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Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com
ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88
www.ijera.com 84|P a g e
Antibacterial Resistance in the Muscles of Chicken, Pig and Beef
Pravin Raj Solomon1
, Wong Sai Ming2
1
faculty Of Biomedical Sciences ,Mahsa University, Kuala Lumpur, Malaysia 59100
2
northumbria Universitykuala Lumpur, Malaysia 59200
ABSTRACT
Though antibiotic drugs are known to improve the health and welfare of food animals , there is parallel risk due
to the development of resistant microorganisms in the body of target animals. Seven meat samples were
procured from wet market in Old Town,Petaling Jaya, Malaysia and assessed for the presence of antibiotic
residues. The samples chosen were chicken parts (skin, muscle and liver) , pig parts (liver, muscle and
intestine) and beef muscle. The results indicated that chicken skin had high level of antibioticresidues which
positively resisted the presence of gram positive, Staphylococcus aureus, S. epidermidisand B. cereus as known
by the zone of inhibition.The beef muscle also held residue which resisted S. aureusChosenbacteriaalong with
the extracts of chicken skin, pig intestine and beef muscle were observed to be resistant totetracycline
hydrochloride, ciprofloxacin hydrochloride monohydrate and their combinations when tested at a concentration
of 1 percent
Keywords- antibiotic drugs, animal feeds, antibiotic residues, meat products,
I. INTRODUCTION
The poultry contributes one-fourth of the
meat that are being produced worldwide. It plays a
major role in human nutrition as a source of
protein. Poultry units in the recent past are able to
produce market ready broiler chickens in not more
than 42 days.
Higher productivity is reasoned for the
usage of antibiotics in feeds as therapeutic agents.
Few of the common antibiotics used in the poultry
are chlortetracycline, bacitracin, avoparcin,
neomycin, oxytetracycline, tylosin, lincosamides,
cephalosporins and virginiamycin.
The advantages of using antibiotics in
poultry are that it helps to produce disease-free
animals capable of growing fast and harboring low
density of microbial pathogens. Antibiotics at a
concentration of 50-100 mg kg-1
in the feed act as
growth promoters and suppressors ofnoxious
microorganisms. Consequently inherent resistance
develops against chosen bacteria which are often
pathogens to human beings[1]. Typically, the
elimination of the susceptible bacteria in poultry
farmingis initiated when a drug or an antibiotic is
applied through feed notably at a dosage that
exceeds a therapeutic index.
Certain microbes are able to withstand the
above concentration. These bacteria will increase
their numbers million fold. Such shift normally
takes place after several days of continued
administration of therapeutics. These resistant
bacteria will eventually become dominant and its
transmittance will occur due to genetically defined
resistant characteristics to the next lineage of the
Strains as well as to other bacterial type by
plasmid-mediated mutation routes [2].
The intransigence of bacteria towards the
antibiotics is the competence of its populace to
endure the aftermath of inhibitory pressure of
antimicrobial agents [3]. Radical and pervasive
usage of antibiotics will result in the development
of a pool of resistant genes in the ambiance.
According to Randall et al.[4] the
fluoroquinoloneswhich being used in broiler
chicken is known to increase the resistance of
Campylobacter.Aarestrupet al.[5] studied the use of
avilamycin in broiler feed which eventually
developed resistance toEnterococcus faecium.Such
resistant microbes may enter into human system
consequent to incomplete cooking or wrong
handling of the animal tissue[6].
The occurrence of resistance in bacteria is
demonstrated by a proliferation of the
microorganisms with a rate higher than that of the
minimal inhibitory concentration (MIC). The latter
is construed as the lowest concentration of
antibiotic needed to hinder 90 percent of the
colonies of a specific organism [7]. Therefore any
gradual increment in the resistance of bacterial
population to antibiotics is a matter of concern [8].
Resistance is often accomplished by
enzymatic action. Staphylococcus, which produces
penicillinase, has the ability to disintegrate the
molecular structure of penicillin by hydrolytic
cleavage, there by developing deliberate resistance.
The resistance is also due to the ability of the
microbes tosustain in the latency of the antibiotic
without a candid interaction.
