Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Effect of Chicken Egg Yolk Antibodies (IgY) against Diarrhea in Domesticated Animals: A Systematic Review and Meta-Analysis

  • Thirumalai Diraviyam,

    Affiliation College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China

  • Bin Zhao,

    Affiliations College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China, College of Science, Northwest A&F University, Yangling, Shaanxi, China

  • Yuan Wang,

    Affiliation College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China

  • Ruediger Schade,

    Affiliation Institute of Pharmacology, Charité - Universitätsmedizin Berlin, Berlin, Germany

  • Antonysamy Michael,

    Affiliation PSG College of Arts and Science, Bharathiar University, Coimbatore, Tamil Nadu, India

  • Xiaoying Zhang

    zhang.xy@nwsuaf.edu.cn

    Affiliation College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China

Abstract

Background

IgY antibodies are serum immunoglobulin in birds, reptiles and amphibians, and are transferred from serum to egg yolk to confer passive immunity to their embryos and offspring. Currently, the oral passive immunization using chicken IgY has been focused as an alternative to antibiotics for the treatment and control of diarrhea in animals and humans. This systematic review was focused to determine the effect of IgY in controlling and preventing diarrhea in domesticated animals including Piglets, Mice, Poultry and Calves.

Methods and Results

Previous research reports focused on treatment effect of Chicken IgY against diarrhea were retrieved from different electronic data bases (MEDLINE, EMBASE, SPRINGER-LINK, WILEY, AGRICOLA, MEDWELL Journals, Scientific Publish, Chinese articles from Core periodicals in 2012). A total of 61 studies in 4 different animal classes met the inclusion criteria. Data on study characteristics and outcome measures were extracted. The pooled relative risk (RR) of 49 studies of different animals [Piglets – 22; Mice – 14; Poultry – 7 and Calves – 6] in meta-analyses revealed that, IgY significantly reduced the risk of diarrhea in treatment group when compare to the placebo. However, the 95% confidence intervals of the majority of studies in animal class piglets and calves embrace RR of one. The same results were obtained in sub group analyses (treatment regiment – prophylactic or therapeutic; pathogen type – bacterial or viral). Perhaps, this inconsistency in the effect of IgY at the individual study level and overall effect measures could be influenced by the methodological heterogeneity.

Conclusion

The present systematic review (SR) and meta-analysis demonstrated the beneficial effect of IgY. This supports the opinion that IgY is useful for prophylaxis and treatment. However, more intensive studies using the gold standard animal experiments with the focus to use IgY alone or in combination with other alternative strategies are indispensable.

Introduction

In a common way antibiotics have been used in animal agriculture for growth promotion (sub-therapeutic doses), disease prevention (prophylactic doses) and for the treatment (therapeutic dose) for more than 50 years and many of the research reports and practical experiences have shown the usage of antibiotic to significantly contribute for the improved performance of animals [1], [2]. However, the use and misuse of in-feed antibiotics have resulted in serious complications due to drug residues in animal products and increased bacterial resistance. The recognition of these dangers prompted the ban on sub therapeutic usage of antibiotics in many developed countries and some of the developing countries are seriously considering a similar ban. Therefore a viable alternative strategy to antibiotics is essentially needed to combat drug-resistance microorganisms and also to treat the diseases that are unresponsive to drug therapy (viral infection) and for individuals with impaired immune systems who are unable to respond to conventional vaccines [3].

A broad range of products as an effective alternative to antibiotics have been focused seriously by the global biomedical research community. Recently, passive immunization using chicken egg yolk immunoglobulin (IgY) has become an attractive approach with considerable attention as it possesses a variety of advantages over mammalian IgG such as convenience, high yield and cost-effectiveness. Oral administration of specific chicken IgY has been shown to be effective against a variety of intestinal pathogens especially diarrheal pathogens in different animal classes and humans such as bovine and human rotaviruses, bovine coronavirus, enterotoxigenic Escherichia coli (ETEC) and Salmonella spp. [4]. Although the beneficial effects of chicken IgY in controlling or preventing the diarrheal disease in animals have been known for more than two decades and reported by many researchers globally, it still remains a difficult task to use chicken IgY as an alternative to conventional treatment with strong scientific conclusion. At this juncture, a meta-analysis is necessary and helpful to summarize the previous research findings and provide a comprehensive conclusion and proper direction for further research. The objective of this SR and meta-analysis is to determine the effect of chicken IgY for the treatment and control of diarrhea in domesticated animals using available research reports on IgY against diarrhea in different animal classes like piglets, mice, poultry and claves.

Materials and Methods

The review protocol is publicly available at CAMARADES (Collaborative Approach to Meta Analysis and Review of Animal Data from Experimental Studies) web site (http://www.camarades.info/index_files/chickenyolkSRt.pdf).

1. Literature search

Previous research reports were retrieved from different electronic data bases including MEDLINE, EMBASE, SPRINGER-LINK, WILEY, AGRICOLA, MEDWELL Journals, Scientific Research Publish and Chinese articles from Core periodicals in 2012 regardless of language and publication status. The search strategies are presented in our review protocol available at CAMARADE as well as in supporting information. Bibliographies of narrative review articles and eligible trials were reviewed manually for the potential studies which cannot be retrieved by the electronic searches. All these literature searches were carried out until September 30, 2013. Besides, the publications in the conference proceedings, dissertation abstracts and other studies that would have to be in “file drawers” (unpublished manuscripts) were also considered for the analyses in order to reduce the risk of missing potential studies.

2. Selection of potential studies

The research studies reported on the effect of IgY antibodies as a treatment agent for controlling and preventing diarrhea in animals were selected on the basis of the title and abstract by 2 independent authors (TD and XYZ). Full articles were reviewed when a decision could not be made using abstract. 2 reviewers independently evaluated the eligibility of each potential full-text article and resolved the disagreement by consensus and discussion with the third party (RS and AM).

