dc.contributor.author
Woshie, Adem Hiko
dc.date.accessioned
2018-06-07T15:18:15Z
dc.date.available
2017-10-23T09:03:24.905Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/876
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-5078
dc.description.abstract
Background: In Ethiopia, little information is available on the status of food
safety. It was the aim of this study to detect points of risk in meat and
product contamination; to assess the prevalence of Salmonella serotypes and E.
coli in meat production and handling chains and to track possible sources and
transmission routes of Salmonella; to evaluate the microbiological quality of
the final product using the Aerobic Plate Count (APC) and the
Enterobacteriaceae count (EBC); and to perform antimicrobial
susceptibility/resistance tests on the isolates. Materials and methods: The
study was conducted from December 2011 to April 2012 in two beef production
and supply lines. The first was the Addis Ababa Abattoir Enterprise (AAAE)
abbatoir with its recipient city butchers’ in Addis Ababa city - “the abattoir
line” - while the second was a beef processing plant located some 47 km out of
Addis Ababa at Bishoftu/Debre Zeit town with its product recipient
supermarkets in Addis Ababa city - “the processing plant line”. For this
purpose, from the abattoir line, different samples were taken along cattle
slaughter steps from the abattoir environment (n=101), animal-related
materials (n=102) and from raw beef from city butchers’ (n=34). Similarly,
samples were collected in the processing plant line along the processing steps
from the processing environment (n=194), animal-related materials (n=118) and
products from 8 selected supermarkets (n=119) . All samples were examined for
Salmonella and E. coli. In addition, samples from the processing plant line
were examined for APC and EBC. Salmonella isolates were serotyped and exposed
to Pulsed Field Gel Electrophoresis (PFGE) using XbaI® enzymatic genomic
digestion. Possible sources and transmission routes of Salmonella serotypes
were tracked based upon genetic similarity and differences of the obtained
same serotype relation. All Salmonella and E. coli isolates were tested for
susceptibility/resistance to antimicrobial agents of six different chemical
classes of drugs and each with their respective concentrations (Oxoid) used
for sensitivity testing. The drugs were β-lactams - amoxicillin (AML 25 μg),
amphenicols - chloramphenicol (C 50 μg), amino glycosides - gentamycin (CN 10
μg) and neomycin (30 μg), tetracycline - oxytetracycline (OT 30 μg),
polymyxins - polymyxin B (PB 300IU), and folate pathway inhibitors -
trimethoprim (W 5 μg) and trimethoprim-sulfamethoxazol (SXT 1.25/23.75 μg).
Within both lines, sampling occasions, locations and directions in the
production, processing and supply of the final product were considered and
taken into account for data management and analysis. Numerical data from
spoilage bacteria counts were calculated in logarithmic function and compared
using single and paired t-tests. Categorical data for prevalence and
antimicrobial susceptibility/resistance were calculated using percentages and
the 95% midprevalence exact confidence interval was used to assess
associations. PFGE data were analyzed using the BioNumerics® 6.6 version.
Results: Abattoir line Spoilage bacteria: Due to non-expected heavy
contamination of the abattoir spoilage bacteria were only assessed at the
processing plant line. Salmonella: 63 isolates resulting in a 26.6% prevalence
were identified in the abattoir line. Salmonella prevalence was higher for
abattoir environment (36.6%) than for animal-related materials (14.7%).
Prevalence at butchers’ was 32.4%, similarly to abattoir environment but not
animal-related materials. Six different serotypes with higher
prevalences/proportions of 11.4%/42.8% for S. Saintpaul, followed by
5.9%/22.2% for S. Muenchen were observed. In this line, a prevalence of S.
Larochelle (4.6%), S. Dublin (1.7%), S. Kastrup (1.3%), S. London (0.24%) and
unidentified ones (1.3%) was found. The PFGE pattern showed 1, 2 and 6
pulsotypes with 1 to 14 ratios of isolates to pulsotypes in serotypes and 1 to
7 pulsotypes with 1 to 2.5 ratios of isolates to pulsotypes in positive
locations. Based on genomic similarity, transmission routes were identified
for S. Saintpaul (SSaX2), S. Muenchen (SMuX1), S. Larochelle (SKLX1) and S.
