Testis development and gonadotropin secretion in broiler breeder males.

One-day-old chicks were used to evaluate testis development and concentrations of luteinizing hormone, follicle-stimulating hormone (FSH), and testosterone during ontogenesis. Males on a conventional breeder program (control) were reared on a 15L:9D photoperiod and ad libitum food and water intake for 2 wk. On the third week, males were placed on a restricted diet and the photoperiod was reduced to 8L:16D. Males on a pedigree breeder program (broilerized) were reared on a 23L:1D photoperiod and unrestricted food and water intake for 6 wk. At 7 wk, males were placed on a restricted diet and the photoperiod was reduced to 8L:16D. On wk 18, both treatment groups were photostimulated (16L:8D) until the end of the experiment (50 wk). After photostimulation, there was an exponential increase in testis weight (TW), FSH, and testosterone concentrations. At 28 wk, TW from broilerized males were significantly heavier than those from control birds, and concentrations of luteinizing hormone, FSH, and testosterone were maximal at that time. After 28 wk, there was a significant decrease in FSH and testosterone concentrations that were associated with reduced TW. No correlation was observed between BW and TW. However, TW was highly correlated with FSH concentrations and daily sperm production. Our data suggest that management and photoperiod had a profound effect on testicular function that was associated with FSH concentrations in male broiler breeders.

Active immunization against ghrelin decreases weight gain and alters plasma concentrations of growth hormone in growing pigs.

Ghrelin has been implicated in the control of food intake and in the long-term regulation of body weight. We theorize that preventing the ability of ghrelin to interact with its receptors, would eventually lead to decreased appetite and thereby decrease body weight gain. To test our hypothesis, pigs were actively immunized against ghrelin. Ghrelin((1-10)) was conjugated to BSA and emulsified in Freund's incomplete adjuvant and diethylaminoethyl-dextran. Primary immunization was given at 19 weeks of age (WOA), with booster immunizations given 20 and 40 days after primary immunization. Body weight (BW) and plasma samples were collected weekly beginning at 19 WOA, and feed intake was measured daily. Fourteen days after primary immunization, the percentage of bound (125)I-ghrelin in plasma from immunized pigs was increased compared with control animals (P<0.001). Voluntary feed intake was decreased more than 15% in animals that were actively immunized against ghrelin compared with controls. By the end of the experiment, immunized pigs weighed 10% less than control animals (P<0.1). Concentrations of GH were increased (P<0.05) in immunized pigs. Apoptosis was not observed in post-mortem samples obtained from the fundic region of the stomach. Our observations suggest that immunization against ghrelin induces mild anorexia. This procedure could potentially be used as a treatment to control caloric intake and obesity.

An inexpensive, simple protocol for DNA isolation from blood for high-throughput genotyping by polymerase chain reaction or restriction endonuclease digestion.

We describe simple, inexpensive, and reliable methods for isolating DNA from avian blood, semen, or feather pulp. The procedures are readily applicable to high-throughput 96-well plate isolation for genotype analysis of chicken DNA based on restriction endonuclease digestion or PCR. Isolation cost is primarily the cost of a deep-well assay block and a few pipet tips; current price is less than 0.10 dollar per sample, providing a significant cost advantage over commercial kits. The procedure employs inexpensive, nonhazardous reagents and yields intact, double-stranded DNA from as little as 2 to 10 microL of avian blood, suitable for RFLP analysis or hundreds of PCR amplifications. We compared our method to published procedures for alkaline extraction from feather pulp and found our method to be more reliable with the advantage of isolating intact DNA sequences that can be easily quantified. With minor modifications, the method can isolate DNA for PCR genotyping from mammalian whole blood.

Immunization of pigs against chicken gonadotropin-releasing hormone-II and lamprey gonadotropin-releasing hormone-III: effects on gonadotropin secretion and testicular function.