RESEARCH ARTICLE OPEN ACCESS
Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com
ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88
www.ijera.com 85|P a g e
Therefore it is felt necessary to investigate
the occurrence of antibiotic residues and antibiotic-
resistant bacterial strains in the meat of poultry,
pork and beef being sold in the open market
II. MATERIALS AND METHODS
This work has the endorsement of the
Research Ethics Committee of the Northumbria
University and was designed so as to qualitatively
evaluate the presence of any antibiotic residues in
the edible parts of animal flesh procured from the
market. In addition to the above a cursory test was
made on theresistance of eight chosen bacteria
(Gram+ive = Staphylococcus aureus, Streptococcus
pyogenes, Streptococcus epidermidis, Bacillus
cereus, Gram-ive= Escherichia coli, Proteus sp.,
Salmonella sp.and Pseudomonas sp.) against two
antibiotics(tetracycline hydrochloride and
ciprofloxacin hydrochloride monohydrate) being
popularly used in the husbandry of poultry and
cattle.
Various parts of poultry (skin, liver, and
muscle), pig (liver, muscle and intestine) and beef
muscle were procured from the wet market in Old
Town, Petaling Jaya, Malaysia.
Meat sample (5g each) was weighed,
macerated in sterile mortar and pestle and
emulsified with 10 mL phosphate-buffered saline
(PBS), centrifuged at 5000 rpm for 10 min. and the
supernatant was sterilized at a pressure of 15 psi
for 15 minutes .
Parallely filter discs were placed in a clean
petridish and sterilized.The sterilizedextract was
then transferred aseptically using a micropipette to
the filter disc.Four types of filter discs(disc soaked
with 80,100,120 and 140 µ L of the sterile extract)
were thus prepared.Mueller –Hinton agar medium
was prepared and platted in petridishes .
The 8 cultures grown in nutrient broths
and incubated at 37C for 24 h.were
individuallylawned on the sterilized Mueller-
Hinton agar (MHA). Thus in each of the above
plates onemicrobial culture was lawned. To that
plates the filter disc incorporated with the tissue
extract was placed .Each plate was demarked as
four quadrates and each quadrate was placed with
any one of the four filter discs of different
concentration obtained from a particular tissue.
Thus there were 56 plates ( 7 tissue
samples and 8 cultures)The plates were then
inverted and incubated for 24 h at 37ºC..On the
expiry of the incubation, the plates were examined.
The presence of antibiotic residues in the disc was
inferred by the development of clear inhibition zone
of a diameter of 0.5 mm or more.
In a next experiment the 8 microbes were
individually cultured in nutrient agar broth.These
cultures in broth were mixed with the sterile tissue
(chicken skin, pig intestineandbeef muscle)
extracts.
The contents were then plated in petri
dishes in nutrient agar medium and incubated for
3 days. There were 72 petri plates (8 cultures,3
tissue extracts ,3 antibiotics and its combination)
Sterile filter discs were also prepared and were
incorporated with 100 µL of 1 percent aquas
solution of the two antibiotics.
These discs were then transferred to the
plates containing the microbial culture and
incubated for 24 h at 37 ºC. The zone of inhibition
was examined.
The compound diffused from the filter
paper in to the agar and consequently no colonies
could grow unless the microbes resist the
antibiotics.
The pig parts showed any antibiotic
resistance neither to the Gram +ive nor to the Gram
–ive bacteria tested.The beef muscle showed
antibiotic resistance against S.aureus and there was
negative impact for other microbial species.
The intensity of the resistance dependa on
the bacteria’s sensitivity to that particular antibiotic.
The absence of growth around the disk was an
indirect measure of the ability of that compound to
inhibit that organisms.
III. RESULTS
The bacterial species employed in this
experiment is given in Table 1. Out of the 8
bacteria tested 4 are Gram positive and the rest are
Gram negative.
Table 2 indicates that the extract of the
chicken skin had antibiotic residues inhibiting
Gram positive bacteria :S.aureus,S. epidermidis and
B cereus while the chicken muscle showed
resistance to the gram positive bacteria S.
aureusalone (Fig-1). The chicken liver did not
show antibiotic resistance to both gram positive and
negative bacteria.
