مولانا محمد جلیل کیرانوی
افسوس ہے کہ گزشتہ ماہ اگست میں حضرت شیخ الہندؒ کے دومنتسبین،مولانا محمد جلیل کیرانوی استاذ اورمولانا محمد مبارک علی نائب مہتمم دارالعلوم دیوبند واصل بحق ہوکر اس جہانِ فانی کوالوداع کہہ گئے۔اناﷲ وانا الیہ راجعون۔ اوّل الذکر (المتولد۱۳۱۸ھ)نے اگرچہ دورۂ حدیث حضرت الاستاذ مولانا محمد انورشاہ کے عہد میں تمام کیا تھا لیکن درحقیقت پروردہ تھے حضرت شیخ الہند کے گھرانے کے ہی۔ نوبرس کی عمر تھی کہ اُن کے والد حضرت ؒ کے سپردکرگئے تھے۔یہ اس آستانۂ قدس کوایسے چمٹے کہ مرتے دم تک اسے نہ چھوڑا۔اس لیے حضرت شیخ الہند کے خادم خاص اور شریکِ جلوت وخلوت تھے اس بناء پر حضرت شیخ الہند کی مشہور’’ریشمی خطوط‘‘والی تحریک کے جزوکل سے خوب واقف اوراس کے محرمِ اسرار تھے۔اس سلسلہ میں انھوں نے بڑے بڑے مصائب اورشدائد برداشت کئے لیکن تحریک کابھید آشکار نہیں کیا۔حضرت ؒ کی وفات کے بعد ادہر ادہرمدرس رہے۔آخر میں دیوبند آگئے تھے اوردرس کی خدمات انجام دیتے تھے۔
[ستمبر۱۹۶۸ء]
This article focus on the literary aspect of Qur’an. Stylistically it has a rich texture, which in itself is a miracle Qur’an is not only the last message of Allah- bearing finality but it is the root source of all forms of human knowledge. It has a pithy style therefore it offers multiple shades of meanings in it. This article focuses on that so as to open up new pathways into the stylistically rich texture of Holy Qur’an.
The present study was designed to compare the sensitivity and specificity of different parasitological and molecular techniques for the detection of Trypanosoma sp. during different seasonsof year 2013 in equines and camels of Dera Ghazi Khan District and to determine the risk factors associated with the spread of trypanosomiasis. The objective of this project was to demonstrate the effect of Trypanosoma sp. on complete blood count (CBC) and selected serum biochemical parameters in camels, horses and donkeys from Southern Punjab (Pakistan). A total of 858 blood samples (291 camels, 284 horses and 283 donkeys) were collected and were subjected to blood smear examination, hematocrit centrifugation technique and Polymerase Chain Reaction (PCR) (by amplifying kinetoplast maxicircle DNA) to determine the prevalence of trypanosomiasis in collected samples. Blood samples were also analyzed for complete blood count and selected serum biochemical parameters (Total Protein, Creatinine, Alanine Transferase (ALT), Aspartate Transferase (AST) and Triglycerides). Out of 291 camel blood samples, 28 (9.62%) generated a 164 bp DNA fragment specific for Trypanosoma sp. Only 6 blood samples from camels (2.1%) were found positive through microscopic examination while 13 (4.46%) were positive for Microhematocrit centrifugation technique. Out of 284 blood samples from horses 16 (5.63%) samples were found Trypanosoma sp. positive by PCR. Only 5 blood samples (1.8%) were found positive through microscopic examination while 9 (3.17%) blood samples from horses were positive for Microhematocrit centrifugation technique. Out of 283 blood samples of donkeys, 19 (6.71%) samples amplified a 164 bp DNA fragment specific for Trypanosoma sp. while only 7 blood samples (2.5%) were found positive through microscopic examination and 9 (3.18%) were found positive for Microhematocrit centrifugation technique. Seasonal prevalence through PCR was 6.9% (5/72) in spring, 13.7% (10/73) in summer, 9.7% (7/72) in autumn and 8.1% (6/74) in winter in camels. Seasonal prevalence through PCR was 4.2% (3/72) in spring, 5.9% (4/68) in summer, 7.04% (5/71) in autumn and 5.48% (4/73) in winter in horses. In donkeys, seasonal prevalence through PCR was 4.76% (3/65) in spring, 8.22% (6/73) in summer, 8.45% (6/71) in autumn and 5.41% (4/74) in winter. No significant association (P˃0.05) of disease was observed with age of all studied animals. Trypanosomiasis was also found not to be associated (P˃0.05) with the gender of equines and camels during present study. A significant increase was detected in white blood cells (WBC) (P˂0.001), neutrophils(P˂0.004) and ALT(P˂0.028) in Trypanosoma sp. positive as compared to the Trypanosoma sp. negative blood samples while a significant decrease in red blood cells (RBC) (P˂0.001), hemoglobin (P˂0.001), lymphocytes (P˂0.003) and packed cell volume (P˂0.001) was observed in blood samples of camels. In horse blood samples, there was also significant increase in WBC (P˂0.001), neutrophils (P˂0.001) and ALT (P˂0.032) and a significant decrease (P˂0.001) in RBC, hemoglobin (P˂0.001), lymphocytes (P˂0.021) and packed cell volume was observed in parasite positive as compared to the parasite negative blood samples. In donkeys, a significant increase was detected in WBC (P˂0.002), neutrophils (P˂0.001) and ALT (P˂0.019) in Trypanosoma sp. positive as compared to the Trypanosoma sp. negative blood samples while a significant decrease in RBC (P˂0.001), hemoglobin (P˂0.003), lymphocytes (P˂0.001) and packed cell volume (P˂0.003) was observed. In conclusion, PCR was found more reliable and sensitive technique than the blood smear examination and microhematocrit centrifugation technique for Trypanosoma sp. detection in blood samples of equines and camels and it is recommended to be used for Trypanosoma sp. detection in epidemiological surveys and control policies in livestock sector to minimize economic losses.