<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/css" href="https://imcjms.com/public/assets/rss.css" ?><rss version="2.0">
<channel>
    <title>IMC Journal of Medical Science</title>
    <link>https://imcjms.com/public</link>
    <description>Ibrahim Medical College Journal of Medical Science</description>

                        <item>
                <title><![CDATA[Listerial contamination of raw beef and chevon in north-central Nigeria]]></title>

                                    <author><![CDATA[Aleruchi Chuku]]></author>
                                    <author><![CDATA[Godwin Attah Obande ]]></author>
                                    <author><![CDATA[Sani Bashir Eya]]></author>
                
                <link data-url="https://imcjms.com/public/registration/journal_full_text/316">
    https://imcjms.com/public/registration/journal_full_text/316
</link>
                <pubDate>Tue, 26 Mar 2019 21:03:53 +0000</pubDate>
                <category><![CDATA[Original Article]]></category>
                <comments><![CDATA[IMC J Med Sci 2019; 13(2): 001]]></comments>
                <description>Abstract
Background and objective: Listeria sp. is a
ubiquitous and frequently isolated foodborne pathogen. The prevalence of Listeria
sp in raw beef and chevon sold in Lafia Nigeria, as well as their
antibiotic susceptibility profile was evaluated.
Methods: A total 104
samples comprising of 52 raw beef and 52 chevon were obtained from street
vendors (hawkers), Shinge abattoir, Lafia old market and Lafia Modern Market.
Isolation of Listeria sp. was
performed on Listeria Selective Agar, following enrichment in supplemented
Listeria Selective Broth. Identification of Listeria
sp. was carried out by cultural and biochemical methods. Antimicrobial
susceptibility of isolated L. monocytogenes was performed by standard disk diffusion method. Chi-square test
was used to determine association between contamination levels at p=0.05.
Results: Seven types
of Listeria sp. were isolated. L. monocytogenes and L. ivanovii were the most frequently isolated
contaminants in all meat types and
from all sample sources. L. monocytogenes was isolated with a frequency of 64.4% (67/104) in the meat samples. Beef samples
had the highest listerial contamination with a frequency of 58.2% (78/134) compared to chevon which
had a listerial frequency of 41.8% (56/134). Resistance of L. monocytogenes to streptomycin and sparfloxacin was 58.2% and
55.2% respectively. Resistance to ampicillin (34.3%) and gentamicin (20.9%) was
also observed. Resistances to multiple antimicrobials were detected in 11 L.
monocytogenes isolates. 
Conclusion: The study
demonstrated that the raw meat sold in Lafia was contaminated with several Listeria sp. L. monocytogenes showed high rate of resistance to several
antimicrobial agents used for the treatment of listerial infection. Appropriate
regulation and monitoring of livestock rearing and meat retailing practices are
advocated to safeguard the health of consumers.
IMC
J Med Sci 2019; 13(2): 001. EPub date: 18 July 2019.&amp;nbsp;DOI: https://doi.org/10.3329/imcjms.v13i2.45274  
Address for Correspondence: Godwin Attah Obande,
Department of Microbiology, Faculty of Science, Federal University Lafia,
Nasarawa state, Nigeria. E-mail: obandegodwins@gmail.com;
+2348039646924
&amp;nbsp;
Introduction
Listeria
monocytogenes is a facultative anaerobic bacterium which can grow and reproduce
inside the host’s cells, making it one of the most virulent food-borne
pathogens. Unlike most other food-borne pathogens it can grow and multiply at a
very low temperatures [1,2]. L. monocytogenes has been
typed into four serotypes of which only three (1/2a, 1/2b, 4b) are involved in
95% of all human listeriosis cases [3].
It
belongs to the genus Listeria which is widely distributed in the
environment. The genus currently includes a total of seven species namely L. monocytogenes, L. ivanovii, L. innocua, L.
seeligeri, L. murrayi, L. grayi and L. welshimeri [4]. Of these species, L. monocytogenes and L. ivanovi are the only species found to
be pathogenic to humans and other animals [5].
