The egg industry in the United States provides both table eggs for consumption and hatching eggs produced for maintenance of future poultry flocks. According to the National Agricultural Statistics Service, the United States produces approximately 99.1 billion table eggs per year (USDA, 2020) to accommodate the average individual consumption of 287.1 eggs annually (AEB, 2019). Furthermore, according to the National Agricultural Statistics Service, in 2019 approximately 14.1 billion eggs were utilized to produce broiler-type and layer-type chicks and replenish the poultry industry needs (USDA, 2020). With the current scale of egg production, ensuring safety of consumers, producers, and animal welfare is crucial.
Between 2009 and 2015, the Centers for Disease Control and Prevention reported that table eggs accounted for 9% of total foodborne illnesses in the United States (Dewey-Mattia et al., 2018). Salmonella enterica serovars Typhimurium and Enteritidis are the major pathogens associated with egg-borne outbreaks. To ensure food safety during table egg processing, distribution, and consumption, eggs are primarily washed with a hot detergent solution and rinsed with a sanitizer solution (O’Bryan et al., 2017). A variety of sanitizers have been investigated including chlorine, hydrogen peroxide, electrolyzed oxidizing water, ozone, UV light, pulsed ultraviolet light, etc., resulting in a range of effectiveness, affordability, and accessibility (Keener, 2017; Vinayananda et al., 2017).
In addition to the food safety concerns of table eggs, decontamination of hatching eggs is also important for maintaining good chick health. When hatching, chicks are exposed to microorganisms present in the environment, including those on the surface of eggshells, some of which can be pathogenic. Pathogenic strains of Escherichia coli can cause significant poultry health problems that result in economic losses because of costs of containment, mortality, and carcass disposal (Shane and Faust, 1996; Mellata, 2013). Commercial decontamination of hatchery eggs is primarily achieved with use of chemical sanitizers (Williams, 1970; Shane and Faust, 1996). Numerous studies have investigated various interventions for decontamination of hatching eggs, including but not limited to chlorine dioxide foam (Patterson et al., 1990), alkylated pyrazines (Kusstatscher et al., 2017), and UV light (Turtoi and Borda, 2014).
Pulsed ultraviolet (PUV) light has emerged as a novel technology that continues to prove effective as an antimicrobial intervention for food surfaces, including shell eggs. Pulsed UV light is termed as a result of the broad spectrum (100–1,100 nm) emitted from a xenon flashlamp that is delivered in a series of pulses (100 ns to 2 ms) with over 50% of the energy originating from the UV region (100–400 nm). The main germicidal mechanism of PUV light is the formation of DNA thymine dimers as a result of UV exposure. Secondary germicidal mechanisms are a result of longer wavelengths in combination with short pulses that produce localized heating and microvibrations, respectively, that contribute to microbial cell membrane collapse and death (Sonenshein, 2003; Krishnamurthy et al., 2010; Cassar et al., 2020). In addition to PUV light’s antimicrobial effectiveness for numerous other foods, it has also been reported to achieve a significant reduction of Salmonella serotypes on the surface of eggshells (Hierro et al., 2009; Keklik et al., 2010; Lasagabaster et al., 2011) and in liquid egg (Ouyang et al., 2020).
Specific to eggshells, Keklik et al. (2010) inoculated a 2 cm2 surface area of shell eggs with Salmonella Enteritidis before treatment with PUV light. By adjusting proximity and duration of exposure to PUV light, microbial reductions ranged from 1.3 to 7.7 Log10 CFU/cm2 after 0.8 to 35.3 J/cm2. Hierro et al. (2009) also investigated the decontamination of Salmonella Enteritidis on the exterior of washed and unwashed shell eggs. Eggs were inoculated by submersion then placed on a quartz glass window between 2 PUV light flashlamps for treatment. The microbial reduction ranged from 0.14 to 2.49 and 0.21 to 1.85 Log10 CFU/cm2 for washed and unwashed eggs, respectively, after 2 to 12 J/cm2 of PUV light exposure. Using the same system as Hierro et al. (2009), Lagasabaster et al. (2011) inoculated the surface of shell eggs with Salmonella Typhimurium before PUV light treatment. After exposure to 2.1 J/cm2 of PUV light, a 5.0 and 4.9 Log10 CFU/cm2 reduction was reported on the surface of washed and unwashed eggs, respectively. Ouyang et al. (2020) used PUV light to inactivate Salmonella Enteritidis inoculated in liquid egg white. After 45.6 J/cm2 of PUV light exposure, a significant reduction of 1.98 Log10 CFU/mL was reported.