The chicken skin extract when mixed with
thebacterial cultures uniformly resisted the
antibiotics:tetracycline hydro-chloride,
ciprofloxacin hydrochloride mono-hydrate and
tetracycline hydrochloride + ciprofloxacin
hydrochloride monohydrate (Table
Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com
ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88
www.ijera.com 86|P a g e
Table 1.Bacterial strains used, their ATCC number
and Gram Status
Table 2. Qualitative assessment of the resistance of
meat extract to eight bacterial cultures
Extract
expressing
resistance
All the cultures when mixed with the
extracts of pig intestine resisted tetracycline
hydrochloride but could not resist ciprofloxacin
hydrochloride monohydrate . When the antibiotics
were mixed 1:1 ratio there was resistance. It clearly
indicates that the effect is singularly caused by
tetracycline hydrochloride even in the combination
of antibiotics In the case of beef extract the
microbes resisted both tetracycline hydrochloride
and ciprofloxacin hydrochloride .However they
could not resist the combination of antibiotics
Table 3. The resistance pattern of the eight bacteria in
combination with the extracts of chicken skin, pig
intestine and beef muscle
Fig1.Culture dishes showing inhibitory zone
around chicken skin extract soaked discs against
Gram+ive bacteria
S. aureus
S. epidermidis
S.pyogenes
B. cereus
Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com
ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88
www.ijera.com 87|P a g e
IV. DISCUSSION
The microbes employed in this evaluation
process have a far reaching pathological
significance.S aureus is known to create
pimples,impetigo, cellulitis,folliculitis and
abscesses.It may also be responsible for
pneumonia. meningitis, osteomyelitis and sepsis.It
secretes extra cellular polysaccharide which can
coat any microbial films very easily.When a
microbial film is caught within such coatings the
nutrient transfer and antibiotic diffusion are
hampered. S.epidermidismay bring skin rashes and
are often resistant to popular antibiotics penicillin,
amoxicillin and methicillin.
S.pyogenes is reported to cause rheumatic
fever.B.cereus is responsible for causing nausea
vomiting and diarrhea.Its spores survive if the food
is cooked at or less than 100°C.The contamination
normally takes a serious turn if the contaminated
food is stored in a temperature range of 10- 50 ºC
for a long time as microbial proliferation takes
place in that range of temp. E.coli is an indicator
microbe for the fecal contamination of the food
stuff.Proteus sp. is implicated as serious cause of
infection in humans along withEscherichia sp. and
Klebsiella sp. Contamination of this pathogen may
occur due to improper handling of food products
Salmonella sp. may also be found in
poultry ,milk and eggs.Vegetables are also prone to
be contaminated by this species
P. aeruginosa is known to develop
resistance through mutation in chromosomally
encoded genes or byhorizontal gene transfer of
antibiotic resistance determinants.Mutation driven
antibiotic resistance in P. aeruginosa may be an
irresistible factor for chronic infection
The increase in bacterial resistance to
antibiotics and rising prevalence of bacterial strains
with critical level of bacterial resistance in the food
product is considered as a severe problem
nowadays. The utilization of antibiotics brings
about an upsurge in resistance to antibiotics not
only in pathogenic bacterial strains but also in
strains forming a part of the endogenous flora of
humans and animals. Multi-resistant bacterial
strains of animal origin may spread in to the human
body by direct contacts or through food from
animal sources.
These resistant strains colonize the human
intestine and the genes coding resistance to
antibiotics can be transferred to bacterial strains
even that belong to natural micro flora [6].The
relation between the application of antibiotics and
the dissemination of bacterial resistance from
animal body to the human beings was described by
Hummel et al.[9].Leveyet al.[10] also confirmed
that in chickens which wasfed with tetracycline,
there was transfer of tetracycline resistance genes
between chicken E. coli strains, from chicken to
chicken and from chicken to man.
An ominous factor in this study is the
demonstration of tetracycline and ciprofloxacin-
resistant strains present in the chicken skin, pig
intestine as well as beef muscle. Development of
bacterial resistance to tetracycline and
ciprofloxacin could have been causeddue to the
repeated administration of the two mentioned
antibiotics.
The qualitative assessment of the presence
of residues as studied showed that, chicken skin
recorded the highest level of antibiotic residues as
evident by the zone of inhibition in Gram positive
bacteria, namely, S. aureus, S. epidermidis and B.
cereus.
The evaluation of antibiotic resistance
incurred a ban on subtherapeutic antibitoic usage in
European Union and the potential for a ban in the
United States as well as in many developed
countries.