L.
monocytogenes is a constant challenge for the food industry, health regulatory
officials and consumers [6] since it remains as one of the most virulent
foodborne pathogens for immunodeficient individuals. It has been extensively
studied over the past few decades due to its high case/fatality rate (20-30%),
chronic infection resulting in high healthcare cost and its ability to survive
for longer periods under adverse environmental conditions than many other
non-spore-forming bacteria [7].
In
man, outbreaks usually occur following consumption of unpasteurized milk,
contaminated cheeses and other dairy products. Reports of outbreaks have also
followed ingestion of undercooked meat and poultry [8]. It is frequently
present in the gut of cattle, poultry and pigs and can be transmitted through
ready-to-eat (RTE) foods or raw meat products [9]. Listeria species are
isolated from a diversity of environmental sources, including decaying
vegetation, soil, water, effluents, variety of foods, and the faeces of humans
and animals [10]. 
L.
monocytogenes is a major contaminant of RTE food and food products. Packaged raw
foods can represent a potential source of contamination, and listeriosis is
associated with the consumption of such undercooked raw foods [11]. Major
changes in food production, processing and distribution, increased use of
refrigeration as a primary preservation method, changes in eating habits
particularly towards ready-to-eat foods are suggested as possible reasons for
the emergence of human food-borne listeriosis [12].
While
several studies have reported antibiotic resistance in bacterial isolates from
human beings, it is becoming evident that food produced from farm animals is no
longer exempted from antibiotic resistant bacteria [13]. Thus, the food
microflora is not separated from its human counterpart in cases of antibiotic
resistance. The occurrence of infection by antibiotic resistant organisms makes
treatment difficult and increases the period of recovery from illness [14].
This situation has been worsened by the indiscriminate use of common broad
spectrum antibiotics as prophylaxis and growth promoters in animal feed, particularly
in developing nations [14,15]. 
There
has been a dearth of information on the epidemiology of listeriosis in most
African countries, including Nigeria [16] with only few reports, when compared
to other developed regions like Europe and United States of America [17]. This
is because the organism seems not to have been given as much attention as is
required [18,19]. Listeriosis is considered a serious health problem due to its
high mortality rate and severity of symptoms. Despite the foregoing and the
continuous observation of the emergence of antibiotic resistant strains of Listeria, there is little or no
documented reports of its prevalence and its antibiotic susceptibility profile
in Lafia of Nasarawa state of Nigeria. 
&amp;nbsp;
Methods
Study
area and period: This study was conducted in Lafia, Nasarawa
state which lies between latitude 8o25’ 40”N to 8o34’
15”N and longitude 8o24’ 25”E to 8o38’ 19”E in the guinea
savannah region of North-Central Nigeria. Lafia is a large town in Nasarawa
state with an estimated population of 330, 712 [20]. The study was carried out
from June to August which witnessed increased slaughtering of animals in
commemoration of the Eid il-Fitr celebration in the month of July, 2016.
Sample
collection: Preliminary investigation identified the Shinge abattoir, open
markets (Lafia old market and Modern
market) and hawkers as major sources of retail fresh raw meat within Lafia.A total of 104
samples comprising of 52 raw beef samples and 52 raw chevon samples were
collected randomly from the four identified sources in the morning hours to
prevent effects of changing temperatures on microbial population. The meat
samples were bought and packaged as they are sold to other consumers,
appropriately labeled and transported within 90 minutes to the laboratory for
analysis. Contamination of the meat samples by other materials or sources such
as collector’s hand was avoided.
Isolation of Listeria sp: Isolation of Listeria
from the meat samples were based on the method described by Ndahi et al.
[21] and Adikwu et al. [19] with some
modifications. Aseptically, 10g of each sample was added to 90 ml Listeria Enrichment
broth (Oxoid, Basingstoke, UK) containing Listeria Selective Enrichment
Supplement. The mixture was homogenized for 2 minutes in a blender (MasterChef)
at room temperature and incubated at 30°C for 24 hours. Listeria species were isolated on Listeria Selective Agar (Oxoid)
using pour plate method, by transferring 1 ml of the overnight supplement culture
into molten Listeria Selective agar and incubating for 48 hours at 37°C, after
which the plates were examined for the presence of listeria-like growths.
Identification
of Listeria sp: Listeria
was identified by standard
methods as previously described [22,23]. Suspected colonies were identified by
Gram stain, motility, catalase reaction, haemolysin production, indole,
urease, CAMP (Christie, Atkins, and Munch-Peterson) and sugar fermentation
(rhamnose, mannose, xylose and mannitol) tests. 
