High genetic diversity among extraintestinal Escherichia coli isolates in pullets and layers revealed by a longitudinal study.

BACKGROUND: Various information about the genetic diversity of Escherichia coli isolates from chickens are available but a detailed epidemiological investigation based upon isolates obtained from interrelated pullet and layer flocks is still missing. Therefore, in the course of a longitudinal epidemiological study on pullets and layers, 144 E. coli isolates from chickens with or without pathological lesions of the reproductive tract were serotyped and genotyped with pulsed-field gel electrophoresis (PFGE). These isolates were collected during rearing, peak and at the end of production. The actual study is the first of its kind so as to elucidate genetic relatedness among extraintestinal E. coli isolated from chickens with varying pathological conditions in interrelated layer farms/flocks at different stages of rearing.
RESULTS: Serotyping revealed that 63.19 % of the isolates could not be assigned to any of the three serotypes tested whereas 30.55 % of the isolates belonged to serotype O1:K1, 4.86 % to O2:K1 and 1.38 % to O78:K80. After macrorestriction digest with XbaI, 91.66 % of the isolates were typeable resulting in 96 distinct PFGE profiles. Among them, five PFGE types included isolates collected from diseased chickens as well as from birds without pathological lesions. This finding shows that pathogenicity of E. coli in layers seems to be largely influenced by concurrent susceptibility factors. Furthermore, in six out of eight cases where two isolates were collected from each of eight birds, different PFGE types were found in the same or different organs of the same bird. The existence of predominant or persistent E. coli genotypes was only observed in two cases.
CONCLUSIONS: It is concluded that extraintestinal E. coli genotypes and serotypes in pullets and layers are heterogenous and also do not maintain a single clonality within the same bird. The facts that E. coli strains did not show any definite clonal population structure based on geographical region, age of the host and pathological lesions should have relevance in further epidemiological studies and control strategies.

Background

Escherichia coli isolates that are extraintestinal in nature are associated with the disease named colibacillosis that can infect all aged groups of chickens [1]. In layers, the pathogen is able to cause a systemic infection leading to fibrinous polyserositis, pericarditis, perihepatitis, salpingitis, peritonitis, salpingoperitonitis and a decrease in egg production ultimately leading to severe economic losses [2-8]. Despite serological diversities, serogroups such as O1, O2 and O78 are mostly implicated in disease conditions [9-11]. Until now, the pathogenicity of E. coli infection in chickens is not well understood. Several putative virulence and virulence-associated genes have been reported in avian pathogenic E. coli (APEC) [1, 11, 12]. However, the fact that a single genetic trait cannot separate disease-associated E. coli from commensal intestinal isolates raised certain concern on the definition of APEC as a single pathotype [13, 14].

From an epidemiological point of view, understanding the clonal population structure of extraintestinal E. coli involving a longitudinal sampling scheme in interrelated rearing and laying flocks has a high priority. Thus we performed a longitudinal study in order to characterize the relatedness among E. coli isolates from systemic organs of pullets and layers kept in alternative housing systems in Austria. Beside the determination of the serotype, pulsed-field gel electrophoresis (PFGE) was applied for genetic fingerprinting which has higher discriminating power compared to other methods such as multilocus sequence typing [15]. PFGE is more applicable to investigate large-scale genomic diversity within a distinct population and has also been previously applied to infer molecular relatedness among APEC isolates in other geographical locations [16-18].

Methods

Flock history, sampling and E. coli isolation

The present investigation was focused on extraintestinal E. coli isolates from pullets and laying hens kept in alternative husbandry system that were located in different provincial states of Austria. Six rearing and eight related layer farms comprising 15 layer flocks were included in the longitudinal study. Rearing farms are designated with letter “R” along with farm numbers as RI – RVI (e. g. RI is rearing farm 1). The layer flocks are designated with letter “L” along with the flock number and the corresponding rearing farm (e. g. L1/I indicate for layer flock 1 that comes from rearing farm 1). Detailed information on farms and flocks is provided in Table 1.