There is growing enthusiasm for
identifying alternatives for antibiotics in feed and
for the ratification of organic farming. Among the
modern substitute feeds for animals,acidifiers are
known to boost the growth of broiler chickens by
lowering the pH of the feed . Thus inimical
bacteriaare prone to be fairly regulated. Probiotics,
which are non-digestible substancesbeneficially
influence the host by selectively stimulating growth
and moderating thebeneficial bacteria in the gut.
Probiotics oftenassist the productivity of
animals through their resistance to diseases caused
especiallydue tocertain microbes such as E. coli,
Salmonella spp., and Clostridium perfringens. The
reduction of enteric disease in poultry and
subsequent contamination of poultry products are
some of their promising characteristics [11]. The
most frequently used organisms in probiotic
framework for poultry species are Bacillus sp.,
Bifidobacteriumsp., Lactobacillussp.,
Streptococcussp.and Enterococcus sp.[12,13]
which are found in large numbers in the gut of
healthy animals and do not appear to affect them
negatively.Present study qualitatively indicates the
resistance of bacteria to some antibiotics in poultry
feeds and underline the need of antibiotic policy
implementation in veterinary medicine, including
monitoring of bacterial strains with varying degree
of innocuous phenotypes of resistance. Strict
adherence of hygiene practice also plays an
essential part in food safety and firmly regulating
the transfer of resistant microbes from meat to
humans. Poultry and beef meats need to be cooked
assiduously to restrain human infection sincedue
cooking procedures at high temperatures destroy
the pathogenic bacteria.. Indispensable hygienic
measures coupled with cautious and more
Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com
ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88
www.ijera.com 88|P a g e
diligentadministration of drugs in animal
husbandryare to be encouraged. It is strongly felt
that the present qualitative evaluation needs to be
validated through quantitative approach so as to
provide a vivid picture on this issue .
REFERENCES
[1]. D. F. Apata, The emergence of antibiotics
resistance and utilization of probiotics for
poultry production.Science Journal of
Microbiology,2, 2012 , 8-13.
[2]. I.M.Gould , The epidemiology of
antibiotic resistance. International journal
of antimicrobial agents,32 (1), 2008 , 82-
89.
[3]. B.H.Catry, L.Devriese,G.Opsomer and De
Kruif,Antimicrobial resistance
inLivestock Journal of veterinary
pharmacology and therapeutics, 26 (2)
,2003,81-93.
[4]. L.P.Randal , A.M. Ridley,S.W.Cooles
,M.Sharma, A.R. Sayers,L.Pumbwe, D.G.
Newell,L.J.Piddock and M.J.Woodward,
Prevalence of multiple antibiotic
resistancein 443 Campylobacter spp.
isolated from humans and animals. The
Journal of antimicrobial chemotherapy, 52
(3),2003,507-510.
[5]. F.M.Aarestrup,F.Bager and J.S.Andersen,
Association between the use of avilamycin
for growth promotion and the occurrence
of resistance among Enterococcus faecium
[6]. from broilers: epidemiological study and
changes over time. Microbial drug
resistance (Larchmont, N.Y.). 6 (1),2000
,71-75.
[7]. .E.V.D .Bogaard, and E.E.Stobberingh,
Epidemiology of resistance to antibiotics.
Links between animals and humans.
International Journal of Antimicrobial
Agents,14 (4), 2000 , 327 – 335.
[8]. A.A.Ojeniyi,Public health aspects of
bacterial drug resistance in modern battery
and town/villagepoultry in the tropics.
ActaveterinariaScandinavica, 30 (2),
1987,127-132.
[9]. M.Kolář, R. Pantůček,J.Bardoň,
I.Vágnerová,H .Typovska,I.Válka, and J
Doskar, Occurrence ofantibiotic-resistant
bacterial strains isolated in poultry. Vet
Med Czech, 47,2002 , 52-59.
[10]. R.Hummel,H.Tschäpe and W.
Witte,Spread of plasmid-mediated
nourseothricin resistance due to antibiotic
use in animal husbandry. Journal of Basic
Microbiology, 26 (8),1986, 461 - 466.
[11]. S.B.Levey, G.B. Fitzgerald and A.B.
Macone, Spread of antibiotic resistanc
Plasmids from chickento chicken and
from chicken to man. Nature ,260 (5546),
1976 ,40 - 42.
[12]. J.A.Patterson andK.M. Burkholder,
Application of prebiotics and probiotics in
poultry production.Poultry Science, 82
(4), 2003 , 627-631.