3. Inclusion criteria

Research reports that were published in English, Chinese and German were selected and included for the analyses, having met the following inclusion criteria: 1) Study with in-vivo animal experiment [should have been conducted with animal ethical committee approval] 2) Study should have evaluated the effect of IgY against diarrhea causing pathogens 3) Study should have used any one formulation of IgY: purified IgY, partially purified IgY, immune yolk (liquid) or immune yolk powder (spray dried or freeze dried) 4) The treatment effect of IgY was assessed using one of the following outcomes: mortality rate, survival rate, fecal score for pathogen excretion, fecal consistency (diarrhea) and body weight 5) Sufficient data should be described including number of animals in each group (treatment and control), pathogen challenge dose and IgY treatment dose with duration, hypothetical consent either prophylactic or therapeutic effect of IgY. PRISMA flow diagram for literature selection, screening and inclusion has been presented in Figure 1 [5].

thumbnail
Figure 1. Summary of literature search, screening and selection.

PRISMA flow diagram represents the literature search in different electronic data base followed by screening and inclusion of eligible studies for systematic review and meta-analysis.

https://doi.org/10.1371/journal.pone.0097716.g001

4. Data extraction

Studies included for qualitative and quantitative analysis were critically assessed by three independent reviewers (TD, XYZ and YW) and the following data were extracted: year of publication with first author, information pertaining to the hypothesis of IgY usage (therapeutic or prophylactic), animals class, breed, age, body weight, type of infection (experimental or natural-field trail), pathogen (bacterial or viral), strain, challenge dose and time, dose of IgY, mode of administration, duration of the treatment, number of animals in control and treatment group, outcome assessment (Table S1, S2, S3 and Table 1). Missing information was discussed with the corresponding authors by contacting through e-mail or telephonic conversation. Reviewers assessed the risk of bias, inconsistency and indirectness of the study included for the systematic review.

thumbnail
Table 1. Characteristics of the included study – Calves.

https://doi.org/10.1371/journal.pone.0097716.t001

5. Assessing the quality of the studies

Potential studies were assessed for methodological quality using the Animal Research: Reporting of In-vivo Experiment (ARRIVE) Guidelines developed as a part of NC3Rs (National Centre for the Replacement, Refinement and Reduction of Animals in Research) to improve the design, analysis and reporting of research using animals [6], [7]. The quality was assessed by evaluating whether the methodology of included studies met the ARRIVE guideline or not. Maximum score of 20 points was attributed to each article. Based on the total score, studies were categorized in to three different groups as good, moderate and poor if the score percentage was ≥75%, ≥65% and ≤55% respectively (Table 2).

thumbnail
Table 2. Quality of Animal Studies: Values are numbers (percentage).

https://doi.org/10.1371/journal.pone.0097716.t002

Risk of bias of the included studies was measured by two reviewers (TD and X-YZ) using the criteria designed already with slight modification (in items 9 and 10) such as the possible presence of selection bias (items 1, 2 and 3), performance bias (items 4 and 7), detection bias (items 5, 6 and 8) and attrition bias (items 9 and 10) [8], [9]. The scores such as “Yes” denotes low risk of bias, “No” denotes high risk of bias, “Unclear” denotes unknown risk of bias, “NA” indicates non applicable (Figure 2).

thumbnail
Figure 2. Risk of bias assessment.

Yes = low risk of bias, No = high risk of bias, Unclear = unclear risk of bias, NA = not applicable.

https://doi.org/10.1371/journal.pone.0097716.g002

6. Data synthesis and statistical analysis

In accordance to the differences between studies such as different doses, formulation of IgY, pathogenic strains used for challenge, duration of treatment, outcome assessment and age of animals; the random-effects meta-analysis was taken in to consideration for calculating the relative risk (RR) and the 95% confidence interval (CI) in trails reporting the binary outcome i.e., number of animals with diarrhea or number of animals died by diarrhea (mortality rate). Since, the number of studies in piglets are relatively higher than other animal class, the subgroup analysis were carried out for the studies reported only in Piglets with following study characteristics, pathogen type – bacterial or viral and treatment regiment – prophylactic or therapeutic. In order to estimate the amount of heterogeneity, Q and I2 value was calculated [10]. The presence of publication bias was assessed by funnel plots and Egger regression test [11]. Meta-analysis was performed by MedCalc Statistical Software version 12.7.7 (MedCalc Software bvba, Ostend, Belgium; 2013) [12]. Forest plot graphical representation was used to display the meta-analysis results (BZ). Other study characteristics and results were summarized narratively with tables and running text.

Results

1. Characteristics of the included studies

A total of 378 records were identified through different database searching: Medline (n = 155); EMBASE (n = 144); Springer link (n = 38), Chinese articles from Core periodicals in 2012 (n = 12); Wiley (n = 4); Agricola (n = 3); other open access journals (n = 16) and conference proceedings (n = 6). After intensive screening and eligibility to met inclusion criteria a total of 61 studies [Piglets – 24; Mice – 15; Poultry – 15 and Calves – 7] [13][73] were included for systematic review, of which 49 records [Piglets – 22; Mice – 14; Poultry – 7 and Calves – 6] were included for meta-analysis (Figure 1). Chinese and German articles were translated by three reviewers (XYZ, YW and RS). The characteristics of each included studies are documented and presented in Table S1, S2, S3 and Table 1.

The study characteristics had considerable difference among the records included for analyses; in particular IgY dose and formulation are not comparatively homologous. Some of the studies mentioned, that IgY administration started before challenging with pathogen (prophylactic effect) whereas in some trials it was after the onset of diarrhea (therapeutic effect). Few studies have reported that IgY administration had begun immediately after challenging. In terms of diarrhea, 12 experiments among different studies were performed to evaluate the effect of IgY in the field (farm) whereas other studies reported the effect of IgY against the experimental diarrhea. In poultry trails, some studies focused to assess the effect of IgY to prevent the possible bacterial contamination (pathogens responsible for diarrhea in animals and humans) in the eggs.

