Soil-transmitted helminth infections constitute a global affliction affecting people and livestock, resulting in a significant disease burden and economic losses in endemic regions. However, control has not been entirely successful and the problem is compounded by the development of resistance to available chemotherapy. Novel alternative compounds are urgently needed, encouraging the screening of largely plant-based sources for anthelmintic effects. Date palm fruit (Phoenix dactylifera) is a popular and nutritious food much coveted for its nutraceutical effect. There are convincing reports documenting the antibacterial, antiviral and antifungal effects of date palm fruit but evidence for any potential anthelmintic effect remains unclear. Here we conducted a systematic review of the published information through an electronic search using six scientific databases; SCOPUS, MEDLINE COMPLETE, OVID, EMBASE, WEB OF SCIENCE and CINAHL COMPLETE. Out of 58 studies that were initially identified only 2 manuscripts fitted our inclusion criteria. The first article reported on the anthelmintic effect of date palm fruit against the rodent nematodes Trichuris muris and Angiostrongylus cantonensis in vitro and in vivo while the second article was based only on in vivo assessment (with coconut) of the effect on the rodent cestode Hymenolepis microstoma. Our review revealed limited anecdotal reports of the anthelmintic effect of date palm fruit against parasitic helminths, however, the majority of reports were inconclusive due to mixed results, limited focus on date palm fruit and lack of any statistical analyses. Rigorous, systematic and fully controlled studies focusing on date palm fruit are needed to validate the anecdotal evidence.

Purpose: To evaluate the activity of the ethanol leaf extract of Piper sarmentosum against toxoplasmosis. Methods: An in vitro anti-Toxoplasma study was conducted using Vero cells as a host for T. gondii. Clindamycin used as the reference drug. Light microscopy technique was used to study the in situ antiparasitic activity of T. gondii. Non-toxic concentrations of the ethanol extract for Vero cells were determined by methyl thiazolyl tetrazolium (MTT) cell proliferation. The presence of Toxoplasma gondii was observed by Giemsa staining. Results: The results showed that significant (p < 0.05) anti-toxoplasma activity of the ethanol extract, though lower than that of clindamycin (control drug), was achieved, with half-maximal inhibitory concentration (IC50) of 12.4 and 7.2 mu g/mL for the extract and reference drug, respectively. After 24 hours of exposure to the extract, the inoculated Vero cells showed lower parasitemia and no remarkable morphological changes. Conclusion: The findings demonstrate that the ethanol extract of P. sarmentosum leaves are active against toxoplasmosis in vitro. However, further studies are required to determine the therapeutic significance of these findings in vivo.

In endemic areas of intestinal parasitic infections, prevalence of Blastocystis sp in animals has not been clearly elucidated. This is the first study of the distribution of Blastocystis sp subtypes in animals reared by Orang Ash population in Pahang, Malaysia during a wet and dry season. Fecal samples of dogs, chickens, goats, ducks, swans, birds and cows were collected and subjected to PCR amplification and sequencing of Blastocystis small subunit rDNA. Of 127 fecal samples collected during the wet season, 9% were positive for Blastocystis sp, with Blastocystis sp ST3 being predominant (16%) followed by ST1 (4%), ST7 (3%), ST4 (2%), ST10 (2%), ST6 (1%), and ST9 (1%). Of 146 fecal samples collected during the dry season 37% were positive, with Blastocystis sp ST3 being predominant (10%) followed by ST1 (8%), ST7 (6%), ST4 (5%), ST8 (3%), ST2 (1%), ST6 (1%), ST9 (1%), and ST10 (1%). High prevalence of Blastocystis sp was observed in dogs and chickens which carried a diverse range of subtypes especially during the dry season. Dogs and chickens might comprise a part of the transmission dynamics of the infection in the population. Health education related to awareness of hygienic practice and disposal of animals waste should be regularly provided and monitored to prevent the transmission of Blastocystis sp infection in this population.