[13]. O.Simon,A.JadamusandW.Vahjen,
Probiotic feed additives-effectiveness and
expected modes ofaction. Journal of
Animal Feed Science, 10, 2001, 51-67.
[14]. S.M.L.Kabir, The role of probiotics in the
poultry industry. International Journal of
MoleculaSciences, 10 (8) ,2009, 3531 –
3546.

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Antibacterial Resistance in the Muscles of Chicken, Pig and Beef

  • 1. Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88 www.ijera.com 84|P a g e Antibacterial Resistance in the Muscles of Chicken, Pig and Beef Pravin Raj Solomon1 , Wong Sai Ming2 1 faculty Of Biomedical Sciences ,Mahsa University, Kuala Lumpur, Malaysia 59100 2 northumbria Universitykuala Lumpur, Malaysia 59200 ABSTRACT Though antibiotic drugs are known to improve the health and welfare of food animals , there is parallel risk due to the development of resistant microorganisms in the body of target animals. Seven meat samples were procured from wet market in Old Town,Petaling Jaya, Malaysia and assessed for the presence of antibiotic residues. The samples chosen were chicken parts (skin, muscle and liver) , pig parts (liver, muscle and intestine) and beef muscle. The results indicated that chicken skin had high level of antibioticresidues which positively resisted the presence of gram positive, Staphylococcus aureus, S. epidermidisand B. cereus as known by the zone of inhibition.The beef muscle also held residue which resisted S. aureusChosenbacteriaalong with the extracts of chicken skin, pig intestine and beef muscle were observed to be resistant totetracycline hydrochloride, ciprofloxacin hydrochloride monohydrate and their combinations when tested at a concentration of 1 percent Keywords- antibiotic drugs, animal feeds, antibiotic residues, meat products, I. INTRODUCTION The poultry contributes one-fourth of the meat that are being produced worldwide. It plays a major role in human nutrition as a source of protein. Poultry units in the recent past are able to produce market ready broiler chickens in not more than 42 days. Higher productivity is reasoned for the usage of antibiotics in feeds as therapeutic agents. Few of the common antibiotics used in the poultry are chlortetracycline, bacitracin, avoparcin, neomycin, oxytetracycline, tylosin, lincosamides, cephalosporins and virginiamycin. The advantages of using antibiotics in poultry are that it helps to produce disease-free animals capable of growing fast and harboring low density of microbial pathogens. Antibiotics at a concentration of 50-100 mg kg-1 in the feed act as growth promoters and suppressors ofnoxious microorganisms. Consequently inherent resistance develops against chosen bacteria which are often pathogens to human beings[1]. Typically, the elimination of the susceptible bacteria in poultry farmingis initiated when a drug or an antibiotic is applied through feed notably at a dosage that exceeds a therapeutic index. Certain microbes are able to withstand the above concentration. These bacteria will increase their numbers million fold. Such shift normally takes place after several days of continued administration of therapeutics. These resistant bacteria will eventually become dominant and its transmittance will occur due to genetically defined resistant characteristics to the next lineage of the Strains as well as to other bacterial type by plasmid-mediated mutation routes [2]. The intransigence of bacteria towards the antibiotics is the competence of its populace to endure the aftermath of inhibitory pressure of antimicrobial agents [3]. Radical and pervasive usage of antibiotics will result in the development of a pool of resistant genes in the ambiance. According to Randall et al.[4] the fluoroquinoloneswhich being used in broiler chicken is known to increase the resistance of Campylobacter.Aarestrupet al.[5] studied the use of avilamycin in broiler feed which eventually developed resistance toEnterococcus faecium.Such resistant microbes may enter into human system consequent to incomplete cooking or wrong handling of the animal tissue[6]. The occurrence of resistance in bacteria is demonstrated by a proliferation of the microorganisms with a rate higher than that of the minimal inhibitory concentration (MIC). The latter is construed as the lowest concentration of antibiotic needed to hinder 90 percent of the colonies of a specific organism [7]. Therefore any gradual increment in the resistance of bacterial population to antibiotics is a matter of concern [8]. Resistance is often accomplished by enzymatic action. Staphylococcus, which produces penicillinase, has the ability to disintegrate the molecular structure of penicillin by hydrolytic cleavage, there by developing deliberate resistance. The resistance is also due to the ability of the microbes tosustain in the latency of the antibiotic without a candid interaction. RESEARCH ARTICLE OPEN ACCESS
