ABSTRACT
This
study was conducted to isolate and identify Salmonella
in feeds, droppings, water and litters in poultry farm in Umudike, Abia State
during the period of July to September, 2018. A total of 45 samples were taken
from four (4) poultry farms located in Umudike area. The samples includes;
poultry feed from feeders (9 samples), droppings (12 samples), litters (12
samples), and drinking water from drinkers (12 samples). Isolation of Salmonella was carried out in
differential and selective medium (SSA) after enrichment in Selenite-F-broth.
After incubation, colonies were identified by cultural characteristics and
biochemical reactions like indole test, hydrogen sulphide production (H2S)
test, citrate utilization test and Gram staining techniques. Twenty three Salmonella spp were isolated (51.1% of the
total isolates). Number of samples without growth was found to be 22(48.89%).
TABLE OF
CONTENTS
title page i
certification ii
dedication iii
acknowledgements iv
table of contents
v
list of tables vi
abstract vii
CHAPTER ONE
1.0 Introduction 1
1.1 Classification of Salmonella 2
1.2
Aim 3
1.2.1
Objectives 3
CHAPTER TWO
2.0 Literature Review 4
2.1 Salmonella 4
2.2 Cultural Characteristics 4
2.3. Biochemical Characteristics 5
2.3.1 Analytical Profile Index (API) for
Enterobacteria 5
2.4 Antigenic Structure 6
2.5 Serological Tests 6
2.6 Pathogenicity of Salmonella
2.7 Drug Susceptibility 7
.2.8 Incidence of Salmonella in Poultry 8
2.9 Incidence of Salmonella in Animal and
Poultry Feeds 9
2.10 Incidence of Salmonella in Man 11
2.11 Control of Salmonella Infection 11
CHAPTER THREE
3.0 MATERIALS AND METHODS 13
3.1Specimen
Collection 13
3.2 Media Preparation 13
3.3.1 Inoculation of Specimens 15
3.4Gram Staining 16
3.41 Biochemical Test 16
3.4.2Indole
Test 16
3.4.3 Citrate Utilization Test 16
3.4.4 Hydrogen Sulphide (H2S) Production 16
CHAPTER FOUR
4.0Results 17 4.1Discussion 22
CHAPTER
FIVE
5.0
Conclusion 24
5.1
Recommendation 24
REFERENCES
LIST OF TABLES
Tables Title Page
1:No.
of Isolates from Different Samples Location 19
2:Morphological
and Biochemical Characteristics
Salmonella spp 21
CHAPTER ONE
1.0 INTRODUCTION
Members
of the family Enterobacteriaceae are Gram-negative, non-spore forming
rods. Some of them are human and animal pathogens producing enteric infections
and food poisoning. The genera of pathogenic importance in poultry include Salmonella
and Escherichia (Dumen et al.,
2015). Salmonella as a group of microorganisms has long been
recognized as an important zoonotic pathogen of worldwide economic significance
in animals, birds and man. They are intestinal bacteria which give rise to
enteritis and typhoid-like disease. The early observation of the disease was
made by Eberth who described the typhoid bacillus in the tissue of a dead
patient, and the organisms was isolated by Salmon in 1885 and named after him (Herikstad et al., 2012). Avian Salmonellosis
is an acute or chronic disease of fowl caused by different species including S.
pullorum (Pullorum disease), S. gallinarum (Fowl typhoid), S.
arizonae (arizonae infection), S. typhimurium, S.
enteritidis and others (paratyphoid infection) (Carter
and Wise, 2014). Salmonellosis in poultry resulted in continuous
increase of public health problems as stated by Dumen
et al., 2015). Contamination of poultry meat with Salmonella was
investigated by many scientists in Sudan as well as in other countries. In the
Sudan, 21 Salmonella enteritidis was isolated from embryonated eggs.
Yagoub and Mohamed studied the occurrence of Salmonella in poultry
carcasses in Khartoum State; twenty three serotypes were identified and most of
them were S. mons and S. amek. S. auganda, and S.
sandiego were also isolated from poultry ration in the Sudan. During 1990s,
S. enteritidis infection increased in Europe (Nilakovic et al., 2010; Pitol et al., 2011).
In Portugal, 57% out of 300 chicken carcasses yielded salmonellae when they
were tested by swabbing method. Demonstrated serotypes were S. enteritidis (66%)
S. derby (4%), S. typhimurium (3%) and S. brado (1%)
(Vose et al., 2010).
1.1 Classification of Salmonella
The
scientific classification of Salmonella was described by (Hafez 2015) as
follows:
Domain:Bacteria
Kindom: Monera
Phylum: Proteobacteria
Class: Gamma Protobacteria
Order: Enterobacteriales
Family: Enterobacteriaceae
Genus: Salmonella
Recent
advances in Salmonella taxonomy divide the genus into two species: Salmonella
bongori and Salmonella enterica (Le Minor and Popoff 2012). S.
bongori contains less than 10 serovars while S. enteric contains
more than 2500 serovars and are divided into six subspecies namely enterica,
salamae, arizonae, diarizonae, houtenae and indica. All centers of disease
control and prevention recommended that Salmonella species should be
named by their genus and serovar e.g. Salmonella typhi instead of Salmonella
entrica subspecies enteric serovar Typhi. Most commonly, the Salmonella
are classified according to serology. The main division is first by the
somatic (O) antigen and by the flagellar (H) antigen. (O) Antigen is of a
lipopolysaccharide nature and (H) antigen of protein nature (Kauffmann White
and Scheme 2010). The genus Salmonella can roughly be classified into 3
groups (Hafez and Jodas 2010). Group I includes highly host adapted and
invasive serovars such as S. gallinarium, S. polurium in poultry and S.
typhi in human. Group II includes non-host adapted and invasive serovars
such as S. typhimurium, S. arizonae and S. entertidis. Group III
contains non-host adapted and non invasive serovars, most of these serovares
are harmless for animals and human.
1.2 Aim
This
work is aimed at examining the occurrence of Salmonella spp in poultry
equipment like litters, poultry droppings and feed
1.2.1 Objectives
The
core objectives of this research are;
To
swab and culture poultry equipment like litters, poultry feed and poultry
droppings
To
isolate Salmonella Spp from the examined poultry equipment, feed and droppings
To
check the rate of occurrence of Salmonella in poultry equipment, feed and
droppings
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