These previous studies mentioned above document the significant reduction of Salmonella on the surface of shell eggs or liquid egg treated with PUV light. This study differs from previous research using a modified commercial egg candling system to convey and rotate eggs under a PUV light flashlamp. The design of the PUV light conveyor system used in this project is an example of how commercially processed eggs could be treated. The objectives of this experiment are 1) to further evaluate the germicidal response on the surface of shell eggs after treatment by pulsed ultraviolet light with the commercial egg conveyor and 2) to evaluate incubation and grow-out parameters of hatching eggs treated with the selected PUV light doses.
Materials and methods
Pulsed Ultraviolet Light System
Pulsed ultraviolet light was generated from a xenon flashlamp connected to a Pulsed Light RC-802 Interweave System (model Z-5000; Xenon Corporation, Wilmington, MA). Eggs were exposed to PUV light using a flashlamp positioned above a modified egg candling conveyor (Figure 1). The 128 cm long by 29 cm wide conveyor was fitted with adjustable braces to support a flashlamp housing and the 40.6 cm xenon gas flashlamp that was centered along the length of the conveyor. The conveyor had a fixed speed of 4.8 cm/s, which resulted in a complete 360° rotation along the equator of the egg approximately every 17 cm. Processing time for a single pass was 26.7 s. The lamp pulsed 3 times (360 μs/pulse) per second emitting a polychromatic spectrum (100–1,100 nm) with over 50% of the total energy deriving from the UV region (Sonenshein, 2003).
The total energy emitted from the PUV flashlamp was measured using a Nova Laser Power/Energy Monitor (P/N 1J06013, OPHIR Optronics Ltd., Wilmington, MA) with a 46 mm aperture pyroelectric metallic absorber (P/N 1Z02860, OPHIR Optronics Ltd.). The power monitor measured the total energy that was delivered across a single plane within the treatment space. To account for the constant rotation of the eggs, the total energy measured was divided in half because only one half of any given egg was exposed to PUV light at any given time on the conveyor.
The eggs used in both the microbial response and hatchability portions of this study were provided by the Hy-Line North America hatchery (Elizabethtown, PA) and produced by 48-week-old Lohmann LSL Light hens. Eggs weighed on average was 60.2 ± 2.0 g and had an average surface area of 71.5 ± 3.8 cm2, which falls within the classification of “Large” eggs (USDA, 2000). Surface area was calculated using a modeling system described by Troscianko (2014). Eggs were not altered in any way before treatment, though eggs with visible surface debris were excluded from the study.
E. coli K12 and Enterococcus faecium (NRRL B-2354) were selected as nonpathogenic model microorganisms as supported by previous research (Boney et al., 2018; Cassar et al., 2019, respectively). E. coli K12 was obtained from the E. coli Reference Center at the Pennsylvania State University (University Park, PA). Naladixic acid and streptomycin sulfate antibiotic resistant (NSR) cultures were prepared as described by Catalano and Knabel (1994), and a working culture of E. coli K12-NSR was derived from a frozen culture prepared by Cassar et al. (2019). Cultures were maintained in tryptic soy broth (BD-Difco, Franklin Lakes, NJ) supplemented with 0.6% of yeast extract and 100 mg/mL of both nalidixic acid and streptomycin sulfate (TSBYE-NS). E. coli K12-NSR was plated on tryptic soy agar (BD-Difco) supplemented with 0.6% of yeast extract and 100 mg/mL of both nalidixic acid and streptomycin sulfate. Working cultures were subcultured every 14 d and maintained in TSBYE-NS at 4°C.
E. faecium (NRRL B-2354) was obtained from the Pennsylvania State University Food Science Culture Collection. Stock cultures were prepared and kept at cryopreservation conditions (−80°C) in sterile Brain Heart Infusion broth (DOT Scientific, Burton, MI) with 20% glycerol. Stock cultures were aseptically transferred to tryptic soy broth supplemented with 0.6% yeast extract (TSBYE) and incubated for 24 h at 37°C to create a working culture. E. faecium was plated on m-Enterococcus agar (Neogen; Lansing, MI). Working cultures were maintained in TSBYE at 4°C and subcultured every 14 d.
