Shamsul Arfin1, Md Abu Sayeed2, Shaharin Sultana3, Amith Kumar Dash4, Md Liakot Hossen1. 1. Department of Physiology, Biochemistry and Pharmacology, Jhenaidah Government Veterinary College, Jhenaidah, Bangladesh. 2. Department of Medicine and Surgery, Jhenaidah Government Veterinary College, Jhenaidah, Bangladesh. 3. Department of Microbiology and Hygiene, Jhenaidah Government Veterinary College, Jhenaidah, Bangladesh. 4. Department of Animal Science and Nutrition, Jhenaidah Government Veterinary College, Jhenaidah, Bangladesh.
Pigeon farming is gaining popularity in Bangladesh. On the entire population of pigeons raised in our country, one would possibly guess, by assessing the amount of pigeons and squabs sold-out in virtually each live bird market, that pigeons contribute considerably to the poultry meat sector within the country [1]. Unfortunately, there is scantly revealed data on the population of pigeons and their common diseases in our country. There may be some printed data on the management sides and breeds of pigeons found in Bangladesh; however, epidemiologic studies relating to the prevalence of different diseases of pigeons within the context of parasitological aspect are incredibly vital to grasp the present state of affairs.Several health issues will have an effect on pigeons; however, parasitic infections will play an important role. The role of pigeons in the transmission of disease to other pigeons, domestic animal, and poultry and especially to human has been well documented by many authors [2,3].Among parasites, protozoa Trichomonas gallinae inhabiting the digestive tract of pigeons are responsible for considerable economic loss [3]. The infected pigeon shows signs of dullness, depression, and diarrhea, characterized by yellow pasty stools [4]. Mortality in naturally infected untreated cases may be high allowing very high morbidity rate that makes this problem more [3].Among protozoa, T. gallinae causes Avian Trichomonasis and affects upper digestive and respiratory tract. Pigeons and doves of the family Columbidae are the most common hosts of the flagellate protozoan T. gallinae, with prevalence up to 100% [5]. The protozoan has been reported in a number of other avian orders worldwide [6,7] such as turkey, chicken, eagles, falcons, and bustards may also be infected [3] In fact, Avian Trichomonasis caused by T. gallinae is a disease of young [3] pigeons, which may result in a high mortality in young pigeons [3,8] within 10 days. A high latent infection rate (up to 90%) has also been reported in [9]. Experimental studies reveal marked difference in pathogenicity and virulence among different strains of T. gallinae [5]. Although the parasite is spread directly, via shared nourishing or from parent to huddling (crop milk) but indirectly via water or food [10] is also possible. Signs of trichomonasis include yellowish caseous lesions and or necrotic ulcerations in the upper digestive and respiratory tracts, a foul cheesy smell originating from the gaze, and sniffing of parts of the head such as the eyes or nose [7].Trichomonas gallinae is an important one infecting pigeons concerning morbidity and mortality rate as well as economic loss in most countries of the world [3,5]. In Bangladesh, the same scenario is also suspected in pigeon but no such type of significant study has been done yet.If the common diseases of pigeons are controlled, their production may be well enhanced. For management and interference of Pigeon’s illness, the primary scientific approach ought to be the entity of the disease and pathologies related to them. Therefore, this study has conducted to estimate the prevalence of T. gallinae infection in pigeons and to determine the spatial factors related with T. gallinae infection in pigeons.
Materials and Methods
Study site
Cross-sectional study for a period of 4 months starting from November 24, 2017 to February 28, 2018 in Abhaynagar and Monirumpur Upazillas under Jessore District has been conducted. The study location has been visualized in the map (Fig. 1).
Figure 1.
Map locating the study site.
Sampling strategy
Twelve smallholder farms from 20 (having at least 15 pigeons) were randomly recruited for this study in which ten farms were located in Abhaynagar upazilla (seven in urban area & three in rural area) and other two located at Monirumpur Upazilla (rural area). Randomly selected five pigeons (minimum with two squabs, one adult male and one adult female) from each farm were evaluated for T. gallinae infection from each farm. Again, the number of birds died during the study period in the sampled farms was also evaluated for this study. According to this, the total sampled pigeons were 60.The study treated a squab up to 6 weeks of age and an adult from 1.5 months to above. The baseline information including farm size and disease history for the pigeons of the study farms were collected through pretested Questionnaire.
Sample collection from live bird
Swab samples from oropharynx and crop were collected following the sample collection procedure described in [2]. Briefly, a sterile cotton swab was bungled up and absorbed into refined water. After the removal of the spare liquid, the swab was inserted in a swirling motion into the oropharynx as well as the crop of each bird. After that, fluid hold in the cotton of swab sticks was pressed on the slide. The slides were identified using a unique identification number maintaining a serial of the sampled farm. Separate swab sticks followed by separate slide were used for oropharyngeal and crop swab samples collected from each bird. After slide preparation, the sample containing slides were transported to the subsequent Upazilla Veterinary Hospital using a cool box for laboratory evaluation.
Sample evaluation
The swab samples were tested by wet mount technique and examined under light microscope for the organism T. gallinae maintaining standard procedure described in [2,11]. Trichomonas gallinae were identified under the field of light microscope at 400× magnification as motile, flagellated protozoa [11].