Dublin (SDuX1). Findings revealed similar pulsotypes over sampling
occasions/batches in different sampling locations for the corresponding
serotypes. Other isolates of the same serotype but of a different pulsotype
were determined as possible sources and/or contaminants of the production line
from other sources. E. coli: With regard to E. coli from this line, an overall
prevalence of 45.1% was observed. This prevalence essentially agreed with
prevalences of the environment (40.6%), animalrelated materials at the
abattoir (52.0%) and with retailed meat at butchers (38.2%). Prevalence at
individual sampling locations ranged from 33.3% in tap water to 55.9% in raw
beef at the abattoir with no principal differences among and between sampled
locations. Processing plant line Parameters tested here were spoilage
bacteria, Salmonella and E. coli. Spoilage bacteria: Highest APC of 5.28±0.24
log10 cfu/cm2 in room floor swabs to lowest 3.99±0.75 log10 cfu/g in spices
wwere observed. EBC ranged from high 3.19±0.55 log10 cfu/cm2 for room floors
to low 2.08±0.19 log10 cfu/g in products at Supermarket-G. The paired t-test
on the count difference (log10 APC – log10 EBC) within locations showed higher
APC than EBC. This difference ranged from 2.75±0.65 cfu/g in products to
1.71±0.70 cfu/g in spices. Using APC, microbiological quality of products in
total was found to be good in 24.4% of cases, 44.5% acceptable and 31.1%
unsatisfactory. In contrast, by EBC 64.7% of products were good and 35.5%
acceptable. Salmonella: A total of 23 Salmonella isolates (5.3% prevalence)
was observed in this line. Prevalence in theenvironment (5.2%) was similar to
that of animal-related materials (10.2%) and final products from supermarkets
(0.8%), but in comparison it was higher in animalrelated materials than in
final products. Only one isolate was observed in a single supermarket, the
others being negative. A total of seven serotypes with a high ratio of
prevalence to proportion (1.4%/26.1%) of S. London was observed. Unidentified
Salmonella strains were also obtained from this line. Possible transmission of
S. London (SLoX1) was observed on the 1st sampling occasion from raw beef
samples to working tables which were also positive on the 2nd sampling
occasion. A similar pulsotype within each of S. Anatum (SAnX1), S. London
(SLoX1) and S. Muenchen (SMuX1) from raw beef on the 1st, 2nd and 6th sampling
occasions was observed, respectively showing that the contaminated meat was
coming from the same sources. E. coli: The overall prevalence along the
processing plant line (46.4%) was found to be the same as the prevalence in
the environment (50.5%) and in animal-related materials at the processing
plant (56.8%) but was higher than in the end products at supermarkets (29.4%).
Differences were not observed between and among locations, with the only
exception beingprocessing plant rooms for whom a higher prevalence was
recorded (75%) than in tap water (23.5%), spices (13.3%), Supermarkets-A and H
(each with 20%) and Supermarket-F (16.7%). There was no difference in
prevalence among and between products from all supermarkets. Antimicrobial
susceptibility/resistance: Salmonella: Susceptibility to PB, CN, C, W and SXT
ranged from 93.2% to 100% and from 30.4% to 50.4% to N for all isolates in
general and for those from the abattoir line and processing plant line in
particular. Susceptibility to OT was 44.2% overall but it was 31.7% and 78.3%
in isolates from abattoir and processing plant lines, respectively. Resistance
was high (53.5%) overall. High (65.1%) resistance to oxytetracycline was found
in isolates from the abattoir line was low (21.7%) in isolates from the
processing plant line. A total of 55 (63.9%) isolates was found to be
resistant to at least one of the antimicrobial agents used in this study. High
resistance was detected in S. Saintpaul (41.8%) and in S. Muenchen (30.9%).