Inoculum Preparation and Inoculation
An inoculum of E. coli K12-NSR was prepared as described by Cassar et al. (2019). The E. coli K12-NSR working cultures were transferred into 1,000 mL TSBYE-NS and incubated at 37°C for 24 h. For E. faecium inoculum, working cultures were transferred to 1,000 mL of TSBYE and incubated at 37°C for 24 h. After incubation, E. coli K12-NSR and E. faecium working cultures were centrifuged at 10°C and 3,330 × g for 30 min, the supernatant was removed, and 1,000 mL of sterile buffered peptone water (BPW; BD) was used to resuspend the pellet, yielding 108 to 109 Log10 CFU/mL. Eggs were removed from cooler storage 6 h before being inoculated to reach room temperature (ca. 20°C). Fifteen eggs were placed into a sterile plastic container positioned in a rotating water-bath (Precision, Winchester, VA) at 100 rpm with room temperature water (ca. 20°). One thousand milliliter of either E. coli K12-NSR or E. faecium inoculum was added to the containers with 15 eggs each. Eggs, submersed for 10 min, were then aseptically transferred to an incubator (37°C) for 30 min to allow surface drying and contribute to microbial surface attachment, resulting in a 104 to 105 Log10 CFU/cm2 population.
Pulsed Ultraviolet Light Treatment System
Inoculated eggs were held for 30 min at ca. 37°C to dry the egg surface and contribute to microbial attachment before PUV light treatment. The flashlamp was positioned parallel to the long axis of the conveyor at 9.5, 14.5, and 19.5 cm above the surface of the eggs to deliver 4.9, 3.1, and 2.4 J/cm2, respectively. The flashlamp was also positioned perpendicular to the long axis of the conveyor at 14.5 cm above the surface of the eggs to deliver 1.0 J/cm2. Four treatment levels were used with 15 eggs in each treatment exposed to a total energy of 1.0, 2.4, 3.1, and 4.9 J/cm2 of PUV light, respectively. Immediately before and following PUV light treatment, the surface temperature of the eggs was measured using a noncontact infrared thermometer (Lasergrip 800; Etekcity, Anaheim, CA).
Using the same modified egg candling conveyor, the xenon flashlamp was positioned 9.5 cm above and parallel to the long axis of the conveyor. At this setting, eggs were passed under the PUV light 1, 5, or 10 times in series to deliver 3 energy treatments of 4.9, 24.4, and 48.8 J/cm2, respectively. A total of 2,000 fertile eggs were used in this phase of the study divided equally into 4 replicates per treatment level (n = 125 eggs/rep) for PUV light treatments of 0 (control), 4.9, 24.4, and 48.8 J/cm2. Similar, to table eggs, fertile egg surface temperatures were recorded following treatment.
Microbial Analysis of Table Eggs
E. coli K12-NSR and E. faecium inoculated eggs were treated separately when evaluating the impact of PUV light on microbial reduction of eggs. At each treatment level, eggs (n = 15) were evaluated for both E. coli K12-NSR and E. faecium. Following treatment, eggs were aseptically transferred to a filtered stomacher bag (Classic 400, Seward Ltd., Worthing, UK), with 70 mL of BPW (Thermo Fisher Scientific, Oxoid Ltd., Basingstoke, UK). Samples were then vigorously shaken by hand for 30 s before being serially diluted in BPW. E. coli K12-NSR and E. faecium samples were plated on tryptic soy agar supplemented with 0.6% of yeast extract and 100 mg/mL of both nalidixic acid and streptomycin sulfate and m-Enterococcus agar plates, respectively, using an autoplater (Autoplate 4000; Spiral Biotech, San Diego, CA) and incubated at 37°C for 24 h. Microbial reductions (Log10 CFU/cm2) were determined by comparing CFU counts of treated samples to the CFU counts of controls (untreated samples). Natural microflora, if present, would have been accounted for when comparing treated samples to controls. For samples that resulted in zero colonies, enrichment was performed by transferring 1 mL from the BPW rinse solution to a 9 mL solution of TSBYE-NS and TSBYE for E. coli K12-NSR and E faecium, respectively. After incubation for 24 h at 37°C, positive enrichment was determined by the presence of microbial growth in the broth. The minimum detection limit was calculated as 1.3 Log10 CFU/cm2 and was subtracted from the initial log concentration number when samples resulted in zero colony plate counts with a positive enrichment.