Table 1

Farms and flocks included in the study

Rearing farm		Layer farm/flock
Farm identificationa	Location	Farm	Flock identificationb	Location	Housing systemc	Flock sized
RI	Lower Austria	1	L1/I	Styria	FR	7500
			L2/I	Styria	FR	3800
			L3/I	Styria	DL	3440
RII	Salzburg	2	L1/II	Carinthia	ORG	3000
		3	L2/II	Lower Austria	ORG	3000
RIII	Styria	4	L1/III	Burgenland	ORG	6000
			L2/III	Burgenland	ORG	6000
			L3/III	Burgenland	ORG	6000
RIV	Upper Austria	5	L1/IV	Lower Austria	DL	5980
			L2/IV	Lower Austria	DL	10890
			L3/IV	Lower Austria	DL	9030
RV	Styria	6	L1/V	Styria	DL	17738
		7	L2/V	Styria	DL	14950
RVI	Burgenland	8	L1/VI	Styria	DL	2950
			L2/VI	Styria	FR	7300

asix rearing farms are indicated as RI - RVI (all birds were kept in deep litter system)

blayer flocks are designated with letter “L” along with flock number/corresponding rearing farm number

chousing system: FR – conventional free range, ORG – organic free range, DL – deep litter

dnumber of birds in each layer flock

In total, 188 birds were sampled for extraintestinal E. coli based on the sampling scheme as shown in Fig. 1. Sampling was performed during rearing (age of birds: 16–19 weeks), at the peak of production (age of birds: 37–42 weeks) and at the end of production (age of birds: 64–80 weeks). In each of the sampling events, five birds per rearing farm/layer flock were necropsied and sampled for extraintestinal E. coli. In two flocks of one layer farm (L2/IV and L3/IV), additional samplings were included at 30–33 weeks of age (eight birds in total) because of increased mortality and drop in egg production. The sampling scheme was focused on the isolation of E. coli from the reproductive organs (ovary and oviduct). Where E. coli could not be isolated from the reproductive tract, isolates from liver, heart or lung were chosen for further investigation. For isolation of E. coli, organ samples were aseptically streaked on McConkey agar (Scharlau, Vienna, Austria) and incubated at 37 °C for 24 h aerobically. On the following day, subcultures were made on Columbia agar supplemented with 5 % sheep blood (COS agar, BioMérieux, Vienna, Austria) and incubated at 37 °C for 24 h aerobically. Most of the isolates were collected from ovary or oviduct (number of isolates n = 106) followed by liver (n = 25), lung (n = 10) and heart (n = 3). Details on E. coli isolates included in the present study are shown in Table 2. Isolates from rearing farms are marked with letter “R” along with farm number and bird number (e. g. RI-1 denotes for E. coli isolate collected from rearing farm 1 and bird number 1). Likewise, isolates from layer flocks are labelled with letter “L” along with flock number/corresponding rearing farm number – time of sampling (A: peak of production, B: end of production, Z1 or Z2: first or second additional samplings) – bird number – organs (only in those birds from where two samples were collected). For instance, L1/I-A-1 denotes for the isolate collected from layer flock 1 that originated from rearing farm 1; at the peak of production; bird number 1. Generally, one E. coli isolate per bird was included for further characterization. However, in the case of eight birds, two isolates per bird from the same or different organs were collected at the same sampling event: L1/III-B-2-ovary1, L1/III-B-2-ovary2; L1/III-B-3-ovary, L1/III-B-3-oviduct; L1/III-B-4-oviduct1, L1/III-B-4-oviduct2; L2/IV-B-1-ovary, L2/IV-B-1-liver; L1/V-A-4-oviduct, L1/V-A-4-ovary; L2/V-B-5-ovary, L2/V-B-5-heart, L1/VI-B-1-ovary, L1/VI-B-1-oviduct; L2/VI-B-2-ovary, L2/VI-B-2-oviduct.

Fig. 1

Sampling scheme for the longitudinal study of extraintestinal Escherichia coli in pullets and layers. Each box represents an individual sampling event and includes the following information: farm/flock identification (rearing farms are indicated as RI - RVI and layer flocks are designated with letter “L” along with flock number/corresponding rearing farm number) – age of birds during sampling (weeks) – number of E. coli isolates in parenthesis

