1. Lethal response of the dengue vectors to the plant extracts from family Anacardiaceae
Ali YOUSAF ; Wan Fatma ZUHARAH ; Wan Fatma ZUHARAH
Asian Pacific Journal of Tropical Biomedicine 2015;5(10):812-818
Objective: To explore the larvicidal activities of different plant parts of Melanochyla fasciculiflora (. M. fasciculiflora), Gluta renghas (. G. renghas), Anacardium occidentale and Mangifera indica from family Anacardiaceae against the laboratory and field strains of dengue vectors Aedes aegypti and Aedes albopictus (. Ae. albopictus). Methods: Leaves and bark parts of study plants were collected from Taman Nageri, Bukit Pancor and Teluk Bahang National Park, Penang, Malaysia. Leaves and stem barks were separated, air dried, ground and extracted with methanol by Soxhlet apparatus. Crude extract was obtained by evaporating the extra solvent in rotary evaporator. The 4th instar larvae from laboratory and field strains were exposed to 50-1. 300 mg/L concentrations according to World Health Organization standard larval bioassay. Larval mortality was recorded after 24 h of exposure. Results: Highest larvicidal activity was exhibited by G. renghas bark extract against Ae. albopictus laboratory strain at 600 mg/L. G. renghas also showed the highest larvicidal activities for other strains as compared to other plant extracts, followed by Mangifera indica and M. fasciculiflora and Anacardium occidentale. Conclusions: Ae. albopictus has been found to be more susceptible as compare to Aedes aegypti in both laboratory and field strains in this study. G. renghas and M. fasciculiflora were tested for the first time and exhibited prompting larvicidal activities against dengue vectors. These results revealed that all the plants especially G. renghas and M. fasciculiflora have the higher larvicidal activities and can be used for the control of dengue vector as a new environment friendly, target specific and low cost phytochemical.
2. Scenario of dengue infection & its control in Pakistan: An up-date and way forward
Muhammad Zubair YOUSAF ; Adeena SIDDIQUE ; Muhammad ALI ; Muhammad Zubair YOUSAF ; Usman Ali ASHFAQ
Asian Pacific Journal of Tropical Medicine 2018;11(1):15-23
Dengue fever is one of the major health problems in tropical and subtropical areas throughout the world. The causative agent of dengue fever is the dengue virus which is an enveloped single stranded RNA virus belongs to the family Flaviviridae and has five distinct serotypes (DENV-1, DENV-2, DENV-3, DENV-4 and DENV-5). Dengue virus is transmitted to human via bite of Aedes aegypti and Aedes albopictus mosquitoes. The clinical symptoms of dengue fever ranging from mild to severe form as dengue hemorrhagic fever and dengue shock syndrome. Pakistan is dengue endemic since 1994 but from 2006, Pakistan faced the worst condition regarding dengue in which thousands of people affected by the disease and hundreds of people lost their lives. DENV-2, DENV-3 and DENV-1 are the prevalent serotypes in Pakistan. Common diagnostic techniques are being used in Pakistan such as enzyme-linked immunosorbent assay, polymerase chain reaction and rapid diagnostic tests, while differential diagnosis, limitations of diagnostic methods and poor health care system are the real challenges in dengue diagnosis. Favorable climatic conditions, unplanned urbanization, travelling etc., are major factors responsible for dengue epidemics in Pakistan. This presentation provides update about dengue circumstances in Pakistan and also describes the way how to improve dengue situation in Pakistan.
3.Molecular detection and characterization of ovine herpesvirus-2 using heminested PCR in Pakistan
Aayesha RIAZ ; Inga DRY ; Robert DALZIEL ; Saif Ur REHMAN ; Muhammad Ali SHAH ; Hafiz Muhammad Naeem AKHTAR ; Arfan YOUSAF ; Ruqia BAIG
Journal of Veterinary Science 2021;22(4):e51-
Background:
Malignant catarrhal fever (MCF) is a highly fatal lymphoproliferative disease of cattle, deer, bison, water buffalo, and pigs caused by the gamma-herpesviruses alcelaphine herpesvirus-1 (AlHV-1) and ovine herpesvirus-2 (OvHV-2).
Objectives:
This study aimed to determine the prevalence of OvHV-2 in sheep, goats, cattle, and buffalo in Rawalpindi and Islamabad, Pakistan, by applying molecular and phylogenetic methods.
Methods:
Blood samples were aspirated from sheep (n = 54), goat (n = 50), cattle (n = 46) and buffalo (n= 50) at a slaughterhouse and several farms. The samples were subjected to heminested polymerase chain reaction (PCR), followed by sequencing and phylogenetic analysis of the OvHV-2 POL gene and the OvHV-2 ORF75 tegument protein gene.
Results:
The highest percentage of MCF positive samples was in sheep (13%), whereas goat, cattle, and buffalo had lower positive percentages, 11%, 9%, and 6.5%, respectively. Four OvHV-2-positive PCR products obtained from sheep samples were sequenced. The sequences obtained were submitted to the NCBI GenBank database (MK852173 for the POL gene;MK840962, MK852171, and MK852172 for the ORF75 tegument protein gene). Phylogenetic analysis revealed a close similarity of study sequences with those of worldwide samples.
Conclusions
This study is the first cross-sectional study on the prevalence and molecular detection of OvHV-2 in apparently healthy cattle and buffalo that could be carrying OvHV-2 acquired from OvHV-2-positive sheep and goats. The results indicate that OvHV-2 is circulating in Pakistan. Further studies are needed to characterize OvHV-2 and elucidate further its prevalence.
4.Molecular detection and characterization of ovine herpesvirus-2 using heminested PCR in Pakistan
Aayesha RIAZ ; Inga DRY ; Robert DALZIEL ; Saif Ur REHMAN ; Muhammad Ali SHAH ; Hafiz Muhammad Naeem AKHTAR ; Arfan YOUSAF ; Ruqia BAIG
Journal of Veterinary Science 2021;22(4):e51-
Background:
Malignant catarrhal fever (MCF) is a highly fatal lymphoproliferative disease of cattle, deer, bison, water buffalo, and pigs caused by the gamma-herpesviruses alcelaphine herpesvirus-1 (AlHV-1) and ovine herpesvirus-2 (OvHV-2).
Objectives:
This study aimed to determine the prevalence of OvHV-2 in sheep, goats, cattle, and buffalo in Rawalpindi and Islamabad, Pakistan, by applying molecular and phylogenetic methods.
Methods:
Blood samples were aspirated from sheep (n = 54), goat (n = 50), cattle (n = 46) and buffalo (n= 50) at a slaughterhouse and several farms. The samples were subjected to heminested polymerase chain reaction (PCR), followed by sequencing and phylogenetic analysis of the OvHV-2 POL gene and the OvHV-2 ORF75 tegument protein gene.
Results:
The highest percentage of MCF positive samples was in sheep (13%), whereas goat, cattle, and buffalo had lower positive percentages, 11%, 9%, and 6.5%, respectively. Four OvHV-2-positive PCR products obtained from sheep samples were sequenced. The sequences obtained were submitted to the NCBI GenBank database (MK852173 for the POL gene;MK840962, MK852171, and MK852172 for the ORF75 tegument protein gene). Phylogenetic analysis revealed a close similarity of study sequences with those of worldwide samples.
Conclusions
This study is the first cross-sectional study on the prevalence and molecular detection of OvHV-2 in apparently healthy cattle and buffalo that could be carrying OvHV-2 acquired from OvHV-2-positive sheep and goats. The results indicate that OvHV-2 is circulating in Pakistan. Further studies are needed to characterize OvHV-2 and elucidate further its prevalence.