Blastocystis sp. is a common intestinal protozoan parasite that colonises humans and various animals, with rodents identified as significant reservoir hosts for zoonotic transmission. This study aimed to investigate the prevalence and subtype distribution of Blastocystis sp. among wild rats in Pulau Pinang, Malaysia, while evaluating the associations with host demographics and geographic factors. A total of 150 rodent faecal samples from 12 sampling sites across Pulau Pinang, Malaysia, were examined using microscopy, DNA extraction, and PCR amplification of the SSU-rRNA gene. The overall prevalence of Blastocystis was 25.3%, with Rattus norvegicus exhibiting the highest infection rate (34.5%), followed by R. rattus (19.4%), and Bandicota bengalensis (16.7%). No infections were reported in B. indica (0.0%). Statistical analysis revealed a significant association between Blastocystis infection and rodent species (c2 = 11.874, df = 3 and p = 0.008), whereas no association was indicated in gender, development stages, and sampling sites. Due to limited funding, sequencing was conducted on ten positive samples that exhibited well-defined bands. Out of ten, three zoonotic subtypes were identified namely, ST1 (allele 4), ST3 (allele 34), and ST4 (allele 94 and 133). The findings of this study emphasise the role of R. norvegicus as the major reservoir host in Pulau Pinang, Malaysia and highlight the zoonotic potential of Blastocystis in urban settings.

Blastocystis is a prevalent infectious agent found in the gastrointestinal tract of humans and animals. While the morphology of Blastocystis has been extensively studied, there is still a lack of comprehensive research on its ultrastructure, especially regarding surface characteristics and their correlation with pathogenic potential. Additionally, the subtyping of Blastocystis does not provide information on the isolate’s pathogenicity. This study aimed to examine the morphology and the cell surface of Blastocystis in avian and non-human primates, including peafowl, pheasant, and lion-headed tamarin. By employing light microscopy and scanning electron microscopy (SEM), this study provides the first evidence of the cellular and surface features of Blastocystis in these animal species. Our findings revealed distinct variations in cell size, shape, and surface morphology among the different host species. Notably, the isolates from peafowl exhibited larger cell sizes compared to the isolates from the pheasant. However, interestingly, both animal species were found to exhibit the same Blastocystis ST6. It was also observed that the surface structure of Blastocystis from different hosts displayed a diverse range of patterns, including mesh-like appearances, deep indentations, and attachments to bacteria. Additionally, findings also revealed the presence of a rough surface structure in peafowl, a characteristic that has been previously linked to pathogenicity and symptomatic infection in animals, as indicated by earlier studies. The findings contribute to our understanding of the morphological features and the surface characteristic of Blastocystis in different host species, shedding light on the parasite’s adaptations and potential implications for host health.

Blastocystis is the most prevalent eukaryotic gastrointestinal symbiont found in humans and animals worldwide. Increased human infection rates are associated with raising concerns about the involvement of the parasite in public health. Over the last decade, the number of linked epidemiology studies has been prudently grown. Microscopy has been used to detect the presence of protozoan and the advent of molecular techniques has made detection easier. However, due to its limited host specificity and zoonotic potential, animals, either livestock or wildlife animals, may serve as a potential reservoir for Blastocystis infection transmission. The approach utilised in this study aided in understanding the distribution and prevalence of Blastocystis in animals, particularly captivated and free-ranging wild animals worldwide due to increased interest. This review will help comprehend the epidemiological aspects, demographic, subtypes, and the zoonotic potential of Blastocystis in wildlife and captive animals.

