong>nocua was less common <strong>an</strong>d the rarest was L. seeligeri. L. monocytogenes was<br />

isolated from bulk milk t<strong>an</strong>k on three farms. R<strong>an</strong>dom amplified polymorphic DNA<br />

(RAPD) assays were used to identify the source <strong>of</strong> <strong>in</strong>fection <strong>in</strong> <strong>dairy</strong> cows <strong>an</strong>d to<br />

determ<strong>in</strong>e the variation between the stra<strong>in</strong>s <strong>of</strong> different orig<strong>in</strong>. In total 113 isolates (40<br />

from the environment <strong>an</strong>d 73 from the <strong>an</strong>imals) were exam<strong>in</strong>ed <strong>an</strong>d 12 different RAPD<br />

patterns were obta<strong>in</strong>ed. The results <strong>in</strong>dicated that different “stra<strong>in</strong>s” exist between <strong>an</strong>d<br />

with<strong>in</strong> farms. There also were similar patterns <strong>of</strong> RAPD between environmental <strong>an</strong>d<br />

<strong>an</strong>imal stra<strong>in</strong>s.<br />

iii

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