Table 2

E. coli isolates and pathological findings in reproductive tract

Farm/flock	Isolate identificationa	Age (weeks)	Reproductive lesions	Serotype	PFGE type
Rearing farm 1
RI	RI-1	18	no	ntb	LA23
	RI-2		no	nt	nt
	RI-3		no	nt	LA20
	RI-4		no	nt	LA19
L1/I-A	L1/I-A-1	42	no	nt	S31
	L1/I-A-2		no	nt	S37
	L1/I-A-5		no	O78:K80	S6
L2/I-A	L2/I-A-1	42	no	O1:K1	S2
	L2/I-A-5		no	O1:K1	S15
L2/I-B	L2/I-B-4	77	oophoritis	nt	S22
	L2/I-B-5		oophoritis	nt	S23
L3/I-B	L3/I-B-1	77	oophoritis and salpingitis	O2:K1	S19
	L3/I-B-2		oophoritis	O2:K1	S19
Rearing farm 2
RII	RII-1	19	no	O1:K1,O2:K1,O78:K80	Sa3
	RII-2		no	O1:K1,O2:K1,	Sa1
	RII-3		no	nt	Sa4
	RII-4		no	O1:K1	Sa5
	RII-5		no	nt	Sa2
L1/II-A	L1/II-A-1	40	no	O1:K1	nt
	L1/II-A-2		no	O1:K1	nt
	L1/II-A-3		no	O1:K1	nt
	L1/II-A-4		no	O1:K1	nt
	L1/II-A-5		no	O1:K1	nt
L2/II-A	L2/II-A-1	38	degeneration of oviduct	O1:K1,O2:K1,	nt
	L2/II-A-2		no	O1:K1,O2:K1,	LA10
	L2/II-A-3		oophoritis	O2:K1	LA6
	L2/II-A-4		oophoritis	O1:K1,O2:K1,O78:K80	LA9
	L2/II-A-5		oophoritis	O1:K1,O2:K1,	LA2
L1/II-B	L1/II-B-1	80	egg peritonitis	nt	Ca4
	L1/II-B-2		no	O2:K1	Ca2
	L1/II-B-3		egg peritonitis	nt	Ca3
	L1/II-B-4		egg peritonitis	nt	Ca5
	L1/II-B-5		egg peritonitis	nt	Ca1
L2/II-B	L2/II-B-1	68	oophoritis	nt	LA17
	L2/II-B-2		oophoritis	nt	LA18
	L2/II-B-3		oophoritis	nt	LA18
	L2/II-B-4		oophoritis	nt	LA7
	L2/II-B-5		oophoritis	nt	LA18
Rearing farm 3
RIII	RIII-1	18	no	nt	S16
	RIII-2		no	nt	S5
	RIII-3		no	nt	S5
	RIII-4		no	O1:K1,O2:K1,	S4
L1/III-A	L1/III-A-1	39	oophoritis	nt	B15
	L1/III-A-3		no	O1:K1	B14
	L1/III-A-5		oophoritis	nt	B3
L2/III-A	L2/III-A-1	39	no	nt	B4
	L2/III-A-2		no	O1:K1	B6
	L2/III-A-3		no	nt	B4
	L2/III-A-4		no	nt	B8
	L2/III-A-5		no	nt	B8
L3/III-A	L3/III-A-1	39	oophoritis	nt	B1
	L3/III-A-2		oophoritis	nt	B1
	L3/III-A-3		oophoritis	nt	B1
	L3/III-A-4		oophoritis	nt	B1
	L3/III-A-5		oophoritis	nt	B17
L1/III-B	L1/III-B-2-ovary1	67	egg peritonitis	O1:K1	B13
	L1/III-B-2-ovary2		egg peritonitis	nt	B12
	L1/III-B-3-ovary		no	O1:K1	B12
	L1/III-B-3-oviduct		no	nt	B12
	L1/III-B-4-oviduct1		no	nt	B5
	L1/III-B-4-oviduct2		no	nt	B11
	L1/III-B-5		degeneration of ovary and oviduct	nt	B10
L2/III-B	L2/III-B-1	67	no	O1:K1	B7
	L2/III-B-2		egg peritonitis	O1:K1	B7
	L2/III-B-3		degeneration of ovary and oviduct	O1:K1	B9
	L2/III-B-4		egg peritonitis	O1:K1	B9
L3/III-B	L3/III-B-3	67	no	O1:K1	B16
	L3/III-B-4		oophoritis	O1:K1	B2
	L3/III-B-5		no	O1:K1	nt
Rearing farm 4
RIV	RIV-1	17	no	nt	Ua2
	RIV-2		no	nt	Ua1
	RIV-3		no	nt	Ua1
	RIV-4		no	nt	Ua3
	RIV-5		no	nt	Ua4
L1/IV-A	L1/IV-A-1	41	no	nt	LA16
	L1/IV-A-2		no	nt	LA15
	L1/IV-A-3		no	nt	LA15
	L1/IV-A-4		no	nt	LA27