The objective of this experiment was to evaluate the effects of active immunization against 2 GnRH isoforms on gonadotropin secretion and testicular function in pigs. Synthetic chicken (c) GnRH-II and lamprey (l) GnRH-III peptides, with the common pGlu-His-Trp-Ser sequence at the N-terminal omitted, were conjugated to BSA. Forty-eight male piglets were randomly assigned to 1 of 4 treatments. Pigs on treatment 1 were actively immunized against cGnRH-II, whereas pigs on treatment 2 were actively immunized against lGnRH-III. Control pigs on treatment 3 were actively immunized against the carrier protein (BSA), and pigs on treatment 4 were castrated and actively immunized against BSA. The BSA conjugate was emulsified in Freund's Incomplete Adjuvant and diethylaminoethyldextran. Primary immunization was given at 13 wk of age (WOA) with booster immunizations given at 16 and 19 WOA. Body weight and plasma samples were collected weekly beginning at 11 WOA. Treatments did not affect BW during the experimental period. Antibody titers were increased in animals immunized against cGnRH-II and lGnRH-III (P < 0.001). Cross-reactivity of the antibodies to mammalian GnRH or between cGnRH-II and lGnRH-III was minimal. Concentrations of testosterone were maximal in control boars (treatment 3) and minimal in control barrows (treatment 4) and immunized pigs (treatment x week; P < 0.01). Immunized animals had concentrations of LH (P < 0.001) and FSH (treatment x week; P < 0.03) that were less than control barrows and similar to control boars. At the end of the experiment, intact (noncastrated) pigs were exsanguinated. Testes were removed immediately; Leydig cells were isolated and treated with 0, 1, or 10 ng/mL of LH. There was an LH x GnRH treatment effect on testosterone concentrations (P < 0.03), indicating that Leydig cells were sensitive to the immunization protocol and doses of LH. Taken together, these data suggest that immunization against GnRH isoforms decreased gonadotropin secretion compared with control barrows. Additionally, immunization against cGnRH-II and lGnRH-III reduced the ability of Leydig cells to respond to LH challenges.

An expressed sequence tag analysis of the chicken reproductive tract transcriptome.

Analysis of the chicken reproductive tract transcriptome is important in comparative biology for analysis of reproductive tract development and evolution. In addition, molecular analysis of the reproductive tract is important for identification of genes affecting fertility in the poultry industry. We sampled the chicken reproductive tract (ovary, oviduct, and testis) transcriptome, generating 5,328 expressed sequence tags that assembled into 4,518 contigs. We identified 475 contigs with no match in the current expressed sequence tag databases or in GenBank. The novel contigs included 31 with no match to the current assembly of the chicken genome, 119 representing spliced transcripts, and 309 that were unspliced. More detailed molecular characterization of the 428 novel contigs present in the assembly will be important to gene discovery and annotation of the chicken and other vertebrate genomes.

Sperm mobility: phenotype in roosters (Gallus domesticus) determined by mitochondrial function.

Previously, inheritance of sperm mobility entailed a maternal additive genetic effect, and sperm ATP content was correlated (r = 0.80) with phenotype. The present study was conducted to determine if mitochondrial function was critical to phenotypic expression. Whereas phenotype was independent of mitochondrial helix length, phenotype was correlated with sperm oxygen consumption (r = 0.83) using random-bred roosters. Aberrant mitochondria characterized immobile sperm, as evidenced by transmission-electron microscopy. Such mitochondria were swollen and contained disorganized cristae. Additional experiments were performed with roosters from lines selected for low or high sperm mobility. A threefold difference in sperm oxygen consumption was observed between lines. Single nucleotide polymorphisms were observed in mitochondrial DNA by sequencing replicate mitochondrial genomes from each line. An A-to-G substitution in the gene encoding tRNA(Arg) was inherited consistently, as evidenced by restriction fragment length polymorphism analysis using two male and two female progeny per family group and 14 family groups per line. Motile concentration in semen from low-line males was half that observed in semen from high-line males, as evidenced by computer-assisted sperm motion analysis. Likewise, 47% of sperm from low-line males contained aberrant mitochondria, compared to 4% for high-line males. In summary, sperm mobility phenotype was dependent on mitochondrial function, which in turn was altered by genetic selection. Fowl deferent duct fluid contains a high concentration of glutamate. We propose that variation in sperm mobility phenotype stems from the extent to which glutamate induces excessive mitochondrial Ca2+ uptake before ejaculation.

