<?xml version="1.0" encoding="UTF-8"?><feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
<title>Department of Microbiology</title>
<link href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/114" rel="alternate"/>
<subtitle/>
<id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/114</id>
<updated>2026-04-23T13:52:50Z</updated>
<dc:date>2026-04-23T13:52:50Z</dc:date>
<entry>
<title>A Comparative Study Of Cartridge Based Nucleic Acid Amplification Testing And Auramine-Rhodamine Stain Microscopy With Culture Method In The Diagnosis Of Pulmonary Tuberculosis</title>
<link href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/4628" rel="alternate"/>
<author>
<name>Dr.Hajra Tasneem Masali</name>
</author>
<id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/4628</id>
<updated>2026-04-02T06:00:26Z</updated>
<published>2019-01-01T00:00:00Z</published>
<summary type="text">A Comparative Study Of Cartridge Based Nucleic Acid Amplification Testing And Auramine-Rhodamine Stain Microscopy With Culture Method In The Diagnosis Of Pulmonary Tuberculosis
Dr.Hajra Tasneem Masali
One of the crucial step for effective tuberculosis management is to choose a Diagnostic&#13;
method with high sensitivity and specificity. But slow growth rate of Tubercle bacilli makes the&#13;
diagnosis more complicated and hence need of hour is improved diagnostic methods to limit&#13;
progression and the spread of the disease. Options available among conventional laboratory&#13;
methods are sputum microscopy and culture methods.&#13;
 Sputum microscopy is rapid, reliable, simple &amp; reasonably costing but has poor&#13;
sensitivity and requires multiple visits leading to higher default rate. Culture method although&#13;
considered gold standard but it takes almost 2-6 weeks’ time to give the result and also requires&#13;
proper infrastructure with technical expertise. But with advancement in technology CBNAAT&#13;
also offer a better option as it is specific, automated technology utilizing DNA - PCR technique&#13;
for identification. It is currently unique in its simplification of molecular testing. It can detect&#13;
both M. tuberculosis and Rifampicin resistance directly from sputum in an assay fetching results&#13;
within two hours
</summary>
<dc:date>2019-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Comparison Of Lowenstein-Jensen Medium, Middlebrook 7h10 Medium And Bact/Alert 3d For Isolation Of Mycobacterium Tuberculosis From Clinical Specimens</title>
<link href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/2446" rel="alternate"/>
<author>
<name>Naveen.G</name>
</author>
<id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/2446</id>
<updated>2026-04-02T08:00:18Z</updated>
<published>2012-01-01T00:00:00Z</published>
<summary type="text">Comparison Of Lowenstein-Jensen Medium, Middlebrook 7h10 Medium And Bact/Alert 3d For Isolation Of Mycobacterium Tuberculosis From Clinical Specimens
Naveen.G
Introduction – Tuberculosis is the most common cause of death due to single infectious agent &#13;
worldwide in adults. India alone accounts for 30% of global tuberculosis burden. There is &#13;
manifest need for method of cultivation of mycobacteria that is reliable, economical and has &#13;
short turnaround time.  &#13;
 &#13;
Objective – Present study was attempted to assess the feasibility of using MB bact and &#13;
middlebrook7H10 as primary isolation medium for mycobacteria. It has been compared with LJ &#13;
medium, the gold standard.  &#13;
 &#13;
Materials and Methods – Various clinical specimens from total of 230 clinically suspected &#13;
cases of TB were studied. All isolates were decontaminated using modified Petroff’s method. &#13;
Each sample was subjected to ZN staining and simultaneously inoculated onto LJ medium, &#13;
middlebrook7H10 medium and MB bact. Growth from the culture were confirmed by ZN &#13;
staining and speciated using biochemical reactions. &#13;
 &#13;
Results – Out of 230 samples screened, 116 isolates were obtained. Of the 116 all of them were &#13;
isolated from MB bact, 82 were isolated by LJ medium and 62 were isolated by &#13;
middlebrook7H10. 82 isolates were obtained by MB bact and LJ medium, 62 were obtained by &#13;
middlebrook7H10 and MB bact, 58 by LJ and middlebrook7H10 and 58 by LJ medium, &#13;
middlebrook7H10 and MB bact. Neither L J medium nor middlebrook 7H 1O medium could &#13;
isolate mycobacteria exclusively. The average isolation time by L J, middlebrook 7H10 medium &#13;
and MB BACT was 30.81 days,31.06 days and 18.70 days.
</summary>
<dc:date>2012-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Serological Markers Hbsag And Hbeag In Chronic Hepatitis B Carriers And Their Correlation With Viral Load By Polymerase Chain Reaction Assay</title>
<link href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/891" rel="alternate"/>
<author>
<name>Borgaonkar, Rasika</name>
</author>
<id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/891</id>
<updated>2026-04-02T06:06:26Z</updated>
<published>2018-01-01T00:00:00Z</published>
<summary type="text">Serological Markers Hbsag And Hbeag In Chronic Hepatitis B Carriers And Their Correlation With Viral Load By Polymerase Chain Reaction Assay
Borgaonkar, Rasika
</summary>
<dc:date>2018-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Seroprevalence of Rubella antibodies in women of reproductive age</title>
<link href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/592" rel="alternate"/>
<author>
<name>Shilpi, Gupta</name>
</author>
<id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/592</id>
<updated>2026-04-02T06:08:51Z</updated>
<published>2015-01-01T00:00:00Z</published>
<summary type="text">Seroprevalence of Rubella antibodies in women of reproductive age
Shilpi, Gupta
</summary>
<dc:date>2015-01-01T00:00:00Z</dc:date>
</entry>
</feed>
