200 research outputs found
Prevalence, antimicrobial resistance and genotyping (AFLP) of thermophilic Campylobacter spp. in broiler flocks and analysis of risk factors for Campylobacter colonisation at flock level
Titelblatt
Persönlicher Dank
Inhaltsverzeichnis
AbkĂŒrzungsverzeichnis
Einleitung
LiteraturĂŒbersicht
Eigene Untersuchungen
Ergebnisse
Diskussion
Schlussfolgerungen
Zusammenfassung
Summary
Quellenverzeichnis
Anhang
Danksagung, Lebenslauf, SelbststÀndigkeitserklÀrungIm Zeitraum von Mai 2004 bis Juli 2005 wurden 279 MasthÀhnchenherden
verschiedener Haltungssysteme auf das Vorkommen von thermophilen Campylobacter
spp. beprobt. Hierzu wurde pro Herde der Blinddarmkot von zehn Tieren als
Pool- und/oder Einzelproben untersucht. Alle gewonnenen Campylobacter- Isolate
wurden durch eine Multiplex- PCR bestÀtigt. 79 Campylobacter- Isolate wurden
durch Mikrodilution auf ihr Verhalten gegenĂŒber acht Antibiotika
(-Kombinationen) getestet, 236 Campylobacter- Isolate wurden mittels der AFLP-
Analyse feintypisiert. Zuletzt wurden 75 Mastanlagen anhand eines Fragebogens
auf mögliche Einflussfaktoren fĂŒr den Campylobacter- Eintrag in die Herden
untersucht. 44% der Herden waren Campylobacter- positiv. C. jejuni wurde mit
77% als dominierende Spezies detektiert, gefolgt von C. coli mit 23%. Das
Vorkommen von Campylobacter spp. in den MasthÀhnchenherden war
jahreszeitlichen Schwankung unterworfen mit hohen PrÀvalenzen in den warmen
Sommer- und Herbstmonaten. Die InnerherdenprÀvalenz variierte von 10% bis
100%. Bei 33% der Herden waren alle zehn Blinddarmpaare positiv. WĂ€hrend in
den Campylobacter- positiven Herden aus konventionellen und Louisiana- StÀllen
vor allem C. jejuni detektiert wurde, war in den Herden aus Freiland- und
biologischer Haltung C. coli vorherrschend. Durch Untersuchung von Poolproben
wurden 93% der durch Einzeluntersuchung als Campylobacter- positiv befundenen
Herden erkannt. Von den 79 untersuchten Campylobacter- Isolaten waren 30%
Ampicillin- resistent, 13% resistent gegen Ampicillin in Kombination mit
Sulbactam, 10% Ceftazidim- resistent, 41% Ciprofloxacin- und NalidixinsÀure-
resistent und 30% Tetrazyklin- resistent. Alle Isolate waren empfindlich
gegenĂŒber Gentamicin. GegenĂŒber Erythromycin waren alle C. jejuni- Isolate
sensibel, wohingegen 28% der C. coli- Isolate resistent waren. Es wurden 34
Cluster fĂŒr 61 C. jejuni- Isolate und 11 Cluster fĂŒr 18 C. coli- Isolate
identifiziert. Dies verdeutlicht die genetische DiversitÀt von Campylobacter
spp. bei MastgeflĂŒgel. Das Vorfinden von dominierenden und wiederkehrenden
AFLP- Genotypen in aufeinander folgenden Herden verdeutlicht das Bestehen von
persistierenden Infektionsquellen in der Umwelt. Das Vorkommen von
Campylobacter- negativen Herden nach Campylobacter- positiven Herden zeigt,
dass eine Infektion der Herde verhindert werden kann. Die PrÀsens von
verschiedenen Campylobacter- Spezies in einer Herde und in aufeinander
folgenden Herden eines Stalles deutet auf verschiedene Infektionsquellen hin
und beschreibt die Dynamik der Kolonisation. Anhand der Fragebogenaktion
konnten drei Einflussfaktoren fĂŒr eine Campylobacter- Belastung von
MasthĂ€hnchenherden erkannt werden: die Haltungsform, die HerdengröĂe und die
TrĂ€nkeform. Andere Variablen, wie HygienemaĂnahmen, Alter, Serviceperiode und
Wasserquelle hatten keinen signifikanten Einfluss auf die Campylobacter-
PrÀvalenz.From May 2004 to July 2005, 279 broiler flocks of different production types
were tested for the presence of thermophilic Campylobacter spp. Of each flock
caecal content of ten chickens was tested. All Campylobacter isolates were
additionally identified by multiplex- PCR. 79 Campylobacter isolates were
tested for susceptibility to eight antimicrobial agents and combinations by
microbroth dilution and 236 Campylobacter isolates were genotyped by AFLP-
analysis, too. To identify potential risk factors for the presence of
Campylobacter spp. at flock level, 75 farms were analysed using farm and flock
specific information obtained from questionnaires. Of all investigated broiler
flocks Campylobacter spp. was detected in 44%. C. jejuni was the most
prevalent species (77%) followed by C. coli (23%). Higher prevalence was
mainly associated with summer and fall. Within- flock prevalence varied from
10% to 100%. In 33% of the Campylobacter positive flocks all ten caecal probes
were positive. Flocks of conventional and Louisiana broiler houses harboured
in most cases C. jejuni, whereas C. coli was the predominant species in flocks
from free range or organic farming. Comparing results of pooled and single
probes, 93% of Campylobacter positive single probes were detected using pooled
probes. Of the 79 (61 C. jejuni, 18 C. coli) chicken isolates 30% (31% bzw.