L2/IV-A	L2/IV-A-2	41	no	O1:K1	LA13
L3/IV-A	L3/IV-A-1	41	degeneration of ovary and oviduct	nt	LA21
	L3/IV-A-2		egg peritonitis	nt	LA21
	L3/IV-A-3		degeneration of ovary and oviduct	nt	LA11
	L3/IV-A-4		degeneration of ovary and oviduct	nt	LA11
	L3/IV-A-5		no	nt	LA4
L1/IV-B	L1/IV-B-1	73	degeneration of ovary and oviduct	nt	LA25
	L1/IV-B-2		oophoritis	nt	LA1
	L1/IV-B-3		oophoritis	nt	nt
	L1/IV-B-4		oophoritis	nt	LA5
	L1/IV-B-5		oophoritis	nt	LA25
L2/IV-B	L2/IV-B-1-ovary	73	oophoritis	nt	LA25
	L2/IV-B-1-liver		oophoritis	O1:K1	LA25
	L2/IV-B-2		oophoritis	O1:K1	LA25
	L2/IV-B-3		oophoritis	O1:K1	LA26
	L2/IV-B-4		oophoritis	O1:K1	LA25
	L2/IV-B-5		oophoritis	nt	LA28
L3/IV-B	L3/IV-B-1	73	oophoritis	O1:K1	LA3
	L3/IV-B-2		oophoritis	O1:K1	LA14
	L3/IV-B-3		oophoritis	O1:K1	LA25
	L3/IV-B-4		oophoritis	nt	LA8
	L3/IV-B-5		oophoritis	O1:K1	LA25
L2/IV-Z1	L2/IV-Z1-1	31	oophoritis	O1:K1,O2:K1,O78:K80	LA22
	L2/IV-Z1-2		no	O1:K1,O2:K1,O78:K80	LA22
	L2/IV-Z1-3		egg peritonitis	O1:K1,O2:K1,O78:K80	LA22
L3/IV-Z1	L3/IV-Z1-2	30	degeneration of ovary and oviduct	O1:K1,O2:K1,	LA24
L3/IV-Z2	L3/IV-Z2-1	33	no	nt	LA12
Rearing farm 5
RV	RV-3	16	no	O1:K1,O2:K1,	nt
	RV-4		no	O1:K1	S7
	RV-5		no	O1:K1	S7
L1/V-A	L1/V-A-2	37	no	O1:K1	nt
	L1/V-A-3-oviduct		no	nt	S1
	L1/V-A-4-oviduct		egg peritonitis	nt	S18
	L1/V-A-4-ovary		egg peritonitis	O1:K1	S7
	L1/V-A-6		egg peritonitis	O1:K1	nt
L1/V-B	L1/V-B-1	64	egg peritonitis	O2:K1	S8
	L1/V-B-2		egg peritonitis	O2:K1	S9
	L1/V-B-3		egg peritonitis	nt	S25
	L1/V-B-5		egg peritonitis	O2:K1	S9
L2/V-A	L2/V-A-3	39	degeneration of ovary	nt	S27
	L2/V-A-4		degeneration of ovary	O78:K80	S29
	L2/V-A-5		no	nt	S3
L2/V-B	L2/V-B-1	74	no	O1:K1	S10
	L2/V-B-2		no	O1:K1	S10
	L2/V-B-3		oophoritis and salpingitis	O1:K1	S10
	L2/V-B-4		oophoritis	nt	S20
	L2/V-B-5-ovary		egg peritonitis	O1:K1	S34
	L2/V-B-5-heart		egg peritonitis	O1:K1	S34
Rearing farm 6
L1/VI-A	L1/VI-A-1	38	no	nt	S36
	L1/VI-A-2		no	nt	S21
	L1/VI-A-4		oophoritis	nt	S11
	L1/VI-A-5		no	nt	S21
L1/VI-B	L1/VI-B-1-ovary	80	degeneration of ovary and oviduct	O1:K1	S33
	L1/VI-B-1-oviduct		degeneration of ovary and oviduct	nt	S12
	L1/VI-B-2		degeneration of ovary and oviduct	O1:K1	S33
	L1/VI-B-3		oophoritis	O1:K1	S26
	L1/VI-B-4		degeneration of ovary and oviduct	nt	S24
	L1/VI-B-5		egg peritonitis	O1:K1	S35
L2/VI-A	L2/VI-A-1	38	no	nt	S17
	L2/VI-A-2		no	nt	S13
	L2/VI-A-4		oophoritis	nt	S32
	L2/VI-A-5		oophoritis, degeneration of oviduct	nt	S17
L2/VI-B	L2/VI-B-2-ovary	80	oophoritis	nt	S28
	L2/VI-B-2-oviduct		oophoritis	O1:K1	S30
	L2/VI-B-4		degeneration of ovary	nt	S14
	L2/VI-B-5		egg peritonitis	O1:K1	S32