Blastocystis sp. is a unicellular, anaerobic intestinal protist regularly reported in humans and various animals worldwide. There seems to be little research on Blastocystis infection in poultry in Malaysia, and none on Blastocystis in quail specifically. In Malaysia, the consumption of quail meat and eggs is rapidly gaining popularity as a significant source of protein. It is, therefore, essential to explore the presence of Blastocystis in Malaysian quails in order to aid in the understanding of Blastocystis in this group of birds and their role in its transmission. Intestinal contents were collected from 90 commercial quails raised on two farms in Penang, Malaysia, in a multi-layer cage system with adequate farm management. Detection of Blastocystis sp. was by cultivation in modified Jones’ medium supplemented with 10% horse serum. Giemsa-stained slides made from positive cultures were used for morphological studies whereas Blastocystis subtyping was conducted by using Polymerase Chain Reaction (PCR). A prevalence of 17.8% (16/90) was recorded for Blastocystis sp. in quail in this study. The most common forms detected in the in vitro culture medium were vacuolar and granular forms with cell diameters ranging from 9.09μm to 33.33μm. None of the quail birds screened had any visible gastrointestinal symptoms or signs. All successfully sequenced isolates were identified as Blastocystis sp. ST6, one of the potentially zoonotic subtypes of Blastocystis. This study posits that the quail birds may serve as reservoirs of zoonotic subtypes of Blastocystis. More studies are required to understand the source of Blastocystis infection to poultry under intensive care and the role of poultry animals in the transmission of Blastocystis to humans.

Accurate diagnosis and prompt treatment are highly essential in the management of malaria, which is one of the deadliest infectious diseases worldwide, particularly in tropical and sub-tropical regions including Nigeria. This study was designed to evaluate the efficacy of malaria histidine-rich protein 2-based rapid diagnostic test (RDT) and microscopy in the diagnosis of falciparum malaria in Nigeria. This was a cross-sectional and hospital-based study. The standard method of microscopy was used as the gold standard. Giemsa stained thick and thin smears were prepared to count and detect malaria parasite species. Also, a malaria histidine-rich protein 2-based RDT was used to detect malaria parasites and diagnostic efficacy were determined through the measure of sensitivity, specificity, Positive Predictive Value (PPV), Negative Predictive Value (NPV), diagnostic accuracy and Youden Index (J). The result showed that out of the total 303 individuals examined, a total malaria prevalence of 67.0% and 68.0% were recorded for microscopy and RDT, respectively. Additionally, the sensitivity (95% C.I), specificity (95% C.I), PPV (95% C.I), and NPV (95% C.I) of RDT compared to microscopy were 97.54 (94.36-98.94), 92.00 (85.00-95.89), 96.12 (92.53-98.02), and 94.85 (88.50- 97.78), respectively. The diagnostic accuracy (95% C.I) and Youden Index (J) were 95.71 (92.77- 97.70) and 0.89, respectively. Conclusively, our study revealed that RDT continues to remain efficacious. Thus, while malaria diagnosis by microscopy which is the gold standard remains the major method of malaria detection, it should be complemented by rapid diagnostic test (RDT), particularly in high malaria endemic regions where mean parasite density of patients are usually high.

Malaria which is caused by parasites of the genus Plasmodium is a devastating parasitic disease of major public health challenge worldwide, particularly Nigeria. This study was carried out to investigate the epidemiology of falciparum malaria among residents of rural and peri-urban communities in Ekiti State, Southwestern Nigeria. Standard parasitological technique of microscopy was employed to determine and identify parasite prevalence and species. A questionnaire was used to collect subject’s information such as age, sex, location, occupation and education. Out of the 300 individuals examined, a total of 283 (93.4%) individuals were infected with malaria parasite. Sex pattern of infection indicated that male had higher malaria prevalence of 95.0% compared to female with the prevalence of 93.3% (P>0.05). The age group 51 to 60 years had the highest malaria parasite prevalence of 100% while age group <10 years has the least malaria parasite prevalence of 86.0% (P>0.05). Similarly, a total mean malaria parasite density of 1455.90 parasite/μL of blood was recorded. The mean malaria parasite density does not significantly vary (P>0.05) among age and sex group. The age group >60 years recorded the highest mean parasite density of 2092.50 parasite/μL of blood while age group <10 has the least mean malaria parasite density of 1044. 42 parasite/μL of blood. In relation to sex, the highest mean malaria parasite density was found among the female (1461.80 parasite/μL of blood) compared to male (1450 parasite/ μL of blood). In the same vein, occupation as a socioeconomic risk factor play a major role with respect to malaria infection. The highest malaria prevalence of 113 (98.26%) was recorded among farmers while the least 34 (85%) was recorded among Civil servants (P<0.05). Thus, it is apparent that falciparum malaria is heavily prevalent in this study area and as such urgent management control measures and interventions should be made available and fully utilized.