Effect of strain, feed allocation program, and age at photostimulation on reproductive development and carcass characteristics of broiler breeder hens.

A study was conducted with broiler breeder pullets to investigate the effects of strain, age at photostimulation (PS), and release from feed restriction at PS on age, BW, ovarian morphology, and carcass characteristics at sexual maturity (point of initiation of lay). Sixty birds of each of 4 strains were used. The 4 types represented a classic strain (A), 2 high-yield strains (B, C), and a roaster strain (D). Photostimulation (8L:16D to 14L:10D) was applied at 2 different ages (21 and 24 wk) to 30 birds of each strain type. Within each of the PS periods, 15 birds of each strain were fed ad libitum (F), and the remaining 15 were feed-restricted (R) following a common feeding schedule. On the day that each bird had its first oviposition, its feed was withdrawn. It was euthanized the following morning by cervical dislocation and organs were collected. Of the 3 main effects, feeding program had the greatest effect on all the parameters measured. Within the 21-wk PS treatment group, R birds reached onset of sexual maturity later than F birds (50.2+/-1.64 vs. 36.6+/-1.01 d, respectively). There were no differences in the age at sexual maturity between R and F birds for the 24-wk PS treatment (28.9+/-0.95 vs. 26.9+/-0.85 for R and F, respectively). These results suggest that by 24 wk, all strains had reached a threshold BW and responded uniformly to PS regardless of feeding program. Feed restriction reduced the number of large yellow follicles (LYF) (diameter >10 mm) (8.43+/-0.23 vs. 9.65+/-0.33 for R and F birds, respectively). Follicle number was not different between birds photostimulated at 21 or 24 wk (9.6+/-0.33 vs. 8.45+/-0.23, respectively). Feed restriction affects sexual development that can be modulated by the PS program.

Field testing the influence of sperm competition based on sperm mobility in breeder turkey toms.

1. Commercial reproduction of turkeys relies on pooling of semen from multiple males for inseminations. Understanding how sperm characteristics influence paternity under commercial breeding conditions is important to improving production efficiency. 2. The objective of this study was to evaluate progeny production of individual toms following commercial practices of pooling semen to determine if sperm mobility influences progeny production in field conditions. 3. A total of 104 toms were evaluated for sperm mobility. A subset of 10 toms were housed together and semen was collected, pooled and used to inseminate hens (n = 28). Hens were inseminated at 30 weeks of age and weekly thereafter. 4. Ejaculates from each tom were evaluated on two separate days for sperm mobility. Semen from each tom was diluted and layered upon 6% (wt/vol) Accudenz solution. The sperm suspension was incubated at 41 degrees C for 5 min and absorbance was measured with a spectrophotometer. 5. Toms were ranked by absorbance and categorised as high or low if mobility score was +/- 1 SD from the flock mean (average). 6. For parentage determination, DNA was extracted from tom, hen and poult blood. Poult parentage (n = 276) was determined at one day of age or at 14 weeks by analysis of marker genotypes that were generated by polymerase chain reaction (PCR) amplification of genomic DNA with selected microsatellite markers. 7. Sperm mobility differed across males with absorbance values ranging from 0.147 to 0.366. 8. Findings demonstrate differences in poult production among individual toms when semen from multiple males was pooled and inseminated. Toms classified as high, average and low produced 55, 41 and 4% of the offspring, respectively. 9. It appears that sperm mobility is a trait that influences sperm competition among toms under field conditions where sperm numbers inseminated from individual toms are not controlled or constant and that toms with low sperm mobility produce few offspring.

