Several factors may influence the amount of protein that reaches the colon after feeding, such as the amount of DM ingested and content and digestibility of protein sources included in the diet. Therefore, the use of highly digestible protein sources results in less flow of protein residues in the large intestine and a possible reduction in production of fermentation metabolites and flatulence in dogs( Reference Hand, Thatcher and Remirllard 1 , Reference Nery, Biourge and Tournier 2 ).
Although digestion and absorption of proteins in the small intestine are efficient processes, substantial amounts of undigested proteins are directed to the large intestine( Reference Blachier, Mariotti and Huneau 3 , Reference Boye, Wijesinha-Bettoni and Burlingame 4 ), where the microbial fermentation of these components results in the production of various putrefaction compounds, such as ammonia, phenols, indoles, SCFA, branched-chain fatty acids, gases (H2, CO2 and methane), biogenic amines (putrescine, cadaverine, histamine, phenylethylamine) and lactate. Some of these compounds influence faecal odour and can be toxic if produced in high concentrations( Reference Kuzmuk, Swanson and Tappenden 5 , Reference Nery, Goudez and Biourge 6 ). Moreover, according to Zentek et al.( Reference Zentek, Marquart and Pietrzak 7 ), the ingestion of diets with high concentrations of proteins favours the growth of undesirable bacteria, such as Clostridium perfringens, and decreases the faecal counts of other beneficial bacteria, resulting in imbalance in the intestinal microbiota and consequent increase in excretion of enterotoxins and other metabolic products related to the increase of the protein decomposition in the colon.
Brachycephalic dog breeds such as French bulldogs have been identified as having faeces with a stronger odour and higher frequency of flatulence. Their typical anatomical characteristics result in aerophagia, predisposing to increased gas production. This gas production is associated with a higher presence of non-assimilated substrates, resulting in flatulence and foul-smelling faeces( Reference Roudebush, Davenport, Remillard, Hand, Thatcher, Remirllard, Roudebush and Novotni 8 , Reference Cave, Washabau and Day 9 ). Degradation of undigested proteins in the colon may be responsible for the strong faecal odour in brachycephalic dogs. Therefore, nutritional strategies based on sources and altered concentrations of protein may be important in reducing the impact of fermentative activity in the colon and thus modulate the composition of the intestinal microbiota. Its metabolic activity and the formation of fermentation products are effects that can be important for the reduction of strong faecal odour in brachycephalic dogs. Zentek( Reference Zentek 10 ) reported that dogs fed with higher digestible proteins had lower amounts of protein in the ileal chyme which would allow the decrease in putrefaction in the posterior intestine, and consequently reduction of the compounds involved in the gases and bad faecal odour. Thus, the improvement of protein quality and the use of different protein sources in dog food will decrease the fermentation products and as a consequence the odour of faeces in dogs of the French bulldog breed.
The objective of the present study was to evaluate the effects of inclusion of various protein sources in dry dog diets on the digestibility of nutrients and faecal fermentation products in adult brachycephalic dogs.
Material and methods
The present study was conducted at the Nutrition Development Center of PremieR Pet, Dourado, São Paulo, Brazil, jointly with the Department of Animal Production and Nutrition at the School of Veterinary Medicine and Animal Science of the University of São Paulo, Pirassununga, São Paulo, Brazil. All care procedures were approved by the Ethics Research Committee on Animal Use of PremieR Pet (CEUA PremieR Pet – protocol no. 028-14).
Animals, facilities and experimental design
Eight healthy adult French bulldog dogs (one male and seven female), intact and neutered, mean weight of 11·09 (sd 2·35) kg, mean age of 2·75 (sd 1·98) years and body condition score between 4 and 5 (9-point body condition score by Laflamme( Reference Laflamme 11 )) were used. Health status was confirmed before the beginning of the experiment by physical, blood and coproparasitological examinations. Dogs were previously dewormed and were up to date with vaccinations. The dogs were housed individually in kennels with solarium (11·2 m2). The animals were distributed in replicate 4 × 4 Latin squares, four treatments (diets) and four periods, totalling eight replicates per treatment. The treatments were balanced by the animals’ body weight. Each experimental period lasted 28 d. The animals were adapted to the diet for 20 d; followed by 5 d of faecal collection for apparent digestibility and faecal score; and 3 d of fresh faeces collection to determine the fermentation products.