  • 2. Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88 www.ijera.com 85|P a g e Therefore it is felt necessary to investigate the occurrence of antibiotic residues and antibiotic- resistant bacterial strains in the meat of poultry, pork and beef being sold in the open market II. MATERIALS AND METHODS This work has the endorsement of the Research Ethics Committee of the Northumbria University and was designed so as to qualitatively evaluate the presence of any antibiotic residues in the edible parts of animal flesh procured from the market. In addition to the above a cursory test was made on theresistance of eight chosen bacteria (Gram+ive = Staphylococcus aureus, Streptococcus pyogenes, Streptococcus epidermidis, Bacillus cereus, Gram-ive= Escherichia coli, Proteus sp., Salmonella sp.and Pseudomonas sp.) against two antibiotics(tetracycline hydrochloride and ciprofloxacin hydrochloride monohydrate) being popularly used in the husbandry of poultry and cattle. Various parts of poultry (skin, liver, and muscle), pig (liver, muscle and intestine) and beef muscle were procured from the wet market in Old Town, Petaling Jaya, Malaysia. Meat sample (5g each) was weighed, macerated in sterile mortar and pestle and emulsified with 10 mL phosphate-buffered saline (PBS), centrifuged at 5000 rpm for 10 min. and the supernatant was sterilized at a pressure of 15 psi for 15 minutes . Parallely filter discs were placed in a clean petridish and sterilized.The sterilizedextract was then transferred aseptically using a micropipette to the filter disc.Four types of filter discs(disc soaked with 80,100,120 and 140 µ L of the sterile extract) were thus prepared.Mueller –Hinton agar medium was prepared and platted in petridishes . The 8 cultures grown in nutrient broths and incubated at 37C for 24 h.were individuallylawned on the sterilized Mueller- Hinton agar (MHA). Thus in each of the above plates onemicrobial culture was lawned. To that plates the filter disc incorporated with the tissue extract was placed .Each plate was demarked as four quadrates and each quadrate was placed with any one of the four filter discs of different concentration obtained from a particular tissue. Thus there were 56 plates ( 7 tissue samples and 8 cultures)The plates were then inverted and incubated for 24 h at 37ºC..On the expiry of the incubation, the plates were examined. The presence of antibiotic residues in the disc was inferred by the development of clear inhibition zone of a diameter of 0.5 mm or more. In a next experiment the 8 microbes were individually cultured in nutrient agar broth.These cultures in broth were mixed with the sterile tissue (chicken skin, pig intestineandbeef muscle) extracts. The contents were then plated in petri dishes in nutrient agar medium and incubated for 3 days. There were 72 petri plates (8 cultures,3 tissue extracts ,3 antibiotics and its combination) Sterile filter discs were also prepared and were incorporated with 100 µL of 1 percent aquas solution of the two antibiotics. These discs were then transferred to the plates containing the microbial culture and incubated for 24 h at 37 ºC. The zone of inhibition was examined. The compound diffused from the filter paper in to the agar and consequently no colonies could grow unless the microbes resist the antibiotics. The pig parts showed any antibiotic resistance neither to the Gram +ive nor to the Gram –ive bacteria tested.The beef muscle showed antibiotic resistance against S.aureus and there was negative impact for other microbial species. The intensity of the resistance dependa on the bacteria’s sensitivity to that particular antibiotic. The absence of growth around the disk was an indirect measure of the ability of that compound to inhibit that organisms. III. RESULTS The bacterial species employed in this experiment is given in Table 1. Out of the 8 bacteria tested 4 are Gram positive and the rest are Gram negative. Table 2 indicates that the extract of the chicken skin had antibiotic residues inhibiting Gram positive bacteria :S.aureus,S. epidermidis and B cereus while the chicken muscle showed resistance to the gram positive bacteria S. aureusalone (Fig-1). The chicken liver did not show antibiotic resistance to both gram positive and negative bacteria. The chicken skin extract when mixed with thebacterial cultures uniformly resisted the antibiotics:tetracycline hydro-chloride, ciprofloxacin hydrochloride mono-hydrate and tetracycline hydrochloride + ciprofloxacin hydrochloride monohydrate (Table