2. Risk of bias and quality of studies

The quality of the included studies as per ARRIVE Guidelines: individual study analysis revealed that none of the studies showed 100% quality, barely very few studies scored more than 90%. In categorization, 52.5% of the studies are good, 34.4% studies are moderate and 13.1% studies are poor. Which indicates that, the nearly 50% of the included studies are relatively low in quality (Table 2). The overall result for the risk of bias assessment for the 61 studies included was presented in Figure 2. The results indicated 49.2% studies reported that experimental groups of animals were randomly assigned, but there was not description regarding the method of randomization. None of the studies discussed about the grouping concealment. Only three of these studies described about the blinded outcome assessment and only one of which provided the complete details. Out of the 10 items, only two items 7 and 8 show the low risk of bias for all the studies and many items are scored as “unclear risk of bias”. These findings clearly state the inadequacy of quality and standard in the reporting of animal studies on effect of IgY against diarrhea in different animal classes. In addition, the existence of these biases in animal experiments possibly influences the outcome of this systematic review and meta-analysis.

3. Effect of chicken IgY against diarrhea in animals

Studies on passive immunization by oral administration of IgY for the treatment and control of diarrhea in different animal classes such as piglets, mice, poultry and calves were selected and statistically analyzed to have comprehensive evidence regarding the effect of IgY. The following results were found for each animal class.

3.1. Effect of IgY against diarrhea in Piglets.

Out of 61studies selected for analysis, 24 studies were reported on IgY effect against diarrhea in piglets, in which 22 studies were included for meta-analysis including 17 studies against bacterial diarrhea and 5 studies against viral diarrhea (a total of 39 experiments). Meta-analysis indicated, that majority of the studies (except 8 experiments) overlaps the RR of 1at 95% confidence interval, even though the overall effect estimate was statically significant (Figure 3 and Table 3; pooled RR,0.30; 95% CI 0.22 to 0.41). The heterogeneity was moderate (Q = 86.63; DF = 37; P<0.0001, I2 = 57.29%). Studies of Zuniga et al 1997 and Girard et al 2006 were not included in the meta-analysis, since they reported the continuous variables such as amount of viable cells in the feces (log colony forming unit g−1) and reduction in the mean percentage of inter-crypt epithelium (ICME); but both the studies supported the oral application of egg yolk antibodies for prevention of infectious diseases caused by enteric pathogens.

thumbnail
Figure 3. Effect of IgY against diarrhea in piglets.

Forest plot demonstrates the relative risk (RR) of individual studies included for meta-analysis under animal class piglets, 95% confidence interval. The diamond represents the global estimate and its 95% confidence interval. The cut off line crossing RR 1 differentiates the study favors IgY treatment group or control group. The line crossing diamond is to determine the number of studies positioned in global RR.

https://doi.org/10.1371/journal.pone.0097716.g003

3.2. Effect of IgY against diarrhea in Mice.

Fifteen records were identified those reported on the effect of IgY against diarrhea in Mice and 14 studies (22 experimental trails) were included for meta-analysis. Results revealed the statistically significant effect of IgY for reducing the risk of diarrhea in intervention group treated with specific IgY compared with the control group at the individual study level (16 experiments out of 22 trials reported in 14 studies) as well as the meta-analysis level (Figure 4 and Table 4; pooled RR, 0.25; 95% CI 0.18 to 0.36). The low level of heterogeneity (Q = 36.17; DF = 21; P = 0.0209, I2 = 41.94%) was observed among the studies. Report of Hirai et al 2010 was not included in the meta-analysis due to lack of description for absolute number of experimental animals (results were presented as percentage of survival), the study demonstrated, that the mixture of anti-Vibrio cholera and anti-cholera toxin subunit-B IgYs could be used to prevent or treat cholera caused by either O1 or O139.

thumbnail
Figure 4. Effect of IgY against diarrhea in mice.

Forest plot demonstrates the relative risk (RR) of individual studies included for meta-analysis under animal class mice, 95% confidence interval. The diamond represents the global estimate and its 95% confidence interval. The cut off line crossing RR 1 differentiates the study favors IgY treatment group or control group. The line crossing diamond is to determine the number of studies positioned in global RR.

https://doi.org/10.1371/journal.pone.0097716.g004

3.3. Effect of IgY against diarrhea in Poultry.

A total of 15 studies demonstrating the effect of IgY against diarrheagenic pathogens in poultry were selected. Of which 8 (>50%) reports were excluded from meta-analysis, because 6 studies presented the outcome measures as graphical representations and statistical derivatives (not absolute number of birds); 2 records were reported the reduction in the possible bacterial contamination of eggs. The meta-analysis showed, that the administration of IgY reduces the risk of event significantly in the treated group when compare to the untreated control (Figure 5 and Table 5; pooled RR, 0.22; 95% CI 0.14 to 0.34). The beneficial effect of IgY could be further supported by the 95% confidence intervals at individual study level (6 experiments reported in the 5 studies) did not embrace a RR of 1. The heterogeneity was low between the included studies (Q = 10.14; DF = 7; P = 0.1807, I2 = 30.98%).

thumbnail
Figure 5. Effect of IgY against diarrhea in poultry.

Forest plot demonstrates the relative risk (RR) of individual studies included for meta-analysis under animal class poultry, 95% confidence interval. The diamond represents the global estimate and its 95% confidence interval. The cut off line crossing RR 1 differentiates the study favors IgY treatment group or control group. The line crossing diamond is to determine the number of studies positioned in global RR.

https://doi.org/10.1371/journal.pone.0097716.g005

3.4. Effect of IgY against diarrhea in Calves.

Six studies were included for meta-analysis out of 7 studies investigated the effect of IgY against diarrhea in calves. As mentioned in the previous animal class, one study was excluded due to insufficient information about the number of animals in the outcome measures. Most of the studies were performed as field trail; it might be the reason that rearing cost of cows to have calves for animal experiment, further the size of the animals is relatively lager. Results revealed, that the 95% confidence intervals of all the studies except one study overlap the RR of 1, hence there is no statistical significance at the individual study level. However, the overall effect estimate and its 95% confidence intervals indicated the beneficial effect of IgY (Figure 6 and Table 6; pooled RR, 0.35; 95% CI 0.21 to 0.57) with very low level of heterogeneity (Q = 3.13; DF = 6; P = 0.7924, I2 = 0.00%).

thumbnail
Figure 6. Effect of IgY against diarrhea in calves.

