Probiotics, belonging to the functional group of
gut

flora stabilisers
within the category of zootechnical feed additives (according to the Regulation
EC No 1831/2003) is a fast growing market. In 2004, the global market value of
probiotics was €32 million, with a forecasted annual growth of approximately 3%.
However, due to the ban of antimicrobial feed additives, the probiotic market in
Western Europe showed an annual growth of more than 7%. In 2006, Western Europe
produced around 296 tons of probiotics, with a value of €15.5 million. With 1012
CFU (equivalent to about 100g) usually added to a ton of mixed feed,
approximately 3 million tons of feed containing probiotics was produced last
year.
Authorised probiotics for pigs Of the 18 authorised probiotics in the EU, 12 are
authorised for pig feed (10 are approved for piglets, 6 for sows and 5 for
fattening pigs). The micro-organisms for pig feed are of various origins
(
Table 1). Most preparations contain defined strains of

bacteria and only three of them contain yeasts.
Bacillus strains are spore forming bacteria and are applied as spore
preparations while enterococci and pediococci do not form spores and are applied
as desiccated vegetative ells. Therefore,
Bacillus probiotics are much
more stable during feed processing (including pelleting and during in-feed
storage). We have found that the recovery of
B. cereus var. toyoi was
95% after pelleting (conditioner 80°C, dye 87°C), while the recovery of viable
counts of an
E. faecium strain decreased with increasing treatment
temperature (
Figure 1). However, the stability of vegetative cells can
be improved by various techniques (soaking on globuli, coating). Although
viability losses can be compensated by initial overdosing during feed production
if the rate of inactivation is known, storage of the complete feed is still a
matter of concern. Bacterial spores, on the other hand, are remarkably stable
during storage in pelleted feed (
Figure 2). Yeasts are the most
sensitive to heat treatment. Probably influenced by their stability
characteristics, sales volume of used probiotic organisms in pig feeding can be
categorised as follows:
Bacillus
spore probiotics > Enterococcus strains (lactic acid bacteria) >
yeast probiotics (viable cells).


Effect on bacterial communities
Considering the fact that bacterial population outnumber
the ingested probiotic bacterium by a factor of 10-1000 in the stomach/small
intestine and more than 104 in the hind gut, one may doubt that any effect could
occur. However, there are a number of studies on the influence of probiotics in
piglets that show significant modifications of bacterial composition and hence
bacterial activity, as well as influences on intestinal immunology, epithelial
physiology and anatomy. Bacillus cereus and Enterococcus faecium, two commonly
used probiotics in pig nutrition, are of completely different origin. Both
species are able to modify bacterial population in young animals, yet their
modes of action may be completely different. In our recent realtime-PCR study
(Vahjen et al., 2006), we found that the ratio of probiotic E.
faecium cells to total Enterococcus spp. cells in the intestine of
suckling and weaned piglets was only in the range of about 0.1 - 12% (Figure
3) and even less for total bacterial cells in the intestine. However, the
same study showed that E. faecalis - not E. faecium - cell numbers
(excluding the probiotic strain) were significantly reduced due to the presence
of the probiotic E. faecium. Thus, one probiotic mode of action of this
strain may be the growth inhibition of similar species, which may trigger
further changes of the bacterial composition. Similar studies on Bacillus
spp.
probiotics are not available; however, classical culturing studies show
decreased growth of enterobacteria and enterococci, but not for total lactic
acid bacteria or other main bacterial groups. As bacilli are alien to the
intestine, the local immune system of the piglet will treat probiotic bacilli as
a potentially pathogenic threat. Indeed, the contact of suckling piglets with a
Bacillus cereus probiotic via mother faeces led to an upregulation of key small
intestinal immune parameters.
Interestingly, the same group found a reduced immune
response in suckling piglets which had contact with E. faecium
probiotic via mother faeces (Scharek et al., 2005). This led to the
assumption that the E. faecium
probiotic itself or the modified bacterial population in mother faeces (mother
sows received the probiotic in feed) were less active in triggering an immune
response in the piglet. Thus, different modes of action regarding the
modification of intestinal bacterial communities can be expected in different
probiotic bacteria.
Effects on pig performance
A summary of 49 peer-reviewed publications on
probiotics in pigs between 1973 and 2007, which covered 11 different bacterial
species in several different strains and in various preparations, yield a very
heterogeneous picture regarding piglet performance and post-weaning
diarrhoea.
Concentrating on weaned piglets, for which the reviewed literature is
reasonably comparable, the relative change (probiotic vs. control group) in
average daily gain (ADG) of post-weaning piglets ranged from -8% to +24% (median
+5.5%), but compromised just 14 trials (35%) with significant positive effects
out of 40 analysed trials.
The relative change in feed conversion ratio (FCR) in these trials ranged
from -12.5 to +5%, had a median change of 0% and was significantly improved
compared to the control group in only 10 trials.
Our own studies, which used Enterococcus
faecium NCIMB 10415 and Bacillus cereus var. toyoi in feed for
sows during gestation/lactation and for piglets pre-/ postweaning, led to an 11%
numerical increase in ADG (P>0.05) and a highly significant improvement of
about 9% for FCR (P<0.01) in the case of the B. cereus strain (Taras et
al
., 2005). E. faecium NCIMB 10415 had no
significant affect on overall performance of weaned piglets in any of three
supplementation initiation variants; although the overall FCR was improved
numerically by about 1%.
Correlation of the ADG in control groups with the
relative ADG differences observed in the respective probiotic groups has led to
the impression that a significant improvement of ADG by probiotics might become
more and more unlikely with increasing ADG in the control group (Figure
4). In addition, it might be suggested that with increasing ADG in the
control group, the magnitude of the probiotic effect decreases. This may
indicate that probiotics work most efficient in young piglets early on in the
development of microbial communities in the gut. Immunological parameters that
exhibited the largest difference to control samples in 14 day old probiotic
piglets measured in one of our own trial might support this hypothesis (Scharek
et al
., 2005).

Effects on post weaning diarrhoea
Of the 49 reviewed publications, 19 trials in
pre-/postweaning piglets considered diarrhoea incidence and 74% of those trials
reported a reduction in diarrhoea incidence. However, a large range from a 78%
increase in the number of affected piglets to total elimination of diarrhoea in
the probiotic group (median 49% reduction) can be observed, although significant
differences were always in favour of the probiotic group (11 trials). Evaluation
of the effect of different starting points of probiotic application with E.
faecium NCIMB 10415 in our own trials demonstrated that the relative
magnitude of the reduction in diarrhoea was frequency largely independent of
dietary probiotic concentration or starting time of supplementation (Figure
5
).

Future developments and potential
Despite the apparent inconsistencies
in conclusions from published research, investigations are undertaken to
genetically engineer probiotics with improved abilities (acid stability,
epithelial adhesion and metabolite profile). The European Union has not yet
implemented regulations for the risk assessment of genetically modified
microorganisms (GMO) in animal nutrition.
Especially when GMOs are used to deliver drugs or vaccines, they could not
be regulated as feed additives but have to be treated as therapeutic agents. For
the development of probiotics with an improved potential, such sophisticated
genetic tools might be unnecessary.
Several work groups isolate novel bacteria from the habitat of interest as
done with the isolation of Bifidobacterium spp. from pigs to test their
probiotic potential. The use of Bifidobacterium spp. and Lactobacillus spp. as
probiotics in pigs might be a further future development if technological
solutions (e.g. drinking water application or non-thermal feed processing) can
be developed, which overcome their instability in common feed processing
techniques.
This article can be found in Feed Mix magazine Vol. 15 nr. 1