Antimicrobial susceptibility
test: Antibiotic susceptibility of the isolated L. monocytogenes was determined by the
Kirby-Bauer disk diffusion method on Mueller-Hinton Agar [19,25]. The
antibiotics used include erythromycin (15µg), streptomycin (10µg), co-trimoxazole
(1.25/23.75 µg), rifampicin (5µg), nalidixic acid (30µg), ciprofloxacin (5µg), ampicillin
(10µg), gentamicin (10µg), chloramphenicol (30µg), sparfloxacin (5µg) and ofloxacin
(5µg). A broth culture of at least 18 hours old was diluted using sterile
distilled water and standardized to match 0.5 McFarland standards
(approximately 108cfu/ml). The culture was inoculated onto dried
Mueller-Hinton Agar (MHA, Oxoid) plate to create a lawn. Antibiotic discs were
then placed on the seeded agar surfaces and the plates incubated for 24 hours
at 37°C, after which the diameter (in mm) of the inhibition zone around each
disk was measured and interpreted according to the Clinical Laboratory Standard
Institute (CLSI) guidelines using the break points of Staphylococcus species [25].
Statistical analysis: IBM SPSS Statistics version
22.0 (IBM Corp., Armonk, NY, USA; 2013) was used to analyse results obtained.
Pearson’s chi-square test was used to determine significance of associations
between variables. A p-value less than 0.05 was considered
statistically significant.
&amp;nbsp;
Results
The prevalence of Listeria species
isolated from 104 samples is shown in Table-1. L. monocytogenes had the
highest prevalence rate of 64.4% (67/104) while L. grayi had the lowest
rate of 2.9% (3/104). L. ivanovii was isolated from 21.2% samples. Mixed
contamination with more than one species was observed in some samples. L.
monocytogenes was isolated from 42 (80.8%) and 25 (48.1%) of beef and
chevon samples respectively. Differences in L.
monocytogenes contamination was statistically significant (p&amp;lt;0.01). Beef samples had the highest listerial presence of
58.2% (78/134) against 41.8% (56/134) in chevon samples.
&amp;nbsp;
Table-1: Types of Listeria species isolated from beef (n=52) and chevon samples
(n=52)
&amp;nbsp;
&amp;nbsp;
Table-2 shows the distribution of Listeria spp
isolated from raw beef samples collected from different locations. L. monocytogenes was most frequently
isolated in sample sources, having a frequency of 76.9% (10/13) in both Shinge
abattoir and Street hawker samples, and 86.4 % (11/13) in samples from Lafia
old market and Lafia modern market. The second most isolated species from
Shinge abattoir and Street hawker samples was L. ivanovii with frequencies of 38.5% (5/13) and 30.8% (4/13)
respectively. L. inocua were the
second most isolated species in both Lafia old market and Lafia modern market
with frequencies of 23.1% (3/13) respectively. At most, only one Listeria spp
type was absent from each sample source. L. monocytogenes, L.
ivanovii and L. innocua were isolated from all the collection sites.
Beef samples from Shinge abattoir had the highest number of listeria
contaminants (28.2%; 22/78), followed by Lafia modern market and street vendors
which had the same number of listeria contaminants (24.4%; 19/78). Lafia old
market had the least number of listeria contaminants (23.1%; 18/78).
Contamination rate in the respective sources were however, not different
statistically (p&amp;gt;0.05).
&amp;nbsp;
Table-2: Distribution of Listeria species in raw beef samples collected from
different locations 
&amp;nbsp;
&amp;nbsp;
Table-3 shows the distribution of Listeria species
in raw chevon samples from the different sample sources. Samples from Shinge
abattoir had the highest number of listerial contaminants (51.8%; 29/56) while
Lafia old market had the least (48.2%; 27/56). L. monocytogenes was most prevalent in both sources (46.2%; 12/26
and 50.0%; 13/26 respectively). No L.
grayi was found in samples obtained from Shinge abattoir. L. welshimeri,
L. grayi and L. murrayi were the least occurring species in samples from Lafia
old market with a frequency of 3.8% (1/26) respectively. Differences in
contamination rates were not statistically significant (p&amp;gt;0.05).