The proportion of Salmonella isolates tested and the corresponding resistant
isolates showed no difference (p>0.05) within origin/source. Strains of higher
resistance were found at the abattoir line (85.5%) than at the processing
plant line (14.5%). Single-drug resistant strains were more frequent (83.6%)
than two-drug resistant ones (12.7%). Multiple drug resistance (MDR) in the
strains was only 3.6%. Resistance to OT was frequently observed. Distribution
of strains resistant to individual drugs in both abattoir and processing plant
lines was 1.8% to each of PB, CN, W and SXT, 5.4% to C, 26.6% to N and 83.6%
to OT, in increasing order. E. coli: Susceptibility of E. coli isolates to PB,
C, CN and SXT ranged from 92.2% to 100%. Furthermore, their susceptibility to
AML was between 70.1% and 79.5% while to OT it spanned between 49.5% and
60.0%. This was true overall for isolates from the abattoir line and the
processing plant line. High frequencies of resistant strains to OT (37.5% to
43.9%) and to AML (18.5% to 26.2%) were observed in total as well as in
individual isolates from abattoir and processing plant lines. A total of 143
(46.6%) isolates were found resistant to at least one of the antimicrobial
agents used in this study. Higher frequencies of resistant strains were
observed at the processing plant line (61.5%) than at the abattoir plant line
(38.5%). Single-drug resistant isolates (55.9%) were more frequent than two-
drug resistant ones (28.7%) and MDR accounted for 15%. Isolates resistant to
OT were frequently observed. The total distribution of strains resistant to
individual drugs both at the abattoir and at the processing plant line showed
differences. The extent of resistance to each drug in increasing order was PB
(1.4%), CN (2.1%), C (8.4%), SXT (16.1%), AML (45.5%) and OT (85.3%).
Discussion: Observation of Salmonella and E. coli in all sampling locations on
one or more sampling occasions in this investigation demonstrated the presence
of zoonotic and spoilage bacteria, particularly with higher loads along the
abattoir line. Higher Salmonella prevalence (26.6%) at the abattoir line than
at the processing plant line (5.3%) identified the abattoir to be the main
source of Salmonella transmission along beef production, processing and
handling lines. In this study, occurrence of S. Kastrup and S. London was
reported for Ethiopia for the first time. With XbaI® PFGE profiles, S. Kastrup
and S. Larochelle showed indistinguishable profiles. Antimicrobial
susceptibility/resistance of Salmonella and E. coli from both studied lines
showed high susceptibility to PB, CN, C, SXT and W. Resistance was high to
oxytetracycline. Conclusions: This investigation involved two beef lines to
study spoilage and zoonotic bacteria and their antimicrobial
susceptibility/resistance. Findings revealed prevalence of the agents and the
need for improvement, regular monitoring and application of HACCP during
production, processing, handling and supply of products. Furthermore,
resistance of Salmonella and E. coli to oxytetracycline was high and accounted
for 83.6% and 85.3%, respectively. This drug is marketed, it is popular and
widely used in the veterinary sector in Ethiopia. The further use of this drug
thus should be questionned in light of the high prevalence of resistant
strains in the country. Future emphasis should be put tohygiene toimprove beef
production line, to antimicrobial susceptibility testing, to further screening
of the present isolates of E. coli strains and to the extension of this type
of study to meat production lines of other food animals of the country.