Forest plot demonstrates the relative risk (RR) of individual studies included for meta-analysis under animal class Calves, 95% confidence interval. The diamond represents the global estimate and its 95% confidence interval. The cut off line crossing RR 1 differentiates the study favors IgY treatment group or control group. The line crossing diamond is to determine the number of studies positioned in global RR.

https://doi.org/10.1371/journal.pone.0097716.g006

3.5. Sub-group analysis.

In order to perform the sub-group analysis, 24 piglets studies were considered, of which 16 studies were selected to evaluate the prophylactic effect of IgY and 14 studies were identified to determine the therapeutic effect of IgY (regardless of pathogen type). There was no statistical significance at individual study level but overall effect estimate did not overlap the RR of 1, thus indicated the intervention is better than the control [prophylactic effect of IgY: pooled RR, 0.38 (95% CI 0.27 to 0.55); therapeutic effect of IgY: pooled RR, 0.11 (95% CI 0.06 to 0.22) (Table 7 and Table 8)]. To assess the difference in the effect of IgY against type of diarrheal pathogen (bacterial or viral) 19 studies of bacterial pathogen and 5 studies of viral pathogen were considered (regardless of treatment strategy – therapeutic or prophylactic). The results suggested no statistical significance at the individual study level but the pooled effect measure showed the significant effect of IgY against both bacterial and viral diarrhea [Bacterial: pooled RR, 0.29 (95% CI 0.213 to 0.40; Viral: pooled RR, 0.45 (95% CI 0.28 to 0.70)]. Heterogeneity was considerably low at all the sub-group analysis.

thumbnail
Table 7. Prophylactic effect of IgY against diarrhea in Piglets.

https://doi.org/10.1371/journal.pone.0097716.t007

thumbnail
Table 8. Therapeutic effect of IgY against Diarrhea in Piglets.

https://doi.org/10.1371/journal.pone.0097716.t008

The pooled effect estimate in all the animal class suggested the beneficial effect of IgY against diarrhea, but majority of effect measure at the individual study level in animal class piglets and calves were not statistically significant at 95% confidence interval. All the studies selected for analysis indicated that, there was no adverse event because of the IgY or immune yolk administration either with feed or drinking water or force feeding. Some of the studies have analyzed the effect of probiotics along with IgY as an agent to enhance the beneficial bacterial population in the gut and decrease the pathogen count synergistically.

4. Publication bias

The presence of publication bias was primarily assessed by Funnel plotting. The asymmetry of funnel plots indicated the presence of publication bias in the study topic. Sometimes asymmetry could be the results of other sources rather than publication bias. In order to test asymmetry of funnel plots, Egger regression test was performed for included studies of each animal class separately. Results revealed that, there was some evidence of publication bias in the meta-analysis of animal class piglets and mice. But, it is difficult to reach any conclusion for meta-analysis of animal class poultry and calves, since the included studies are less in number (data not shown).

Discussion

The prime findings of this SR and meta-analysis reveal that, the use of IgY as an alternative treatment approach could reduce the risk of diarrhea in domesticated animals with the statistically significant overall effect measure (pooled RR). The result was consistence across all the animal class including piglets, mice, poultry and calves. In addition, the 95% confidence intervals of majority of the studies in animal class mice and poultry did not embrace the RR of 1, thus indicates the statistical significance of IgY effect at individual study level. Despite, the animal class piglets and calves showed no evidence of the same effect at study level. Subgroup analyses using the studies reported in piglets also demonstrate the significant effect of IgY at meta-analysis level but failed to show the same evidence in individual studies. The genetic heterogeneity of animals might be the reason for differences in the statistical data between individual study level and overall effect measures of animal class piglets and calves. Overall outcome of the review shows that, the pooled RR of every analyses are significantly evidence the effect of IgY for reducing the deleterious events (morbidity or mortality) in treated animals when compare to the untreated control. This finding strengthens one of the promising approaches of antibody engineering, to apply IgY for treating and controlling the gastrointestinal infections in farm animal by oral passive immunization.

Diarrhea in young animals is one of the most important diseases that affect livestock industry and continuing to cause high economic losses worldwide due to increased mortality, medication costs, feed conversion rates and decreased weight gain. Normally these diseases are being controlled by administering antibiotics. Nevertheless, the problem of antibiotic resistance has increased dramatically during the past three decades; this may turn into successful treatment more difficult or sometimes impossible and prompted the ban on sub therapeutic use of antibiotics in livestock. Noticeably the sale of antibiotics used in veterinary medicine declined worldwide, for instance 16% of the decline in the sales from 2010 to 2011was reported by European surveillance of veterinary antimicrobial consumption, whereas the Swissmedic declared the fall of 8% in veterinary antibiotics sale in Switzerland during 2012 [74], [75]. Further, the development of novel antimicrobial agents has drastically declined, nevertheless only two new systemic classes of antibiotics (oxazolidinones and cyclic lipopeptides) and two topical classes of antibiotics (pseudomonic acids and pleuromutilins) were introduced in the market during the past 30 years [76]. As a result, the recent scientific publications are pointing out the need for next generation antibiotics. Therefore, new treatment approaches to substitute antibiotics are currently indispensable for combating pathogens. At this juncture, the beneficial effect of IgY likely to be considered for further investigation as a viable alternative to antibiotics. In addition to the bacterial and viral diarrheal diseases in live stock, some economically important intestinal diseases are caused by several different protozoan species; for instance, avian coccidiosis is caused by Eimeria protozoa in the poultry worldwide. In recent years, IgY has also been focused as an alternative control method for the prevention and treatment of protozoan diseases by oral passive immune therapy. Reports on this approach are also clearly evidence the significant protective effect of IgY against Eimeria tenella and Eimeria maxima in chicks. This provide a strong suggestion, that the passive immunization using IgY could be extended to many other gastro intestinal tract diseases caused by microorganisms irrespective of their types and groups [77][79].