Evaluation of dead bird
Postmortem was performed for dead pigeons as described in [12]. In brief, the general body condition of the dead bird was examined and observed whether any exudation from the natural opening was present or not. Then, the bird was placed on its right aspect with the head pointed toward the examiner. The head was opened and also the blunt, a part of the scissors, was inserted into oral fissure to chop and open. This method was continuing down the neck to open the esophagus and crop, oral cavity, and pharynx for the identification of the inflammation caused by T. gallinae.Again, the swabs samples were collected from oropharynx and crops, and the microscopic slide was produced. The slide was evaluated under light microscope for the identification of T. gallinae considering their characteristics including elongated ellipsoid shape, presence of an obvious undulating membrane associated with four free anterior flagella and showed rolling jerky movement.
Statistical analysis
Obtained data were recorded into Microsoft Excel spreadsheet. The data were cleaned and forwarded to STATA 13.2 for descriptive statistics.
Results and Discussion
The overall prevalence of T. gallinae was 57.4% in which 70% among squabs followed by 50% among male pigeons and 46.7% among female pigeons. This findings notify that squabs are mostly susceptible, which may be due to the chance of being infected from their parents through shared feed and water where those are naturally occurred [11,13] (Table 1).
Table 1.
Frequency of T. gallinae in live pigeons of the study.
Type of Pigeon
Frequency
Percentage
95% CI
Squabs (n = 20)
14
70
45.7–88.1
Adult male (n = 12)
6
50
21.1–78.9
Adult female (n = 15)
7
46.7
21.3–73.4
Total (n = 47)
27
57.4
42.2–71.7
Among dead pigeons (N = 13), the prevalence of T. gallinae was 69.2% in which 87.5% of squabs similarly 50% and 33.3% of adult male and female, respectively. These findings are in line with [7,14] who revealed that T. gallinae infection as being a primary reason of death in squab similarly [3,7,13] reported that T. gallinae can cause up to 90% loss among young pigeons. This study identified the prevalence among adult bird is a bit lower than the study conducted in [5] and [13] but a bit higher than the study conducted in [7]. Again, some other studies conducted in [3] and [4] reported 90% prevalence of T. gallinae among dead young pigeons. These studies suggested that a substantial amount of infection is persisting among the pigeon population, which may cause death at a high rate among both juvenile and young adults (Table 2).
Table 2.
Frequency of T. gallinae in dead pigeons.
Type of Pigeon
Frequency
Percentage
95% CI
Squabs (n = 8)
7
87.5
47.3–99.7
Adult male (n = 2)
1
50
1.3–98.7
Adult female (n = 3)
1
33.3
0.08–90.6
Total (n = 13)
9
69.2
38.6–90.9
The overall prevalence (N = 60) of T. gallinae infection was 60% (95% CI: 46.5–72.4) in which squab, adult male, and adult female level prevalence were 75% (95% CI: 55.1–89.3), 50% (95% CI: 23.0–76.9), and 44.4% (95% CI: 21.5–69.2), respectively.There was no significant difference in the occurrence of T. gallinae between live and dead squab, which is in line with the study conducted in [15]. Again, there was no any significant association of T. gallinae infection between live and dead male as well as live and dead female. These similar findings have been reported by many study conducted in [16] female in this observation. [7,13,17] found that an overall scenario of 60% pigeons was positive to T. gallinae infection. [7,11,13] observed that the prevalence of T. gallinae in adult pigeons was 76% [3] and found no significance difference in the prevalence of T. gallinae between male (77.7%) and female (79.5%). Similarly, [2,7,11,13] also did not find any substantial variance in the prevalence of T. gallinae between male and female (Table 3).The overall prevalence of T. gallinae in rural area (64%) was insignificantly higher than the estimated prevalence 57.1% in urban area of Jessore district. These findings are different than the study conducted in [5] who revealed higher prevalence of T. gallinae in urban pigeons rather than rural area pigeons. This dissimilarity may be due to the difference in small sample size and atmosphere of the study areas. Again, the prevalence of T. gallinae was inconsequentially higher at Abhaynagar upazilla in contrast to Monirampur upazilla (30%) of Jessore district. The study has been conducted for a very limited period with small sample size. Therefore, further study with a well-structured sample size is recommended.
Table 3.
Univariate association between live and dead pigeon according to different age group and spatial factors.
Type
Category (n)
Positive (%)
Negative
p-value
Squab (n = 28)
Live (20)
14 (70)
6
0.6
Dead (8)
7 (87.5)
1
Adult male
Live (12)
6 (50)
6
1.0
Dead (2)
1 (50)
1
Adult female
Live (15)
7 (46.7)
8
1.0
Dead (3)
1 (33.3)
2
Sex
Male (14)
7 (50)
7
1.0
Female (18)
8 (44.4)
10
Industrialization
Urban (35)
20 (57.1)
15
0.8
Rural (25)
16 (64)
9
Administrative division
Abhaynagar (50)
33 (66)
17
0.07
Monirampur (10)
3 (30)
7
Conclusion
The study revealed that Trichomonasis is a major threat to pigeons. Squabs were found more susceptible to the infection than adults. The cause of the death of most squabs might be due to T. gallinae infection. The comparative study in between urban and rural area expressed that the pigeons of rural areas were more susceptible to T. gallinae than the urban area.
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