Most poultry farms in Malaysia preferred rearing chickens either for eggs or/and meat than turkeys. This is due to several challenges such as parasitic load and heat stress in rearing turkey. Blastocystis is one of the most common protozoan parasites infecting poultry. As no study was conducted on Blastocystis infection in turkey in Malaysia, this study aims to determine the current status, the morphological characteristics and subtyping of Blastocystis from turkey reared either in closed house or free-range system in Penang, Malaysia. It was found that the prevalence of Blastocystis sp. infection in turkeys were moderately high with 41.6% (25/60) in the closed house and 45.0% (45/100) in free-range system as infection was higher in the female turkeys with no gastrointestinal signs and symptoms. Vacuolar form was the most common form found in the in vitro culture ranged between 5 to 20 μm in diameter with a rough surface coat and undulating cell surface viewed under the scanning electron microscope. Meanwhile, the ultrastructure of the cells from turkey isolates were varies with partially expanded electron-opaque vacuoles to electron-dense in fully distended vacuoles. Interestingly, sequence analysis for 30 positive Blastocystis isolates from turkeys revealed one subtypes with three alleles namely, ST7 allele 99 (73.4%, n=22), ST7 allele 100 (23.3%, n=7) and ST7 allele 101 (3.3%, n=1). Findings from this study added to our understanding on Blastocystis infection in turkey production.

Indigenous chicken (Gallus domesticus) is reared for both its meat and eggs. Most consumers prefer the meat probably due to its specific texture and taste. The study was conducted to determine the presence of helminth parasites of 240 indigenous chickens (Gallus domesticus) obtained randomly from 12 divisions in Penang Island, Malaysia. Necropsy findings revealed 14 endoparasite species which parasitized these chickens namely, Acuaria hamulosa, Acuaria spiralis, Amoebotaenia sphenoides, Ascaridia galli, Brachylaima sp., Capillaria spp., Gongylonema ingluvicola, Heterakis gallinarum, Hymenolepis sp., Oxyspirura mansoni, Raillietina echinobothrida, Raillietina tetragona, Syngamus trachea and Tetrameres americana. The high abundance of helminth species observed in this study may be attributed to the free-range scavenging production system, where these indigenous chickens were exposed to intermediate or paratenic hosts of helminths which infect poultry. Besides, sustainable methods of helminthic control measure are necessary in order to enhance indigenous chicken production and eventually improve the economy of the rural farmers.

An investigation was undertaken for screening and isolating nematophagous-fungi from the faecal samples of various grazing animals and soils in Malaysia. Total of 111 faeces and 50 soil samples were collected and the samples were cultured on 2% water agar plates. The growth of nematophagous-fungi was stimulated by sprinkling-baiting technique. The conidia of suspected nematophagous-fungi were inoculated on 2% water agar plates. All isolated were maintained on 2% cornmeal agar plates. Verticillium spp., Fusarium spp. and Arthrobotrys spp. were identified from the faecal and soil samples. 62.5% of the faecal samples and 100% of the soil samples were shown to be positive with nematophagous-fungi. This study highlights the present of nematophagous-fungi population in faecal and soil samples. Much study remains to be done to better understanding some fungi especially their mode of action and their predatory behaviour against parasitic nematodes.

Blastocystis infection is widely reported in wildlife, livestocks and in non-human primates however, occurrence in Malaysian wildlife is scarce