In recent decades, a number of IgY or hyper immune egg products are available in the market for the betterment of overall health in humans, livestock and companion animals. As a result, many biological companies are now focusing their attention to establish IgY production, especially for animal feed supplementation. Results of this SR is relatively supports those commercial products unless otherwise manufactured with scientific approach.

Regarding the study quality and risk of bias, none of the studies were scored 100% as per ARRIVE Guidelines. Of course it was not possible for the earlier reports to have contained the standard protocol for animal experiment, but some of the recent studies also did not fit the standards. Only very few recent reports have strictly followed the proper guidelines for the intervention of therapeutic events in animals. The risk of bias assessment showed, that majority of the items had unclear risk of bias out of 10 items (considered for the study). These findings exhibit the inadequacy of reporting or designing animal experiments in scientific publications. Further, it enforces the need and importance of proper animal experiments in future pre-clinical trials to reduce the bias by outlining transparency in objective and methodology.

The methodological heterogeneity among the included studies, especially the dose and formulation of IgY (purified form or immune yolk/egg) was fairly considerable. With respect to reduction of the possible heterogeneity between the studies, the binary outcome such as the number of animals that died (mortality) due to diarrhea and the number of animals that exhibited diarrhea during and after treatment with IgY were considered as primary outcome measures for the meta-analysis. However, the two animal class (pigs and calves) and subgroup analyses showed statistical significance in overall random effect, but not at individual study level. This would have possibly influenced by several factor including the poor animal experimental design, the difference in the effect of IgY between primary outcomes measures taken into consideration for this SR and other continuous variables, the divergence in biological response of each animal class towards a particular treatment strategy.

In terms of limitations to this SR, the inclusion of four different animal classes in a single study has driven the reviewers to consider some homologous binary outcome measures between the studies. Some other continuous variables with respect to pathogenesis of diarrhea such as fecal consistency, number of bacteria or viral particle excreted per g of feces, differences in the body weight gain were not included in the meta-analysis. As a consequence, the reliability of the conclusion (the pooled effect size) of this meta-analysis is relatively low. This limitation is also applicable for subgroup analysis. The further crucial scrutiny by separate meta-analysis of each animal class with the focus to analyze multiple outcome measures is warranted.

In conclusion, the present SR and meta-analysis demonstrated the beneficial effect of IgY in controlling and preventing the diarrhea in domesticated animals. This supports the opinion that IgY is useful for prophylaxis and treatment of gastrointestinal infection by oral passive immunization as an alternative strategy to antibiotics. However, the further investigations are indispensable for the robustness of IgY application are indispensable to optimize the effective IgY dose with suitable formulation in order to withstand in the gastric environment; to determine the combinatorial effect of IgY with other alternative therapeutic strategies including probiotics and plant extracts for the improved performance. The gold standard animal experiments are necessarily to be conducted as per guidelines.

Supporting Information

Table S1.

Characteristic of the included studies – Piglets.

https://doi.org/10.1371/journal.pone.0097716.s001

(DOC)

Table S2.

Characteristic of the included studies – Mice.

https://doi.org/10.1371/journal.pone.0097716.s002

(DOC)

Table S3.

Characteristic of the included studies – Poultry.

https://doi.org/10.1371/journal.pone.0097716.s003

(DOC)

Checklist S1.

PRISMA Checklist for SR and Meta-analysis.

https://doi.org/10.1371/journal.pone.0097716.s004

(DOC)

Protocol S1.

Systematic Review protocol (publicly available in CAMARADES site).

https://doi.org/10.1371/journal.pone.0097716.s005

(DOC)

Acknowledgments

We would like to express our sincere gratitude to all authors who were published their findings in the study topic and for their kind response to provide additional data. We also thank Dr. Sential Rajan, Senior Research Fellow, PSG College of Arts and Science, Coimbatore, India for language corrections and proof reading the manuscript.

Author Contributions

Conceived and designed the experiments: XYZ TD. Performed the experiments: TD XYZ YW RS. Analyzed the data: TD YW XYZ RS AM BZ. Contributed reagents/materials/analysis tools: TD BZ. Wrote the paper: TD XYZ BZ. Contributed for manuscript improvement technically and proof reading as well: RS AM.

