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Avian Parasitology in Captive Psittaciformes: A Study of Ascaridia spp. Infections in Gujranwala, Punjab, Pakistan

PJN_43_1_01-08

Avian Parasitology in Captive Psittaciformes: A Study of Ascaridia spp. Infections in Gujranwala, Punjab, Pakistan

Shahzadi Sarrah Atique and Ishrat Aziz*

Department of Biological Sciences, Virtual University of Pakistan.

Abstract | Infections caused by Ascaridia spp. are commonly referred to as ascaridiosis. In parrots, diarrhea, weight loss, lethargy, intestinal blockage, and respiratory distress are examples of clinical signs of illness. In the present study, the prevalence and detection of Ascaridia spp. infection have been investigated in 110 parrots across nine species housed at the RASSA Bird Aviary and farm in Gujranwala, Punjab, Pakistan. The species examined included the Grey Parrot (Psittacus erithacus) (n=14), Cockatiel (Nymphicus hollandicus) (n=12), Senegal Parrot (Poicephalus senegalus) (n=12), Rump Parrot (Psephotus haematonotus) (n=14), Indian Ringneck Parrot (Psittacula krameri) (n=10), Lovebird (Agapornis spp.) (n=12), Sun Conure (Aratinga solstitialis) (n=10), Alexandrine Parrot (Psittacula eupatria) (n=14), and Australian Budgerigar (Melopsittacus undulatus) (n=12). In total, 45 out of 110 birds tested positive for Ascaridia spp., with a prevalence of 40.9%. Specifically, Ascaridia galli and Ascaridia platyceri were identified as the predominant parasites. The prevalence of Ascaridia galli was highest in Grey Parrots (21.4%), followed by Rump Parrots (21.4%), Alexandrine Parrots (14.3%), Sun Conures (10.0%), Indian Ringneck Parrots (10.0%), and Senegal Parrots (8.3%). No Ascaridia galli infections were detected in Cockatiels, Lovebirds, and Australian Budgerigars. The prevalence of Ascaridia platyceri was highest in Grey Parrots (50.0%), followed by Senegal Parrots (41.7%), Rump Parrots (28.6%), Alexandrine Parrots (28.6%), Sun Conures (30.0%), Cockatiels (25.0%), Lovebirds (25.0%), Australian Budgerigars (25.0%), and Indian Ringneck Parrots (20.0%).Notably, this study represents the first report of Ascaridia platyceri in Pakistan, highlighting its previously undocumented presence in the region. These findings emphasize the significant presence of Ascaridia spp. in captive parrots and highlight the need for effective management strategies to ensure their health and welfare.


Received | October 27, 2024; Accepted | December 02, 2024; Published | February 06, 2025

*Correspondence | Dr. Ishrat Aziz, Department of Biological Sciences, Virtual University Of Pakistan, Kala Shah Kaku Campus, Near Judicial Academy Pakistan; Email: [email protected]

Citation | Atique, S.S. and I. Aziz. 2025. Avian parasitology in captive Psittaciformes: A study of Ascaridia spp. infections in Gujranwala, Punjab, Pakistan. Pakistan Journal of Nematology, 43(1): 01-08.

DOI | https://dx.doi.org/10.17582/journal.pjn/2025/43.1.1.8

Keywords | Ascaridia spp., Psittaciformes, Direct microscopy, Floatation method, Ascaridia galli, Ascaridia platyceri

Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



Introduction

Ascaridia is a large nematode (roundworm) genus in the superfamily Ascaridoidea that parasitizes several different vertebrate hosts, such as birds (Aldamigh et al., 2024). There are a wide variety of species in the genus Ascaridia at least 15 have been recognized so far. Remarkably, five of these species show host selectivity and pathogenicity by favoring parrots (Psittaciformes) as hosts (Soulsby, 1982). Some Ascaridia that are unique to parrots consist of A. platyceri, A. nicobarensis, A. ornata, A. sergiomeirai, and A. hermaphrodita. Parrots can still become infected with different Ascaridia species, though. Parrots are known to harbor A. galli and A. columbae, which are known to prey on gallinaceous and columbiform birds, respectively (Kajerová et al., 2004). According to their morphology, Ascaridia are distinguished by their long, cylindrical bodies that are designed for parasitism in the gastrointestinal system of their hosts (Samour, 2016). Ascaridia spp. eggs have an elliptical form and a strong, thick shell, which helps them withstand harsh environments better (Zajac and Conboy, 2012).