In the tropics, there are too few studies on isolation of Biastocystis sp. subtypes from water sources; in addition, there is also an absence of reported studies on the occurrence of Blastocystis sp. subtYPes In water during different seasons. Therefore, this stud)/ was aimed to determine the occurrence of Blastocystis sp. subtypes in river water and other water sources that drained aboriginal vicinity of highly endemic intestinal parasitic infections during wet and dry seasons. Water samples were collected from six sampling Points of Sungai Krau (K1-K6) and a Point at Sungai Lompat (K7) and ()the: water sources around the aboriginal villages. The water samples were collected during both seasons, wet and dry seasons. Filtration of the water samples were carried out using a flatbed membrane filtration system. The extracted DNA from concentrated water sediment was subjected to single round polymerase chain reaction and positive PCR products were subjected to sequencing. All samples were also subjected to filtration and cultured on membrane lactose glucuronide agar for the detection of faecal coliforms. During wet season, Blastocystis sp. ST1, ST2 and ST3 were detected in river water samples. Blastocystis sp. ST3 occurrence was sustained in the river water samples during dry season. However Blastocystis sp. ST1 and ST2 were absent during dry season. Water samples collected from various water sources showed contaminations of Blastocystis sp. ST1, ST2, ST3 and ST4, during wet season and Blastocystis sp. ST1, ST3, ST8 and ST10 during dry season. Water collected from all river sampling points during both seasons showed growth of Escherichia coli and Enterobacter aerogenes, indicating faecal contamination. In this study, Blastocystis sp. ST3 is suggested as the most resistant subtype able to survive in any adverse environmental condition. robust and Restriction and control of human and animal faecal contaminations to the river and other water

Acanthamoeba species are ubiquitous free-living protozoa that can be found worldwide. Occasionally, it can become parasitic and the causative agent of acanthamoebic keratitis (AK) and Granulomatous Amoebic Encephalitis (GAE) in man. A total of 160 environmental samples and 225 naturally-infected animal corneal swabs were collected for Acanthamoeba cultivation. Acanthamoeba was found to be high in samples collected from environments (85%, 136/160) compared to infected animal corneas (24.89%, 56/225) by microscopic examination. Analysis of nucleotide sequence of 18S rRNA gene of all the 192 cultivable Acanthamoeba isolates revealed 4 genotypes (T3, T4. T5 and T15) with T4 as the most prevalent (69.27%, 133/192) followed by T5 (20.31%), T15 (9.90%) and T3 (0.52%). Genotype T4 was from the strain of A. castellanii U07401 (44.27%), A. castellanii U07409 (20.83%) and A. polyphagaAY026243 (4.17%), but interestingly, only A. castellanii U07401 was detected in naturally infected corneal samples. In environmental samples, T4 was commonly detected in all samples including dry soil, dust, wet debris, wet soil and water. Among the T4, A. castellanii (U07409) strains were detected high occurrence in dry (45%) followed by aquatic (32.50%) and moist (22.50%) samples but however A. castellanii (U07401) strains were dominant in dry samples of soil and dust (93.10%). Subsequently, genotype T5 of A. lenticulata (U94741) strains were dominant in samples collected from aquatic environments (58.97%). In summary, A. castellanii (U07401) strains were found dominant in both environmental and corneal swab samples. Therefore, these strains are possibly the most virulent and dry soil or dusts are the most possible source of Acanthamoeba infection in cats and dogs corneas.

Many modern-day diagnostic tests for parasitic diseases rely on conventional labour-intensive technologies such as serology and microscopy. Although major advances have been recorded in the diagnosis of infectious diseases in humans, parasitic diseases continue to present challenges, particularly in resource-poor countries, and this is mainly attributable to war and famine. Factors such as poverty, deteriorated health facilities and destruction of infrastructure are the consequence of the lack of suitable sanitary practices and proper hygiene, especially in refugee camps, that adversely promote infectious diseases to migrants, particularly among vulnerable children. Generally, the gastrointestinal tract is the predilection site for most helminths and protozoa. They are therefore regarded as a serious public-health problem, as they cause malabsorption, malnutrition and blood loss, leading to anaemia or even death. In addition to their health effects, parasitic infections cause physical and mental impairment in children, retard their educational achievements and hinder economic development.