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Advanced Techniques in Diagnostic Microbiology

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22<br />

Review of Molecular <strong>Techniques</strong><br />

for Sexually Transmitted<br />

Diseases Diagnosis<br />

ANGUS C.T. LO ANDKAI MAN KAM<br />

Introduction<br />

Sexually transmitted diseases (STDs) constitute the most common <strong>in</strong>fectious diseases<br />

around the world and bear significant consequences for both the <strong>in</strong>dividual<br />

and public health of the community. More than 20 STDs have now been identified,<br />

and they affect more than 13 million men and women <strong>in</strong> the United States<br />

each year (CDC, 2002). Data from the Centers for Disease Control and Prevention<br />

(CDC) show that more than 7 million cases of Chlamydia trachomatis <strong>in</strong>fection<br />

and more than 350,000 cases of Neisseria gonorrhoeae <strong>in</strong>fection were reported <strong>in</strong><br />

2000 (CDC, 2001). In the past decade, the rapid development of molecular techniques<br />

has gradually shifted the paradigm of laboratory diagnosis from traditional<br />

biological to molecular amplification and detection of major causative agents of<br />

sexually transmitted <strong>in</strong>fections.<br />

A milestone <strong>in</strong> biotechnology that heralded the beg<strong>in</strong>n<strong>in</strong>g of molecular diagnostics<br />

was the development of the polymerase cha<strong>in</strong> reaction (PCR) by Mullis<br />

and colleagues (Saiki et al., 1988). S<strong>in</strong>ce then, numerous molecular detection techniques<br />

have been designed to detect specific nucleic acids without rely<strong>in</strong>g on the<br />

ability to culture or directly observe <strong>in</strong>tact organisms. As a result, str<strong>in</strong>gency <strong>in</strong><br />

transport of cl<strong>in</strong>ical samples, <strong>in</strong> terms of preserv<strong>in</strong>g organism viability, has become<br />

less strict. With automation, a faster turn-around time of molecular tests became<br />

an advantage that significantly enhances this paradigm shift. Silent pathogens such<br />

as human papillomavirus (HPV) that cannot be cultivated <strong>in</strong> vitro can now be detected<br />

and typed by us<strong>in</strong>g molecular detection techniques that can also determ<strong>in</strong>e<br />

oncogenic potential and prognostic outcome of different <strong>in</strong>fections. These powerful<br />

molecular techniques have a significant impact on strategies and public health<br />

programs designed for the control and prevention of STDs worldwide.<br />

An estimated 50% of STDs occur asymptomatically, and this forms a major<br />

reservoir of <strong>in</strong>fectious source that persists <strong>in</strong> the community. More sensitive detection<br />

techniques are often required for detect<strong>in</strong>g asymptomatic <strong>in</strong>dividuals with low<br />

microbial load (Yoshida et al., 2002). Currently available molecular techniques us<strong>in</strong>g<br />

nucleic acid amplification can now offer high sensitivity <strong>in</strong> screen<strong>in</strong>g for these<br />

<strong>in</strong>fections and disrupt the transmission cha<strong>in</strong>s with<strong>in</strong> the community. This would,<br />

353

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