The fascinating order of avian wonders known as Psittaciformes, which includes the majestic macaws and the endearing cockatiels, has a long history of being held in captivity and has developed a bond with humans (Eberhard, 2016). Psittaciformes, the family of birds generally referred to as parrots, includes more than 400 species, such as lorikeets, parakeets, cockatoos, and macaws. According to historical records, parrots were domesticated as pets by several ancient civilizations, such as the Greeks, Romans, and Egyptians (Collar, 1997). According to Pires (2012), the Psittaciformes trade is a significant market in terms of economics. Parrots support plant species dispersal and forest regeneration by eating fruits and excreting seeds in various places (Galetti, 1993).

Psittaciformes are particularly significant in Pakistan and the South Asian area. Native species are found in Pakistan including the three types of parakeets: Plum-headed (Psittacula cyanocephala), Rose-ringed (Psittacula krameri), and Alexandrine (Psittacula eupatria). These species are not only essential to the regional ecosystems but also hold significant cultural importance (Roberts, 1991). According to Bird Life International (2020), native parrots of Southeast Asia include the Red-breasted parakeet (Psittacula alexandri), Blossom-headed parakeet (Psittacula roseata), and Blue-rumped parrot (Psittinus cyanurus). Their high value in the pet trade contributes to the economic benefits of the communities where they are bred and sold (Pires, 2012). Understanding parasite illnesses like as Ascaridia spp. infections is crucial since Psittaciformes health is closely related to their survival and ecological roles (Anderson, 2000). The occurrence of gastrointestinal nematodes, particularly Ascaridia spp., in captive environments poses significant concerns for the welfare and health of our avian companions. An infection of Ascaridia usually results in ascaridiosis. Ascaridia spp. infections affect more than only particular bird species such as chickens, pigeons, doves, and turkeys (Sadaf et al. 2021).

In Psittaciformes, Ascaridia are primarily transmitted through the ingestion of contaminated food or water, as well as through the birds grooming and feather maintenance activities (Soulsby, 1982). Clinical signs of infection in birds might include diarrhea, weight loss, lethargy, and in extreme cases, intestinal obstruction (Samour, 2016). According to Permin and Hansen (1998), a reliable method of diagnosing Ascaridia infections is to use microscopic methods, to look for eggs in fecal flotation. This technique enables early diagnosis and management by detecting infections even in asymptomatic birds (Soulsby, 1982). Fecal flotation technique help to recover parasite eggs, such as Ascaridia spp., from fecal samples (Höglund et al., 2023). Microscopic investigation focuses on these catch to provide a thorough study and confirmation. When combined, these techniques serve as the first diagnosis’ detection, rapidly spotting possible infestations and opening the door to more research. Effective detection methods for these parasite illnesses can lead to improved health management and conservation measures for Psittaciformes (Samour, 2016).

Materials and Methods

Study area

The study took place at the RASSA bird aviary and farm, located in Bakhtay Wala, Gujranwala, Punjab, Pakistan. Fecal samples were gathered from the birds and analysis was conducted at the biology department’s lab located at the Gujranwala campus (VGJW01) of Virtual University of Pakistan.

Study period

The study was conducted over a span of approximately four weeks, from April 18th to May 17th, 2024.

Sample collection

Fecal samples were obtained from a total of 110 parrots representing nine species under the order Psittaciformes. These species included the Alexandrine Parakeet (Psittacula eupatria) mostly blue, white, yellow and spangle in color variation, African Grey Parrot (Psittacus erithacus), Sun Conure (Aratinga solstitialis), Senegal Parrot (Poicephalus senegalus), Plum-headed Parakeet (Psittacula cyanocephala), Australian Budgerigar (Melopsittacus undulatus), Cockatiel (Nymphicus hollandicus), Indian Ringneck Parakeet (Psittacula krameri), Lovebirds (Agapornis spp.) and their variations. To collect the samples, the following steps were undertaken: The parrots were provided with clean food and water to avoid contamination. All parrots were kept in separate caged in pairing. Sticks were used to gather samples from the cage bottoms. Each sample was individually bagged in a polyethylene plastic clear bag labeled with key information of the species and gender of the parrots. Within an hour of collection, the samples were taken to laboratory for examination.