28%) were ampicillin resistant, 13% (8% bzw. 28%) were resistant against a
combination of ampicillin and sulbactam, 10% (8% bzw. 17%) were ceftazidime
resistant, 41% (39% bzw. 44%) were ciprofloxacin and nalidixic acid resistant
und 30% (30% bzw. 33%) were tetracycline resistant. All strains were
susceptible against gentamicin. All C. jejuni strains were susceptible against
erythromycin, whereas 28% of C. coli strains were resistant. From 61 C.
jejuni- isolates and 18 C. coli isolates 34 AFLP- cluster respectively 11
AFLP- cluster were identified, demonstrating the genetic diversity of
Campylobacter spp. isolated from poultry. Dominant and reiterating AFLP-
genotypes in successive flocks show the presence of persistent sources of
Campylobacter spp. in the environment. Colonisation with sporadic isolates was
also found. Campylobacter negative flocks followed Campylobacter positive
flocks demonstrating, that it is possible to prevent a Campylobacter
infection. Different Campylobacter species within a flock and in successive
flocks may be caused by different sources of infections and describe the
dynamic of colonisation. Three risk factors for Campylobacter colonisation
were identified: production system, flock size and water system
The effect of short-term heat acclimation with a permissive dehydration stimulus in female team sports players
Introduction: Repeated heat exposure can facilitate physiological adaptation to heat during intermittent exercise; however, there is limited information available regarding female cohorts. This has implications on the health and safety guidelines for females during heat exposure. Studies using short-term heat acclimation (STHA) with permissive dehydration have reported improved physiological response and performance during heat exposure but have tended to use male participants. Therefore, the aim of this study was to investigate the efficacy of STHA over 5-days using the controlled hyperthermia technique (with permissive dehydration), on an intermittent heat stress test (HST), using a female cohort and controlling for menstrual cycle.Methods: Eight healthy, active, moderately trained females (mean [SD]; age 22.6 [3.0] y; height 166.2 [6.0] cm; body mass 62.3 [9.0] kg; VO2 max 43.2 [8.2] mL.kg-1.min-1). The HST (31.0ËC, 50% RH) consisted of 9x5min (45 mins) of intermittent exercise (individualised standing, walking, jogging, low-, medium-, and high-intensity running on a motorised treadmill) finishing with a 6s maximal sprint on a cycle ergometer. The exercise intensities were adapted from the match-play dynamics of female collegiate football players. Participants completed two HSTs (HST1 and HST2), separated by one week, with no STHA, as a control (C) trial. This was followed by 90 mins dehydration (no fluid), heat acclimation for 5 consecutive days (39.5ËC, 60% RH), using the controlled hyperthermia technique (rectal temperature [Tre] 38.5ËC). Participants completed a final HST (HST3), within one week of the STHA. The HST2 and HST3 trials were in the same week of each participantâs menstrual phase determined by self-reported menstrual cycle and plasma 17ÎČ-estradiol.Results: Post (HST3) vs. Pre- (HST2) STHA, showed a reduced rectal temperature (Tre) at 45-min by 0.20ËC (95%CI: -0.31 to -0.05ËC; p = 0.01; d = 1.13); mean skin temperature ( sk T ) (-0.47; -0.82 to -0.12°C; P = 0.02; d = 1.06) and mean body temperature ( b T ) (-0.21; -0.31 to -0.11°C; P = 0.001; d = 1.28). There was limited change (P > 0.05) for these measures in the HST1 vs. HST2 C trial. Resting cardiac frequency decreased by 11 b.min-1 (-16 to -5 b.min-1; P = 0.004; d = 0.81) and by 3 b.min-1 at 45-min (-8 to 0 b.min-1; P = 0.07; d = 0.65). There was an increase in percentage plasma volume (%PV) change post-STHA by 8.65% (-1.21 to 18.51%; P = 0.007; d = 1.26) but limited change in C (P > 0.05). There was an increase in mean average power (MAvP) across all 9 sprints by 41W (3 to 80W; P = 0.04; d = 0.18) but limited change in C (P > 0.05).Discussion and conclusion: Short-term heat acclimation (5 days), with permissive dehydration, using the controlled-hyperthermia technique leads to physiological adaptation during intermittent exercise in the heat, in moderately trained females when controlling for menstrual cycle
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