Salt
|
Description
|
Mode
of Action
|
Withdrawal
Time
|
Avilamycin
|
Avilamycin is an orthosomycin antibiotic complex
produced by the fermentation of Streptomyces viridochromogenes. Avilamycin is
primarily active against gram-positive bacteria.
|
Avilamycin inhibits protein synthesis. It
is thought to bind to 50S ribosomal subunit. It prevents the association of
IF2 which inhibits the formation of the mature 70S initiation complex and the
correct positioning of the tRNA in the aminoacyl site.
|
NIL
|
Bacitracin
(ZB,
BMD)
|
Bacitracin is a mixture of related cyclic
peptides produced by organisms of the licheniformis group
of Bacillus subtilis var Tracy,
These peptides
disrupt Gram-positive bacteria by interfering with cell
wall and peptidoglycan synthesis.
|
Bacitracin interferes with
the dephosphorylation of C55-isoprenyl pyrophosphate, also
known as bactoprenol, a membrane carrier molecule that transports the
building-blocks of the peptidoglycan bacterial cell
wall outside of the inner membrane
|
It does not absorb in the intestine. So, it
has no WHP
|
Chlortetracycline
|
Chlortetracycline belong to one of the important classes of broad-spectrum
antibiotics. Two of the more common semisynthetic tetracyclines that have
been marketed for decades are doxycycline and minocycline. The tetracyclines
inhibit bacterial growth by inhibiting bacterial protein synthesis by
preventing the association of aminoacyl-tRNA with bacterial ribosomes
|
Chlortetracycline, like other
tetracyclines, competes for the A site of the bacterial ribosome. This
binding competes with tRNA carrying amino acids preventing the addition of
more amino acids to the peptide chain. This inhibition of protein synthesis
ultimately inhibits growth and reproduction of the bacterial cell as
necessary proteins cannot be synthesized.
|
It has withdrawal time of 1-5 days
|
Colistin Sulphate
|
Colistin, also known as polymyxin E, is
an antibiotic produced by certain
strains of the bacteria Paenibacillus polymyxa. Colistin is a
mixture of the cyclic polypeptides colistin
A and B and belongs to the class of polypeptide antibiotics known as polymyxins. Colistin is effective against most Gram-negative bacilli.
|
Colistin is a polycationic peptide and has both hydrophilic and lipophilic moieties. These cationic regions interact with
the bacterial outer membrane, by displacing magnesium and calcium bacterial counter
ions in the lipopolysaccharide. Hydrophobic/hydrophilic
regions interact with the cytoplasmic membrane just like a detergent, solubilizing the membrane
in an aqueous environment. This effect is bactericidal even in an
isosmolar environment.
|
7 Days
|
Enramycin
|
Enramycin or Enduracidin is a polypeptide
antibiotic produced by Streptomyces fungicidus. Enramycin is
widely used as a feed additive for pigs and chickens to prevent necrotic
enteritis induced by Gram-positive gut pathogens.
It improves weight gain and feed conversion
|
Enramycin acts as an inhibitor of the
enzyme, MurG, which is essential for cell wall biosynthesis
in Gram-positive bacteria. MurG catalyzes the transglycosylation
reaction in the last step of peptidoglycan biosynthesis. Inhibiting
this step greatly compromises cell wall integrity leading to cell lysis.
|
7 days
|
Flavomycin
|
Bambermycin (flavomycin) is a complex
of antibiotics obtained from Streptomyces bambergiensis and Streptomyces
ghanaensis used as a food additive for poultry. Bambermycin is
predominately effective against Gram-positivepathogenic bacteria
|
Flavomycin inhibits the transglycosylation step of
peptidoglycan biosynthesis, a structural component of the bacterial cell
wall. This causes accumulation of cell wall intermediates, and leads to lysis
and cell death.
|
Nil
|
Lincomycin
|
Lincomycin is a lincosamide antibiotic that comes
from the actinomycete Streptomyces lincolnensis. Lincomycin
is a narrow spectrum antibiotic with activity against Gram-positive and cell
wall-less bacteria including pathogenic species of Streptococcus, Staphylococcus, and Mycoplasma
|
Lincomycin inhibits protein synthesis
in susceptible bacteria by binding to the 50 S subunits of bacterial
ribosomes and preventing peptide bond formation upon transcription.
|
Nil
|
Neomycin
|
A component of neomycin that is
produced by Streptomyces fradiae. On hydrolysis it yields neamine and
neobiosamine B.
|
Neomycin is a bactericidal
aminoglycoside antibiotic that binds to the 30S ribosome of susceptible
organisms. Binding interferes with mRNA binding and acceptor tRNA sites and
results in the production of non-functional or toxic peptides.
