Abstract The trend towards tunnel farming and hydroponic systems is increasing owing to the climatic changes as well as the need to increase crop yield. Hydroponic is a technique of growing plants without soil. Tunnel farming and hydroponic system requires controlled environmental parameters like temperature, humidity and soil moisture for better production of crops. This paper presents an effective method, named, ACHPA (Automatically Controlled Hydro-Ponic Agriculture) scheme that monitor and controls environmental parameters using sensors and controller. ACHPA provides better environmental control over traditional manual monitoring and controlling, thus yield high-quality crops. Sensor based monitoring and control system regulates the temperature and humidity of the tunnel to yield better. For the sake of saving water, an efficient method of drip irrigation is implemented which delivers water directly to the plants rather than being sprayed on as in conventional farming method. The proposed system here is tested for controlled environment and observations recorded for crop analysis purpose. This makes an effective solution to growing highly efficient, good quality and disease free crop production.

Plasmodium vivax and Plasmodium falciparum are becoming resistant to drugs including antifolates, sulphonamides and chloroquine. This study was focused at sequence analysis of resistant genes of these parasites against sulphadoxine-pyrimethamine and chloroquine, from Bannu, Pakistan. Known mutations were detected at codons 57, 58 and 117 of pvdhfr gene of P. vivax, while none of the isolates had any pvdhps mutation. Similarly P. falciparum isolates exhibited double 59R + 108N mutations in pfdhfr, and single 437G in pfdhps thus demonstrating the existance of triple mutant 59R + 108N + 437G haplotype in this region. The key chloroquine resistance mutation, 76T in pfcrt was observed in 100% of the P. falciparum isolates, with haplotype SVMNT which is also associated with resistance to amodiaquine. Some novel mutations were also observed in pvdhfr and pfdhfr genes.

Background: The Bemisia tabaci is one of the most devastating pests of agricultural crops and ornamental plants worldwide. The genetic diversity and biotype status of the Bemisia tabaci in Pakistan was assessed by using random amplified polymorphic DNA-polymerase chain reaction (RAPD-PCR). A total 80 samples of B. tabaci collected from 14 districts of the Punjab province and 7 districts of the Sindh province were included. Results: All 10 primers screened in this study generated 151 scorable amplification products, of which 117 or 77% were polymorphic. Pairwise Nei and Li’s similarity had ranged from 0.25 to 0.88 among all individuals analyzed. Based on Nei and Li’s similarity coefficients Bemisia populations were grouped into 3 main clusters and clearly distinguished the non B biotype from the B biotype. Conclusion: The level of similarity among populations of same biotypes was high whereas between populations of non B and B biotypes appeared to be less closely related. This analysis showed that non B biotype is prevalent in both provinces however B biotype is restricted to few locations in Sindh. This monitoring of the spread of B. tabaci in Pakistan will assist in the establishment of appropriate management strategies.

O gene da proteína A foi usado como marcador genético para a caracterização de isolados de Staphylococcus aureus resistentes à meticilina (SAMR). De um total de 130 isolados de Staphylococcus aureus, 90 foram identificados como SAMR e 81 destes puderam se caracterizar por tipificação spa. Todos estes isolados foram obtidos de cinco Hospitais Nacionais da Comunidade. Utilizaram-se dois jogos diferentes de cevadores para amplificar a região-X do gene da proteína A nas cepas de SAMRUn conjunto de cevadores, spa-F/spa-R tem identificado três tipos de repetições diferentes, a saber, 7 repetições (spa 2), 8 repetições (spa 3) e 10 repetições (spa 4) e outro conjunto de cevadores, spa-1113F/spa-1514R tem identificado 4 tipos de repetições diferentes, a saber, 6 repetições (spa 1), 15 repetições (spa 6), e 17 repetições (spa 7) e 19 repetições (spa 8). Foi identificada a repetição 11 (spa 5) com ambos os conjuntos de cevadores. Os tipos de SAMR esporádicos que tinham as repetições 6, 7, 10, 17 e 19 foram pouco prevalecentes enquanto que os SAMR epidêmicos com 8, 11, e 15 repetições foram mais prevalecentes e são considerados envolvidos na transmissão entre os pacientes dentro dos diferentes hospitais. Este trabalho conclui que a técnica spa é o suficientemente eficiente como para diferenciar as cepas epidêmicas, esporádicas e aquelas que se transformam lentamente de esporádicas em epidêmicas.