Use of ultrasonography to characterize ovarian status in chicken.

Much research has been conducted to investigate the effects of environmental and nutritional treatments on ovarian development in poultry. However, to investigate the ovary, the hen must be killed, and thus, lifelong egg production can only be inferred. To date, the ability to noninvasively determine ovarian status has not been available. Improvements in ultrasound technology now make it possible to observe ovarian condition in vivo, thereby allowing for repeated sampling of the same bird over an entire egg production cycle. In the current study, large yellow follicles (LYF; diameter greater than 10 mm) were characterized in broiler breeder hens using Aloka ultrasound diagnostic equipment. Ultrasound images were used to determine the number and diameter of the LYF as well as the presence of an egg in the oviduct. Immediately following ultrasonography, hens were killed and dissected to determine the number and diameter of LYF. From the ultrasound images, the number of LYF +/- 1 was predicted with 96.3% accuracy in Experiment 1 and 93.3% accuracy in Experiment 2. Diameter measurements were used to classify follicles hierarchically. Of the birds determined via dissection to have multiple hierarchies, 77.8% were identified with ultrasound. All regressing or regressed ovaries were correctly identified with ultrasound.

Identification of epididymal stones in diverse rooster populations.

The epididymal region of the male reproductive tract is essential for sperm maturation, and dysfunction of this region results in infertility. Adult roosters have been observed to develop epididymal stones and consequently have reduced fertility. Efferent ductule cysts were first observed in White Leghorn roosters ages 18 to 26 wk. By 26 wk of age, the cysts had become solid, irregularly shaped, yellow-green stones primarily containing calcium (48%). The number and size of stones (9 to 160 microm, largest diameter) increased with age in affected males. Incidence ranged from 0 to 94% within rooster flocks surveyed. Stones have also been observed in broiler breeder roosters. Histological analysis of Leghorn and broiler breeder reproductive tracts revealed chronic inflammation with abundant interstitial mononuclear cell infiltrates. The normal, highly folded structure of efferent ductules was replaced by a thin, eroded epithelial layer with few luminal sperm. Abnormal areas were found interspersed with normal areas of epithelium. Broiler breeder male fertility trials demonstrated that birds with stones compared with normal males had reduced fertility following both natural mating (24.8+/-10.5% vs. 66.1+/-7.2%) and artificial insemination (47.8+/-16% vs. 82.0+/-6%). At 62 wk of age, testis weight (14.2+/-1.4 g vs. 20.5+/-1.2 g), daily sperm production (8.1+/-1.3 x 10(8) vs. 12.3+/-0.8 x 10(8) sperm per testis per day), and circulating testosterone concentrations (0.9+/-0.3 vs. 2.6+/-0.4 ng/mL) were all significantly reduced in males with stones. In conclusion, we are reporting a new dysfunction of the rooster reproductive tract that affects diverse bird populations and decreases fertility.

Circadian rhythm of the preovulatory surge of luteinizing hormone and its relationships to rhythms of body temperature and locomotor activity in turkey hens.

Simultaneous measurements of plasma LH, body temperature, and locomotor activity were made in laying turkey hens and are reported. Blood samples were remotely collected using a jugular cannula system, and body temperature and locomotor activity were remotely monitored using a radiotelemetry system in freely moving laying turkeys. Under a photoschedule of 14L:10D, the period for preovulatory surges of LH was 25.7 +/- 0.4 h while the periods for peak body temperature and onset of sustained locomotor activity were 24.9 +/- 0.4 and 25.7 +/- 0.5 h, respectively. During exposure to constant light, the periods for preovulatory surges of LH, peak body temperature, and onset of sustained locomotor activity increased to 27.9 +/- 0.9, 26.7 +/- 0.7, and 27.4 +/- 0.7 h, respectively. With the 14L:10D photoschedule, initiation of LH surges was restricted to the scotophase, but after 8 days of constant light, initiation of LH surges had dispersed throughout the 24-h subjective day and night. With constant light, the amplitude of the peak body temperature rhythm decreased, while the duration of the locomotor activity rhythm became broadened and, in some birds, disorganized. Peak body temperature and onset of locomotor activity rhythms and LH surges did not coincide, even though peak body temperature, onset of locomotor activity, and LH surges had similar periods. It is concluded that 1) the photoschedule influences the periods of the LH surge, peak body temperature, and onset of locomotor activity; and 2) a specific or direct relationship between the rhythms of LH surge, body temperature, and locomotor activity remains to be determined in laying turkey hens.