Diets
Four extruded isonutrient diets were produced to meet the adequate intake of the requirements for the maintenance of adult dogs( 12 ), containing: brewer's rice, beet pulp, cellulose, chicken fat, fish oil, egg powder, brewer's yeast, palatability enhancer, potassium chloride, mineral–vitamin premix, magnesium oxide, salt, dicalcium phosphate, calcium carbonate and antioxidant. The diets presented contained 13 % of protein from different sources (poultry meal (PM); wheat gluten (WG); PM + WG (50 % PM and 50 % WG); PM + WG + liver hydrolysed protein (HP) (PM, WG and HP, with 33·33 % inclusion of each)). The diets’ proximate analyses composition means were approximately: 23 % protein, 16 % fat, 3 % crude fibre, 6 % ash, 7 % moisture, 54 % N-free extract and 3·9 kcal/kg (16·3 kJ/kg). To verify if the extrusion processing conditions were able to cook the starch, the degree of gelatinisation of the starch was determined by the amyloglucosidase method described by Sá et al.( Reference Sá, Vasconcellos and Brunetto 13 )
Food intake and digestibility experiment
The total faecal collection method was used to perform the coefficients of total tract apparent digestibility (CTTAD) assay( 14 ), consisting of an initial phase of 20 d of adaptation to the diet, followed by 5 d of faecal collection. The animals were fed twice per d (07·00 and 16·30 hours) and received water ad libitum. The amount of food offered and refused was recorded at each meal. The amount of food offered was calculated by formula: 130 × body weight0·75 = kcal/d (544 × body weight0·75 = kJ/d), based on the energy requirement prediction equation for maintenance of active adult dogs( 12 ). The food offered was weekly adjusted to keep the animals’ body weight stable.
The faeces were individually collected, weighed and kept in a freezer (−20°C) for further analysis. After the collection period, the faecal samples were thawed, homogenised, and pooled for each animal and period. Faecal samples were dried in a forced-air oven (320SE; Fanem) at 55°C for 72 h. Dried faeces and feed samples were then ground in a cutting mill with a 1 mm screen sieve (MOD 340; ART LAB). The qualitative analysis of the faeces was determined over the stool collection period for digestibility, scoring from 1 (watery stools) to 5 (very hard and resected stools)( Reference Carciofi, Takakura and De-Oliveira 15 ). Based on laboratory results, the CTTAD of DM, crude protein, ether extract in acid hydrolysis, organic matter, N-free extract and gross energy were calculated according to the equation of Pond et al.( Reference Pond, Church and Pond 16 )
Diets and faeces were submitted to DM, crude protein, ether extract in acid hydrolysis, crude fibre and ash analyses according to the Association of Official Analytical Chemists (AOAC)( 17 ). Gross energy was determined in a bomb calorimeter (1281; Parr Instrument Company). All analyses were conducted in duplicate and were repeated when CV was greater than 5 %.
Fermentation metabolites
Fresh faeces were collected up to 30 min after defecation. Faecal pH was determined by digital pH meter (DM-20; Digimed) in a solution of faeces and distilled water (2 g/18 ml)( Reference Walter, Silva and Perdomo 18 ). Lactic acid concentration was measured by spectrophotometry at 565 nm (QUICK-Lab; DRAKE Eletrônica Comércio LTDA)( Reference Pryce 19 ). Faeces were diluted in distilled water (3 g/9 ml).
For SCFA and branched-chain fatty acid determinations, 3 g faeces were diluted in 9 ml of 16 % formic acid, kept in a refrigerator, homogenised daily and centrifuged for 15 min at 15°C and 5000 rpm. This procedure was repeated three times using only the supernatant fraction and stored in a freezer (−15°C). SCFA and branched-chain fatty acids were determined by GC, according to methodology described in the literature( Reference Erwin, Marco and Emery 20 ).
The biogenic amine profile was determined using 0·5 g faeces preserved in 7 ml of 5 % trichloroacetic acid. The samples were then centrifuged and filtered according to Vale & Gloria( Reference Vale and Gloria 21 ). Identification of the amines was performed by HPLC (Shimadzu Corporation).
Ammonia concentration was determined using 3 g faeces acidified with 9 ml of 16 % formic acid. The samples were centrifuged and stored according to the methodology described for SCFA determination. Aliquots of 2 ml were diluted in 13 ml distilled water and distilled in N distillation. The distillation was carried out with 5 ml of 2 m-potassium hydroxide solution and the titration with hydrochloric acid (0·005 mol/l)( Reference Vieira 22 ).
Statistical analysis
The data were analysed considering a duplicate 4 × 4 Latin square design. Treatments were compared by ANOVA and, in case of significant effects, we used Tukey's test for post hoc group comparisons. The analyses were performed by PROC MIXED, using version 9.3 of SAS software( 23 ). The model contemplated the treatment as fixed effect, and the animal and the period as random effects. Statistical significance was set at P < 0·05.