&amp;nbsp;
Table-3: Distribution of Listeria species in raw
chevon samples collected from Shinge and Lafia old market
&amp;nbsp;
&amp;nbsp;
A total 67 L.
monocytogenes isolates were tested for susceptibility to different
antimicrobial agents. Resistance to nalidixic acid, co-trimoxazole and sparfloxacin was 100%, 58.2% and 55.2%
respectively (Table-4). Susceptibility rate of 76.1%, 65.7%, 61.2% and 55.2% was observed with
rifampicin, ampicillin, gentamicin and erythromycin respectively. Eleven L.
monocytogenes strains showed resistance to more than one antibiotic.
&amp;nbsp;
Table-4: Susceptibility pattern of L. monocytogenes to selected antimicrobial
agents (N=67)
&amp;nbsp;
&amp;nbsp;
Discussion
Results of this study revealed a high
prevalence of L. monocytogenes in raw beef and chevon sold in Lafia. The
prevalence rate of Listeria species observed in this study was lower
than the 95.8% prevalence rate reported in vegetable salads in Zaria, Kaduna
state
[24] but higher than the 39.6%
and 7.8% observed in Sokoto [26]
and in Makurdi, Benue state [19].
The high L. monocytogenes contamination observed in the raw meat samples
was in concordance with an earlier report where 14 out of the 15 Listeria species
isolated were L. monocytogenes [27].
Similarly, the high prevalence of L. monocytogenes in beef samples
confirms an earlier report [17].
The present study appears to be the first
investigation regarding presence of Listeria
sp in retailed meat within Nasarawa state. The high prevalence of Listeria in the two widely consumed
meats raises an issue of serious public health importance. It is possible that
cases of listeriosis may have been misdiagnosed across health centers in the
study area since they do not include investigations for listeria infection in
clinical specimens. Some of the symptoms associated with the disease onset such
as gastroenteritis, headache, fatigue, muscular and joint pain are similar to
those of typhoid fever [28].
Moreover, not much appears to be known about this organism in Nigeria and most
African countries [16]. 
The least common listeria isolate was L. grayi while the most
observed was L. monocytogenes. This was in contrast with an earlier
report [26]where L. seeligeri and L. innocua were the
least and the most observed listerial contaminants respectively. Listerial
contamination of beef was highest in samples from the Shinge abattoir.
Contamination was higher in beef than chevon, an observation that was also
reported by earlier studies [22,29].
Although not determined in this study, the difference in contamination between
the two meat types might have been influenced by factors such as pH and water
activity (aw). For instance, L.
monocytogenes is known to survive at a pH of &amp;lt;4.3 and water activity of
&amp;lt;0.930 [30]. The high rate of Listeria
contaminants identified in beef samples from this source could be due to
unhygienic practices such as slaughtering and preparing of meat on bare floor, poor
drainage system, use of contaminated water, poor facility maintenance,
illiteracy and lack of hygiene awareness by the handlers, as well as improper
storage facilities. Vending of these meats is mostly done without any covering,
thus exposing the meats to high rate of microbial contamination. Adoption of
proper methods during slaughtering of animals have been suggested as a means of
considerably reducing presence of listeria in meats [31,32].
Chevon samples from Lafia old market had less
listerial contaminants than those from Shinge abattoir. This could be due to
double-washing process practiced in Lafia old market; the meats are washed
after slaughtering and before sales to butchers (retailers), unlike at Shinge
abattoir where this is not practiced. The practice of repeated washing might
have enhanced the removal of surface contaminants from the meat obtained from
Lafia old market. 