Incubation and Grow-Out of Hatching Eggs
After PUV light treatment, fertile eggs were placed in a commercial incubator (Chick Master, Englewood, NJ) and incubated for 18 d. From the set day through day 18 of incubation, eggs were rotated 45° every hour at 37.6°C and 47.5% relative humidity. From day 18 until hatch, eggs were incubated in a commercial hatcher (Chick Master) maintained at 36.8°C and 65% relative humidity. Percent fertility was determined manually using an egg candler to observe embryonic development after 5 d of incubation. After 21 d of incubation, the percent hatch and hatchability were measured and recorded as a percentage of chicks from all set eggs and the percentage of chicks from the fertile eggs set, respectively. Hatched treatment chicks were randomly distributed to pullet rearing cages with 25 chicks per cage and 20 replicate cages per treatment. Chicks were fed a commercial pullet starter crumble diet. Average bird weight was calculated by dividing cage weight by the number of birds in each respective cage. Weights were recorded immediately after hatch and at day 7 and day 42 of rearing. Additionally, percent livability was calculated at 7 and 42 d of rearing as a percentage of chicks placed. The procedures followed during this study and the training of the personnel were approved by The Pennsylvania State University Institutional Animal Care and Use Committee, IACUC #01193.
Data analysis was performed using the Statistical Analysis Software 9.4 (SAS, Cary, NC). Table egg parameters were evaluated using a 1-way ANOVA (PROC GLM) for the effect of PUV light on microbial reduction and change in surface temperature with 15 measurements per treatment. Fertile eggs were evaluated for percent fertility, hatch, hatchability, and livability at 7 and 42 d using PROC GLM with an ARC SIN transformation of the percentage data. PROC GLIMIX was used to evaluate average bird weight at 1, 7, and 42 d of age. Tukey’s multiple comparison test was used to separate means when the F-test was significant, P ≤ 0.05 (Steel and Torrie, 1960).
Results and discussion
Microbial Response after PUV Light Treatment
The Log10 reduction of E. coli K12-NSR and E. faecium on the surface of shell eggs was evaluated after PUV light treatment. For eggs inoculated with E. coli K12-NSR, there was a significant reduction after exposure to PUV light (P < 0.05). Microbial reduction was quantified by comparing PUV-treated samples to untreated (control) samples. Microbial reduction was ≥3.43, ≥4.00, ≥3.76, and ≥4.54 Log10 CFU/cm2 after 1.0, 2.4, 3.1, or 4.9 J/cm2 treatment, respectively (Table 1). At each treatment level, at least 1 egg resulted in positive growth on selective agar. Therefore, for samples that did not produce any colonies, but had a positive enrichment, a final microbial reduction was calculated by subtracting the minimum detection limit (1.3 Log10 CFU/cm2) from the initial log concentration. After 4.9 J/cm2 of PUV light exposure, there was complete surface inactivation of E. coli K12-NSR with no growth in selective enrichment. Reduction of E. coli K12-NSR observed on the surface of eggs after a total energy of 4.9 J/cm2 was significantly greater compared with eggs treated with 1.0 and 3.1 J/cm2 (P < 0.05). There was no significant difference in reduction of E. coli K12-NSR for eggs treated with 1.0, 2.4, and 3.1 J/cm2 (P > 0.05).