Protein A gene was used as a genetic marker for the characterization of Pakistani methicillin resistant Staphylococcus aureus (MRSA) isolates. Out of a total of 130 Staphylococcus aureus isolates, 90 were identified as MRSA and of these 90 MRSA, 81 MRSA isolates were characterized by spa typing. All of these isolates were collected from five National Community Hospitals. Two different sets of primers were used to amplify the X-region of Protein A gene in MRSA strains. One set of primers i.e, spa-F/spa-R identified three types of different repeats viz., 7 repeats (spa 2), 8 repeats (spa 3) and 10 repeats (spa 4) and another set of primers i.e. spa-1113F/spa-1514R identified 4 types of different repeats viz., 6 repeats (spa 1), 15 repeats (spa 6), and 17 repeats (spa 7) and 19 repeats (spa 8). Repeat 11 (spa 5) was identified with both sets of primers. Sporadic MRSA types carrying 6, 7, 10, 17 and 19 repeats were less prevalent, while the epidemic MRSA with 8, 11 and 15 repeats were more prevalent and considered to be involved in transmission among the patients within different hospitals. Research work concludes that spa technique is efficient enough to differentiate spa strains carrying variations in general and those slowly transforming from sporadic to epidemic outbreak in particular.

El gen de la proteína A se usó como marcador genético para la caracterización de aislados de Staphylococcus aureus resistentes a la meticilina (SAMR). De un total de 130 aislados de Staphylococcus aureus, 90 fueron identificados como SAMR y 81 de éstos se pudieron caracterizar por tipificación spa. Todos estos aislados fueron obtenidos de cinco Hospitales Nacionales de la Comunidad. Se utilizaron dos juegos diferentes de cebadores para amplificar la región-X del gen de la proteína A en las cepas de SAMR. Un conjunto de cebadores, spa-F/spa-R ha identificado tres tipos de repeticiones diferentes, a saber, 7 repeticiones (spa 2), 8 repeticiones (spa 3) y 10 repeticiones (spa 4) y otro conjunto de cebadores, spa-1113F/spa-1514R ha identificado 4 tipos de repeticiones diferentes, a saber, 6 repeticiones (spa 1), 15 repeticiones (spa 6), y 17 repeticiones (spa 7) y 19 repeticiones (spa 8). Se identificó la repetición 11 (spa 5) con ambos conjuntos de cebadores. Los tipos de SAMR esporádicos que portaban las repeticiones 6, 7, 10, 17 y 19 fueron poco prevalentes mientras que los SAMR epidémicos con 8, 11, y 15 repeticiones fueron más prevalentes y se los consideró involucrados en la transmisión entre los pacientes dentro de los diferentes hospitales. Este trabajo concluye que la técnica spa es lo suficientemente eficiente como para diferenciar las cepas epidémicas, esporádicas y aquéllas que se transforman lentamente de esporádicas a epidémicas.

Malaria is one of the serious diseases threatening human health in Pakistan and contributes to a large proportion of the total malaria deaths in South Asia. However, little is known about the nature and extent of genetic diversity of the malarial parasites circulating in Pakistan. This study was designed to assess the infection status of Plasmodium and the genetic diversity of Plasmodium vivax and Plasmodium falciparum by analyzing msp-3α, msp-3β and msp-1, msp-2 genes respectively using allele specific nested PCR and RFLP assays. For this purpose, 130 field isolates were collected from the individuals who exhibited clinical symptoms associated with malaria in the Kohat region of Khyber Pakhtoonkhwa (KPK), Pakistan. Among 130 blood samples collected, P. vivax was detected in 105/130 (80.8%) and P. falciparum in 21/130 (16.2%). Mixed infections with both parasites were detected in 4/130 (3%) of the isolates. A large number of distinguishable alleles were found for msp genetic markers: 10 alleles for msp-3α and seven for msp-3β with one mixed infection in case of msp-3β. The genotyping of P. falciparum showed that K1+MAD20 mixed genotype was dominant in msp-1 and FC27 in msp-2. The results collectively suggest that P. vivax and P. falciparum populations in this region are highly polymorphic and mixed infections are prevalent.

Genetic diversity underlies the improvement of crops by plant breeding. Land races of rice (Oryza sativa L.) can contain some valuable alleles not common in modern germplasm. The aim here was to measure genetic diversity and its effect on agronomic traits among rice land-race genotypes grown in Pakistan. Diversity was measured using thirty-five microsatellite markers and seventy-five genotypes. Among the markers used a total of 142 alleles were detected at 32 polymorphic SSR loci, while three loci were monomorphic in Pakistani rice landraces. The number of alleles identified by each marker ranged from 2 to 13 with a mean of 4.4. Size differences between the smallest and largest alleles varied from 11bp to 71bp. Polymorphism information content ranged from 0.124 to 0.836, with an average of 0.569. At nine microsatellite loci, basmati-type landraces amplified more different alleles than those in the coarse-type. DNA markers RM70 and RM72 divided the rice landraces on the basis of days to flowering. A dendrogram based on total microsatellite polymorphism grouped 75 genotypes into four major clusters at 0.40 similarity coefficient, differentiating tall, late maturing and slender aromatic types from the short, early and bold non-aromatic ones. It inferred that Pakistani landraces have diverse genetic bases and can be utilized in future breeding programs. The DNA markers developed will assist in genotype identification, purity testing and plant variety protection.