Findings also showed that the isolated L.
monocytogenes was either sensitive or intermediate sensitive to most of the
antimicrobial agents tested. Susceptibility to some antibiotics and the
multiple antimicrobial resistance observed in this study is similar to earlier
reports [19,21,24]. Almost all the
studied strains were susceptible to a wide range of antibiotics but completely
resistant to nalidixic acid. This observation is in agreement with the earlier
reports [33,34]. Resistance to
nalidixic acid justifies addition of nalidixic acid into selective media for
the isolation of L. monocytogenes. Susceptibility to ampicillin, erythromycin, chloramphenicol, co-trimoxazoleand
gentamicin, observed in this study is similar to that reported by Troxiler et al. [35] and Hansen et
al. [36]. Listeriosis is treated
usually with β-lactam antibiotics like ampicillin or penicillin alone, or
combined with an aminoglycoside (usually gentamicin) [37]. However, about 20-34% of the isolated L. monocytogenes were resistant to ampicillin, gentamicin and erythromycin in this study. This
portends a serious public health issue. Around Lafia, meat is prepared by
roasting, apart from boiling and frying; sometimes, this may not be enough to
destroy deep listerial contaminants, leaving consumers of such products at risk
of foodborne diseases. 
The resistance pattern observed in the present
study could be attributed to the irrational use of the antibiotics in cattle
and goat by the animal rearers or veterinary quacks [26]. Misuse of antibiotics as growth promoters can
confer selective pressure on bacteria [38],
making those increasingly resistant to conventional antibiotics. Although not
determined experimentally, horizontal gene transfer among bacteria in the
environment could also been responsible for antibiotic resistance as observed
in this study [38,39].
&amp;nbsp;
Conclusion
Listeria
contamination of raw beef and chevon sold in Lafia is alarming. Unhygienic
practices amongst meat handlers at the collection site could be the major
source of contamination. Use of contaminated water, washing without addition of
disinfectant, lack of awareness, improper storage facilities, poor equipment
maintenance and dirty environment were factors believed to be the major causes
and sources of listerial contamination observed in this study. 
&amp;nbsp;
Authors’ contributions
GAO
conceived the idea of the study. AC, GAO and SBE designed the study. SBE and
GAO conducted the study. GAO performed statistical analysis of data. AC, SBE
and GAO wrote, reviewed and approved the final manuscript.
&amp;nbsp;
Conflict of interest
The
authors hereby, declare that no conflict of interest exists.
&amp;nbsp;
References
1.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Huss, HH, Reilly A, Embarek PKB. Prevention and control of hazards in seafood.
Food Control. 2000; 11(2): 149-56. 
2.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Jeyaletchumi P, Tunung R,
Margaret SP, Son R, Farinazleen MG, Cheah YK. Review article: Detection of Listeria
monocytogenes in foods. Int Food Res J. 2010; 17: 1-11. 
3.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Wang W,
Zhou X, Suo Y, Deng X, Cheng M, Shi C, Shi X. Prevalence, serotype diversity,
biofilm-forming ability and eradication of&amp;nbsp;Listeria monocytogenes&amp;nbsp;isolated from
diverse foods in Shanghai, China.&amp;nbsp;Food Control.&amp;nbsp;2017; 73B: 1068–1073.
4.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Gebretsadik S, Kassa T,
Alemayehu H, Huruy K, Kebede N. Isolation and characterization of Listeria
monocytogenes and other Listeria species in foods of animal origin
in Addis Abada, Ethiopia. J Infect Public Health. 2011; 4(1): 22- 29.

5. Robinson RK, Batt CA,
Patel PD. (eds). Encyclopedia of Food Microbiology. San Diego, CA: Academic
Press; 2000.
6.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Selby, TL, Berzins A,
Gerrard DE, Corvalan CM, Grant AL, Linton RH. Microbial heat resistance of Listeria
monocytogenes and the impact on ready-to-eat meat quality after
post-package pasteurization. Meat Science. 2006; 74(3): 425-34.
7.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Fenlon DR. Listeria
monocytogenes in the natural environment. In: Ryser ET, Marth EH,
editors. Listeria, Listeriosis and food safety. New York: Marcel Dekker;
1999. pp. 21-37.
8.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Ryser ET, Arimi SM, Bunduki
MM, Donnelly CW. Recovery of different Listeria ribotypes from naturally
contaminated, raw refrigerated meat and poultry products with two primary
enrichment media. Appl Environ Microbiol. 1996; 62: 1781-7.
9.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Jones AD, Seeliger HPR. The
Genus Listeria. In: Balows A, Trüper HG, Dworkin M, Harder W, Schleifer KH, editors. Prokaryotes: a handbook on the biology of bacteria: Ecophysiology,
isolation, identification, applications. 2nd Ed. New York, NY: Springer
Verlag; 1992. pp. 1595-1616.