Results
The body weight of the animals did not change during the study. Food intake did not differ between diets (P > 0·05; Table 1). The PM, WG, PM + WG and PM + WG + HP diets presented, respectively, 91·0, 87·4, 98·5 and 77·7 % gelatinisation of starch. Animals fed the PM + WG diet had a greater CTTAD for DM (P < 0·05) and those fed the WG diet for organic matter (P < 0·05). A higher CTTAD for crude protein was observed for the WG and PM + WG diets compared with the PM and PM + WG + HP diets. Feeding the PM + WG + HP diet resulted in lower faecal score and pH compared with other diets. Also faecal volume was smaller with the PM + WG diet compared with the other diets (g faeces/100 g food on a DM basis). However, faecal fermentation metabolites did not differ among diets (Table 2).
Nutrient intake, coefficients of apparent total tract digestibility, metabolisable energy and faecal traits of French bulldogs fed experimental diets with different protein sources
(Mean values and pooled standard errors; n 8 dogs per diet)
PM, poultry meal; WG, wheat gluten; HP, hydrolysed protein.
a,b,c Mean values within a row with unlike superscript letters were significantly different (P < 0·05; Tukey's test).
* To convert kcal to kJ, multiply by 4·184.
Fermentation products: lactic acid, faecal ammonia, SCFA, branched-chain fatty acids (BCFA) and biogenic amines of French bulldogs fed experimental diets with different protein sources
(Mean values and pooled standard errors; n 8 dogs per diet)
PM, poultry meal; WG, wheat gluten; HP, hydrolysed protein.
Discussion
The crude protein CTTAD of the four experimental diets were high (Table 1), indicating good utilisation of the protein sources evaluated in the study. However, higher CTTAD were observed in the diets formulated with higher proportions of WG (WG and PM + WG diets). Stool production was greatest in the PM treatment, having a possible relationship with the low CTTAD of the protein, besides the other nutrients. Nery et al.( Reference Nery, Biourge and Tournier 2 ) evaluated diets formulated with PM and WG, together (WPMP) and separated and in different concentrations (WGLP: inclusion of 22 % dietary protein; WGHP: inclusion of 39 % dietary protein; WPMP: 29 % dietary protein). These authors found higher coefficients of apparent digestibility of protein in WGLP (86·6 %), in WPMP (91·4 %) and WPMP (86·2 %) comparing with only PM (82·2 %) diets. In the present study, the WG-based diet was formulated with 21 % protein content and 13 % of the total protein on a DM basis came from gluten. The results of protein digestibility for the WG (88·08 %) and PM + WG (88·5 %) diets were similar or even better compared with the study cited. Partially, these best results may be related to the quality of the ingredients used in food formulation. However, the lower apparent digestibility coefficients of the PM + WG + HP diet, which were not expected, could be explained by lower starch gelatinisation (77·7 %). The influence of starch gelatinisation on improving protein digestibility has been studied by Loureiro et al.( Reference Loureiro, Roberti and Pacheco 24 )
Some authors( Reference Weber, Hernot and Nguyen 25 , Reference Hernot, Biourge and Martin 26 ) have reported that the ideal faecal score and pH values are expected with higher-quality protein at lower concentrations. This results in a reduction of colonic fermentation similar to that observed in the present study. Faecal scores did not differ among PM, WG and PM + WG treatments, but were similar to previous research with several breeds and sizes of dogs( Reference Nery, Goudez and Biourge 6 ). This previous study found a high water content in the faeces of dogs fed with PM and lower moisture in the faeces of dogs fed diets containing WG. The low-protein fermentation in the present study is probably related to the lower flow of undigested proteins in the large intestine, due to the low protein content in the diets and the high digestibility of the same ones.
The study presented some limitations related to the lack of information in the literature about digestibility in brachycephalic dogs, and the use of WG in pet food as a protein source. These limitations restricted the discussion and references in the study. Also, the inclusion of a non-brachycephalic breed as a control in the study might have demonstrated differences between the breeds in this paper.
Conclusion
The WG used as the sole source of protein or in combination with PM increased protein digestibility. However, this effect was not able to alter the fermentation parameters measured.
Acknowledgements
The first author (M. I. G. U.) acknowledges the scholarship granted by CAPES (Brazilian Federal Agency for Support and Evaluation of Graduate Education).
Grandfood Ind Com LTDA provided the animals, raw materials and facilities used in this study. Grandfood Ind Com LTDA played no role in the study design, sample collection, data analysis and interpretation, and in the decision to submit the manuscript for publication.
M. I. G. U. was responsible for planning the study, conducting the analysis, and writing and editing the manuscript. L. F. O. M. and D. F. S. were responsible for planning the study and manufacturing the diets. M. M., K. M. S. and M. C. E. were responsible for compiling the data and reviewing the manuscript. J. C. C. B. was responsible for data analysis. M. A. B., C. F. F. P. and L. F. A. were responsible for planning the study and composing and reviewing the manuscript.
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