References

  1. 1. Turner J, Dritz S, Minton J (2001) Review: Alternatives to conventional antimicrobials in swine diets. The Professional Animal Scientist 17: 217–226.
  2. 2. Cromwell GL (2002) Why and how antibiotics are used in swine production. Animal biotechnology 13: 7–27.
  3. 3. Kovacs-Nolan J, Mine Y (2012) Egg yolk antibodies for passive immunity. Annual Review of Food Science and Technology 3: 163–182.
  4. 4. Xu Y, Li X, Jin L, Zhen Y, Lu Y, et al. (2011) Application of chicken egg yolk immunoglobulins in the control of terrestrial and aquatic animal diseases: a review. Biotechnology advances 29: 860–868.
  5. 5. Moher D, Liberati A, Tetzlaff J, Altman DG (2009) Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Annals of internal medicine 151: 264–269.
  6. 6. Hooijmans C, Ritskes-Hoitinga M (2013) Progress in Using Systematic Reviews of Animal Studies to Improve Translational Research. PLoS medicine 10: e1001482.
  7. 7. Kilkenny C, Browne W, Cuthill IC, Emerson M, Altman DG (2010) Animal research: reporting in vivo experiments: the ARRIVE guidelines. British journal of pharmacology 160: 1577–1579.
  8. 8. Egger M, Smith GD, Altman D (2008) Systematic reviews in health care: meta-analysis in context: BMJ Publishing group.
  9. 9. Hooijmans CR, de Vries RB, Rovers MM, Gooszen HG, Ritskes-Hoitinga M (2012) The Effects of Probiotic Supplementation on Experimental Acute Pancreatitis: A Systematic Review and Meta-Analysis. PloS one 7: e48811.
  10. 10. Vesterinen H, Sena E, Egan K, Hirst T, Churolov L, et al. (2014) Meta-analysis of data from animal studies: A practical guide. Journal of neuroscience methods 221: 92–102.
  11. 11. Egger M, Smith GD, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. British medical journal 315 (7109): 629–634.
  12. 12. MedCalc Statistical Software version 12.7.7 (2013) MedCalc Software bvba, Ostend, Belgium; http://www.medcalc.org.
  13. 13. Yokoyama H, Peralta RC, Diaz R, Sendo S, Ikemori Y, et al. (1992) Passive protective effect of chicken egg yolk immunoglobulins against experimental enterotoxigenic Escherichia coli infection in neonatal piglets. Infect Immun 60: 998–1007.
  14. 14. Kellner J, Erhard MH, Renner M, Losch U (1993) Therapeutischer Einsatz von spezifischen Eiantikörpern bei Saugferkeldurchfall - ein Feldversuch, [A field trial of the treatment of diarrhea in piglets with specific egg antibodies]. Jahrgang (49) January 94: 31–34.
  15. 15. Erhard MH, Bergmann J, Renner M, Hofmann A, Heinritzi K (1996) Prophylaktische Wirkung von spezifischen Dotterantikörpern bei Escherichia coli K88 (F4)-bedingten Durchfallerkrankungen von Absatzferkeln, [Prophylactic effect of specific egg yolk antibodies in diarrhea caused by Escherichia coli K88 (F4) in weaned piglets]. Zentralbl Veterinarmed A 43: 217–223.
  16. 16. Imberechts H, Deprez P, Van Driessche E, Pohl P (1997) Chicken egg yolk antibodies against F18ab fimbriae of Escherichia coli inhibit shedding of F18 positive E. coli by experimentally infected pigs. Vet Microbiol 54: 329–341.
  17. 17. Yokoyama H, Hashi T, Umeda K, Icatlo FC Jr, Kuroki M, et al. (1997) Effect of oral egg antibody in experimental F18+ Escherichia coli infection in weaned pigs. J Vet Med Sci 59: 917–921.
  18. 18. Zuniga A, Yokoyama H, Albicker-Rippinger P, Eggenberger E, Bertschinger HU (1997) Reduced intestinal colonisation with F18-positive enterotoxigenic Escherichia coli in weaned pigs fed chicken egg antibody against the fimbriae. FEMS Immunol Med Microbiol 18: 153–161.
  19. 19. Xiao C, Zhou SL (1998) Study and application of the chicken yolk antibodies against ETEC. Chinese Journal of Veterinary Science and Technology 28: 21–13.
  20. 20. Marquardt RR, Jin LZ, Kim JW, Fang L, Frohlich AA, et al. (1999) Passive protective effect of egg-yolk antibodies against enterotoxigenic Escherichia coli K88+ infection in neonatal and early-weaned piglets. FEMS Immunol Med Microbiol 23: 283–288.
  21. 21. Yang BL, Zhang YF, Wu JM (2002) Research of hyperimmunized yolk antibodies for prevention and treatment of Piglet dysentery. Animal Science & Veterinary Medicine 10: 37–38.
  22. 22. Xu FZ, Wang J, Yang B, Song W, Lai P, et al. (2002) Preparation and application of chicken egg yolk immunoglobulins against enterotoxigenic escherichiacoli in piglets. Acta Agriculturae Boreali-Sinica 17: 108–112.
  23. 23. Owusu-Asiedu A, Baidoot SK, Nyachoti CM, Marquardt RR (2002) Response of early-weaned pigs to spray-dried porcine or animal plasma-based diets supplemented with egg-yolk antibodies against enterotoxigenic Escherichia colil. J Anim Sci 80: 2895–2903.
  24. 24. Owusu-Asiedu A, Nyachoti CM, Marquardt RR (2003) Response of early-weaned pigs to an enterotoxigenic Escherichia coli (K88) challenge when fed diets containing spray-dried porcine plasma or pea protein isolate plus egg yolk antibody, zinc oxide, fumaric acid, or antibiotic. J Anim Sci 81: 1790–1798.
  25. 25. Owusu-Asiedu A, Nyachoti CM, Baidoo SK, Marquardt RR, Yang X (2003) Response of early-weaned pigs to an enterotoxigenic Escherichia coli (K88) challenge when fed diets containing spray-dried porcine plasma or pea protein isolate plus egg yolk antibody. J Anim Sci 81: 1781–1789.
  26. 26. Chernysheva LV, Friendship RM, Dewey CE, Gyles CL (2004) The effect of dietary chicken egg-yolk antibodies on the clinical response in weaned pigs challenged with a K88+ Escherichia coli isolate. Journal of Swine Health and Production 12: 119–121.
  27. 27. Girard F, Batisson I, Martinez G, Breton C, Harel J, et al. (2006) Use of virulence factor-specific egg yolk-derived immunoglobulins as a promising alternative to antibiotics for prevention of attaching and effacing Escherichia coli infections. FEMS Immunol Med Microbiol 46: 340–350.