Table 1. Microbial reduction on the surface of table eggs after treatment by PUV light (±SD).
|Microorganism||Energy(J/cm2)||Reduction(Log₁₀ CFU/cm2)||CFU observed(% no-growth)1||Selective enrichment(% positive)2||General enrichment(% positive)3|
|1.0||≥3.43 ± 0.55b||60%||93%||100%|
|2.4||≥4.00 ± 0.79ab||73%||53%||60%|
|3.1||≥3.76 ± 0.61b||80%||53%||60%|
|4.9||≥4.54 ± 0.38a||100%||0%||20%|
|Enterococcus faecium||1.0||2.03 ± 0.32c||0%||n/a||100%|
|2.4||2.81 ± 0.63b||0%||n/a||100%|
|3.1||2.98 ± 0.64b||13%||n/a||100%|
|4.9||3.52 ± 0.47a||13%||n/a||100%|
a-cMeans within microorganism without common superscripts are significantly different (P < 0.05).
Abbreviations: PUV, pulsed ultraviolet; TSBYE-NS, tryptic soy broth supplemented with 0.6% of yeast extract and 100 mg/mL of both nalidixic acid and streptomycin sulfate
Percent of agar plates (n = 15) that did not result in growth of colony forming units.
TSBYE-NS for selective enrichment of E. coli K12-NSR.
TSBYE for general enrichment for E. coli and E. faecium.
For eggs inoculated with E. faecium, there was significant reduction after exposure to PUV light (P < 0.05). Microbial reduction observed was 2.03, 2.81, 2.98, and 3.52 Log10 CFU/cm2 after 1.0, 2.4, 3.1, or 4.9 J/cm2 treatment, respectively (Table 1). Reduction of E. faecium observed on the surface of eggs after a total energy of 4.9 J/cm2 was significantly greater compared with eggs treated with 1.0, 2.4, and 3.1 J/cm2 (P < 0.05). There was no significant difference in reduction of E. coli K12-NSR for eggs treated with 2.4 and 3.1 J/cm2 (P > 0.05).
Though evaluated separately, E. coli K12-NSR and E. faecium appear to have differing germicidal responses after exposure to PUV light at equal energy when initial inoculation concentrations were similar. For eggs inoculated with E. coli K12-NSR, every treatment level had agar plates with no colony growth. At 1.0, 2.4, 3.1, and 4.9 J/cm2 of total energy, 60, 73, 80, and 100% of TSBYE-NS plates did not result in the growth of E. coli colonies. In comparison, E. faecium resulted in colony growth on m-Enterococcus agar at all treatment levels. At 4.9 J/cm2 of total energy, E. coli K12-NSR resulted in a reduction of ≥4.54 Log10 CFU/cm2 compared with 3.52 Log10 CFU/cm2 for E. faecium. The difference in observed germicidal response is likely associated with the physiological differences between the microorganisms. E. coli K12-NSR are gram-negative and rod shaped, whereas E. faecium are gram-positive and cocci shaped. The thicker layer of cell wall peptidoglycan associated with gram-positive bacteria may be contributing a protective benefit against the effects of PUV light exposure. Koutchma (2009) reported that gram-positive bacteria are more resistant to conventional UV light than gram-negative bacteria. Rowan et al. (1999) and Anderson et al. (2000) both concluded that susceptibility of microorganisms to PUV light was greater for gram-negative bacteria compared with gram-positive bacteria.
Regardless of germicidal response differences observed between E. coli K12-NSR and E. faecium, reductions from this study are similar to previous shell egg decontamination research with PUV light. Keklik et al. (2010) reported between 1.3 to 5.3 Log10 CFU/cm2 reduction of Salmonella Enteritidis on 2.0 cm2 portions of eggshells exposed to 1.2 to 24.8 J/cm2 of PUV light, without any visible damage to the surface of the egg. It was reported that greater exposures, 24.8 to 35.3 J/cm2, resulted in surface temperature increases of 13.3°C to 16.3°C. Hierro et al. (2009) and Lasagabaster et al. (2011) inoculated the entire surface of shell eggs with Salmonella Enteritidis and Salmonella Typhimurium, respectively, before treatment using a benchtop PUV light system. In these studies, PUV flashlamps were positioned above and below a single egg held stationary in a fixed position. After 12 J/cm2 of PUV exposure, Hierro et al. (2009) reported that the reduction of Salmonella Enteritidis on unwashed eggs was 2.49 Log10 CFU/cm2, with 80% of the samples achieving the maximum observable decontamination of 3.6 Log10 CFU/cm2. At 2.1 J/cm2 energy of PUV light, Lasagabaster et al. (2011) reported a 4.9 Log10 CFU/cm2 reduction of S. Typhimurium on unwashed eggs. The findings of the current study are mostly consistent with the reports cited above, but further work directly comparing benchtop and conveyor PUV light systems may be illuminating.