10.&amp;nbsp; Kuhn M, Goebel W. Molecular
virulence determinants of Listeria monocytogenes. In: Ryser ET, Marth
EH, editors. Listeria, listeriosis and food safety. Boca Raton: CRC
Press Taylor and Francis Group; 2007. pp. 111-155.
11.&amp;nbsp; Centers for Disease Control and Prevention (CDC). National Listeria
Surveillance Annual Summary, 2008. Atlanta, Georgia: US Department of Health
and Human Services, CDC, 2011.
12.&amp;nbsp; Chodorowska M, Kuklinska D.
Virulence factors of Listeria monocytogenes and pathogenesis, clinical
symptoms and antibiotic therapy of listeriosis. Post Mikrobiol. 2002; 41: 37-49.
13.&amp;nbsp; Teuber M. Spread of
antibiotic resistance with food borne pathogens. Cell Mol Life Sci. 1999;
56(9-10): 755-63.
14.&amp;nbsp; Harakeh S, Saleh I, Zouhairi
O, Baydoun E, Barbour E, Alwan N. Antimicrobial resistance of Listeria
monocytogenes isolated from dairy-based food products. Sci Total Environ.
2009; 407(13): 4022-7. 
15.&amp;nbsp; Bondarianzadeh D. Food risk
to babies listeriosis. Nutrition Today. 2007; 42: 236-9.
16.&amp;nbsp; Enurah LU, Aboaba OO,
Nwachukwu SCU, Nwosuh CI. Antibiotic resistant profiles of food (fresh raw
milk) and environmental (abattoir effluents) isolates of Listeria
monocytogenes from the six zones of Nigeria. Afr J Microbiol Res.
2013; 7(34): 4373-8.
17.&amp;nbsp; Molla B, Yilma R, Alemayehu
D. Listeria monocytogenes and other Listeria species in retail
meat and milk products in Addis Ababa, Ethiopia. Ethiop J Health Dev.
2004; 18(3): 131-212.
18.&amp;nbsp; Ishola OO, Mosugu JI, Adesokan HK. Prevalence and antibiotic
susceptibility profiles of Listeria monocytogenes contamination of chicken
flocks and meat in Oyo State, south-western Nigeria: Public health
implications. J Prev Med Hyg. 2016; 57(3): E157-E163.
19.&amp;nbsp; Adikwu Peter, E.U. Umeh, E.T. Azua and Godwin Attah Obande. Prevalence and
Antimicrobial Susceptibility of Listeria monocytogenes Isolated from
Beef, Pork and Chicken Sold in Makurdi Metropolis. Br Microbiol Res J. 2016;
14(5): 1-7.
20.&amp;nbsp; National Population
Commission. Federal Republic of
Nigeria Official Gazette Number 2. Volume 96, 2nd
February 2009.
21.&amp;nbsp; Ndahi MD, Kwaga JKP, Bello M, Kabir J, Umoh VJ, Yakubu
SE, Nok AJ. Prevalence and antimicrobial susceptibility
of Listeria monocytogenes and methicillin-resistant Staphylococcus
aureus strains from raw meat and meat products in Zaria, Nigeria. Lett
App Microbiol. 2013; 58(3): 262-269.
22.&amp;nbsp; Al-Nabulsia AA, Osailia
TM, Awada AA, Olaimatb AN, Shakera RR, Holley RA. Occurrence and antibiotic
susceptibility of Listeria monocytogenes isolated from raw and processed meat
products in Amman, Jordan. CYTA-J Food.
2015; 13(3): 346–352. 
23.&amp;nbsp; Food and Agriculture
Organization. Quality assurance for microbiology in feed analysis laboratories,
by R.A. Cowie. Edited by Harinder P.S. Makkar. FAO Animal Production and
Health Manual No. 16. Rome. 2013.
24.&amp;nbsp; Ieren II, Bello M, Kwaga JKP.
Occurrence and antibiotic resistance profile of Listeria monocytogenes
in salad vegetables and vegetable salads sold in Zaria, Nigeria. Afr J Food
Sci. 2013; 7(9): 334-338. 
25.&amp;nbsp; Clinical and Laboratory
Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing;
Twenty-Fourth Informational Supplement. CLSI document M100-S24. Wayne,
PA. 2014.