  • 3. Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88 www.ijera.com 86|P a g e Table 1.Bacterial strains used, their ATCC number and Gram Status Table 2. Qualitative assessment of the resistance of meat extract to eight bacterial cultures Extract expressing resistance All the cultures when mixed with the extracts of pig intestine resisted tetracycline hydrochloride but could not resist ciprofloxacin hydrochloride monohydrate . When the antibiotics were mixed 1:1 ratio there was resistance. It clearly indicates that the effect is singularly caused by tetracycline hydrochloride even in the combination of antibiotics In the case of beef extract the microbes resisted both tetracycline hydrochloride and ciprofloxacin hydrochloride .However they could not resist the combination of antibiotics Table 3. The resistance pattern of the eight bacteria in combination with the extracts of chicken skin, pig intestine and beef muscle Fig1.Culture dishes showing inhibitory zone around chicken skin extract soaked discs against Gram+ive bacteria S. aureus S. epidermidis S.pyogenes B. cereus
  • 4. Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88 www.ijera.com 87|P a g e IV. DISCUSSION The microbes employed in this evaluation process have a far reaching pathological significance.S aureus is known to create pimples,impetigo, cellulitis,folliculitis and abscesses.It may also be responsible for pneumonia. meningitis, osteomyelitis and sepsis.It secretes extra cellular polysaccharide which can coat any microbial films very easily.When a microbial film is caught within such coatings the nutrient transfer and antibiotic diffusion are hampered. S.epidermidismay bring skin rashes and are often resistant to popular antibiotics penicillin, amoxicillin and methicillin. S.pyogenes is reported to cause rheumatic fever.B.cereus is responsible for causing nausea vomiting and diarrhea.Its spores survive if the food is cooked at or less than 100°C.The contamination normally takes a serious turn if the contaminated food is stored in a temperature range of 10- 50 ºC for a long time as microbial proliferation takes place in that range of temp. E.coli is an indicator microbe for the fecal contamination of the food stuff.Proteus sp. is implicated as serious cause of infection in humans along withEscherichia sp. and Klebsiella sp. Contamination of this pathogen may occur due to improper handling of food products Salmonella sp. may also be found in poultry ,milk and eggs.Vegetables are also prone to be contaminated by this species P. aeruginosa is known to develop resistance through mutation in chromosomally encoded genes or byhorizontal gene transfer of antibiotic resistance determinants.Mutation driven antibiotic resistance in P. aeruginosa may be an irresistible factor for chronic infection The increase in bacterial resistance to antibiotics and rising prevalence of bacterial strains with critical level of bacterial resistance in the food product is considered as a severe problem nowadays. The utilization of antibiotics brings about an upsurge in resistance to antibiotics not only in pathogenic bacterial strains but also in strains forming a part of the endogenous flora of humans and animals. Multi-resistant bacterial strains of animal origin may spread in to the human body by direct contacts or through food from animal sources. These resistant strains colonize the human intestine and the genes coding resistance to antibiotics can be transferred to bacterial strains even that belong to natural micro flora [6].The relation between the application of antibiotics and the dissemination of bacterial resistance from animal body to the human beings was described by Hummel et al.[9].Leveyet al.[10] also confirmed that in chickens which wasfed with tetracycline, there was transfer of tetracycline resistance genes between chicken E. coli strains, from chicken to chicken and from chicken to man. An ominous factor in this study is the demonstration of tetracycline and ciprofloxacin- resistant strains present in the chicken skin, pig intestine as well as beef muscle. Development of bacterial resistance to tetracycline and ciprofloxacin could have been causeddue to the repeated administration of the two mentioned antibiotics. The qualitative assessment of the presence of residues as studied showed that, chicken skin recorded the highest level of antibiotic residues as evident by the zone of inhibition in Gram positive bacteria, namely, S. aureus, S. epidermidis and B. cereus. The evaluation of antibiotic resistance incurred a ban on subtherapeutic antibitoic usage in