Age of birds, lesions in the reproductive tract, serotypes and PFGE types of each E. coli isolates are provided in the corresponding vertical line

aisolates identification: isolates from rearing farms are marked with letter “R” along with farm number and bird number. Likewise, isolates from layer flocks are labelled with letter “L” along with flock number/corresponding rearing farm number – time of sampling (A: peak of production, B: end of production, Z1 or Z2: first or second additional samplings) – bird number – organs (only in those birds from where two samples were collected)

bnon-typeable

Additionally, gross pathological lesions of the reproductive tract were recorded. Pullets from all six rearing farms did not show any gross pathological lesions. At the peak of production, some E. coli isolates originated from birds showing lesions in the reproductive tract, including egg peritonitis, inflammation of ovary and/or oviduct and degeneration of ovary and/or oviduct in 5, 17 and 7 birds respectively. Also, at the end of production, egg peritonitis, inflammation of ovary and/or oviduct and degeneration of ovary and/or oviduct were recorded in 15, 40 and 9 birds, respectively. In additional samplings, gross pathological lesions found in the reproductive tract comprised egg peritonitis in one bird, inflammation of ovary and/or oviduct in two birds and degeneration of ovary and oviduct in one bird.

Subtyping of E. coli isolates

Serotyping was performed on 144 E. coli isolates applying a slide agglutination test to Escherichia coli O1:K1, O2:K1 and O78:K80 antisera following supplier’s guidelines (Animal Health and Veterinary Laboratory Agency, Weybridge, Surrey, UK).

For PFGE, E. coli isolates were grown on COS agar at 37 °C for 24 h. The plug preparation and PFGE was performed according to the standardized Pulsenet International protocol for E. coli O157:H7, E. coli non-O157, Salmonella serotypes, Shigella sonnei and Shigella flexneri (http://www.pulsenetinternational.org/assets/PulseNet/uploads/pfge/PNL05_Ec-Sal-ShigPFGEprotocol.pdf; accessed on 18.12.2015). The macrorestriction digest was performed applying XbaI (50 U/sample; Thermo Fisher Scientific, Fermentas; Waltham, Massachusetts, USA) at 37 °C for 2–3 h. Restricted samples were separated in a 1 % (w/v) SeaKem Gold agarose gel (Lonza Group AG, Basel, Switzerland) in 0.5 × TBE buffer at 6 V/cm on a Chef DR III system (Bio-Rad Laboratories, Inc.). A linear ramping factor with pulse times from 2.2 to 54.2 s at 14 °C and an inclined angle of 120° was applied for 22.5 h. The gels were stained with ethidium bromide (Sigma Aldrich, Vienna, Austria), digitally photographed with Gel Doc 2000 (Bio-Rad Laboratories, Inc.) and normalized as TIFF images (BioNumerics 6.6 software Applied Math NV, Sint-Martens-Latem, Belgium) applying the PFGE global standard Salmonella ser. Braenderup H9812. In order to identify indistinguishable PFGE types, a Dice co-efficient similarity of 100 % was used.

E. coli confirmation of non-typeable genotypes

Partial sequencing of 16S rRNA gene was done in PFGE non-typeable isolates (n = 12) as described previously [19]. For this purpose, strains were grown on COS agar plates at 37 °C for 24 h. DNA extraction was done from two to three colonies using DNeasy Blood and Tissue Kit (QIAGEN, Hilden, Germany) following manufacturer’s recommendation. PCR was performed with a set of primers: 16S F 5’-GGCGGCRKGCCTAAYACATGCAAGT-3’ and 16S R 5’-GACGACARCCATGCASCACCTGT-3’. Amplification was carried out in 25 μl reaction volume consisting of 12.5 μl of HotStarTaq Master Mix (Qiagen, Hilden, Germany), 8 μl of nuclease free distilled water, 1 μl of each forward and reverse primers (10pmol/μl) and 2.5 μl of DNA template. The PCR thermocycler was programmed as: initial denaturation at 95 °C for 15 min followed by 40 cycles of heat denaturation at 94 °C, annealing at 60 °C for 1 min and extension at 72 °C for 1.5 min. Final elongation was performed at 72 °C for 10 min. The PCR products were visualized by agarose gel electrophoresis. The gel slices were cut and purified using QIAquick® gel extraction kit (QIAGEN, Germany). Samples were then dispatched to LGC genomics GmbH (Berlin, Germany) for sequencing. The data obtained were processed with software Accelrys Gene v2.5 (Accelrys Inc) and analyzed with BLAST search in NCBI database.