Qualitative analysis of fecal samples

In order to do qualitative analysis on the samples, as mentioned in William (2001), a two-step approach was used. The method was based on direct microscopic examination and a simple fecal flotation technique.

Direct microscopic examination

The material used in direct microscopic examination, include fecal samples, glass slides and coverslips, toothpicks, a compound light microscope.

A 500mg fecal sample was carefully deposited on a clean glass slide with a toothpick. With the help of a toothpick, thoroughly mix the sample after adding one or two drops of water. To prevent air bubbles, a coverslip was carefully placed on top of the preparation. The prepared slide was examined under a microscope at 10x and 40x magnifications for Ascaridia spp. and other parasites.

Simple fecal flotation technique

According to Bowman (2014), simple flotation method was also used alongside direct microscopic examination to detect nematode eggs.

Simple fecal flotation method required Materials i.e., fecal samples, glass slides, coverslips, saturated sodium chloride solution, test tubes with racks, and a microscope.

1g of fecal sample was thoroughly mixed with a 10% sodium chloride solution. A cotton cloth was used to filter the mixture and transfer it to a test tube. More saline solution was poured into the tube to form a convex meniscus at the top. The test tube was covered with a coverslip and left undisturbed in the test tube rack for 15 minutes. After the incubation period, the coverslip was gently removed from the test tube and placed on a fresh, sterilized glass microscope slide. The slide was then observed under the microscope at both 4x and 10x magnifications for the presence of nematode eggs.

Results and Discussion

This study employed qualitative investigation (direct microscopic approach and simple flotation method) to explore the prevalence and identification of Ascaridia spp. infection in 110 Psittaciformes from nine distinct species, as indicated in Table 1. The combined use of direct microscopy and flotation techniques revealed infections caused by Ascaridia species, with the most common being Ascaridia galli and Ascaridia platyceri.

In total, 45 out of 110 birds tested positive for Ascaridia spp with a prevalence of 40.9%. A breakdown of the overall prevalence by species is presented in Table 2.

 

Table 1: Parrot species and gender distribution of examined birds.

Common name

Scientific name

Total birds

Males

Females

Grey parrot

Psittacus erithacus

14

7

7

Cockatiel

Nymphicus hollandicus

12

6

6

Senegal parrot

Poicephalus senegalus

12

6

6

Rump parrot

Psephotus haematonotus

14

7

7

Indian ringneck parrot

Psittacula krameri

10

5

5

Love bird

Agapornis spp.

12

6

6

Sun conure

Aratinga solstitialis

10

5

5

Alexandrine parrot

Psittacula eupatria

14

7

7

Australian Budgerigars

Melopsittacus undulatus

12

6

 

Table 2: Overall prevalence of Ascaridia spp. in parrots examined.

Common name

Total birds

Positive birds

Prevalence (%)

Grey parrot

14

10

71.4

Cockatiel

12

3

25.0

Senegal parrot

12

6

50.0

Rump parrot

14

7

50.0

Indian ringneck parrot

10

3

30.0

Love bird

12

3

25.0

Sun conure

10

4

40.0

Alexandrine parrot

14

6

42.9

Australian Budgerigars

12

3

25.0

Overall

110

45

40.9

 

Table 3: Prevalence of Ascaridia galli.

Species

Total birds

Positive birds

Prevalence (%)

Grey parrot

14

3

21.4

Cockatiel

12

0

0.0

Senegal parrot

12

1

8.3

Rump parrot

14

3

21.4

Indian ringneck parrot

10

1

10.0

Love bird

12

0

0.0

Sun conure

10

1

10.0

Alexandrine parrot

14

2

14.3

Australian Budgerigars

12

0

0.0

Overall

110

11

 

Table 4: Prevalence of Ascaridia platyceri.