  28. 28. Chu W-H, GAO G-F (2006) Application of Chicken Egg Yolk Immunoglobulins Against Enterotoxigenic Escherichia coli in Piglets. Chinese Journal of Veterinary Science 26: 616–618.
  29. 29. Li XY, Jin LJ, Uzonna JE, Li SY, Liu JJ, et al. (2009) Chitosan-alginate microcapsules for oral delivery of egg yolk immunoglobulin (IgY): in vivo evaluation in a pig model of enteric colibacillosis. Vet Immunol Immunopathol 129: 132–136.
  30. 30. Sarandan M, Sarandan H, Tirziu E, Pop C (2010) Inhibition of E. coli F4+ adhesion to the piglet's intestinal brush border by specific IgY antibodies. Lucrari stiintifice medicina veterinaria, 2010, xliii 1: 279–284.
  31. 31. Liou J-F, Shiau J-W, Tai C, Chen L-R (2011) Production of egg yolk immunoglobulin against Escherichia coli from White Leghorn and Lohmann chickens. Journal of Animal and Veterinary Advances 10: 2349–2356.
  32. 32. Kweon CH, Kwon BJ, Woo SR, Kim JM, Woo GH, et al. (2000) Immunoprophylactic effect of chicken egg yolk immunoglobulin (Ig Y) against porcine epidemic diarrhea virus (PEDV) in piglets. J Vet Med Sci 62: 961–964.
  33. 33. Song WP XF, Wang JL, Yang B, Lai PA (2003) Effect of IgY Treatment on Porcine Epidemic Diarrhea Virus (PEDV) in Piglets. Acta Agriculturae Boreali-Sinica 18: 114–115.
  34. 34. Zuo Y, Fan J, Fan H, Li T, Zhang X (2009) Prophylactic and therapeutic effects of egg yolk immunoglobulin against porcine transmissible gastroenteritis virus in piglets. Frontiers of Agriculture in China 3: 104–108.
  35. 35. Cui HZ JH, Zhang JL, Zhang H, Qin GX (2012) Study and application of the hyperimmunized yolk antibodies against TGEV and PEDV in piglets China Animal Husbandry & Veterinary Medicine. 39: 173–175.
  36. 36. Vega CG, Bok M, Vlasova AN, Chattha KS, Fernández FM, et al. (2012) IgY antibodies protect against human Rotavirus induced diarrhea in the neonatal gnotobiotic piglet disease model. PloS one 7: e42788.
  37. 37. Peralta R, Yokoyama H, Ikemori Y, Kuroki M, Kodama Y (1994) Passive immunisation against experimental salmonellosis in mice by orally administered hen egg-yolk antibodies specific for 14-kDa fimbriae of Salmonella enteritidis. Journal of medical microbiology 41: 29–35.
  38. 38. Yokoyama H, Umeda K, Peralta RC, Hashi T, Icatlo FC, et al. (1998) Oral passive immunization against experimental salmonellosis in mice using chicken egg yolk antibodies specific for Salmonella enteritidis and S. typhimurium. Vaccine 16: 388–393.
  39. 39. Jacoby HI, Moore G, Wnorowski G (2001) Inhibition of diarrhea by immune egg: a castor oil mouse model. Journal of Nutraceuticals Functional and Medical Foods 3: 47–54.
  40. 40. Wang Q, Hou X-j, Cai K, Li T, Liu Y-n, et al. (2010) Passive protection of purified yolk immunoglobulin administered against Shiga toxin 1 in mouse models. Canadian journal of microbiology 56: 1003–1010.
  41. 41. Hirai K, Arimitsu H, Umeda K, Yokota K, Shen L, et al. (2010) Passive oral immunization by egg yolk immunoglobulin (IgY) to Vibrio cholerae effectively prevents cholera. Acta Med Okayama 64: 163–170.
  42. 42. Neri P, Tokoro S, Kobayashi R, Sugiyama T, Umeda K, et al. (2011) Specific egg yolk immunoglobulin as a new preventive approach for Shiga-toxin-mediated diseases. PloS one 6: e26526.
  43. 43. Parma Y, Chacana P, Rogé A, Kahl A, Cangelosi A, et al. (2011) Antibodies anti-Shiga toxin 2 B subunit from chicken egg yolk: isolation, purification and neutralization efficacy. Toxicon 58: 380–388.
  44. 44. Feng Y, Liu W, Shi D (2013) Effectiveness of Egg Yolk Antibody Against Shiga Toxin II Variant Toxicity In Vitro and In Vivo. Current microbiology: 1–6.
  45. 45. Bartz CR, Conklin RH, Tunstall CB, Steele JH (1980) Prevention of murine rotavirus infection with chicken egg yolk immunoglobulins. Journal of Infectious Diseases 142: 439–441.
  46. 46. Hatta H, Tsuda K, Akachi S, Kim M, Yamamoto T, et al. (1993) Oral passive immunization effect of anti-human rotavirus IgY and its behavior against proteolytic enzymes. Bioscience, biotechnology, and biochemistry 57: 1077.
  47. 47. Kuroki M, Ikemori Y, Yokoyama H, Peralta RC, Icatlo Jr FC, et al. (1993) Passive protection against bovine rotavirus-induced diarrhea in murine model by specific immunoglobulins from chicken egg yolk. Veterinary microbiology 37: 135–146.
  48. 48. Sarker SA, Pant N, Juneja LR, Hammarström L (2007) Successful treatment of rotavirus-induced diarrhoea in suckling mice with egg yolk immunoglobulin. Journal of health, population, and nutrition 25: 465.
  49. 49. Nguyen HH, Tumpey TM, Park H-J, Byun Y-H, Tran LD, et al. (2010) Prophylactic and therapeutic efficacy of avian antibodies against influenza virus H5N1 and H1N1 in mice. PloS one 5: e10152.
  50. 50. Liou J-F, Chang C-W, Tailiu J-J, Yu C-K, Lei H-Y, et al. (2010) Passive protection effect of chicken egg yolk immunoglobulins on enterovirus 71 infected mice. Vaccine 28: 8189–8196.
  51. 51. Buragohain M, Dhale GS, Ghalsasi GR, Chitambar SD (2012) Evaluation of Hyperimmune Hen Egg Yolk Derived Anti-Human Rotavirus Antibodies (Anti-HRVIgY) against Rotavirus Infection. World 2: 73–84.
  52. 52. Tsubokura K, Berndtson E, Bogstedt A, Kaijser B, Kim M, et al. (1997) Oral administration of antibodies as prophylaxis and therapy in Campylobacter jejuni-infected chickens. Clinical & Experimental Immunology 108: 451–455.
  53. 53. Fulton R, Nersessian B, Reed W (2002) Prevention of Salmonella enteritidis infection in commercial ducklings by oral chicken egg-derived antibody alone or in combination with probiotics. Poultry science 81: 34–40.