Antimicrobial resistance (AMR)

Sixteen E. coli isolates originating from eight birds (two isolates per bird from the same or different organs) were investigated for the potential difference in AMR among strains isolated from the same organ (2 birds) or from different organs of the same bird (6 birds). The antimicrobial susceptibility test was performed using the disk diffusion method on Mueller-Hinton Agar (BioMeriéux, Vienna, Austria) according to Bauer et al. [20]). The following antimicrobials were tested: aminopenicilline [amoxicillin and ampicillin (each 10 μg)], aminoglycoside [gentamicin (10 μg), neomycin (30 μg)], tetracyclines [tetracycline and doxycycline (each 30 μg)], co-trimoxazole [sulphamethoxazole and trimethoprim (25 μg)], macrolide (tylosin 30 μg), quinolone [oxolinic acid 2 μg, enrofloxacin (5 μg)], cephalosporine [ceftiofur (30 μg)], polymyxin [colistin (10 μg)] and aminocyclitol [spectinomycin (100 μg)]. Multidrug resistance (MDR) among avian E. coli was defined as resistance to three or more classes of antimicrobial agents.

Results

Serotyping revealed that 44 isolates (30.55 %) were grouped as O1:K1 while 7 (4.86 %) and 2 (1.38 %) strains belonged to O2:K1 and O78:K80, respectively. Furthermore, 91 isolates (63.19 %) could not be assigned to a definite serotype using these three antisera as they did not show agglutination (n = 79) or reacted positive with more than one anti-serum used (n = 12). Isolates that did not show agglutination with any or reacted positive with more than one anti-serum were assigned as non-typeable (Table 2). The PFGE analysis of 132 E. coli isolates resulted in a heterogenous PFGE cluster: 96 E. coli profiles were obtained after macrorestriction digest applying XbaI while 12 isolates were non-typeable. The dendrogram obtained from the cluster analysis is shown in Fig. 2.

Fig. 2

PFGE cluster analysis of Escherichia coli isolates from pullets and layers (restriction enzyme XbaI). The TIFF images were compared using BioNumerics 6.6 software (Applied Math NV, Sint-Martens-Latem, Belgium), and normalized using the PFGE global standard Salmonella ser. Braenderup H9812. Pattern clustering was performed using the unweighted pair group method using arithmetic averages (UPGMA) and the Dice correlation coefficient was applied with a position tolerance of 1.0 %. Information provided adjacent to the dendrogram include the PFGE-type in combination with areas of isolation (S: Styria, LA: Lower Austria, Ua: Upper Austria, Sa: Salzburg, B: Burgenland, Ca: Carinthia), number of isolates (n) in each PFGE type, organs of isolation (source) and serotype [not applicable (na) are untypeable isolates]. Furthermore, E. coli isolation was classified according to the absence (1) or presence (2) of lesions in the reproductive tract

The most abundant E. coli PFGE-profile was LA25 (n = 8) which included strains from three layer flocks (L1/IV-B, L2/IV-B and L3/IV-B) that originated from a single rearing farm (RIV). All these isolates were associated with lesions in the reproductive tract. Likewise, B1 included four isolates from birds with inflammation of ovaries in the same flock (L3/III-A). Furthermore, E. coli genotypes which caused reproductive tract lesions in more than one laying bird at one sampling occasion from the same flock were: B9 (n = 2), LA11 (n = 2), LA18 (n = 3), LA21 (n = 2), S19 (n = 2), S33 (n = 2), S34 (n = 2) and S9 (n = 2).

Interestingly, E. coli genotypes B7 (n = 2), B12 (n = 3), LA22 (n = 3), S10 (n = 3) and S17 (n = 2) included isolates from both normal and diseased chickens. S5 (n = 2), Ua1 (n = 2), B4 (n = 2), B8 (n = 2), LA15 (n = 2) and S21 (n = 2) were present in pullets or layers without clinical signs. PFGE type S7 included three E. coli isolates that were collected from two pullets without pathological lesions and one laying hen with egg peritonitis originating from the same rearing farm.

DNA sequencing

The non-typable isolates were confirmed by partial sequencing of 16S rRNA gene as E. coli (99-100 % identity). Accession numbers of the isolates to the European Nucleotide Archive are as follows: RI-2: LT548255, L1/II-A-1: LT548253, L1/II-A-2: LT548254, L1/II-A-3: LT548256, L2/II-A-1: LT548257, L3/III-B-5: LT548258, RV-3: LT548251, L1/V-A-2: LT548250, L1/V-A-6: LT548252. Following three isolates had 100 % identity with the existing database: L1/II-A-4: JQ975905.1, L1/II-A-5: JQ975905.1, L1/IV-B-3: KU560507.1.