|
Nil
|
Nosiheptide
|
Nosiheptide is a sulfur-containing
cyclic polypeptide, is highly active against Gram-positive bacteria and few
Gram-negative bacteria, especially Clostridium Perfringens, Staphylococcus
Aureus. Nosiheptide acts bacteriostatically in low dose and bactericidally in
high dose.
|
Nosiheptide inhibits bacterial protein synthesis by
inhibiting function of elongation factors Tu and G and greatly reduce the
synthesis of guanosine penta- and tetraphosphates in response to
stringent factor.
|
7 Days
|
Tylosin
|
Tylosin is an antibiotic and a bacteriostatic feed
additive used in veterinary medicine. It has a broad spectrum of activity against Gram-positive organisms
and a limited range of Gram-negative organisms.
|
Tylosin has
a bacteriostatic effect on susceptible organisms, caused by
inhibition of protein synthesis through binding to the 50S subunit
of the bacterial ribosome.
|
5 Days
|
Tiamulin
Hydrogen Fumarate
|
Tiamulln
is a semi-synthetic derivative of pleuromutilin. It is the only member of the
pleuromutili ln class of the diterpenic antibiotics which is approved for use
at mts time. It is typically available for oral use as the Tiamulin base or
the hydrogen fumarate salt. In some references Tiamulln is considered with
the macrolide group of antibiotics.
|
Tiamulin affects bacterial protein synthesis. It has a
strong affinity for the 50S ribosomal sub-unit resulting in breakdown in the
peptide chain immediately following initiation.
|
3 Days
|
Virginiamycin
|
Virginiamycin is
a streptogramin antibiotic similar
to pristinamycin and quinupristin/dalfopristin. It is a combination of pristinamycin IIA(Virginiamycin M1) and Virginiamycin S1.
|
virginiamycin
M blocks the elongation of polypeptide chains by inhibiting both the binding
of aminoacyl-tRNA to ribosomes directed by elongation factor Tu (EF-Tu) and
the peptidyl transferase reaction.
|
Nil
|
Many factors affect milk quality, including weather, hygiene, animal genetics and product handling. Diet often plays a critical role as well. Deficiencies in energy or essential nutrients can hamper cows’ resistance to mastitis pathogens. Maintaining the cow’s immune system can help her ward off bacterial challenges that cause high SCC.
RFCs support the immune system
One management solution to consider for bolstering immunity is feeding Celmanax to your lactating cows. The Refined Functional Carbohydrates (RFCs) in Celmanax support the immune system to help cows become more resilient against environmental challenges, including bacteria that impact milk quality. RFCs also optimise digestion and mitigate aflatoxins that can carry over in milk when cows eat contaminated feedstuffs.
Somatic cell count reduction
Research shows how improved immunity translates into higher milk quality. In three separate studies (Study 1, Study 2, Study 3), cows fed RFCs had numerically lower SCCs compared with control groups without the feed additive (Figure 1).
Figure 1 – Celmanax effect on SCC (x 1,000 CELLS/ML).
Preventing aflatoxins in milk
Another milk quality concern is potential carryover of aflatoxin in milk, caused by Aspergillus flavus fungus and related species of moulds in feed. Although many types of mycotoxins occur commonly in feed, a specific concern for dairy feed is aflatoxin B1, which converts to the metabolite aflatoxin M1 during digestion. Aflatoxin M1 can then transfer to the cow’s milk. At high levels, aflatoxin M1 is toxic to humans and animals.
It’s important to know that thresholds limits for aflatoxin M1 in milk vary from country to country. For example, in Europe the maximum aflatoxin M1 content allowed in milk is 50 parts per trillion (ppt), while the US maximum is 500 ppt. Milk with levels exceeding this amount must be discarded. If your lactating cows eat feed containing aflatoxins at 20 parts per billion (ppb) or greater, realise that their milk may exceed the tolerance levels for aflatoxins in milk1.
Mycotoxin contamination
Regardless of the tolerance levels in your region, it’s important to consider the risk of aflatoxin contamination. The levels of feed contamination vary from year to year based on growing conditions, but mycotoxins are almost always present. A 10-year study2 of mycotoxins in feed, involving 72,821 samples from 100 countries, found that mycotoxin contamination is the rule rather than the exception.
In research at 2 dairy production sites affected by alflatoxins, feeding RFCs helped mitigate aflatoxins carried over in milk. Cows in the study consumed feed contaminated with about 10 ppb of alfatoxin B1. As a result, a significant number of them secreted aflatoxin M1 in their milk – more than 40% of the herd at one of the sites.
Figure 2 – Celmanax mitigation of aflatoxin M1 in milk.
The study showed that supplementing rations with RFCs effectively blocked the transfer of aflatoxin M13 to the milk of cows fed the contaminated feed. Within 3 to 7 days of starting on the feed additive, the cows in the study no longer secreted aflatoxin M1 into milk (Figure 2).
RFCs work in synergy to help cows overcome multiple environmental stressors to maintain health and productivity – as well as milk quality.