de
dc.description.abstract
Hintergrund: Für Äthiopien existieren nur wenige Informationen zur
Lebensmittelsicherheit. Ziele der vorliegenden Untersuchung waren: \-
Abschätzung der Salmonella- und E. coli-Prävalenz in Fleischproduktions- und
–bearbeitungsketten mit Zurückverfolgung der Transferrouten von Salmonella, \-
Beurteilung der mikrobiologischen Qualität des Endprodukts mit Hilfe von
Gesamtkeimzahl (GKZ) und Enterobacteriaceae-Zahl (EBZ) sowie \- Resistenztests
an den gewonnenen Isolaten Material und Methoden: Die Untersuchungen wurden
von Dezember 2011 bis April 2012 in zwei Fleischproduktionsketten in Äthiopien
durchgeführt. Die „Abattoir Line“ wurde aus dem städtischen Schlachthof in
Addis Ababa (Addis Ababa Abattoir Entreprise (AAAE)) sowie Verkaufsstätten
gebildet, die Fleisch direkt von diesem Schlachtbetrieb für den Weiterverkauf
erhielten. Die „Processing Plant Line“ bestand aus dem Zerlege- und
Verarbeitungsbetrieb in Bishoftu / Debre Zeit mit 3 unterschiedlichen
Zulieferschlachtbetrieben sowie Supermärkten in Addis Ababa, die fertige
Produkte aus dem Bearbeitungsbetrieb erhielten. In der „Abattoir Line“ wurden
entlang der Schlachtlinie an unterschiedlichen Positionen Proben genommen (n =
101) sowie Proben von Tieren bzw. den Schlachttierkörpern (n = 102). In den
Verkaufsstätten wurden Fleischproben genommen (n = 34). In der „Processing
Plant Line“ wurden von den einkommenden Tierkörpern (n = 118) und
Umgebungsproben an unterschiedlichen Positionen im Verarbeitungsbetrieb (n =
194) genommen. In insgesamt 8 Supermärkten wurden Produktproben (Mortadella)
(n = 119) entnommen. Alle Proben wurden auf Salmonella und E. coli untersucht,
die Proben der „Processing Plant Line“ wurden zusätzlich auf GKZ und EBZ
geprüft. Die Salmonella-Isolate wurden serotypisiert und mit Hilfe einer
Pulsfeldgelelektrophorese (XbaI) mögliche Übertragungsrouten mit Hilfe
bestimmter Serotypen verfolgt. Die gewonnenen Salmonella und E. coli-Isolate
wurden auf antimikrobielle Resistenzen / Empfindlichkeiten gegenüber sechs
Chemotherapeutika überprüft: β-Laktame: Amoxicillin (AML 25 μg); Amphenicole:
Chloramphenicol (C 50 μg); Aminoglykoside: Gentamycin (CN 10 μg), Neomycin (30
μg); Tetracycline: Oxytetracyclin (OT 30 μg); Polymyxine: Polymycin B (PB 300
IU) und Folsäureinhibitoren: Trimethoprim (W 5 μg), Trimetoprim-
Sulfamethoxazol (SXT 1,25/23,75 μg). Ergebnisse: Abattoir Line Salmonella:
Insgesamt wurden 63 Salmonella-Isolate in der „Abattoir Line“ gewonnen, dies
entsprach einer Prävalenz von 26,6 % (Umgebungsproben: 36,6 %, Tierproben:
14,7 %; Proben aus den Verkaufsstätten: 32,4 %). Sechs unterschiedliche
Serotypen wurden gefunden: S. Saintpaul, S. Muenchen, S. Larochelle, S.
Dublin, S. Kastrup und S. London sowie unidentifizierbare Serotypen. Mit Hilfe
der PFGE konnten bei S. Saintpaul, S. Muenchen, S. Larochelle und S. Dublin
jeweils ähnliche Pulstypen, die auf eine genetische Verwandtschaft der
jeweiligen Serotypen hinweisen, identifiziert werden. Für diese Serotypen
wurden mögliche Transferrouten gezeigt. E. coli: Für E. coli lag die Prävalenz
bei 45,1 % (Umgebungsproben: 40,6 %, Tierproben: 52 %; Metzgereien: 38,2 %).
Processing Plant Line Hygieneparameter GKZ: Die GKZ lag zwischen 3,99 ± 0,75
log10 KbE/g (Gewürze) und 5,28 ± 0,24 log10 KbE/cm2 (Bodentupferproben). Die
EBZ lag zwischen 2,08 ± 0,19 log10 KbE/g (Produktproben aus Supermarkt G) und
3,19 ± 0,55 log10 KbE/cm2 (Bodentupferproben). Salmonella: Insgesamt wurden 23
Salmonella-Isolate in der „Processing Plant Line“ gefunden (Prävalenz: 5,3 %).