Energy and Temperature Profiles During Pulsed UV Treatment
Owing to the broad-spectrum energy delivered by the PUV lamp, surface temperature of eggs was measured immediately following treatment. Treatment by PUV light produced a significant (P < 0.05) increase in the surface temperature of the eggs. The initial surface temperature of the eggs was 21.5 ± 1.1°C. After 1.0, 2.4, 3.1, and 4.9 J/cm2, surface temperature increased 0.24°C, 0.26°C, 0.61°C, and 1.20°C, respectively (Table 2). In another study, the change in temperature on the surface of eggs treated with a total energy of 2.1 to 10.5 J/cm2 was reported to increase 1.2°C to 4.2°C, respectively (Lasagabaster et al., 2011). The apparent difference in egg surface temperatures between previous and current studies may be because of thermodynamic differences in the PUV light systems. Using an enclosed PUV light benchtop system, such as the one used by Lasagabaster et al. (2011), the opportunity for heat to build up in the treatment space is much greater compared with the open system evaluated in this study. In the current study, eggs are exposed to radiant energy on only one side as they rotate. The other, shaded side may be able to cool slightly while it is away from the illumination.
Table 2. Temperature change on the surface of table eggs after PUV light treatment (±SD).
|Treatment (J/cm2)||Temperature (Δ°C)|
|1.0||0.24 ± 0.15c|
|2.4||0.26 ± 0.18c|
|3.1||0.61 ± 0.32b|
|4.9||1.20 ± 0.29a|
a-cMeans without common superscripts are significantly different (P < 0.05).
Abbreviations: PUV, pulsed ultraviolet.
Hatching Egg Response after PUV Light Treatment
Parameters of commercial hatchery performance including fertility, percent hatch, hatchability, and livability were evaluated after PUV light treatment of fertile eggs. The most favorable microbial reduction response was observed at 4.9 J/cm2 for both E. coli K12 NSR and E. faecium; therefore, it was chosen as the minimum PUV light exposure level for treating hatching eggs. Additionally, in an effort to expose any adverse effects of PUV light treatment on fertile eggs, 24.4 and 48.8 J/cm2 were evaluated as extreme treatment conditions.
Immediately after PUV light treatment of hatching eggs, the surface temperature was measured. As previously observed, increasing PUV light exposure significantly increased the egg surface temperature (P < 0.05). The initial surface temperature was 19.5°C ± 2.4°C and increased 1.3, 4.4, and 7.8°C after exposure to a PUV light of 4.9, 24.4, and 48.8 J/cm2, respectively (Table 3). The greatest change in hatching egg surface temperature, observed at 48.8 J/cm2, resulted in a final temperature of 29.4°C ± 2.4°C. This final egg treatment temperature of 29.4°C is lower than commercial incubation temperatures set at approximately 37.5°C. These results indicate that at low levels of exposure, PUV light raises egg temperature to a degree that is not expected to affect hatching performance. Though, after prolonged exposure to PUV light, the rise in temperature may be undesirable.
Table 3. Temperature change on the surface of hatching eggs after PUV light treatment (±SD).
|4.9 J/cm2||1.3 ± 0.09c|
|24.4 J/cm2||4.4 ± 2.0b|
|48.8 J/cm2||7.8 ± 1.9a|
a-cMeans without a common superscript are significantly different (P < 0.05).
Abbreviation: PUV, pulsed ultraviolet.
There was no significant effect of PUV light on percent fertility, hatch, hatchability, or livability of fertile eggs exposed to 4.9, 24.4, and 48.8 J/cm2 of PUV light (P > 0.05; Table 4). Averaged across all treatments, fertility and hatch were 92.4 and 87.8%, respectively, whereas hatchability was 94.4%. However, there appeared to be a numerical difference in percent hatchability between the untreated and treated eggs (P = 0.086). Untreated eggs resulted in a 90.4% hatchability, whereas treated eggs resulted in 86.0, 87.0, and 87.6% hatchability after 4.9, 24.4, and 48.8 J/cm2 of PUV light exposure. After 1 and 6 wk, average chick livability was 99.3 and 98.5%, respectively. Pulsed UV light treatment did not contribute to teratogenic effects on developing embryos even at high treatment levels. The absence of teratogenic effects is similar to findings for fertile eggs exposed to continuous UV light by Scott (1993), for 1, 3, or 5 min of UV light before incubation with no adverse effects on embryonic development reported.