Efficacy of sperm mobility assessment in commercial flocks and the relationships of sperm mobility and insemination dose with fertility in turkeys.

Our objectives were to evaluate: 1) the efficacy of the Sperm Mobility Test on commercial turkey farms, and 2) the influence of sperm mobility phenotype on fertility when insemination parameters are varied. In research flocks, differences in sperm mobility among toms are predictive of fertility. We wanted to test the efficacy of this sire selection test in practical, real-world situations, evaluating its usefulness in terms of assessing large numbers of toms, different strains of turkeys, and variable management practices. Utilizing field study results, controlled studies were then conducted to improve test parameters. For the field trials, semen from each of 405 breeder toms (11 strains or lines) was evaluated either in duplicate (n = 285) or in triplicate (n = 120). Sperm mobility was normally distributed among all toms tested, except for one strain. Because the sperm mobility indices for toms evaluated in these field trials were higher than those observed in research flocks, the Sperm Mobility Test was modified to increase the separation between high and low sperm mobility phenotypes by increasing the concentration of Accudenz. To determine the effects of sperm mobility and insemination dose on sustained fertility through time, hens from a research flock were inseminated twice before the onset of lay with sperm from toms classified as high-, average-, or low-mobility in concentrations of 25 to 400 million sperm per artificial insemination dose, and egg fertility was evaluated over a 5-wk period. Toms with the high-mobility sperm phenotype maintained higher fertility (P < 0.05) over the 5-wk period at all insemination doses compared with toms with low-mobility sperm. Toms with high-mobility sperm sired equal numbers of poults in a sperm competition study in which numbers favored low-mobility toms by 3:1. These results demonstrate that the Sperm Mobility Test can be used for on-farm evaluation of semen quality of toms in commercial flocks and that sperm mobility influences fertility and sire fitness.

Sperm mobility: A primary determinant of fertility in the domestic fowl (Gallus domesticus).

Previous research demonstrated that sperm mobility is a quantitative trait of the domestic fowl. The trait is quantified by measuring the absorbance of an Accudenz solution after overlay with a sperm suspension and brief incubation at body temperature. In the present work, average and high sperm mobility phenotypes (n = 30 males per phenotype) were selected from a base population. Differences were found between sperm oxygen consumption (p < 0.0001), acylcarnitine content (p < 0.05), linear velocity (p < 0.001), and straightness (p < 0.001), a trajectory variable measured with the Hobson SpermTracker. Oxygen consumption and stearoylcarnitine content of sperm from the high-mobility phenotype were twice those observed with sperm from average males, implying a pivotal role for mitochondria. On the basis of these results, a graded relationship was predicted between fertility and sperm mobility. Males (n = 48) were chosen at random from another base population, sperm mobility was measured per male, and each ejaculate was used to inseminate 8-12 hens (8 x 10(7) viable sperm per hen). When fertility was plotted as a function of sperm mobility, data points approximated a skewed logistic function. The hypothesis that vaginal immunoglobulins constitute an immunological barrier to sperm transport was tested and rejected. Therefore, we concluded that sperm mobility is a primary determinant of fertility in the fowl.

Effects of transient treatment with 6-N-propyl-2-thiouracil on testis development and function in breeder turkeys.