Für S. London, S. Anatum und S. Muenchen konnten mögliche Transferrouten
identifiziert werden. E. coli: Für E. coli lag die Prävalenz bei 46,4 %
(Umgebungsproben: 50,5 %; Tierproben: 56,8 %; Produktproben: 29,4 %).
Empfindlichkeitsprüfungen gegenüber Chemotherapeutika: Salmonella:Die
Empfindlichkeit von den aus beiden Linien gewonnenen Salmonella-Isolaten
gegenüber PB, CN C, W und SXT schwankte zwischen 93,2 und 100 %; gegenüber N
zwischen 30,4 und 50,4 %. Insgesamt 55 Isolate waren gegen mindestens ein
Chemotherapeutikum resistent (63,9 %). E. coli: Von den gefundenen E. coli-
Isolaten waren 92,2 bis 100 % empfindlich gegenüber PB, C, CN und SXT.
Insgesamt waren 143 Isolate gegen mindestens ein Chemotherapeutikum resistent
(46,6 %). 83,6 % der Salmonella-Isolate bzw. 85,3 % der E. coli-Isolate waren
gegenüber Oxyterazyklin resistent. Diskussion: Salmonella und E. coli wurden
an unterschiedlichen Probenahmetagen innerhalb beider Ketten gefunden, die
Nachweisrate in der „Abattoir Line“ war höher (26,6 %) als in der Processing
Plant line (5,3 %). Erstmals in Äthiopien wurden S. Kastrup und S. London
nachgewiesen. Die XbaI® PFGE Profile beider Serotypen waren nicht
unterscheidbar. Bezüglich der Antimikrobiellen Empfindlichkeit / Resistenz war
bei Salmonella und E.coli eine hohe Empfindlichkeit gegenüber PB, CN, C, SXT
und W erkennbar sowie eine hohe Resistenz gegenüber Oxytetracyclin.
Schlussfolgerungen: Diese Untersuchung bezog sich auf zwei Prozeßlinien
(Schlacht- und Verarbeitungslinie) und auf Zoonoseerreger, Verderbsmikroflora
und das Resistenzgeschehen. Die Ergebnisse lassen die Notwendigkeit
regelmäßiger Kontrollen, so etwa eines HACCP- Systems erkennen. Es ergab sich
eine hohe Resistenz gegemnüber Oxytetracyclin in beiden Linien (83,6% und
85,3%). Oxytetracyclin ist in Äthiopien häufig in Benutzung, was angesichts
der hohen Resistenzen hinterfragt werden sollte. In Bezug auf die Hygiene
sollten die Abläufe verbessert werden, es sollten Resistenztests und
Untersuchungen auf die nähere Natur der auftretenden E.coli durchgeführt
werden. Untersuchungen wie die hier vorgelegte Studien sollten auch in anderen
Nutztier- Linien durchgeführt werden.
de
dc.format.extent
xlvii, 152 Seiten
dc.rights.uri
http://www.fu-berlin.de/sites/refubium/rechtliches/Nutzungsbedingungen
dc.subject
pulsed field electrophoresis
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::630 Landwirtschaft::630 Landwirtschaft und verwandte Bereiche
dc.title
Zoonotic and spoilage bacteria in a meat production and a processing line in
Ethiopia
dc.contributor.firstReferee
Prof. Dr. Reinhard Fries
dc.contributor.furtherReferee
Prof. Gobena Ameni
dc.contributor.furtherReferee
Univ.-Prof. Dr. Marcus Doherr
dc.date.accepted
2017-09-27
dc.identifier.urn
urn:nbn:de:kobv:188-fudissthesis000000105668-4
dc.title.translated
Zoonose- und Verderbnisserreger in zwei Fleisch produzierenden und
verarbeitenden Linien in Äthiopien (Rind)
de
refubium.affiliation
Veterinärmedizin
de
refubium.mycore.fudocsId
FUDISS_thesis_000000105668
refubium.note.author
Mensch und Buch Verlag
refubium.mycore.derivateId
FUDISS_derivate_000000022486
dcterms.accessRights.dnb
free
dcterms.accessRights.openaire
open access