  54. 54. Gürtler M, Methner U, Kobilke H, Fehlhaber K (2004) Effect of orally administered egg yolk antibodies on Salmonella enteritidis contamination of hen's eggs. Journal of Veterinary Medicine, Series B 51: 129–134.
  55. 55. Kariyawasam S, Wilkie B, Gyles C (2004) Resistance of broiler chickens to<i> Escherichia coli</i> respiratory tract infection induced by passively transferred egg-yolk antibodies. Veterinary microbiology 98: 273–284.
  56. 56. Adriana C (2007) The use of the specific anti-salmonella polyclonal antibodies isolated from hen eggs, in Salmonellosis prophylaxis. Lucrari Stiintifice: Zootehnie si Biotehnologii. 40.
  57. 57. Rahimi S, Shiraz ZM, Salehi TZ, Torshizi MAK, Grimes JL (2007) Prevention of Salmonella infection in poultry by specific egg-derived antibody. International Journal of Poultry Science 6: 230–235.
  58. 58. Chalghoumi R, Marcq C, Théwis A, Portetelle D, Beckers Y (2009) Effects of feed supplementation with specific hen egg yolk antibody (immunoglobin Y) on Salmonella species cecal colonization and growth performances of challenged broiler chickens. Poultry science 88: 2081–2092.
  59. 59. Tamilzarasan K, Dinakaran AM, Selvaraju G, Dorairajan N (2009) Efficacy of egg yolk immunoglobulins (IGY) against enteric pathogens in poultry. Tamilnadu Journal of Veterinary and Animal Sciences 5: 264–268.
  60. 60. Mahdavi A, Rahmani H, Nili N, Samie A, Soleimanian-Zad S, et al. (2010) Effects of dietary egg yolk antibody powder on growth performance, intestinal Escherichia coli colonization, and immunocompetence of challenged broiler chicks. Poultry science 89: 484–494.
  61. 61. Wu GM WZ, Zhang GR, Zhang HJ, Liu J (2013) The preparation of chicken egg yolk immunoglobulins powder Feed additives against Salmonella pullorum. Heilongjiang Animal Science And veterinary Medicine: 140–142.
  62. 62. Muhammad K, Rabbi F, Hussain I, Riaz A, Saeed K, et al. (2001) Passive immunization against Infectious Bursal Disease in chicks. Int J Agric Biol 3: 413–415.
  63. 63. Malik MW, Ayub N, Qureshi IZ (2006) Passive immunization using purified IgYs against infectious bursal disease of chickens in Pakistan. Journal of veterinary science 7: 43–46.
  64. 64. Rahimi S, Salehifar E, Ghorashi SA, Grimes JL, Torshizi MAK (2007) The effect of egg-derived antibody on prevention of avian influenza subtype H9N2 in layer chicken. International Journal of Poultry Science 6: 207–210.
  65. 65. El-Ghany WA (2011) Comparison Between Immunoglobulins IgY and the Vaccine for Prevention of Infectious Bursal Disease in Chickens. Global Veterinaria 6 (1): 16–24.
  66. 66. Farooq A, Rabbani M, Muhammad K, Akram Z, Ahad A, et al. (2012) Passive immunization in infectious bursal disease virus infected birds using chemically purified immune yolk immunoglobulins (IgY). Afr J Microbiol Res 6: 2993–2998.
  67. 67. Özpinar H, Erhard M, Aytug N, Özpinar A, Baklaci C, et al. (1996) Dose-dependent effects of specific egg-yolk antibodies on diarrhea of newborn calves. Preventive Veterinary Medicine 27: 67–73.
  68. 68. Cook S, Bach S, Stevenson S, DeVinney R, Frohlich A, et al. (2005) Orally administered anti-Escherichia coli O157: H7 chicken egg yolk antibodies reduce fecal shedding of the pathogen by ruminants. Canadian journal of animal science 85: 291–299.
  69. 69. Germine SS, Ebied MH, Ibrahim FK, Mettias KN, Daoud AM (2011) Field evaluation of egg yolk antibodies in prevention and treatment of Enteric colibacillosis in calves. Benha veterinary medical journal (special issue I): 108–114.
  70. 70. Kuroki M, Ohta M, Ikemori Y, Peralta R, Yokoyama H, et al. (1994) Passive protection against bovine rotavirus in calves by specific immunoglobulins from chicken egg yolk. Archives of virology 138: 143–148.
  71. 71. Ikemori Y, Ohta M, Umeda K, Icatlo Jr FC, Kuroki M, et al. (1997) Passive protection of neonatal calves against bovine coronavirus-induced diarrhea by administration of egg yolk or colostrum antibody powder. Veterinary microbiology 58: 105–111.
  72. 72. Kuroki M, Ohta M, Ikemori Y, Icatlo Jr F, Kobayashi C, et al. (1997) Field evaluation of chicken egg yolk immunoglobulins specific for bovine rotavirus in neonatal calves. Archives of virology 142: 843–851.
  73. 73. Vega C, Bok M, Chacana P, Saif L, Fernandez F, et al. (2011) Egg yolk IgY: protection against rotavirus induced diarrhea and modulatory effect on the systemic and mucosal antibody responses in newborn calves. Veterinary immunology and immunopathology 142: 156–169.
  74. 74. European Medicines Agency (2013) European Surveillance of Veterinary Antimicrobial Consumption, Sales of veterinary antimicrobial agents in 25 EU/EEA countries in 2011, 613 (EMA/236501/2013).
  75. 75. The Federal Authorities of the Swiss Confederation website. Available: http://www.admin.ch/aktuell/00089/index.html?lang=en&msg-id=50349. Accessed 2013 Oct 11.
  76. 76. Lee C-R, Cho IH, Jeong BC, Lee SH (2013) Strategies to Minimize Antibiotic Resistance. International journal of environmental research and public health 10: 4274–4305.
  77. 77. Lee SH, Lillehoj HS, Park DW, Jang SI, Morales A, et al. (2009) Protective effect of hyperimmune egg yolk IgY antibodies against Eimeria tenella and Eimeria maxima infections. Veterinary parasitology 163(1): 123–126.
  78. 78. Lee SH, Lillehoj HS, Park DW, Jang SI, Morales A, et al.. (2009) Induction of passive immunity in broiler chickens against Eimeria acervulina by hyperimmune egg yolk immunoglobulin Y. Poultry science, 88(3): , 562–566.
  79. 79. Xu JJ, Ren CZ, Wang SS, Liu DD, Cao LQ, et al.. (2013) Protection Efficacy of Multivalent Egg Yolk Immunoglobulin against Eimeria tenella Infection in Chickens. Iranian journal of parasitology, 8(3): , 449.