26.&amp;nbsp; Yakubu Y, Salihu MD, Faleke
OO, Abubakar MB, Junaidu AU, Magaji AA, Gulumbe ML, Aliyu RM. Prevalence and
antibiotic susceptibility of Listeria monocytogenes in raw milk from cattle
herds within Sokoto Metropolis, Nigeria. Sokoto J Vet Sci. 2012; 10(2): 13-17.
27.&amp;nbsp; Meti
M, Govind V, Sundaresan G, Appa RV, Narendra BR. Isolation and detection of Listeria
monocytogenes in chicken meat marketed in retail outlets by using simplex
PCR. J Entomol Zool Stud. 2017; 5(5): 434-437.
28.&amp;nbsp; Liu D, Busse HJ.
Listeria. In: Liu D, editor. Molecular detection of food-borne pathogens.
United Kingdom: CRC Press; 2009.
29.&amp;nbsp; Islam MS, Husna AA, Islam
MA, Khatun MM. Prevalence of Listeria monocytogenes in Beef, Chevon and Chicken
in Bangladesh. Am J Food Sci Health.
2016; 2(4): 39-44.
30.&amp;nbsp; Vermeulen A, Gysemans
KPM, Bernaets K, Geeraerd Ah, Van Impe JF, Debevere J, Devlieghere F. Influence
of pH, water activity and acetic acid concentration on Listeria monocytogenes
at 7°C: data collection for the development of a growth/no growth model. Int J Food Microbiol. 2007; 114(3): 332-341. 
31.&amp;nbsp; Keeratipibul S, Techaruwichit P. Tracking
sources of Listeria contamination in a cooked chicken meat factory by
PCR-RAPD-based DNA fingerprinting. Food Control.
2012; 27(1): 64-72.
32.&amp;nbsp; Kurpas M, Wieczorek K, Osek J. Ready-to-eat meat products as a source of
Listeria monocytogenes. J Vet Res.
2018; 62(1): 49-55.
34.&amp;nbsp; Ennaji H, Timinouni M, Ennaji
M, Hassar M, Cohen N. Characterization and antibiotic susceptibility of
Listeria monocytogenes isolated from poultry and red meat in Marocco. Infect
Drug Resist. 2008; 1: 45-50.
34.&amp;nbsp; Marius EC, Lorena AM, Tatiana
VD, Alexandru R, Alina MB. Antibiotic Susceptibility Profiles of Listeria
monocytogenes strains isolated from food products and clinical samples. Rev
Rom Med Lab. 2014; 22(2): 255-261.

35.&amp;nbsp; Troxler R, von Graevenitz A,
Funke G, Wiedemann B, Stock I. Natural antibiotic susceptibility of Listeria
species: L. grayi, L. innocua, L. ivanovii, L. monocytogenes, L.
seeligeri and L. welshimeri strains. Clin Microbiol Infect.
2000; 6(10): 525-535.
36.&amp;nbsp; Hansen JM, Gerner-Smidt P,
Bruun B. Antibiotic susceptibility of Listeria monocytogenes in Denmark,
1958-2001. APMIS. 2005; 113(1):
31-36.
37.&amp;nbsp; Ramaswamy
V, Cresence VM, Rejitha J, Mohandas UL, Dharsana KS, Suryaprasad PP, Helan MV.
Listeria: Review of epidemiology and pathogensis. J Microbiol Immunol Infect. 2007; 40(1): 4–13.
38.&amp;nbsp; Indrawattana N, Nidabbhasobon T, Sookrung N,
Chongsa-Nguan M, Tungtrongchitr A, Makino S, Tungyong W, Chaicumpa W.
Prevalence of Listeria monocytogenes in raw meats marketed in Bangkok and
characterization of the isolates by phenotypic and molecular methods. J Health Popul Nutr. 2001; 29(1): 26–38. 
39.&amp;nbsp; Charpentier E, Courvalin P. Antibiotic
resistance in Listeria spp. Antimicrob
Agents Chemother. 1999; 43(9): 2103–2108.</description>

            </item>
            
    <copyright>2026 Ibrahim Medical College. All rights reserved.</copyright>
</channel>
</rss>