Species

Total birds

Positive birds

Prevalence (%)

Grey parrot

14

7

50.0

Cockatiel

12

3

25.0

Senegal parrot

12

5

41.7

Rump parrot

14

4

28.6

Indian ringneck parrot

10

2

20.0

Love bird

12

3

25.0

Sun conure

10

3

30.0

Alexandrine parrot

14

4

28.6

Australian Budgerigars

12

3

25.0

Overall

110

34

30.9

 

The prevalence varied among the species, with Grey Parrots (71.4%) having the highest infection rate, followed by Senegal Parrots (50%) and Rump Parrots (50%). Cockatiels (25%), Indian Ringnecks (30%), Lovebirds (25%), Sun Conures (40%), Alexandrine Parrots (42.9%), and black Australian Budgerigars (25%) showed lower infection rates. The infestation rates of Ascaridia galli are shown in Table 3, and the infestation rates of Ascaridia platyceri are shown in Table 4. The identification of Ascaridia spp. was based on the information provided by Kajerová et al. (2004), which helped identify two Ascaridia species:Ascaridia platyceri (Figures 1, 2) and Ascaridia galli (Figures 3, 4). The identification was made using microscopic examination with 4X and 10X lenses and compared with existing morphological descriptions from previous studies (Kajerová et al., 2004). The ova of Ascaridia galli (Figure 5), identified through fecal flotation, exhibit an ellipsoidal shape with a thick, striated outer shell, facilitating their recognition and differentiation from other parasites.

 

 

 

 

This research investigated the prevalence and detection of infections with Ascaridia spp. in Psittaciformes in captivity within Gujranwala, Punjab, Pakistan. Two Ascaridia species, A. galli and A. platyceri, were identified as the predominant parasites based on morphological characteristics. Some Ascaridia species exhibit a preference for Psittaciformes, but the genus has a broader host range as documented by Aldamigh et al. (2024), Kajerová et al. (2004), with Ascaridia platyceri being one of them, A. gallican also infect Psittaciformes if kept near gallinaceous birds (Galosi et al., 2015). Theprevalence of Ascaridia spp. varied among different Psittaciformes species (Table 2). Grey Parrots showed the highest infection rate (71.4%), followed by Senegal Parrotsand Rump Parrots (50% each). Cockatiels, Indian Ringneck Parrots, Love Birds, Sun Conures, Alexandrine Parrots, and

 

Australian Budgerigars exhibited lower infection ratesranging from 25% to 42.9%. Ascaridia galli infections were notably prevalent in Grey Parrots (21.4%), while Ascaridia platyceri infections were prominent in Grey Parrots (50%) and Senegal Parrots (41.7%). Our findings on the prevalence and identification of Ascaridia spp. infections in Psittaciformes are consistent with prior research confirming the significant presence of Ascaridia spp. in Psittaciformes across various regions conducted in this field. In Pakistan, a study conducted in Gujranwala and Jhang, Punjab, showed a prevalence of 33.93% for Ascaridia species in captive parrots. Another study by Khan et al. (2010) in Lahore Zoo, Punjab, Pakistan, reported 26.14% prevalence of Ascaridia galli in lovebirds, ringneck parrots, cockatiels, Australian Budgerigars, Alexandrine parrots, bluefronted amazons, eclectus parrots, and grey parrots belonging to the order Psittaciformes. In Chattogram, Bangladesh, a study found a prevalence of 9.09% of Ascaridia spp. in cockatiels, budgerigars, cockatoos, macaws, grey parrots, lovebirds, lories, and rosellas belonging to the order Psittaciformes as pet birds (Bayzid et al., 2022). A study from the state of Bagmati, Kathmandu Valley, Nepal, found that in Psittaciformes, the prevalence of Ascaridia species was the highest among the various gastrointestinal parasites identified. This study included captive-bred exotic birds from 16 different species (Chokhal et al., 2023). The Ascaridia species showed a prevalence rate of 23% across all examined samples. This indicates that Ascaridia species are particularly common among parrots and other birds in the Psittaciformes order, making it the most prevalent helminth parasite found in this group. In the Alipore Zoological Garden, India, 176 out of 392 birds tested positive for parasitic infections. Among Psittaciformes (including grey parrots, blue and yellow macaws, red and blue macaws, hill mynas, bare-eyed cockatoos, cockatiels, Greater Sulphur-crested cockatoos, smaller Sulphur-crested cockatoos, Goffin’s cockatoos, Moluccan cockatoos, and citron-crested cockatoos),48 out of 122 birds tested positive for Ascaridia spp., with a prevalence of 23.98%. Ascaridia spp. ova with prevalence 32.9% were found to be the most often observed gastrointestinal parasite infection in caged birds (Mondal and Manna, 2019).