European Union and the potential for a ban in the United States as well as in many developed countries. There is growing enthusiasm for identifying alternatives for antibiotics in feed and for the ratification of organic farming. Among the modern substitute feeds for animals,acidifiers are known to boost the growth of broiler chickens by lowering the pH of the feed . Thus inimical bacteriaare prone to be fairly regulated. Probiotics, which are non-digestible substancesbeneficially influence the host by selectively stimulating growth and moderating thebeneficial bacteria in the gut. Probiotics oftenassist the productivity of animals through their resistance to diseases caused especiallydue tocertain microbes such as E. coli, Salmonella spp., and Clostridium perfringens. The reduction of enteric disease in poultry and subsequent contamination of poultry products are some of their promising characteristics [11]. The most frequently used organisms in probiotic framework for poultry species are Bacillus sp., Bifidobacteriumsp., Lactobacillussp., Streptococcussp.and Enterococcus sp.[12,13] which are found in large numbers in the gut of healthy animals and do not appear to affect them negatively.Present study qualitatively indicates the resistance of bacteria to some antibiotics in poultry feeds and underline the need of antibiotic policy implementation in veterinary medicine, including monitoring of bacterial strains with varying degree of innocuous phenotypes of resistance. Strict adherence of hygiene practice also plays an essential part in food safety and firmly regulating the transfer of resistant microbes from meat to humans. Poultry and beef meats need to be cooked assiduously to restrain human infection sincedue cooking procedures at high temperatures destroy the pathogenic bacteria.. Indispensable hygienic measures coupled with cautious and more
  • 5. Pravin Raj Solomon1. Int. Journal of Engineering Research and Applications www.ijera.com ISSN: 2248-9622, Vol. 6, Issue 4, (Part - 4) April 2016, pp.84-88 www.ijera.com 88|P a g e diligentadministration of drugs in animal husbandryare to be encouraged. It is strongly felt that the present qualitative evaluation needs to be validated through quantitative approach so as to provide a vivid picture on this issue . REFERENCES [1]. D. F. Apata, The emergence of antibiotics resistance and utilization of probiotics for poultry production.Science Journal of Microbiology,2, 2012 , 8-13. [2]. I.M.Gould , The epidemiology of antibiotic resistance. International journal of antimicrobial agents,32 (1), 2008 , 82- 89. [3]. B.H.Catry, L.Devriese,G.Opsomer and De Kruif,Antimicrobial resistance inLivestock Journal of veterinary pharmacology and therapeutics, 26 (2) ,2003,81-93. [4]. L.P.Randal , A.M. Ridley,S.W.Cooles ,M.Sharma, A.R. Sayers,L.Pumbwe, D.G. Newell,L.J.Piddock and M.J.Woodward, Prevalence of multiple antibiotic resistancein 443 Campylobacter spp. isolated from humans and animals. The Journal of antimicrobial chemotherapy, 52 (3),2003,507-510. [5]. F.M.Aarestrup,F.Bager and J.S.Andersen, Association between the use of avilamycin for growth promotion and the occurrence of resistance among Enterococcus faecium [6]. from broilers: epidemiological study and changes over time. Microbial drug resistance (Larchmont, N.Y.). 6 (1),2000 ,71-75. [7]. .E.V.D .Bogaard, and E.E.Stobberingh, Epidemiology of resistance to antibiotics. Links between animals and humans. International Journal of Antimicrobial Agents,14 (4), 2000 , 327 – 335. [8]. A.A.Ojeniyi,Public health aspects of bacterial drug resistance in modern battery and town/villagepoultry in the tropics. ActaveterinariaScandinavica, 30 (2), 1987,127-132. [9]. M.Kolář, R. Pantůček,J.Bardoň, I.Vágnerová,H .Typovska,I.Válka, and J Doskar, Occurrence ofantibiotic-resistant bacterial strains isolated in poultry. Vet Med Czech, 47,2002 , 52-59. [10]. R.Hummel,H.Tschäpe and W. Witte,Spread of plasmid-mediated nourseothricin resistance due to antibiotic use in animal husbandry. Journal of Basic Microbiology, 26 (8),1986, 461 - 466. [11]. S.B.Levey, G.B. Fitzgerald and A.B. Macone, Spread of antibiotic resistanc Plasmids from chickento chicken and from chicken to man. Nature ,260 (5546), 1976 ,40 - 42. [12]. J.A.Patterson andK.M. Burkholder, Application of prebiotics and probiotics in poultry production.Poultry Science, 82 (4), 2003 , 627-631. [13]. O.Simon,A.JadamusandW.Vahjen, Probiotic feed additives-effectiveness and expected modes ofaction. Journal of Animal Feed Science, 10, 2001, 51-67. [14]. S.M.L.Kabir, The role of probiotics in the poultry industry. International Journal of MoleculaSciences, 10 (8) ,2009, 3531 – 3546.