The results of antibiotic resistance tests are shown in Table 3. These E. coli isolates were considered for the test in order to investigate similarities or differences in antibiotic sensitivity profiles between two strains collected from the same bird. All isolates were resistant to tylosin. Additionally, MDR was observed in three isolates originating from different birds. Two of these were resistant to five antibiotic substances {aminopenicilline (amoxicillin and ampicillin), tetracycline, doxycycline, sulphamethoxazole and trimethoprim} and the other to three antibiotic substances (oxolinic acid, doxycycline and neomycin). The following pair of isolates had non-identical pattern of resistance towards several antimicrobials used: 1) L1/III-B-2-ovary1 and L1/III-B-2-ovary2: amoxicillin; 2) L1/III-B-3-ovary and L1/III-B-3-oviduct: ampicillin, amoxycillin, doxycycline, tetracycline and sulphamethoxazole + trimethoprim; 3) L1/III-B-4-oviduct1 and L1/III-B-4-oviduct2 : ampicillin, amoxycillin, doxycycline, tetracycline and sulphamethoxazole + trimethoprim; 4) L2/IV-B-1-ovary and L2/IV-B-1-liver : amoxicillin; 5) L1/V-A-4-oviduct and L1/V-A-4-ovary : oxolinic acid; 6) L2/V-B-5-ovary and L2/V-B-5-heart : doxycycline, enrofloxacin, neomycin; 7) L1/VI-B-1-ovary and L1/VI-B-1-oviduct : oxolinic acid; 8) L2/VI-B-2-ovary and L2/VI-B-2-oviduct : amoxicillin and doxycycline.

Table 3

Antibiotic resistance test of 16 Escherichia coli isolates collected from 8 birds (two isolates per bird)

Antibiotics	Isolates
	L1/III-B-2-ovary1	L1/III-B-2-ovary2	L1/III-B-3-ovary	L1/III-B-3-oviduct	L1/III-B-4-oviduct1	L1/III-B-4-oviduct2	L2/IV-B-1-ovary	L2/IV-B-1-liver	L1/V-A-4-oviduct	L1/V-A-4-ovary	L2/V-B-5-ovary	L2/V-B-5-heart	L1/VI-B-1-ovary	L1/VI-B-1-oviduct	L2/VI-B-2-ovary	L2/VI-B-2-oviduct
Ampicillin	I	I	I	R	R	S	S	S	I	I	S	S	I	I	I	I
Amoxycillin	I	R	I	R	R	I	S	I	I	I	I	I	I	I	R	I
Ceftiofur	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S
Colistin	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S
Doxycycline	I	I	S	R	R	S	S	S	S	S	S	R	S	S	I	S
Enrofloxacin	S	S	S	S	S	S	S	S	S	S	S	I	S	S	S	S
Gentamicin	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S
Neomycin	S	S	S	S	S	S	S	S	S	S	S	R	S	S	S	S
Oxolinic acid	S	S	S	S	S	S	S	S	S	R	R	R	R	S	S	S
Tetracycline	S	S	S	R	R	S	S	S	S	S	S	I	S	S	S	S
Tylosin	R	R	R	R	R	R	R	R	R	R	R	R	R	R	R	R
Spectinomycin	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S	S
Sulphamethoxazole + trimethoprim	S	S	S	R	R	S	S	S	S	S	S	S	S	S	S	S

Each isolate ID is designated with letter “L” along with the number of layer flock and rearing farm – A (sampling at the peak of production) or B (sampling at the end of production) – number of sampled bird – organ of isolation – isolate number (in case when two isolates were collected from the same organ). Antibiotic resistance pattern of two isolates from the same bird are in bold letter and highlighted if they showed different sensitivity to antimicrobials used. S: sensitive, I intermediate, R: resistant

Discussion

An infection with E. coli in layers is regarded as one of the major problems in global poultry industry that might cause reproductive disorders referred as salpingitis/peritonitis/salpingoperitonitis and peritonitis syndrome ultimately leading to severe economic losses on commercial farms [6]. In this regards, an epidemiological knowledge of the disease and disease causing agent is fundamental in order to develop effective control and prophylactic strategies. Here, we studied molecular epidemiology of E. coli isolates collected from pullets and layers in a longitudinal sampling study in Austria. Data obtained from genetic fingerprinting by PFGE were analyzed together with serotypes, geographical regions of isolation, and concurrent pathological lesions in each of the sampled birds.