In Chennai, India, the analysis of the 44 Psittaciformes samples was conducted by Prathipa et al. (2013), who found a prevalence of 11.20% for Ascaridia spp. with 5 out of 44 birds testing positive. In Nigeria, 2 out of 18 birds of three species (Senegal Parrot, Grey Parrot, Rose-ringed Parakeet) from the order Psittaciformes tested positive for Ascaridia spp. with a prevalence of 20.0%, indicating the second highest infection rate (Otegbade and Morenikeji, 2013). Research conducted in Italy by Papini et al. (2012) found that 6.8% of pet and zoo birds in the country were infected with Ascaridia spp. In serbia, the prevalence of Ascaridia spp. in zoo birds ranged from 10.25% to 10.78% (Ilić et al., 2018). In the Czech Republic, researchers discovered new cases of the nematode parasite Ascaridia platyceri in parrots. The parasite was discovered in 38 of these birds. Nine of the 15 distinct species of Psittaciform birds that had the parasite were novel hosts for A. platyceri, according to research conducted by Kajerová et al. (2004). Research carried out in northern Brazil by Lima et al. (2016) discovered that 40% of the parrots analyzed had Ascaridia spp. infection. Ascaridia infections have been shown to cause serious, frequently fatal diseases in captive psittacine, resulting in severe damage to the intestines and liver. These results emphasize the significance of effective management and preventative steps to mitigate the negative health effects of these parasites of captive birds (Greiner and Ritchie, 1994; Kajerová et al., 2004). Infections caused by Ascaridia spp., commonly referred to as ascaridiosis. Ascaridia spp. is the largest nematodes found in birds, often reside in small, harmless amounts in their tiny intestines. Even though ascaridiosis is often minor and may not manifest any clinical signs (Höglund et al., 2023). Severe infestations can cause a number of extremely dangerous health problems. Among these are anemia, a severe inflammatory reaction, and maybe even death Fagerholm and Overstreet (2009). Interestingly, none of the birds examined in this study displayed visible signs of Ascaridia spp. infection, even though they carried the parasite. Furthermore, when foraging on contaminated surfaces or substrates in their environment, parrots may inadvertently eat infected eggs, which can contribute to the spread of Ascaridia spp. and Ascaridia spp. infections in parrots can cause symptoms including weight loss, lethargy, and stomach issues. Severe cases may cause intestinal blockage or anemia, two potentially fatal outcomes Respiratory problems might also arise in severe situations. To reduce these risks, it is imperative to implement effective management methods, such as routine screening, hygienic practices, and perhaps preventive therapies depending on data on area prevalence (Greiner and Ritchie, 1994).

Limitations

Acknowledging the limitations of our study is crucial, particularly the dependence on qualitative techniques for parasite identification.

Conclusions and Recommendations

The study conducted at RASSA bird aviary in Gujranwala, Punjab, Pakistan, investigated Ascaridia spp. infections in 110 Psittaciformes across nine species. Using direct microscopic examination and flotation techniques, Ascaridia galli and Ascaridia platyceri were identified as predominant parasites. Overall, 40.9% of birds tested positive, with varying prevalence among species. This study underscores the significant presence of Ascaridia spp. in captive parrots and highlights the importance of effective management strategies to safeguard their health and welfare.

Acknowledgements

I sincerely thank Dr. Ishrat Aziz, my research supervisor at the Virtual University of Pakistan, for her invaluable guidance, support, and encouragement throughout this project. I also extend my gratitude to the owner of RASSA Birds Farm and Aviary for their cooperation and assistance in making the birds and samples accessible, which was essential for the success of this research.

Novelty Statement

In a pioneer revelation, this study documents the first-ever presence of Ascaridia platyceri in Psittaciformes (parrots) in Pakistan, uncovering a striking 40.9% prevalence of Ascaridia spp. such as Ascaridia galli and Ascaridia Platyceri ,highlighting Ascaridia platyceri and Ascaridia galli as a major threat to captive parrot populations. This critical discovery not only fills a vital knowledge gap but also urges aviculturists and veterinarians to rethink preventive measures and protect these vibrant birds from the growing menace of ascaridiosis essential reading for those dedicated to parrot health and conservation!

Author’s Contribution

Shahzadi Sarrah Atique: Designed the study, performed the research, and prepared the manuscript.

Ishrat Aziz: Supervisor, provided guidance throughout the research process.

Conflict of interest

The authors have declared no conflict of interest.

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Pakistan Journal of Zoology

November

Pakistan J. Zool., Vol. 56

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