Table 4. Percent fertility, hatchability, and livability of eggs that received PUV light treatment (±SD).
|Treatment||% Fertility||% Hatchability1||% Hatch2||Livability %|
|1 wk||6 wk|
|Control||93.2 ± 1.5||97.0 ± 0.9||90.4 ± 2.1||99.3 ± 1.6||96.7 ± 5.6|
|4.9 J/cm2||92.0 ± 1.7||93.5 ± 2.2||86.0 ± 0.5||99.4 ± 2.0||98.0 ± 4.1|
|24.4 J/cm2||93.2 ± 1.9||93.3 ± 2.8||87.0 ± 3.8||99.2 ± 1.7||98.2 ± 2.4|
|48.8 J/cm2||93.2 ± 4.2||94.0 ± 1.9||87.6 ± 4.9||99.1 ± 2.0||98.1 ± 2.8|
Percent of fertile eggs.
Percent of set eggs.
Average chick weights at hatch and after 7 and 42 d of age are reported in Table 5. There were no significant differences among treatment groups on the day of hatch and after 42 d of grow out (P > 0.05). However, there were significant differences among treatment groups after 7 d of rearing (P < 0.05). Eggs treated with 4.9 J/cm2 of PUV light resulted in chicks that weighed significantly less compared with all other treatment groups (P < 0.05). There is no obvious explanation for this observation, and this treatment difference did not continue into the 42-day body weight. Averaged across all treatment groups, the chicks weighed 39.6, 69.4, and 471.6 g on the day of hatch and after 7 and 42 d of grow-out, respectively.
Table 5. Bird weight after hatch from eggs that received PUV light treatment (±SD).
|Treatment||Average bird weight|
|Day 1||Day 7||Day 42|
|Control||39.44 ± 1.44||70.41 ± 3.01a||477.09 ± 28.37|
|4.9 J/cm2||39.58 ± 0.92||65.43 ± 4.86b||469.83 ± 20.49|
|24.4 J/cm2||39.94 ± 1.24||72.34 ± 4.95a||469.47 ± 29.83|
|48.8 J/cm2||39.53 ± 0.89||69.40 ± 6.56a||470.48 ± 25.51|
a-bMeans without a common superscript are significantly different (P < 0.05).
Abbreviation: PUV, pulsed ultraviolet.
In a study by Patterson et al. (1990), chlorine dioxide solution proved to be an effective decontamination intervention for hatching eggs, but extreme concentrations negatively affected both fertility and hatchability. Unlike the negative impacts of chlorine dioxide, PUV light appears to have no real negative effects on incubation or rearing parameters.
At the minimum PUV light level evaluated (1.0 J/cm2), PUV light treatment achieved significant microbial reductions of ≥3.43 and 2.03 Log10 CFU/cm2 for E. coli K12-NSR and E. faecium, respectively, on the surface of shell eggs. At an extreme exposure level (48.8 J/cm2), PUV light treatment had no adverse effects on fertility, percent hatch, and livability of fertile eggs. Pulsed ultraviolet lights effect on hatchability was inconclusive and should be further evaluated. These results indicate that PUV light is an effective antimicrobial treatment for all eggs, intended for consumption or commercial incubation. Further research is necessary to determine if interior egg characteristics are altered when PUV light is delivered to the exterior shell surface. Before commercial implementation, it would be beneficial to evaluate the effectiveness of PUV light using actual pathogenic strains that might be found on eggs.
This work was partially supported by the USDA National Institute of Food and Agriculture Federal Appropriations, Project PEN04696 and the Penn State College of Agricultural Sciences, Undergrade Student Research Program. Also, the authors would like to thank Hy-Line North America (Elizabethtown, PA) for supplying the eggs used in this study and Xenon Corporation (Wilmington, MA) for the technical assistance with the PUV light technology.
The authors declare no conflicts of interest.