In total, more than half of the E. coli isolates (n = 91/144) could not be assigned to a single serotype using antibodies against O1:K1, O2:K1 and O78:K80. Furthermore, for those isolates that could be assigned to one of the named serotypes, no correlation was found between a specific serotype and the occurrence of lesions in birds. In previous studies, it was also shown that E. coli isolates collected from diseased birds display a high serological diversity [16, 21, 22], demonstrating as high as 62 different O serogroups [21]. Thus classifying E. coli strains into a definite serotype might sometimes be somewhat challenging. Hence, our finding is in agreement with a previous notion that serotyping alone might not be helpful as a tool for characterization of E. coli [16].

In this study, the PFGE subtyping of E. coli isolates (n = 132) resulted in 96 XbaI profiles. Exclusively in two events, the same PFGE profile was seen in isolates from different sampling dates in mutually related farms/flocks, indicating potential E. coli persistence. The PFGE-type S7 (n = 3) included isolates from pullets (n = 2, rearing farm RV) without pathological lesions and from one layer in the corresponding flock L1/V suffering from egg peritonitis and fibrinous oophoritis at the peak of production. In the second case, PFGE type S32 contained two isolates from the same layer flock (L2/VI) at the peak and end of production. One bird sampled at the peak of production showed inflammation of the ovary whereas egg peritonitis was diagnosed in the other birds necropsied at the end of production. These results indicate that some E. coli genotypes may retain in certain flocks at different stages of rearing but the associated pathological outcomes in birds can vary.

The genomic profile of extraintestinal E. coli with PFGE further revealed that strains collected from birds with pathological lesions can have 100 % genetic identity with strains that were collected from healthy birds. For instance, in PFGE type S10 (n = 3) in flock L2/V, two birds did not have any lesions while one had oophoritis and salpingitis. Likewise in PFGE type B7 (n = 2) in L2/III, one bird showed no lesions while in contrast, the other had egg peritonitis. Also, remaining isolates could not be grouped into distinct clonal clusters based on presence or absence of pathological lesions in sampled birds. This finding is in agreement with a previous study in broilers where authors have reported a high heterogenecity of E. coli isolates in broilers [13, 23]. It can be hypothesized that pathogenicity of extraintestinal E. coli in chickens is highly dependent on concurrent environmental and host susceptibility factors. Providing a suitable opportunity in certain circumstances, E. coli residing in clinically healthy chickens might turn up into pathogenic. The hypothesis is further supported by an earlier finding in broiler that many collibacillosis associated isolates might not be clearly distinguished solely on the basis of presence of virulence associated genes as compared to intestinal commensal E. coli [13].

In the present study, we found no evidence for clonality of E. coli with respect to geographical locations of farms. Previously, Ewers et al. (2004) found only a limited number of E. coli clones to be distributed in poultry production in Germany [16]. In another study, it was reported that chickens with peritonitis in a single flock were likely to be infected by the same E. coli strain [24]. Different to this, we did not find clonality of E. coli isolates in birds from the same flock showing gross pathological lesions in the reproductive tract thus maintaining a high heterogenicity of PFGE types. Interestingly, we further noticed that a single bird can harbour two different PFGE types of E. coli in the same or different organs. Thus, the study demonstrated that a layer can be infected simultaneously by different E. coli genotypes. A similar finding was previously reported in broilers [18]. However, in another study in layers, one PFGE type was found to be present in bone marrow of an individual bird [17]. It might be that in some organs E. coli isolates possess less or no genetic diversity due to an adaptation process, which should however be further elucidated. In the present study, we also tested antibiotic susceptibility of 16 isolates that were collected from eight birds. All the isolates were sensitive to ceftiofur, colistin, gentamicin and spectinomycin but the resistant rate to tylosin was found 100 %. Mixed results were obtained for other antibiotics tested. MDR was seen in 3/16 isolates showing resistance to as high as five different antibiotics used. Although the number of isolates included for antimicrobial susceptibility test in the actual study is not very high, it already provides an indication for the problem of antibiotic resistance in E. coli towards commonly used antimicrobials. In a recent report from China, E. coli isolates collected from chickens were sensitive to relatively newer antibiotics such as cephalosporin but MDR rate was as high as 80.25 % [11]. The results from the present study further indicate that isolates collected from the same bird may not necessarily have identical antibiotic sensitivity profiles. Thus it can be suggested that testing of the antibiotic sensitivity profile from just one isolate per bird might not be enough to decide the most appropriate treatment.

Conclusions

Serotyping, antibiotic resistance test and genotypic fingerprinting of extraintestinal E. coli revealed that isolates exhibit high diversities within and between birds. As one bird can harbour different E. coli types an appropriate number of isolates should be considered for epidemiological studies and antibiotic sensitivity test.