Experiments were conducted to address recent reports of precocial testis development or testicular hypertrophy induced by the anti-thyroid agent 6-N-propyl-2-thiouracil (PTU) in domestic fowl and rodents. In three experiments, PTU was administered to male turkeys during different stages of development. The PTU was given in the feed at a concentration of either 0.1 or 0.5% and effects on thyroid hormones were measured. Periods of PTU treatment were 8 to 16 or 10 to 18 wk of age (Experiment 1); 0 to 8, 0 to 16, and 8 to 16 wk of age (Experiment 2); and 8 to 16 and 20 to 35 wk of age (Experiment 3). Data were collected to determine the effect of PTU treatment on testicular growth (weight), sexual maturation (semen onset and plasma testosterone concentrations), and early adult testicular function in terms of semen quantity (semen volume and sperm concentration) and quality (sperm viability and fertilizing ability). The 0.1% PTU treatment at 8 to 16 wk of age in Experiment 1 resulted in greater testis weights and sperm production than those of untreated controls at 24 wk of age. The difference was absent by 36 wk of age. Likewise, in Experiment 2, onset of semen production was advanced by about 2 wk by the 8 to 16 wk treatment as compared to untreated controls (23.3 vs 25.9 wk), although, at 32 and 36 wk of age neither the quantity nor quality of semen were significantly affected. Also in Experiment 2, 0.1% PTU treatment from 0 to 8 or 0 to 16 wk of age delayed the onset of semen production and depressed semen volumes at 32 and 36 wk of age without affecting semen quality. In Experiment 3, the mean age at the onset of semen was not significantly affected by 0.5% PTU treatment from 8 to 16 or 20 to 35 wk of age. In addition, semen volume and quality at 32 and 36 wk of age was similar to controls. It was concluded that antithyroid treatment with PTU was dependent on dose and time of treatment for effects on both sexual development and early reproductive performance. Precocial development and associated hypertrophy of the testes occurred but was transient. Thereafter, during initial reproductive function, semen quantity and quality were normal.

Electrocardiographic evaluation of broilers following unilateral occlusion of an extrapulmonary primary bronchus.

This study was conducted to provide a comprehensive evaluation of both the amplitudes and durations of the Lead II electrocardiogram (ECG) in nonascitic and ascitic broilers. At 14 d of age, male and female broiler chicks were sham-operated (SHAM, n = 27), or pulmonary hypertension was initiated by occluding one extrapulmonary primary bronchus (BRONCHUS CLAMP, n = 57). Lead II ECG and BW were recorded on Days 28 (ECG1) and 42 (ECG2), necropsies were conducted on all birds dying after Day 28, and final necropsies were conducted on Day 49. Data collected at necropsy included the presence (ASCITIC) or absence (NONASCITIC) of ascites, sex, and ventricular weights for calculating the right:total ventricular weight ratio (RV:TV), which serves as a reliable index of pulmonary hypertension. In each bird, three consecutive ECG1 and ECG2 wave cycles were quantified for both amplitude and duration of the following wave segments: Rb-R, R-S, S-R', R'-R'b, and S-T. The S wave amplitude was calculated by subtracting R-S from Rb-R and heart rate (HR) was measured from the peak of one T wave to the peak of the next. In the majority of comparisons, ASCITIC and BRONCHUS CLAMP broilers had larger S, R'-R'b, and S-T amplitudes, longer R-S, R'-R'b, and S-T durations, and a slower HR than NONASCITIC and SHAM broilers, regardless of sex. The differences in ECG wave forms and durations between ASCITIC and NONASCITIC broilers were greater on Day 42 (ECG2) than on Day 28 (ECG1), but when both ECG were used to develop a regression equation to estimate RV:TV, the R2 was 0.79. The most important Lead II ECG parameters associated with the development of ascites were an increasingly negative S wave amplitude and greater amplitudes and durations for R'-R'b and S-T as well as a decrease in the HR.

Electrocardiographic and genetic evaluation of giant jungle fowl, broilers, and their reciprocal crosses following unilateral bronchus occlusion.

Electrocardiography is useful as a noninvasive technique for detecting right ventricular hypertrophy in birds developing pulmonary hypertension (PH) and pulmonary hypertension syndrome (PHS, ascites). The objective of this study was to identify every aspect of the Lead II ECG wave form (amplitude or duration) that can be correlated with right ventricular hypertrophy [increased right:total ventricular weight ratios (RV:TV)] indicative of PH across a broad genetic background. Sham operations were conducted, or PH was induced by occluding one extrapulmonary primary bronchus in 14-d-old chicks produced from matings of broilers (B x B), Giant Jungle Fowl (J x J), and their reciprocal crosses (B x J and J x B). Standard three-lead electrocardiograms (ECG) were recorded on Days 28 and 42, and final necropsies were conducted to evaluate the incidence of ascites, confirm sex, and obtain ventricular weights for calculating RV:TV. Ascites did not develop in the J x J, and one each of the B x J and J x B chicks developed ascites; consequently, only data from birds that did not develop ascites were compared. Heart rate was recorded, and the following amplitudes and durations were measured or calculated for three consecutive wave cycles of the Lead II ECG: base of R to the peak of R (RbR), peak of R to base of S (RS), base of S to peak of R' (SR'), S, peak of R' to base of R' (R'R'b), and base of S to peak of T (ST). Differences between the ECG of sham and bronchus clamp groups were more prominent in B x B and B x J than in J x B, and bronchus occlusion did not affect the ECG, growth, or RV:TV ratios of J x J. In contrast, sex influences were more prominent in J x J and J x B than in B x J and B x B. These observations suggest a paternal pattern of inheritance for Lead II ECG wave forms, with crosses sired by broilers (B x B, B x J) exhibiting susceptibility to PH and few ECG differences related to sex, whereas crosses sired by Giant Jungle Fowl U x J, J x B) exhibited resistance to PH and numerous ECG differences related to sex.

Evaluation of the duration of sperm fertilizing ability in five lines of commercial broiler breeder and Delaware cross males.

The ability to characterize the reproductive potential of male fowl can be affected by a number of factors, including age, type, insemination scheme, and number of sperm inseminated. Fertility is a complex interaction of traits involving two individuals of differing genetic composition: In modern broiler breeders, selected predominantly for growth and carcass characteristics, fertility problems may be exacerbated. In order to evaluate the male components of fertility, an experiment investigating the effects of male line on both average fertility and the duration of fertility was completed. Male chicks from five commercial broiler breeder male lines or sired by subfertile Delaware cross roosters were reared to adulthood. Between 30 and 60 wk of age, semen was collected from five males per line, extended and used to inseminate each of 10 to 12 hens from four broiler breeder female lines or Single Comb White Leghorn hens with 80 x 10(6) live sperm. Following a single insemination eggs were collected for 21 d and fertility determined by visual inspection following 4 d incubation. The percentages of live sperm and overall fertility data for the replicate trials were analyzed, following transformation, with a linear model and daily fertility data were analyzed by iterative least squares regression. Whereas there were large differences in fertility among individual males (durations from 3.4 to 14.5 d) within a line, there were no significant male line or replicate effects on overall fertility or the duration of fertility. However, there was a significant (P < 0.05) line-dependent reduction in the percentage of live sperm in broiler breeder males, with the subfertile Delaware cross males being intermediate. There were no significant female line or replicate effects on the duration of fertility; however, there were significant female line effects on overall fertility at both 7 and 21 d. These data suggest that although individual males varied widely, there were no male line effects on the duration of fertility in the lines of broiler breeders evaluated when analyzed by iterative least squares. Furthermore, these data suggest that although females may have significant affects on overall fertility, the duration of fertility appears to be a predominantly male characteristic. Therefore, iterative least squares regression may be a useful tool for identifying males with superior sperm fertilizing ability.